Red Seaweed-Derived Compounds as a Potential New Approach for Acne Vulgaris Care

Januário, Adriana P.; Félix, Rafael; Félix, Carina; Reboleira, João; Valentão, Patrícia; Lemos, Marco F. L.

doi:10.3390/pharmaceutics13111930

Open AccessReview

Red Seaweed-Derived Compounds as a Potential New Approach for Acne Vulgaris Care

by

Adriana P. Januário

^1,2,*

,

Rafael Félix

^1,2

,

Carina Félix

¹,

João Reboleira

¹,

Patrícia Valentão

²

and

Marco F. L. Lemos

^1,*

¹

MARE—Marine and Environmental Sciences Centre, ESTM, Instituto Politécnico de Leiria, 2520-641 Peniche, Portugal

²

REQUIMTE/LAQV, Laboratório de Farmacognosia, Faculdade de Farmácia, Universidade do Porto, 4050-313 Porto, Portugal

^*

Authors to whom correspondence should be addressed.

Pharmaceutics 2021, 13(11), 1930; https://doi.org/10.3390/pharmaceutics13111930

Submission received: 31 October 2021 / Revised: 9 November 2021 / Accepted: 9 November 2021 / Published: 15 November 2021

(This article belongs to the Special Issue Herbal Extracts and Natural Compounds: Nutraceutical and Pharmaceutical Aspects Volume II)

Download

Browse Figures

Versions Notes

Abstract

:

Acne vulgaris (AV) is a chronic skin disease of the pilosebaceous unit affecting both adolescents and adults. Its pathophysiology includes processes of inflammation, increased keratinization, sebum production, hormonal dysregulation, and bacterial Cutibacterium acnes proliferation. Common AV has been treated with antibiotics since the 1960s, but strain resistance has emerged and is of paramount concern. Macroalgae are known producers of substances with bioactive properties, including anti-viral, antibacterial, antioxidant, and anti-inflammatory properties, among several others. In particular, red algae are rich in bioactive compounds such as polysaccharides, phenolic compounds, lipids, sterols, alkaloids, and terpenoids, conferring them antioxidant, antimicrobial, and anti-inflammatory activities, among others. Thus, the exploration of compounds from marine resources can be an appealing approach to discover new treatment options against AV. The aim of this work is to provide an overview of the current knowledge of the potentialities of red macroalgae in the treatment of AV by reviewing the main therapeutic targets of this disease, and then the existence of compounds or extracts with bioactive properties against them.

Keywords:

acne pathophysiology; antibacterial; bioactive compounds; Cutibacterium acnes; inflammation; Rhodophyta; seaweed extracts

Graphical Abstract

1. Introduction

Acne vulgaris (AV) is a chronic disease of the pilosebaceous unit, and the most common skin disease in the world. It affects up to 85% of adolescents in the Occidental countries, and it can occur during adulthood in about 50% of people [1,2], having an incidence of nearly 9.4% of the worldwide population and being the eighth most prevalent disease in the world [3]. Acne deeply impacts quality of life through the manifestation of pimples, blackheads and scars on the face, upper chest and back, which can be painful and negatively affect the self-perception of beauty, leading to distress, anxiety, and depression [4,5,6]. Lesions associated with AV vary between non-inflammatory (white- and blackheads) and inflammatory (papules, pustules, and nodules), with different degrees of severity [5,6]. The main factors involved in acne pathogenesis are hormonal disequilibrium, exacerbated sebum production, follicular keratinization, and Cutibacterium acnes proliferation (formerly Propionibacterium acnes), resulting in an immune response and consequent inflammation [4]. Acne is the cause of 14% of primary care and 27% of dermatology consultations in the US, and first line treatment implies long periods of the use of antibiotics (up to three months, each time), oral and/or topical, usually complemented with retinoids, benzoyl peroxide, and oral contraceptives, among others [7]. In the last few years, C. acnes’ resistance to the antibiotics most often used in acne treatment (erythromycin, clindamycin, and tetracycline, for example) has emerged [8,9]. Moreover, about 80% of treatments in women fail in multiple intake sequences of systemic antibiotics, and 30–40% fail after one course of the retinoid isotretinoin, one of the most successful drugs applied in cases of severe acne [10,11]. Therefore, the development of novel therapeutic approaches is of the utmost importance, for example, through the discovery of novel antibacterial and anti-inflammatory natural compounds.

Macroalgae are sessile marine organisms that live in a dynamic environment, being forced to adapt to fluctuations of biotic and abiotic factors, such as light, nutrients, salinity, temperature and predation. Seaweeds produce compounds to survive in response to those variations [12]. Moreover, marine macroalgae are considered to be among the finest sources of biologically active compounds of non-animal origin, having several valuable properties, including antioxidant, antimicrobial, anti-inflammatory, and antiviral properties [13], among others. Several classes of compounds are responsible for such bioactivities, e.g., proteins and peptides, poly- and oligosaccharides, fatty acids, sterols, phenolic compounds, pigments, vitamins, and minerals [14]. In particular, red algae species, the oldest division (Rhodophyta) of lower plants [15], are renowned producers of both anti-inflammatory metabolites (MAAs—mycosporine-like amino acids [16], phycocyanin [17], allophycocyanin [18], carotenoids [19], porphyrans [20]) and antimicrobials (diterpenes [21], monoterpenes [22], phenolic compounds [23], sterols [24], polysaccharides [25], fatty acids [26]). Because red seaweeds are so rich in bioactive compounds, including antibacterial and anti-inflammatory compounds, they seem to represent a promising source of natural, as opposed to conventional, anti-acne compounds or extracts. According to what has been mentioned, the goal of this review is to provide a compilation of compounds and extracts derived from red macroalgae that can hereafter be applied to AV research care.

2. Research Methodology

In order to compose this literature revision, Web of Science, Scopus, and Google Scholar databases were consulted up to 24 September 2021, using a Boolean search, and all of the publications identified from the following strings were analysed: (acne vulgaris AND (patho* OR inflamm* OR acnes OR epidermidis OR keratinization OR cornification OR comedo* OR hormone* OR sebum)) for Section 3; ((rhodophyta OR “red macroalg*” OR “red seaweed*”) AND (acnes OR epidermidis)) for Section 4.1; ((rhodophyta OR “red macroalg*” OR “red seaweed*”) AND (inflamm*)) for Section 4.2; and ((rhodophyta OR “red macroalg*” OR “red seaweed*”) AND (sebum OR hormon* OR testosterone OR androgen* OR estrogen* OR progesterone OR “growth factor*” OR “growth hormone*” OR hyperkeratinization OR cornification OR comedo*)) for Section 4.3.

3. Pathophysiological Targets for the Management of Acne Vulgaris

A thorough literature analysis revealed that the general pathogenesis of AV is well established and amply described, but there is not yet a consensus regarding the whole pathophysiology, mechanisms, and order of events that lead to AV lesions. More recent reviews and research articles focus on the role of immune and inflammatory responses, bacterial dysbiosis, and the interplay between all of these factors [27,28,29], as opposed to older studies in which Cutibacterium acnes, sebum, and hormones were usually the main characters [3,30,31]. There have been several advances in the understanding of the role of each aspect in the cascade of events in AV, and the dominant factors and triggers that are interconnected in a highly complex manner are the following: (a) hormonal influence, mostly due to excessive androgen production and growth factors; (b) hyperseborrhea, triggered by the hormonal stimulation of the sebaceous glands; (c) comedogenesis, hyperkeratinization and the formation of comedones due to excessive sebum accumulation and abnormal epithelial desquamation; (d) microbial proliferation and dysbiosis, especially involving C. acnes, owing to a lipid-rich and anaerobic environment in the pilosebaceous unit; and (e) immune response and inflammation, as a consequence of pro-inflammatory molecules and activated pathways induced by the bacterium, hormonal disequilibrium, changes in sebum composition, and cytokine secreted by keratinocyte hyperproliferation and keratinization [3,4,6,28,29,30,32,33,34,35,36,37,38] (Figure 1). Acne-related factors are detailed below.

3.1. Hormonal Influence

Endogenous hormones—such as androgens, estrogen, progesterone, and insulin-like growth factors (IGFs), among others—play a critical role in the acne pathogenesis flow. Individuals that suffer from acne usually have high levels of androgens, progesterone, insulin, and IGFs, and, on the contrary, low levels of estrogen [6,39,40,41].

Androgens are the most important hormones controlling sebaceous gland activity, because they affect the sebaceous gland enlargement, sebocyte proliferation, and lipid metabolism, thus playing a crucial role in acne pathogenesis [42]. Free androgens are produced by the adrenal gland and gonads, but the most involved in acne are the androgens locally produced in the sebaceous glands. Inside the sebaceous glands is dehydroepiandrosterone sulphate (DHEAS), an adrenal precursor hormone that, by the action of steroid sulfatase, is converted into dehydroepiandrosterone (DHEA). The steroid metabolizing enzyme pathway expressed in the sebaceous glands seems to be initiated by 3β-hydroxysteroid dehydrogenase, which converts DHEA into androstenedione, then 17β-hydroxysteroid dehydrogenase converts androstenedione into testosterone, and finally, 5α-reductase converts testosterone into 5α-dihydrotestosterone (5α-DHT). DHT is three to ten times more potent than testosterone [43] when it comes to androgen receptors interaction, wherein the activity of 5α-reductase has a tremendous impact because its increased activity leads to the bigger size proportions of sebaceous glands. Furthermore, DHT increases lipidic production, not only by increasing the proliferation of sebocytes but also through the magnification of the mRNA levels of proteins involved in cholesterol, fatty acid, and triglyceride synthesis [6,44,45].

The growth hormone (GH) is secreted by the pituitary gland and can be found in sebaceous glands and hair follicles [46]. Diseases involving GH excess, such as acromegaly, are frequently associated with sebum overproduction, leading to acne development [44]. Furthermore, GH stimulates the production of IGFs, and, in particular, women evidencing acne lesions have higher levels of IGF-1, compared with androgens, sebaceous gland growth, and lipogenesis [42,47,48]. Naturally, IGF-1 levels tend to rise during puberty by the action of increased GH secretion, the same as for the levels of testosterone [49]. Features directly related to acne include the IGF-1 capacity to stimulate adrenal synthesis, resulting in increased androgen levels; IGF-1 also induces the proliferation of sebocytes; receptors of IGF-1 are expressed in sebaceous glands and hair follicles; IGF-1 mediates lipogenesis by the influence on the increasing expression of sterol regulatory element-binding proteins (SREBPs) transcription factor, which regulates the geneses involved in lipidic biosynthesis, and also by activating MAPK/ERK (mitogen-activated protein kinase/extracellular signal-regulated kinase) pathways; IGF-1 is able to stimulate 5α-reductase, sebocyte proliferation, and androgen receptor signal transduction [6,44].

For over six decades, oral contraceptive pills containing estrogens have been taken by women, not only as contraceptive method but also to suppress sebum production due to AV-related complaints [50]. Estradiol is the most abundant and potent estrogen. In particular, 17β-estradiol is produced through the aromatase enzyme into testosterone, and can be converted into estrone, a less potent estrogen, by 17β-hydroxysteroid dehydrogenase, with both enzymes being present in gonads, placenta, and skin [51]. Moreover, 17β-estradiol is the most potent sex steroid hormone, being 100 to 1000-times more potent compared to its androgen parents [52]. Estrogens’ roles include the influence on lower sebum segregation, including the opposition of androgens inside the sebaceous gland, because both hormones are able to activate the signaling pathways of estrogen receptor α (ERα), Erβ, and the androgen receptor, in sebocytes; the inhibition of testosterone’s gonadal production; decreasing free testosterone by increasing the production of sex hormone-binding globulin (SHBG); and downregulating the genes involved in sebaceous glands’ growth and production of lipids [6,44]. Several studies indicate that estrogens have anti-inflammatory roles in acne events; in particular, 17β-Estradiol inhibits interferon-γ in human keratinocytes [53]; and estrogens block proinflammatory cytokines (IL-1, IL-6, and TNF-α) and NF-κB [54,55], and repress macrophage activation and monocyte recruitment in inflammatory occasions [56,57,58].

3.2. Seborrhoea

The typical regions of the skin that are affected by acne are the face and upper torso, as they are densely populated by sebaceous glands [3]. Those glands are cutaneous appendages that secrete an oily substance (sebum) within hair follicles through sebaceous ducts [59]. Sebum is a mixture of lipids—namely a combination of wax esters, triglycerides, steroid esters, and squalene [60]—protecting the skin against friction due to natural lubrication; by acting as a barrier, it retains water molecules helping to keep the skin moist and healthy [42]. However, hyperseborrhea, excessive sebum production associated with overactive sebaceous glands, is a major etiopathogenetic factor directly associated with AV, because it contributes to all three mechanisms described below—comedogenesis, microbial proliferation, and inflammation—whereas the disease is not seen in the absence of sebum [4].

It is possible that not only the amount of sebum is a key factor in acne; the alteration of sebum composition may also have a determinant role. For instance, lipidic fractions of sebum are proinflammatory, contributing to the inflammatory cell and tissue process, ultimately resulting in the development of acne lesions [60,61]. For example, squalene peroxide induces inflammatory responses in keratinocytes by increasing IL-6 production and lipoxygenase (5-LOX) activation [62]. Moreover, modifications in the sebum ratio of saturated/unsaturated fatty acid are triggers of innate immunity response and follicular inflammation, being a main character in early inflammatory pathways of acne [47,60]. Additionally, changes in the oxidant/antioxidant ratio also represent a cause for acne’s initial development [32]. Further acne-related lipid-enzymes are liver X receptor-α (LXR-α) and cyclooxygenase 2 (COX-2), which regulate inflammation and lipid synthesis. LXR-α is expressed in sebaceous glands, sweat glands, and hair follicles, and controls the transcription of the genes involved in fatty acid and lipid synthesis. During inflammatory events, COX2 release is stimulated by cytokines that were activated by NF-κB [63].

3.3. Comedogenesis

Increased androgen production, the accumulation of sebum, and the adhesiveness of keratinocytes lead to follicle blockage and the occlusion of the pilosebaceous ducts, resulting in the formation of microcomedones that are the primary type of acne lesions [7,64]. These hard structures, microcomedones, are formed within the hair follicle, more precisely in the infundibulum, and are connected with the sebaceous gland via a keratinized duct. The set of the hair follicle and sebaceous gland constitutes the pilosebaceous unit [59]. As a pleomorphic disorder of the pilosebaceous unit, acne microcomedones evolve into comedones owing to sebum and keratin accumulation accompanied by follicle expansion [58], and these can be closed (white heads) or open (blackheads), but they may progress to inflammatory lesions, such as pustules, papules, cysts, and nodules [30], eventually leaving scars [6].

Keratinocyte IL-1 secretion is another triggering step in the comedogenesis process, mostly as a consequence of C. acnes-mediated Toll-like receptor (TLR) activation. IL-1 also contributes to sebocytes hypercornification. Comedone formation is a result of a combination of some factors, such as the response to androgen production; sebum alteration, production, and oxidation; C. acnes proliferation, and recruitment of cytokines to the pilosebaceous unit [7].

3.4. Microbial Proliferation

The skin microbiome is composed of commensal microbes of which the ultimate function is to maintain skin homeostasis, representing the resident microbiome (usually harmless and non-pathogenic), but also of other microbes that commonly are pathogenic and temporary, representing the transient microbiome. Despite that, the microbiome at AV lesions is usually constituted by C. acnes and Staphylococcus epidermidis, which together set the resident microbiome, while the transient pathogen is typically Staphylococcus aureus [65,66]. Although the resident microbes are usually non-pathogenic, it is accepted that both C. acnes and S. epidermidis—in an acne context—become pathogenic, either through hyperproliferation or by other mechanisms [65,67]. On the other hand, though they are commonly called “acne-related bacteria”, new insights show that S. epidermidis has a beneficial role in acne through an anti-C. acnes action when controlling C. acnes hyperproliferation, and by suppressing C. acnes-induced IL-6 and TNF-α production in keratinocytes [65,67]. The activation of TNF-α stimulates lipogenesis through JNK (c-Jun N-terminal kinase), a family member of the MAPK, PI3K (phosphoinositide 3-kinase), and protein kinase B (PKB) pathways [38]. While this information is available now, in recent past years S. epidermidis’ role was a controversial topic in which the discussion relied on whether it may become pathogenic in an acne context or not, being considered a target which needed to be eliminated in an acne context by some researchers, possibly supported by being the most frequent cause of nosocomial infections, having immune invasion capacity, and being a producer of lipolytic enzymes that may damage follicles, leading to comedogenesis [67,68].

Cutibacterium acnes is the main bacterium linked to acne pathogenesis and is one of the main triggers associated with the disease [4]. It is a Gram-positive, anaerobic, and lipophilic diphtheroid. Commensal, and an abundant member of the skin microbiota [69], the bacterium’s natural habitat is the pilosebaceous follicles, and in regular, non-pathogenic situations, this diphtheroid helps to maintain the homeostasis of a healthy skin [34]. Nevertheless, this bacterium can induce the production of proinflammatory molecules while converting triglycerides (from sebum) into free fatty acids [7]. Its pathogenic features also include infectious mechanisms, such as chemo-attractive mediators’ production, biofilm formation, and the release of virulence factors that mediate the immune response, among others [35,69]. The hyperproliferation of C. acnes is another factor of AV due to the secretion of propionic acid that influences the formation of comedones, which ultimately leads to keratinocyte differentiation [69]. Cutibacterium acnes creates a biofilm by attaching to and growing on the surface of corneocytes, producing extracellular polymers contributing to the process of microcomedones formation [33]. Furthermore, C. acnes is capable of activating several pathways leading to the release of cytokines (IL-1, IL-6, IL-8, IL-10, IL-12, and TNF-α) that activate the immune system to produce inflammation via different pathways, including Toll-like receptors that induce the liberation of antimicrobial peptides (human β-defensin-1 and human β-defensin-2) and trigger matrix metalloproteinases, lipases, proteinases, and hyaluronidases backing dermal matrix destruction, which together lead to acne inflammation and the formation of scars [32,70]. A change of paradigm has come from recent research that points out a specific influence of C. acnes in acne lesions. Not the number of bacterial cells is important, but instead the loss of balance between diverse C. acnes phylotypes that trigger the immune system activation, consequently undergoing inflammation, particularly due to a predominance of C. acnes phylotype IA1 [65].

3.5. Inflammatory Response

The AV pathophysiological cascade ends with the inflammatory process, but, at the same time, it also follows the whole process from the beginning, by activating the immune system and/or by the release of molecules that activate inflammatory pathways [71]. There are many inflammatory mediators involved, as mentioned before, e.g., proinflammatory lipids (at the hyperseborrhea process), cytokines (mostly involved by recruitment of C. acnes), and chemokines (stimulated by bacterial antigens). There is also the role of proinflammatory cathelicidins, peptides from macrophage lysosomes, and members of the immune system with immunomodulatory and antimicrobial functions [7].

It seems that the main factor influencing the inflammatory process is the activation of the immune system by C. acnes, when the bacterium overpopulates sebocytes, through TLRs and nod-like receptors (NLRs) that segregate IL-1 and other cytokines, activating inflammatory pathways [7]. Furthermore, the keratinocyte stimulated-C. acnes production of reactive oxygen species (ROS) induces nitric-oxide production in macrophages, contributing to the magnification of the inflammatory response [69].

4. Seaweed Extracts and Compounds to Address AV Disease

Considering the stated pathophysiological mechanisms of AV, this work will further address the potential uses of red macroalgae against all five of the therapeutic targets described above. The first three processes listed (Section 3.1 hormonal influence, Section 3.2 seborrhoea, Section 3.3 comedogenesis) are harder to analyze in vitro, and this is reflected in the much smaller number of studies targeting these processes. However, numerous studies have identified red seaweeds as significant producers of valuable metabolites with antibacterial and anti-inflammatory activities, thus representing a potential resource in the battle against AV, a chronic disease of which the management involves the mitigation of these symptoms.

4.1. Antibacterials from Red Macroalgae

The antibacterial activity of red seaweed extracts and/or compounds against C. acnes and S. epidermidis is summarized in Table 1. Keeping in mind that the role of S. epidermidis is still controversial in acne pathology, a literature revision about compounds and extracts from red seaweeds that inhibit the growth of this bacterium was included in this table. However, one should acknowledge that these studies were bioprospecting natural products against this species, and therefore generating the presented data, whereas nowadays, given the recent discovery of a positive role of S. epidermidis as an anti-C. acnes agent, it might be more interesting to find the extracts that do not inhibit this species, or that do so to a lower extent than against C. acnes.

Staphylococcus aureus is a common human pathogen which has also been associated with AV pathology on several occasions [72]. There are plenty of research articles proving that red seaweeds are an excellent source of anti-S. aureus compounds, exploiting the potential of, for example, Laurencia johnstonii, Laurencia obtusa var. pyramidata, Gracilaria dendroides, Grateloupia turuturu, Corallina officinalis, and Rissoella verruculosa [73,74,75,76,77,78,79,80]. Such studies were not included in the summarized Table 1, because that would result in hundreds of entries; this has been reviewed quite recently [81].

Research concerning bioactives to inhibit the growth of C. acnes and S. epidermidis resulted in the study of 28 different species of red seaweeds. Though Rhodophyta is the largest group of macroalgae, including about 7000 species [82], the fact that only 28 of them have been studied for this purpose shows that there is still room to proceed with studies to discover antibacterials from this macroalgae which are applicable in AV (specific towards C. acnes).

When it comes to C. acnes, there is a great lack of knowledge, wherein only five studies have approached the antibacterial capacity of 11 red macroalgal species but, notwithstanding, reported results show great capacity of growth inhibition. One example is a methanol crude extract of Symphyocladia latiuscula, having an MIC (minimal inhibitory concentration) of 0.16 mg·mL⁻¹ [83] for a compound isolated from Osmundaria serrata, lanosol ethyl ether, which showed MIC at 0.08 mg·mL⁻¹ and MBC (minimal bactericidal concentration) at 0.5 mg·mL⁻¹ [23]. The study by Choi and co-workers [83] employed methanol solid–liquid extractions from S. latiuscula, resulting in an extract capable of inhibiting C. acnes growth. This seaweed is known to have high amounts of bromophenols, which can explain the antibacterial effect, because these compounds are known to be toxic to some bacteria [83]. The work of Barreto and Meyer (2006) aimed to isolate lanosol ethyl ether from O. serrata, which is a brominated phenol and a halogenated metabolite, showing high bacteriostatic and mild bactericidal activity [23]. Organobromine compounds are naturally produced by seaweeds for chemical defense and are usually found in Rhodophyta. Besides lanosol, examples include acetogenins (brominated nonterpenoid metabolites), which are mainly found in the genus Laurencia [84]; bromoform from Asparagopsis taxiformis [85]; brominated monoterpenes, also in the genus Laurencia [86], but also in Plocamium cartilagineum [84]; and indoles from Rhodophyllis membranacea [84]. These bromine compounds confer several bioactivities, including antimicrobial, antioxidant, anticancerogenic, and anti-diabetic activities [87], emphasizing the high value of red seaweed-derived compounds. Another example showing the antibacterial activity conferred by organobromine compounds is the study by [88], which used Asparagopsis armata supercritical CO₂ extractions to find an inhibition halo of 23 mm (at 10 mg·mL⁻¹) in contact with a C. acnes culture. Such results seem to be in accordance with a variety of cosmeceutical products which recently became available in the market that incorporate A. armata extracts. For instance, ASPAR’AGE™, formulated by SEPPIC (La Garenne-Colombes, France), promises a lotion with an extract containing MAAs that reduce the visible effects of age, and Asparcid P^®, from Exsymol (Monaco-Ville, Monaco), claims to possess cytostimulating action and antimicrobial activity.

Regarding S. epidermidis, there are few studies searching antibacterials from 19 different red macroalgae, probably because this bacterium is a pathogen when the immune system is compromised and is not only involved in acne pathophysiology but also, above all, a relevant matter of concern when it comes to severe hospital-acquired infections from decades ago [89], wherein the research material is more abundant, but unrelated to the present work. A study of 1991 showed an inhibitory halo of 7.5 mm when a piece (3 mm) of Polysiphonia fibrillosa was in contact with an S. epidermidis culture [90]. It is possible that this antibacterial activity may be due to bromophenolic compounds, because other studies reported those properties in the extracts of other species belonging to the genus Polysiphonia, namely a Polysiphonia decipiens compound that was a mild growth inhibitor towards S. aureus, Bacillus subtilis, Micrococcus luteus, Proteus vulgaris, and Salmonella typhimurium [91], and Polysiphonia denudata and Polysiphonia denudata f. fragilis effective against S. aureus and Escherichia coli [92]. More recently, a bromophenol (bis (2,3-dibromo-4,5-dihydroxybenzyl) ether) isolated from Rhodomela confervoides showed MIC at 35 µg·mL⁻¹ [93] exhibiting the highest antibacterial activity (Table 1). The Rhodomela genus is another example containing high levels of brominated compounds—in this case, a bromophenol—and the first two marine dibromophenols were isolated from this genus in 1967, more specifically, from the red algae Rhodomela larix [94].

Different extracts and compounds can be obtained or isolated by using several solvents of extraction and/or isolation procedures. So far, the most-used solvents to obtain crude extracts and isolated compounds with antibacterial properties, when facing the growth of C. acnes or S. epidermidis, are methanol, ether, acetone, toluene, chloroform, and hexane (Table 1). Given the limited variety of red macroalgae explored for this purpose, according to the research, the genus Laurencia was the most often used in crude extracts. Laurencia species have been studied for years, revealing this to be a very rich genus in bioactive metabolites, such as diterpenes, triterpenes, sesquiterpenes, steroids, aromatic compounds, and indoles, among others [95], and sesquiterpenoids are the main constituents from this genus [96]; among other properties, they are known to possess potent antibacterial activities against methicillin-resistant S. aureus (MRSA), penicillin-resistant Streptococcus pneumoniae, and vancomycin-resistant Enterococcus faecalis [97]. From a crude methanol extract of R. confervoides, ten bromophenols were isolated, confirming the reputation of the richness in bromophenol metabolites of the genus Rhodomela [93,94].

Oddly, no work with aqueous extracts addressing the discovery of antibacterials, regarding C. acnes and S. epidermidis, was found. This type of extraction, besides being industry-friendly [98], is a method of obtaining antibacterial bioactives from Rhodophyta, as it allows the recovery of polysaccharides and MAAS, for example, that successfully inhibit E. coli, S. aureus, multidrug-resistant Salmonella, and Vibrio harveyi [77,99]. Another industry- and environmentally friendly way to obtain extracts is using ethanol as extracting solvent, or even by obtaining essential oils, a technique known as solvent-free extraction. Ethanolic extracts from Gracilaria textorii, Gracilaria verrucosa, Grateloupia angusta, Grateloupia crispata, Grateloupia elliptica, and Meristotheca papulose all showed C. acnes growth inhibition, in a study by Lee et al. [100] aiming to find anti-C. acnes capacity in Korean edible seaweeds. Ethanolic extractions can retrieve, among others, phenolic compounds, sterols, and carotenoids [98], and the antibacterial properties of these have been attested [24,101,102]. Essential oil with anti-S. epidermis activity was obtained from L. obtusa [78], corroborating the renowned antimicrobial properties of essential oils obtained from Rhodophyta [103,104,105].

Table 1’s outcomes reveal that both the red seaweeds extracts and the compounds have antibacterial activity against acne-related bacteria. Despite this, there is still plenty of room to study a wide variety of Rhodophyta species, using extractions with different solvents, and isolating its compounds, in order to obtain a more diverse range of compounds and assess their antibacterial potential in an AV context. Furthermore, it is important to understand how different compounds could interfere in the inhibition of bacterial growth, and to study their mechanisms of action. Beyond this, it is also crucial to analyze further how the skin microbiome would be affected by the compounds and, ultimately, to perform in vivo studies to prove compounds’ efficiency.

Table 1. Antibacterial compounds and extracts derived from red seaweeds which are effective on Cutibacterium acnes and Staphylococcus epidermidis growth. SLE: solid–liquid extraction; UE: ultrasonic extraction; SM: steam distillation; MeOH: methanol; MIC: minimum inhibitory concentration; MBC: minimal bactericidal concentration; IC50: half-maximal inhibitory concentration; * Staphylococcus epidermidis clinical isolate; NA: not applicable.

Red Macroalgal Species	Compound or Extract (Technique)	Concentration/ Volume Tested	Antibacterial Assay	Outcome	Reference
Cutibacterium acnes
Asparagopsis armata	Supercritical extract	5 mg·mL⁻¹	Disc Diffusion	Zone of inhibition 17.33 ± 0.58 mm	[88]
Asparagopsis armata	Supercritical extract	10 mg·mL⁻¹	Disc Diffusion	Zone of inhibition 23.00 ± 1.00 mm	[88]
Gracilaria textorii	EtOH (UE)	0–1.024 μg·mL⁻¹	MIC	Inhibitory concentration > 1.024 μg·mL⁻¹	[100]
Gracilaria verrucosa	EtOH (UE)	0–1.024 μg·mL⁻¹	MIC	Inhibitory concentration > 1.024 μg·mL⁻¹	[100]
Grateloupia angusta	EtOH (UE)	0–1.024 μg·mL⁻¹	MIC	Inhibitory concentration > 512 μg·mL⁻¹	[100]
Grateloupia crispata	EtOH (UE)	0–1.024 μg·mL⁻¹	MIC	Inhibitory concentration > 512 μg·mL⁻¹	[100]
Grateloupia elliptica	EtOH (UE)	0–1.024 μg·mL⁻¹	MIC	Inhibitory concentration > 512 μg·mL⁻¹	[100]
Meristotheca papulosa	EtOH (UE)	0–1.024 μg·mL⁻¹	MIC	Inhibitory concentration > 256 μg·mL⁻¹	[100]
Osmundaria serrata	Lanosol ethyl ether	25 to 0.01 mg·mL⁻¹	MBC	Bactericidal concentration 0.50 ± 0.29 mg·mL⁻¹	[23]
Osmundaria serrata	Lanosol ethyl ether	25 to 0.01 mg·mL⁻¹	MIC	Inhibitory concentration 0.08 ± 0.02 mg·mL⁻¹	[23]
Plocamium telfairiae	EtOH (UE)	0–1.024 μg·mL⁻¹	MIC	Inhibitory concentration > 256 μg·mL⁻¹	[88]
Sphaerococcus coronopifolius	12S-hydroxy-bromosphaerol	0.1–200 µM	IC50	Inhibitory concentration 10.88 (7.83–15.12) µM	[106]
	12R-hydroxy-bromosphaerol	0.1–200 µM	IC50	Inhibitory concentration 8.75 (6.51–11.77) µM	[106]
	Bromosphaerol	0.1–200 µM	IC50	Inhibitory concentration 14.06 (10.41–19.00) µM	[106]
Symphyocladia latiuscula	MeOH (SLE)	1 mg·disc⁻¹	Disc Diffusion	Zone of inhibition 3.5 ± 1.3 mm	[83]
	MeOH (SLE)	5 mg·disc⁻¹	Disc Diffusion	Zone of inhibition 8.8 ± 0.8 mm	[83]
	MeOH (SLE)	19.5 μg–10 mg·mL⁻¹	MIC	Inhibitory concentration 0.16 mg·mL⁻¹	[83]
Staphylococcus epidermidis
Asparagopsis taxiformis (Falkenbergia-phase)	MeOH (SLE)	120 µL	Well Diffusion	Zone of inhibition 21 ± 2.31 mm	[107]
Bryothamnion seaforthii	Lectin	125; 250 μg·mL⁻¹	Microdilution (Growth Inhib)	Inhibitory concentration 10–40%	[108]
Chondrus crispus	NA	NA	Piece of algae (3 cm)	Zone of inhibition 6.8 mm	[90]
Chondrus crispus	MeOH (SLE)	100 µ (of 4 mg·mL⁻¹)	Disc Diffusion	Zone of inhibition 21 mm	[90]
Cystoclonium purpureum	NA	NA	Piece of algae (3 cm)	Zone of inhibition 8.2 mm	[90]
Gracilaria corticata	MeOH:toluene 3:1 (SLE)	120 µL	Well Diffusion	Zone of inhibition ± 4 mm	[109]
Gracillaria gracilis	Diethyl ether (SLE)	25 µL	Disc Diffusion	Zone of inhibition 15 mm	[110]
Grinnellia americana	NA	NA	Piece of algae (3 cm)	Zone of inhibition 7 mm	[90]
Hypnea musciformis	Lectin	250 μg·mL⁻¹	Microdilution (Growth Inhib)	Inhibitory concentration 10–40%	[108]
Hypnea pannosa	MeOH:toluene 3:1 (SLE)	120 µL	Well Diffusion	Zone of inhibition ± 7.5 mm	[109]
Jania rubens	MeOH (SLE)	2 mg·disc⁻¹	Disc Diffusion	Zone of inhibition 6.5 mm	[111]
	MeOH (SLE)	4 mg·disc⁻¹	Disc Diffusion	Zone of inhibition 11 mm	[111]
	Chloroform (SLE)	4 mg·disc⁻¹	Disc Diffusion	Zone of inhibition 10 mm	[111]
Laurencia majuscula	Elatol	30 mg·disc⁻¹	Disc Diffusion	Zone of inhibition 19–24 mm *	[112]
Laurencia majuscula	Elatol	1–4 mg·mL⁻¹	MIC	Inhibitory concentration 2 mg·mL⁻¹ *	[112]
Laurencia obtusa	Essential oil	0.1 µL	Disc Diffusion	Zone of inhibition 9 mm	[78]
	Essential oil	0.2 µL	Disc Diffusion	Zone of inhibition 10 mm	[78]
	Essential oil	0.4 µL	Disc Diffusion	Zone of inhibition 11 mm	[78]
	Chloroform (SLE)	2 mg·disc⁻¹	Disc Diffusion	Zone of inhibition 6.5 mm	[78]
	Hexane (SLE)	2 mg·disc⁻¹	Disc Diffusion	Zone of inhibition 6.5 mm	[78]
Laurencia obtusa var. pyramidata	Chloroform (SLE)	2 mg·disc⁻¹	Disc Diffusion	Zone of inhibition 6.5 mm	[78]
Laurencia obtusa var. pyramidata	Hexane (SLE)	2 mg·disc⁻¹	Disc Diffusion	Zone of inhibition 6.5 mm	[78]
Laurencia sp.	MeOH (SLE)	120 µL	Well Diffusion	Zone of inhibition 11 ± 2.56 mm	[107]
Plocamium angustum	Costatone C	0.5–129 µg·mL⁻¹	MIC	Inhibitory concentration 64 µM	[113]
Polysiphonia fibrillosa	NA	NA	Piece of algae (3 cm)	Zone of inhibition 7.5 mm	[90]
Rhodomela confervoides	3-bromo-4-[2,3-dibromo-4,5-dihydroxyphenyl] methyl-5-(hydroxymethyl) 1,2-benzenediol	35–140 μg·mL⁻¹	Microdilution (MIC)	Inhibitory concentration 140 μg·mL⁻¹	[93]
	3-bromo-4-[2,3-dibromo-4,5-dihydroxyphenyl] methyl-5-(hydroxymethyl) 1,2-benzenediol	35–140 μg·mL⁻¹	Microdilution (MIC)	Inhibitory concentration >140 μg·mL⁻¹ *	[93]
	3-bromo-4-[2,3-dibromo-4,5-dihydroxyphenyl] methyl-5-(ethoxymethyl) 1,2-benzenediol	35–140 μg·mL⁻¹	Microdilution (MIC)	Inhibitory concentration 140 μg·mL⁻¹	[93]
	3-bromo-4-[2,3-dibromo-4,5-dihydroxyphenyl] methyl-5-(ethoxymethyl) 1,2-benzenediol	35–140 μg·mL⁻¹	Microdilution (MIC)	Inhibitory concentration 140 μg·mL^{−1 *}	[93]
	3-bromo-4-[2,3-dibromo-4,5-dihydroxyphenyl] methyl-5-(methoxymethyl) 1,2-benzenediol	35–140 μg·mL⁻¹	Microdilution (MIC)	Inhibitory concentration 70 μg·mL⁻¹	[93]
	3-bromo-4-[2,3-dibromo-4,5-dihydroxyphenyl] methyl-5-(methoxymethyl) 1,2-benzenediol	35–140 μg·mL⁻¹	Microdilution (MIC)	Inhibitory concentration 70 μg·mL^{−1 *}	[93]
	4,40-methylenebis [5,6-dibromo-1,2-benzenediol]	35–140 μg·mL⁻¹	Microdilution (MIC)	Inhibitory concentration 140 μg·mL¹	[93]
	4,40-methylenebis [5,6-dibromo-1,2-benzenediol]	35–140 μg·mL⁻¹	Microdilution (MIC)	Inhibitory concentration 140 μg·mL⁻¹ *	[93]
	bis (2,3-dibromo-4,5-dihydroxybenzyl)ether	35–140 μg·mL⁻¹	Microdilution (MIC)	Inhibitory concentration 35 μg·mL⁻¹	[93]
	bis (2,3-dibromo-4,5-dihydroxybenzyl)ether	35–140 μg·mL⁻¹	Microdilution (MIC)	Inhibitory concentration 140 μg·mL⁻¹ *	[93]
Sphaerococcus coronopifolius	12S-hydroxy-bromosphaerol	0.1–200 µM	Microdilution (IC50)	Inhibitory concentration 10.07 (7.84–12.94) µM	[106]
	Sphaerococcenol A	0.1–200 µM	Microdilution (IC50)	Inhibitory concentration 56.58 (41.01–78.06) µM	[106]
	12R-hydroxy-bromosphaerol	0.1–200 µM	Microdilution (IC50)	Inhibitory concentration 5.61 (4.18–7.53) µM	[106]
	Bromosphaerol	0.1–200 µM	Microdilution (IC50)	Inhibitory concentration 9.05 (7.05–11.63) µM	[106]
Symphyocladia latiuscula	MeOH (SLE)	19.5 μg·mL⁻¹–10 mg·mL⁻¹	MIC	Inhibitory concentration 0.63 mg·mL⁻¹	[83]

4.2. Anti-Inflammatory Extracts and Compounds from Red Macroalgae

The literature revision regarding both anti-inflammatory compounds and extracts from Rhodophyta resulted in 75 research articles, which are summarized in Table 2. These papers included 56 different red macroalgal species, wherein the Gracilaria genus was the most abundant, resulting in 31 outcomes. Regarding species, G. verrucosa, Porphyra dentata, and Pyropia yezoensis had the highest scores, presenting 14, 10, and 9 results, respectively.

As mentioned across Section 3, inflammatory responses occur during all of the stages of AV lesions’ formation. These include increasing androgen production that leads to the higher activity, size, and enlargement of the sebaceous glands, consequently producing more sebum; increased lipid synthesis due to LXR-α, COX2, and NF-κB action; inflammatory sebum lipid fractions; the increased segregation of growth hormones, which stimulates the production of IGF’s, consequently activating MAPK/ERK pathways; and C. acnes activation of a vast array of cytokines (IL-1, IL-6, IL-8, IL-10, IL-12 and TNF-α), TLR’s, and β-defensins. Relevant studies targeting some of these inflammatory markers are included in Table 2 and are detailed hereafter.

Rhodophyta species are known for the rich composition in polysaccharides of their cell walls and intercellular matrix. These include non-sulphated polysaccharides (agars and carrageenans), sulphated galactans, and neutral-structural polysaccharides (cellulose, mannans, and xylans) [15]. The analyses of Table 2 reveal that polysaccharides are the compounds that appear in greater quantity, representing the greater number of studies that have reported anti-inflammatory compounds from red seaweed. Isolated compounds classified as polysaccharides by the authors revealed several anti-inflammatory properties, namely the degranulation of basophils inhibition (Chondrus verrucosus ([114]), the reduction of paw edema (Porphyra vietnamensis [115], Digenia simplex [116]) and leukocyte infiltrations (D. simplex [116]), the inhibition of IL-1β, TNF-α (D. simplex [116]; Gracilaria lemaneiformis [117]), NO, PGE2, COX-2 and ROS (Gracilaria lemaneiformis [117]) production, and NF-κB expression (Porphyridium sp. [118]). Furthermore, cellulose microfibril from Gelidium amansii lead to JNK1/2 and p38 inhibition [119], and cellulose nanocrystals from the same seaweed revealed COX-2 and ERK1/2 inhibition [120]. Sulphated polysaccharide outcomes include reduced neutrophil (Agardhiella ramosossima [121]) and leukocyte (Gracilaria birdae [122], Gracilaria caudata [123], Gracilaria cornea [124], Hypnea musciformis [125]) migration/infiltration; reduced paw oedema (Agardhiella ramosossima [121], Gelidium crinale [126], Gracilaria birdiae [122], Gracilaria caudata [123], Gracilaria cornea [124] Hypnea musciformis [125]); NO and TLR4 inhibition (Gelidium pacificum [127]); IL-1β and TNF-α inhibition (Gracilaria caudata [123], Solieria filiformis [128]); and COX-2 and 5-LOX inhibition (Gracilaria opuntia, Kappaphycus alvarezii [129]). These studies included red seaweed compounds which were able to inhibit ILs and TNF-α, which are important triggers of the inflammatory pathways involved in AV, among others. These markers of inflammation are able to activate macrophages that excessively induce the release of pro-inflammatory cytokines and other mediators of inflammation, wherein PGE2 is an inflammatory mediator generated by the COX2 conversion of arachidonic acid [130], NO is a known endogenous free radical and a pro-inflammatory mediator [131], interleukins induce the synthesis of acute phase proteins [132], and TNF-α is one of the most important pro-inflammatory cytokines that participates in vasodilatation, edema formation, and the expression of adhesion molecules that leads to leukocyte adhesion to epithelium [133]. In fact, species belonging to the genera Gracilaria and Gelidium seem to be a good source of compounds, in particular sulphated polysaccharides and agaro-oligosaccharides (non-sulphated polysaccharides), which resulted in ILs and TNF-α inhibition. Specific examples include Gracilaria lemaneiformis isolated agaro-oligosaccharides evaluated in LPS-stimulated RAW264.7 [117] that inhibited several inflammatory triggers, as did sulphated galactan from Kappaphycus alvarezii [129]. Furthermore, porphyran extracted from P. yezoensis supressed IL-6, IL-12, and TNF-α expression in the lipopolysaccharide-induced activation of dendritic cells in mice [134]. Sulphated galactans from both red algae possess anti-inflammatory activity due to the suppression of COX-2 and 5-LOX, and, in accordance with the study of de Sousa et al. [126], the same type of compounds isolated from Gelidium crinale reduced paw oedema on rat-stimulated paw oedema. Curiously, sulphated polysaccharides, such as carrageenan from red seaweed, have been employed for decades to induce local inflammation in in vivo studies using rats, by stimulation through TLR4 signalling pathways [135,136], as a study using kappa/beta-carrageenan proved in human blood cells by the increase of the IL-10 marker [137]. Thus, cases reported where sulphated galactans are anti-inflammatory lead to the conclusion that the subtle differences in the chemical structure of sulphated polysaccharides, among red macroalgal species, profoundly impact their immunomodulatory properties.

Seaweeds usually contain a low quantity of lipids, but despite that, they synthesize important ones, such as omega-3 and -6, unsaturated fatty acids (UFA), polyunsaturated fatty acids (PUFA), highly unsaturated fatty acids (HUFA), and monounsaturated fatty acids (MUFA) [138]. Two studies reported lipid compounds that showed anti-inflammatory activities (Table 2). For example, in lipopolysaccharide (LPS)-stimulated mouse macrophage cell line RAW 264.7 combined with Gracilaria verrucosa, Hung et al. determined that there was significant reduction of NO, TNF-α and IL-6 with the 14 lipid compounds (20 µg·mL⁻¹), including prostaglandins, ceramides, fatty acids, and oxygenated fatty acids [139]. These pro-inflammatory mediators were successfully inhibited by the positive influence of the algal compounds and extracts, confirming their anti-inflammatory properties in the most-used cell line when it comes to biological inflammatory assays [140].

Red macroalgae are a source of metabolites, including halogenated compounds, such as terpenoids and derivatives [141]. Studies show that isolated diterpenes, diterpenoids, and meroterpenoids have anti-inflammatory properties (Table 2). It should be noted that COX-2 and 5-LOX are fundamental enzymes involved in lipid synthesis and are therefore triggers on the AV cascade. Once again, three Gracilaria species showed promising results, in this case, by the inhibition of both enzymes. The newly described salicornolides (A, B, and C) from G. salicornia successfully inhibited both anti-inflammatory markers [142], in the same way that three compounds from the same algae did, which were classified as a one diterpenoid and two 2H-chromenyl derivatives [143]. Similarly, three different compounds—namely an oxygenated meroterpenoid (from Kappaphycus alvarezii [144]), a methylfuran derivative (Gracilaria opuntia [145]), and a halogen derivative [146]—were able to inhibit both enzymes, except for the methylfuran derivative, which only inhibited 5-LOX [145]. Furthermore, a diterpene from Laurencia glandulifera, classified as Neorogioltriol, showed the ability to inhibit not only COX-2, but also NO, TNF-α, NF-κB, and the reduction of paw edema [141].

Seaweeds also synthesize phenolic compounds including phlorotannins, bromophenols, and mycosporine-like amino acids (MAAs) [12]. Found especially in Rhodophyta species are bromophenol, flavonoids, bromated compounds, and MAAs, as they also present anti-inflammatory activities (Table 2). Nuclear factor NF-κB is, perhaps, the most significant transcription factor associated with AV, because it transcribes numerous inflammatory genes, including TNF-α, IL-1, IL-6, and IL-8 [147,148,149]. Porphyra species seem to be an excellent source of metabolites which are able to inhibit the transcription factor. For example, a study by Kazłowska et al. [150] demonstrated that a methanol extract, catechol, and rutin (flavonoid), from P. dentata, were able to inhibit NF-κB, and these two phenolic compounds additionally inhibited iNOS and reduced NO levels. A report on Porphyra-334 also showed NF-κB inhibition in an LPS-challenged RAW264.7 cell line [151]. Likewise, two studies using P. yezoensis showed similar results in other cell lines. P. yezoensis aqueous protein extract downregulated MAPK and NF-κB in the HK2 human proximal tubular epithelial cell line [152]; extracted MAAs obtained through an ethanol extraction, and reduced the expression of IL-1β, IL-6, IL-10, NF-κB in the skin of male ICR mice [153]. Other species can be included as containers of compounds which are able to inhibit NF-κB, including G. lanceolata [154], L. glandulifera [141], Polysiphonia morrowii [155], and Pyropia yezoensis [156]. In this latter study, the use of methanol extracts from P. yezoensis revealed TARC (thymus and activation-regulated chemokine) and MDC (macrophage-derived chemokine) expression inhibition, ERK (extracellular signal-regulated kinase), JNK (c-Jun N-terminal kinase), p38 inhibition, and nuclear factors NF-κB and IkB-α downregulation, when using the cell line HaCaT induced with interferon (IFN)-ϒ and HaCaT induced with TNF-α [156]. HaCaT are immortalized human skin keratinocytes that produce pro-inflammatory cytokines affecting the development of inflammatory skin disorders [119]. Pyropia yezoensis is rich in bioactive compounds such as amino acids, polysaccharides, phytosterols, and pigments. The study by Ha et al. [156] in keratinocytes, using that macroalgae, vouched for the anti-inflammatory activity of its extracts by suppressing pro-inflammatory chemokines. Although MAAs are presented here as anti-inflammatory agents, in accordance with most of the studies we found, a report by Becker et al., (2016) proved that not all MAAs are anti-inflammatory; some are pro-inflammatory, even when the chemical structure is similar. This is the case of shinorine and porphyra-334 isolated from P. yeozensis, where porphyra-334 inhibited NF-κB and supressed IDO-1, and on the contrary, when using shinorine in LPS-stimulated RAW264.7, the result was the increase of NF-κB and the suppression of IDO-1 [151].

Other algae species that should be highlighted are Palmaria palmata, Pyropia yezoensis, and Laurencia okamurae. Palmaria palmata thermolysin-digested water extract reduced NO, TNF-α, and IL-6 on LPS-stimulated RAW264.7, and also reduced the paw oedema of rat carrageenan-induced paw oedema [157]; the seaweeds’ phenolic extract reduced ROS, NO, MPO, IL-8, IL-1Β, IL-6, TNF-α, and downregulated TLR4 on LPS-stimulated primary human neutrophils cell line [158]; the lipid extract of the same algae downregulated the expression of 14 pro-inflammatory genes (TLR1, TLR2, TLR4, TLR8, TRAF5, TRAF6, TNFSF18, IL6R, IL23, CCR1, CCR4, CCL17, STAT3, and MAP3K1) in LPS-stimulated Human THP-1 macrophages [159]. Pyropia yezoensis isolated peptide PPY1 inhibited NO, ROS, iNOS, COX-2, IL-1Β, and TNF-α, and downregulated p38 and MAPK in LPS-stimulated RAW264.7 [160]. A strong activity was also found in an ethyl acetate extract from L. okamurae at 25 µg·mL⁻¹, using LPS-stimulated RAW264.7, inhibiting the production of NO, prostaglandin E2 (PGE2), IL-6, and TNF-α [161].

The final highlight of the results in Table 2 should be given to a relevant number of studies that were condcted in vivo using mice and rats. Most of the reports described the reduction of paw oedema [115,121,126,141,157,162,163,164,165,166,167] and reduced leukocyte influx/migration [168], or even both [116,122,123,124,125,169,170], proving that red seaweed-derived compounds are effectively anti-inflammatory. Though a significant number of compounds isolated from Rhodophyta have proven to be anti-inflammatory, both in vitro and in vivo, the opportunity to investigate how these compounds behave in individuals suffering from AV remains open. Successful anti-inflammatory in vitro studies on inflammatory markers involved in the AV cascade show a promising potential for human clinical trials.

Table 2. Anti-inflammatory compounds and extracts derived from red seaweeds which are effective on different inflammation models. SLE: solid–liquid extraction; SPE: solid-phase extraction; MeOH: methanol; HaCat: immortalized human skin keratinocyte cell line; RAW264.7: macrophage cell line; HK2: human proximal tubular epithelial cell line; NO: nitric oxide; JNK: c-Jun N-terminal kinase; IL: interleukin; TNF: tumor necrosis factor; iNOS: inducible nitric oxide synthase; NF-κB: nuclear factor kappa B; MAPK: mitogen-activated protein kinase; TARC: thymus and activation-regulated chemokine; MDC: macrophage-derived chemokine; ERK: extracellular signal-regulated kinase; n.d.: not described; TMJ: temporomandibular joint; SRBC: sheep red blood cells. PGE2: prostaglandin E2; PMNs: polymorphonuclear leukocytes; MPO: myeloperoxidase; GVHD: graft-vs-host disease; BDMC: bone-marrow derived dendritic cells; THP-1: human THP-1 macrophages; RAW 264.7: mouse macrophage cell line; n.d.: not defined.

Red Macroalgal Species	Compound or Extract (Technique)	Concentration Tested	Anti-Inflammatory Assay	Outcome	Reference
Agardhiella ramosissima	Sulfated polyssacharide	30 mg·kg⁻¹	Swiss mice: carrageenan, dextran, serotonin and histamine induced paw oedema; carrageenan induced peritonitis	Reduced neutrophil migration in peritonitis model; Reduced paw oedema	[121]
Amansia multifida	Ethanol:water 7:3 (SLE)	2.5, 5, 10 mg·kg⁻¹	Swiss mice: carrageenan induced peritonitis; carrageenan induced paw oedema.	Reduced neutrophil migration in peritonitis model; Reduced paw oedema	[162]
Amansia multifida	Lectin	0.1, 0.3, 1 mg·kg⁻¹	Swiss mice: carrageenan-induced peritonitis; carrageenan-, compound 48/80-, histamine- and PGE2-induced paw oedema	Inhibition of paw oedema for all stimulators, inhibition of neutrophil migration, increase in GSH levels, inhibition of TNF-α and IL-1β	[163]
Asparagopsis taxiformis	Water (SLE)	n.d.	Enzymatic activity	COX-2 inhibition	[171]
Asparagopsis taxiformis	Ethanol:water 96:4 (SLE)	1 mg·mL⁻¹	Enzymatic activity	COX-2 inhibition	[172]
Bryothamnion triquetrum	Lectin	1, 5, 10 mg·kg⁻¹	Swiss mice: carrageenan induced peritonitis; carrageenan and dextran induced paw oedema	Reduction of oedema; Reduction of leukocyte infiltrations. IL-1β and TNF-α inhibition	[169]
Chondrus crispus	Lipid extract	3 μg·mL⁻¹ total fatty acids	LPS-stimulated THP-1	TLR1, TLR2, TLR4, TLR8, TRAF5, TRAF6, TNFSF18, IL6R, IL23, CCR1, CCR4, CCL17, STAT3, MAP3K1 downregulation	[159]
Chondrus verrucosus	Polyssacharides	100, 200, 400 µg·mL⁻¹	A23187-stimulated RBL-2H3 cells	Degranulation of basophils inhibition	[114]
Coelarthrum muelleri	MeOH (SLE)	n.d.	Carrageenan-induced rat paw oedema	Reduction of oedema	[164]
Delesseria sanguinea	Sulfated Polysaccharides	n.d.	Enzymatic activity	Elastase inhibition	[173]
Dichotomaria obtusata	MeOH (SLE)	0.0005–2 mg·ear⁻¹ 12.5–100 mg·kg⁻¹	Cenpalab mice: croton oil induced ear oedema	Reduced ear oedema	[174]
Dichotomaria obtusata	Water (SLE)	12.5, 25 and 50 mg·kg⁻¹	Cenpalab mice: TPA-induced ear oedema	Reduction of oedema	[175]
Digenia simplex	Polysaccharide	10, 30 and 60 mg·kg⁻¹	Swiss mice: carrageenan-induced peritonitis; carrageenan-dextran-, serotonin-, histamine- and bradykinin-induced paw oedema	Reduction of oedema; Reduction of leukocyte infiltrations; Inhibition of IL-1β and TNF-α	[116]
Eucheuma cottonii	MeOH:Water 1:1 (SLE)	150, 300 mg·kg⁻¹	Sprague-Dawley rats: ovalbumin induced asthma	Reduced lung inflammation and blood cells migration and positively modulated several inflammatory markers	[165]
Eucheuma cottonii	MeOH:Water 1:1 (SLE)	150, 300 mg·kg⁻¹	Sprague-Dawley rats: SRBC induced paw oedema	Pro-inflammatory at 150 mg·kg⁻¹ Anti-inflammatory at 300 mg·kg⁻¹	[165]
Eucheuma denticulatum	Ethanol (SLE) and SPE fractions	1–100 µg·mL⁻¹	TNF-γ- and LPS-stimulated RAW264.7	Non-inflammatory morphology conserved; NO, TNF-α, IL-1β, IL-6 and MCP-1 inhibition	[176]
Gelidium amansii	Cellulose microfibril	n.d.	HaCaT	JNK1/2 and p38 inhibition	[119]
	Cellulose nanocrystal	n.d.	UVB-stimulated HaCaT	AP-1, COX-2, c-Jun translocation inhibition; phosphorilation of ERK1/2/B-Raf, JNK1/2/MKK4/7, Akt and EGFR inhibition	[120]
	Cellulose nanocrystal	40 and 200 mg·kg⁻¹	UVB-stimulated mice	Epidermal thickening and COX-2 inhibition	[120]
	Hot water (SLE) partitioned with Ethanol	n.d.	LPS-stimulated RAW264.7	Reduced TNF-α, IL-1β and IL-6	[177]
Gelidium crinale	Sulfated galactan	0.01, 0.1 and 1 mg·kg⁻¹	Wistar rats: several stimulatory agents of paw oedema	Reduced paw oedema	[126]
Gelidium pacificum	Sulfated Polysaccharides	0–300 µg·mL⁻¹	LPS-stimulated THP-1	NO, TLR4, MyD88 and TRAF6 inhibition	[127]
Gelidium sesquipedale	Ethanol (SLE)	1 mg·mL⁻¹	Enzymatic activity	COX-2 inhibition	[178]
Gloiopeltis furcata	Ethyl acetate (SLE)	50 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, PGE2, IL-6, TNF-α inhibition	[161]
Gracilaria birdiae	Sulfated Polysaccharide	5, 10, 20 mg·kg⁻¹	Wistar rats: carrageenan-induced peritonitis; carrageenan- and dextran-induced paw oedema	Reduced paw oedema and leukocyte migration	[122]
Gracilaria caudata	Sulfated Polysaccharides	2.5, 5 and 10 mg·kg⁻¹	Swiss mice: carrageenan, dextran, bradykinin and histamine paw oedema; carrageenan induced peritonitis	Reduction of oedema (some inducers). Reduction of leukocyte infiltrations. IL-1β and TNF-α inhibition	[123]
Gracilaria changii	MeOH (SLE)	10 µg·mL⁻¹	PMA-differentiated U937	Inhibition of TNF-α and IL-6	[179]
Gracilaria cornea	Sulfated Polysaccharides	3, 9, 27 mg·kg⁻¹	Wistar rats: carrageenan-induced peritonitis; carrageenan and dextran induced paw oedema	Leukocyte infiltration and oedema reduction.	[124]
Gracilaria lemaneiformis	Agaro-oligosaccharides	12.5, 25, 50 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, PGE2, COX-2, TNF-α, IL-1β and IL-6 inhibition	[117]
Gracilaria lemaneiformis	Agaro-oligosaccharides	12.5, 25, 50 µg·mL⁻¹	LPS-stimulated zebrafish embryo	NO and ROS inhibition	[117]
Gracilaria opuntia	Sulfated galactan	n.d.	Enzymatic activity	Inhibition of COX-2 and 5-LOX	[129]
	2-acetoxy-2-(5-acetoxy-4-methyl-2-oxotetrahydro-2H-pyran-4-yl)ethyl 4-(3-methoxy-2-(methoxymethyl)-7-methyl-3,4,4a,7,8,8a-hexahydro-2H-chromen-4-yloxy)-5-methylheptanoate	n.d.	Enzymatic activity	Inhibition of COX-2 and 5-LOX	[144]
	3-(2-ethyl-6-((3Z,7Z)-1,2,5,6-tetrahydroazocin-5-yl)hexyl) morpholin-6-one	n.d.	Enzymatic activity	Inhibition of COX-2 and 5-LOX	[146]
	2-(3-ethyl-9-(2-methoxyethoxy)-1-oxo-2,3,4,9-tetrahydro-1H-xanthen-2-yl) ethyl-5-hydroxy-9-methoxy-7,8-dimethyl-8-(5-methylfuran-2-yl) nona-3,6-dienoate	n.d.	Enzymatic activity	Inhibition of 5-LOX	[145]
Gracilaria salicornia	Ethyl acetate:MeOH 1:1 (SLE)	n.d.	Enzymatic activity	Inhibition of COX-2 and 5-LOX	[143]
	Methyl-16(13–>14)-abeo-7-labdene-(12-oxo) carboxylate	n.d.	Enzymatic activity	Inhibition of COX-2 and 5-LOX	[143]
	4′-[10′-[7-hydroxy-2,8-dimethyl-6-(pentyloxy)-2H-chromen-2-yl]ethyl]-3′,4′-dimethyl-cyclohexanone	n.d.	Enzymatic activity	Inhibition of COX-2 and 5-LOX	[180]
	3′-[10′-(8-hydroxy-5-methoxy-2,6,7-trimethyl-2H-chromen-2-yl)ethyl]-3′-methyl-2′-methylene cyclohexyl butyrate	n.d.	Enzymatic activity	Inhibition of COX-2 and 5-LOX	[180]
	Salicornolides A-C	n.d.	Enzymatic activity	Inhibition of COX-2 and 5-LOX	[142]
Gracilaria sp.	Lipid extract	100 µg·mL⁻¹	LPS-stimulated RAW264.7	NO inhibition	[181]
Gracilaria sp.	Ethanol (SLE)	5 and 10% (w/w) of cream	UVB-irradiated mice	Reduction of epidermal erosion and thickening induced by UVB radiation	[182]
Gracilaria verrucosa	(5Z,13E)-(8R,12R,15S)-15-Hydroxy-9-oxoprosta-5,13-dienoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	Methyl-(5Z,13E)-(8R,12R,15S)-15-hydroxy-9-oxoprosta-5,13-dienoate	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	(E)-(8R,12R,15S)-15-Hydroxy-9-oxoprost-13-enoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	(Z)-(8R,12S)-9,15-Dioxoprost-5-enoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	(2R,3S)-2-Formamido-1,3-dihydroxyoctadecane	20 µg·mL⁻¹	LPS-stimulated RAW264.7	IL-6 reduction	[139]
	(E)-9-Oxohexadec-10-enoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	10-Oxohexadecanoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	(E)-(S)-10-Hydroxyhexadec-8-enoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	(E)-10-Oxooctadec-8-enoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	(E)-9-Oxooctadec-10-enoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	(E)-(R)-10-Hydroxyoctadec-8-enoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	10-Oxooctadecanoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	11-Oxooctadecanoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
	12-Oxooctadecanoic acid	20 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, TNF-α, IL-6 reduction	[139]
Grateloupia elliptica	Ethyl acetate (SLE)	50 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, PGE2, IL-6, TNF-α inhibition	[161]
Grateloupia lanceolata	Ethanol:water 7:3 (SLE)	0–100 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, IL-1Β, p38 MAPK/ERK/JNK and NF-κB inhibition	[154]
Grateloupia turuturu	Lipids	12.5–250 µg·mL⁻¹	Enzymatic activity	COX-2 inhibition	[183]
Grateloupia turuturu	Hydroethanolic and water SLEs	0.02–0.2 mg·mL⁻¹	LPS-stimulated RAW264.7	NO inhibition	[184]
Hypnea cervicornis	Agglutinin	0.3–3 mg·kg⁻¹	Wistar rats: Zymosan-induced arthritis	Reduced leukocyte influx. iNOS and TNF-α inhibition.	[168]
Hypnea cervicornis	Agglutinin	0.1–10 mg·kg⁻¹	Wistar rats: carrageenan-, ovalbumin- and PGE2-induced inflammation	Inhibition of neutrophil migration; increase in NO	[185]
Hypnea musciformis	Sulfated polysaccharide	10 mg·kg⁻¹	Swiss mice: carrageenan-induced peritonitis; carrageenan- and dextran-induced paw oedema	Reduced leukocyte influx; Reduced paw oedema; IL-1β inhibition	[125]
Kappaphycus alvarezii	Sulfated galactan	n.d.	Enzymatic activity	Inhibition of COX-2 and 5-LOX	[129]
	(3S, 4R, 5S, 6Z)-3-((R)-hexan-2′-yl)-3,4,5,8-tetrahydro-4-methyl-2H-oxocin-5-yl acetate	n.d.	Enzymatic activity	Inhibition of 5-LOX	[186]
	2-ethyl-6-(4-methoxy-2-((2-oxotetrahydro-2H-pyran-4-yl)methyl)butoxy)-6-oxohexyl 5-ethyloct-4-enoate	n.d.	Enzymatic activity	Inhibition of 5-LOX	[187]
	4-(2-chloroethyl)-5-7-(methoxymethyl) undec-3-enyl) cyclooct-4-enone	n.d.	Enzymatic activity	Inhibition of COX-2 and 5-LOX	[188]
Laurencia glandulifera	Neorogioltriol	0.5–1 mg·kg⁻¹	Rats: carrageenan induced paw oedema	Reduction of paw oedema	[141]
Laurencia glandulifera	Neorogioltriol	12.5–62.5 µM	LPS-stimulated RAW264.7	NO, COX-2, TNF-α and NF- kB inhibition	[141]
Laurencia okamurae	Ethyl acetate (SLE)	25 µg·mL⁻¹	LPS-stimulated RAW264.7	NO, PGE2, IL-6, TNF-α inhibition	[161]
Laurencia snackeyi	5β-hydroxypalisadin B	0.25, 0.1 and 1 µg·mL⁻¹	LPS-induced zebrafish embryo	NO and ROS inhibition; Improved survival, heart rate and yolk sac oedema size	[189]
Lithothamnion muelleri	Whole seaweed	1% (w/w) in diet	GVHD mice model	Reduced IFN-γ, TNF-α, CCL2, CCL3, CCL5.	[190]
Melanothamnus afaqhusainii	MeOH (SLE)	n.d.	Carrageenan- induced rat paw oedema	Reduction of oedema	[164]
Palmaria palmata	Ethyl acetate LLE of MeOH:Chloroform (SLE)	n.d.	LPS-stimulated RAW264.7	NO and iNOS inhibition	[191]
	Thermolysin-digested water extract	100–1000 µg·mL⁻¹	LPS-stimulated RAW264.7 and carrageenan-induced paw oedema	Reduction of NO, TNF-α and IL-6; Reduction of paw oedema	[157]
	Phenolic Extract (LLE of MeOH SLE)	25, 50 and 100 µg·mL⁻¹	LPS-stimulated primary human neutrophils	Reduction of ROS, NO, MPO, IL-8, IL-1β, IL-6 and TNF-α; Downregulation of TLR4	[158]
	Lipid extract	3 μg·mL⁻¹ total fatty acids	LPS-stimulated THP-1	TLR1, TLR2, TLR4, TLR8, TRAF5, TRAF6, TNFSF18, IL6R, IL23, CCR1, CCR4, CCL17, STAT3, MAP3K1 downregulation; IL-6 and IL-8 inhibition	[159]
Polysiphonia morrowii	Bis (3-bromo-4,5-dihydroxybenzyl) ether	0.1, 1, 2 µM	LPS-stimulated RAW264.7	NO, iNOS, COX-2, PGE2, TNF-α, IL-6 and IL-1β inhibition	[192]
Polysiphonia morrowii	3-bromo-5-(ethoxymethyl)-1,2-benzenediol	12.5–50 µM	LPS-stimulated RAW264.7 and Zebrafish embryos	NO, ROS, iNOS, COX-2 and NF-κB inhibition	[155]
Porphyra columbina	Protein fraction	n.d.	Several cell lines	IL-10 elicitation; pro-inflammatory cytokines inhibition	[193]
Porphyra dentata	MeOH (SLE)	25, 50, 100, 200 µg·mL⁻¹	LPS-stimulated RAW264.7	NO reduction	[150]
	MeOH (SLE)	50, 100, 200 µg·mL⁻¹	LPS-stimulated RAW264.7	iNOS inhibition	[150]
	MeOH (SLE)	200 µg·mL⁻¹	LPS-stimulated RAW264.7	NF-κB inhibition	[150]
	Catechol	6 µg·mLl⁻¹	LPS-stimulated RAW264.7	NO reduction	[150]
	Catechol	1–11 µg·mL⁻¹	LPS-stimulated RAW264.7	iNOS inhibition	[150]
	Catechol	11 µg·mL⁻¹	LPS-stimulated RAW264.7	NF-κB inhibition	[150]
	Rutin	250 µg·mL⁻¹	LPS-stimulated RAW264.7	NO reduction	[150]
	Rutin	80–250 µg·mL⁻¹	LPS-stimulated RAW264.7	iNOS inhibition	[150]
	Rutin	250 µg·mL⁻¹	LPS-stimulated RAW264.7	NF-κB inhibition	[150]
	Hesperidin	250 µg·mL⁻¹	LPS-stimulated RAW264.7	NO reduction	[150]
Porphyra dioica	Lipid extract	3 μg·mL⁻¹ total fatty acids	LPS-stimulated THP-1	TLR1, TLR2, TLR4, TLR8, TRAF5, TRAF6, TNFSF18, IL6R, IL23, CCR1, CCR4, CCL17, STAT3, MAP3K1 downregulation	[159]
Porphyra sp.	Shinorine	12.5–200 µg·mL⁻¹	LPS-stimulated THP-1 and THP-1-Blue	NF-κB increase and IDO-1 suppression	[151]
Porphyra sp.	Porphyra-334	12.5–200 µg·mL⁻¹	LPS-stimulated THP-1 and THP-1-Blue	NF-κB inhibition and IDO-1 suppression	[151]
Porphyra tenera	Several enzymatic extracts	62.5, 125 and 250 μg·mL⁻¹	LPS-stimulated RAW264.7	NO reduction	[194]
Porphyra umbilicalis	Hydroethanolic and water SLEs	0.005–0.02 mg·mL⁻¹	LPS-stimulated RAW264.7	NO reduction	[184]
Porphyra vietnamensis	MeOH:Water 4:1 (Soxhlet)	200 mg·kg⁻¹	Wistar rats: Carrageenan-induced paw oedema	Reduction of paw oedema	[115]
Porphyra vietnamensis	Precipitated polysaccharide	250 mg·kg⁻¹	Wistar rats: Carrageenan-induced paw oedema	Reduction of paw oedema	[115]
Porphyra yezoensis	Aqueous protein extract (SLE)	25, 50, 100 µg·mL⁻¹	HK2	MAPK and NF-κB downregulation	[152]
Porphyra yezoensis	MAAs (EtOH, SLE)	5, 10, 20 µg·mL⁻¹	Male ICR mice (skin)	IL-1β, IL-6, IL-10, NF-κB expression reduction	[153]
Porphyridium cruentum	Sulfoglycolipid fraction	n.d.	Activated peritoneal mono nuclear cells from Wistar rats	Inhibition of Superoxide generation	[195]
Porphyridium sp.	Polysaccharide	50–500 µg·mL⁻¹	HCAEC induced with angiotensin II	Inhibition of adhesion molecules and NF-κB expression; increase in aantioxidant system activity	[118]
Porphyridium sp.	Polysaccharide	0.005–1% w/v	fMLP-stimulted PMNs	Inhibition of PMN chemotaxis	[196]
Pterocladiella capillacea	Ethanol (SLE)	1 mg·mL⁻¹	Enzymatic activity	COX-2 inhibition	[178]
Pterocladiella capillacea	Lectin	8.1 mg·kg⁻¹	Wistar rats: carrageenan-induced paw oedema and peritonitis	Reduced paw oedema and leukocyte migration.	[170]
Pyropia yezoensis	MeOH (SLE)	40, 200, 1000 µg·mL⁻¹	HaCaT induced with IFN-ϒ	TARC and MDC expression inhibition	[156]
	MeOH (SLE)	40, 200, 1000 µg·mL⁻¹	HaCaT induced with TNF-α	TARC and MDC expression inhibition	[156]
	MeOH (SLE)	40, 200, 1000 µg·mL⁻¹	HaCaT induced with IFN-ϒ	ERK, JNK, p38 inhibition	[156]
	MeOH (SLE)	40 µg·mL⁻¹	HaCaT induced with TNF-α	ERK inhibition	[156]
	MeOH (SLE)	1000 µg·mL⁻¹	HaCaT induced with TNF-α	JNK and p38 inhibition	[156]
	MeOH (SLE)	40, 200, 1000 µg·mL⁻¹	HaCaT induced with IFN-ϒ	NF-κB and IkB-α inhibition	[156]
	Peptide PPY1	250–1000 ng·mL⁻¹	LPS-stimulated RAW264.7	NO, ROS, iNOS, COX-2, IL-1β and TNF-α inhibition; p38 and MAPK downregulation	[160]
	Porphyran	0–100 µg·mL⁻¹	C57BL/6 mice derived, LPS-stimulated BDMCs	Supression of CCR7, IL-6, IL-12 and TNF-α expression	[134]
	Porphyran	0–100 mg·kg⁻¹	LPS-stimulated C57BL/6 mice	Supression of Th1 and Tc1 cells differentiation	[134]
Sarcodia ceylanica	Ethyl acetate LLE of Ethanol (95% v/v) SLE	10, 20, 50 µg·mL⁻¹	LPS-stimulated RAW264.7	iNOS and COX-2 inhibition	[166]
Sarcodia ceylanica	Ethyl acetate LLE of Ethanol (95% v/v) SLE	20, 50 mg·kg⁻¹	Wistar rats: carrageenan-induced paw oedema	Reduced paw oedema	[166]
Solieria filiformis	Lectin	1, 3, 9 mg·kg⁻¹	Wistar rats: carrageenan induced peritonitis; carrageenan, dextran, bradykinin, histamin and serotonin induced paw oedema.	Reduced neutrophil migration in peritonitis model; Reduced paw oedema	[167]
	Lectin	10 µg·mL⁻¹	BALB/c mice splenocytes	IL-6 and IL-10 production (Th2 immune-response stimulators)	[197]
	Sulfated polysaccharide	0.03, 0.3, 3 mg·kg⁻¹	Wistar rats: formalin induced TMJ inflammation	Reduced IL-1β and TNF-α	[128]
Solieria robusta	MeOH (SLE)	n.d.	Carrageenan- induced rat paw oedema	Reduction of oedema	[164]
Tichocarpus crinitus	Kappa/beta Carrageenan	n.d.	Human blood cells	Increase in IL-10	[137]
Vidalia obtusaloba	Vidalols A and B	n.d.	PMA-induced mouse ear oedema; enzymatic activity	Reduction of oedema and inhibition of Phospholipase A₂	[198]

4.3. Extracts and Compounds from Red Macroalgae Targeting Other Mechanisms of AV

The literature search on anti-sebum compounds or extracts from Rhodophyta, even when it comes to macroalgae in general, revealed a complete absence of published studies. Despite this fact, SEPPIC (La Garenne-Colombes, France), a cosmetic company, own red seaweed-incorporating products in the market claiming to possess anti-sebum properties. The incorporation of macroalgal extracts in the skincare line product WESOURCE (SEPPIC) revealed an anti-sebum effect (34% reduction after 56 days), observed when oily skinned volunteers were tested using CONTACTICEL™ (SEPPIC, La Garenne-Colombes, France) [199], a skin-care product that contained extracts from Acrochaetium moniliforme, a red seaweed product under the patent WO2016162648A1. Furthermore, similar results were obtained with a brown seaweed, revealing in vivo sebum regulation—29.3% lower sebum in 23 days—providing visible mattifying effects on volunteers subjected to Laminaria saccharina extract [199]. Because both cosmetic products are effective in the reduction of facial sebum, using active ingredients obtained from two macroalgae, despite no scientific publications being found, at least some red and brown seaweeds may be considered to have anti-sebum properties in vivo.

Hyperlipidaemia, a condition characterized by high levels of lipids in the blood, e.g., cholesterol, was associated with patients exhibiting acne. In accordance with this, high levels of triglycerides (TG), low-density lipoprotein cholesterol (LDL), and high-density lipoprotein cholesterol (HDL) were found in the blood of both male and female subjects [200,201]. A study by Liu et al. (2017) showed the improvement of carbohydrate and lipid metabolism in rats which were hyperlipidaemia-induced by high fructose (HF) intake, when fed with a Gelidium amansii-supplemented diet. Gelidium amansii supplementation resulted in the decrease of glucose, leptin, insulin, and TNF-α blood levels [202]. Moreover, it also reduced the accumulation of hepatic lipids, namely TG and the total cholesterol (TC) content, while increasing the excretion of bile acid and faecal lipids [202]. Further studies are required to prove Rhodophyta’s anti-hyperlipidaemia properties, but evidence already shows the potential of using this biomass to reduce the lipid levels in acne patients. A significant finding in this study, besides the clear improvement in lipid metabolism, lies in the fact that TNF-α rat blood levels decreased due to G. amansii supplementation, corroborating previous results in which algae extract reduced TNF-α, IL-1 and IL-6 levels in LPS-stimulated RAW264.7 [177]. Because TNF-α is known to have an important role in oxidative stress, and in the initiation of inflammatory and immunological processes [203,204] which are also involved in acne pathophysiology, G. amansii represents an opportunity to address multi targets of AV disease.

In order to the present the knowledge and data search criteria used, no scientific papers were found concerning red seaweed-derived compounds targeting acne-involved hormones, keratinization/cornification, or comedogenesis.

The anti-sebum property of red seaweeds is a relevant topic on the AV battle, because the disease is not observed in its absence. Being a precursor of the AV cascade, it is of utmost concern to study the potential of Rhodophyta, and also other macroalgae, to inhibit the hyperproduction of sebum, and how it may contribute to the avoidance of the stimulation of sebaceous glands.

5. Conclusions

Compounds found in macroalgal species are valuable for pharmaceuticals, cosmetics, feeds, and foods due to their valuable and recognized bioactive properties. Red macroalgal species are suitable candidates to the field of drug discovery, because they are abundant in fatty acids, pigments, phenolic compounds, and polysaccharides with therapeutic interest.

A literature revision on antibacterials that inhibit the growth of Cutibacterium acnes and Staphylococcus epidermidis found in the phylum Rhodophyta revealed a limited number of research papers, and more importantly, that a very large portion of Rhodophyta species remains unstudied for this purpose. Despite the relatively few reports, the available research showed that red seaweed possesses potent anti-C. acnes and S. epidermidis activity. On the contrary, the given number of studies concerning the anti-inflammatory capacity of isolated compounds and extracts, both in vitro and in vivo, revealed a significant potential for those macroalgae to be used in the mitigation of inflammatory pathways in AV. Unfortunately, there is as yet no published data concerning research on the other three AV pathophysiological targets (hormones, keratinization, or sebum), but some cosmetic anti-sebum products produced with macroalgae extracts are already in the market, confirming that at least some Rhodophyta compounds have anti-sebum properties, which should trigger further research into this topic. Red seaweed-derived compounds are the most studied in anti-inflammatory contexts, and on the contrary, there is as yet no knowledge related to AV-related hormones and comedogenesis. As we mentioned, and because AV pathophysiology is multi-factorial, there is a need to research the diversity of red algae compounds with antibacterial activity in acne-related bacteria, and to perform in vivo clinical trials of anti-inflammatory compounds in AV patients, in vitro assays to understand inhibition of hyperplasia by the compounds, and hormonal and comedogenesis evaluations to better understand the mechanisms of action.

Red seaweed derived compounds, namely polysaccharides, terpenoids, fatty acids, and phenolic compounds, represent good sources of antibacterial and anti-inflammatory compounds with the potential to be applied in acne vulgaris research for new treatments. In a pathology with great psychological and high-cost impacts in the society, those compounds represent the possibility to alleviate the consequences of the most prevalent skin disease.

Author Contributions

Conceptualization, A.P.J., R.F., C.F. and M.F.L.L.; methodology, R.F. and A.P.J.; investigation, A.P.J.; figure, J.R.; writing—original draft preparation, A.P.J. and R.F.; writing—review and editing, A.P.J., C.F., P.V. and M.F.L.L.; supervision, P.V. and M.F.L.L.; project administration, M.F.L.L.; funding acquisition, M.F.L.L. All authors have read and agreed to the published version of the manuscript.

Funding

This study had the support of the Fundação para a Ciência e a Tecnologia (FCT) Strategic Projects UID/MAR/04292/2020 and UIDB/50006/2020 granted to MARE and REQUIMTE, respectively; the grant awarded to A.P.J. (2020.08202.BD); and project MARINE INVADERS (POCI-01-0145-FEDER-031144). The authors also wish to acknowledge the support of the European Union through EASME Blue Labs project AMALIA, Algae-to-MArket Lab IdeAs (EASME/EMFF/2016/1.2.1.4/03/SI2.750419). The project was also partially funded by RDandT co-promotion project ORCHESTRA (POCI-01-0247-FEDER-070155) through COMPETE, Portugal 2020 and FCT, and COSMOS (MAR-04.03.01-FEAMP-0370) through GAL PESCA OESTE and MAR2020 in the framework of PORTUGAL2020 and the European Maritime and Fisheries Fund.

Conflicts of Interest

The authors declare no conflict of interest.

References

Adamski, Z.; Gornowicz-Porowska, J.; Sobkowska, D.; Kaszuba, K.; Czajkowski, R. Acne–Therapeutic challenges to the cooperation between a dermatologist and a cosmetologist. Adv. Dermatol. Allergol. 2021, 38, 21–31. [Google Scholar] [CrossRef]
Patel, D.J.; Bhatia, N. Oral Antibiotics for Acne. Am. J. Clin. Dermatol. 2021, 22, 193–204. [Google Scholar] [CrossRef]
Tan, J.; Bhate, K. A global perspective on the epidemiology of acne. Br. J. Dermatol. 2015, 172, 3–12. [Google Scholar] [CrossRef]
Aydemir, E.H. Acne vulgaris. Türk Pediatri Arşivi 2017, 49, 13–16. [Google Scholar] [CrossRef]
Kim, S.; Park, T.H.; Kim, W.I.; Park, S.; Kim, J.H.; Cho, M.K. The effects of green tea on acne vulgaris: A systematic review and meta-analysis of randomized clinical trials. Phytotherapy Res. 2021, 35, 374–383. [Google Scholar] [CrossRef]
Arora, M.K.; Yadav, A.; Saini, V. Role of hormones in acne vulgaris. Clin. Biochem. 2011, 44, 1035–1040. [Google Scholar] [CrossRef]
Greydanus, D.E.; Azmeh, R.; Cabral, M.D.; Dickson, C.A.; Patel, D.R. Acne in the first three decades of life: An update of a disorder with profound implications for all decades of life. Dis. Mon. 2021, 67, 101103. [Google Scholar] [CrossRef]
Adler, B.L.; Kornmehl, H.; Armstrong, A.W. Antibiotic Resistance in Acne Treatment. JAMA Dermatol. 2017, 153, 810–811. [Google Scholar] [CrossRef]
Karadag, A.S.; Kayıran, M.A.; Wu, C.; Chen, W.; Parish, L.C. Antibiotic resistance in acne: Changes, consequences and concerns. J. Eur. Acad. Dermatol. Venereol. 2021, 35, 73–78. [Google Scholar] [CrossRef] [PubMed]
Leyden, J.J.; del Rosso, J.Q.; Baum, E.W.; Mcguigan, K.A. The Use of Isotretinoin in the Treatment of Acne Vulgaris Clinical Considerations and Future Directions. J. Clin. Aesthetic Dermatol. 2014, 7, S3. [Google Scholar]
Tan, A.; Schlosser, B.; Paller, A. A review of diagnosis and treatment of acne in adult female patients. Int. J. Women’s Dermatol. 2018, 4, 56–71. [Google Scholar] [CrossRef]
Cotas, J.; Leandro, A.; Pacheco, D.; Gonçalves, A.M.M.; Pereira, L. A Comprehensive Review of the Nutraceutical and Therapeutic Applications of Red Seaweeds (Rhodophyta). Life 2020, 10, 19. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Hentati, F.; Tounsi, L.; Djomdi, D.; Pierre, G.; Delattre, C.; Ursu, A.V.; Fendri, I.; Abdelkafi, S.; Michaud, P. Bioactive Polysaccharides from Seaweeds. Molecules 2020, 25, 3152. [Google Scholar] [CrossRef]
Pereira, A.; Fraga-Corral, M.; Garcia-Oliveira, P.; Lourenço-Lopes, C.; Carpena, M.; Prieto, M.; Simal-Gandara, J. The Use of Invasive Algae Species as a Source of Secondary Metabolites and Biological Activities: Spain as Case-Study. Mar. Drugs 2021, 19, 178. [Google Scholar] [CrossRef]
Usov, A.I. Polysaccharides of the red algae. In Advances in Carbohydrate Chemistry and Biochemistry; Elsevier: Amsterdam, The Netherlands, 2011; Volume 65, pp. 115–217. [Google Scholar]
Lawrence, K.P.; Long, P.F.; Young, A.R. Mycosporine-Like Amino Acids for Skin Photoprotection. Curr. Med. Chem. 2019, 25, 5512–5527. [Google Scholar] [CrossRef] [PubMed]
Romay, C.; Gonzalez, R.; Ledon, N.; Remirez, D.; Rimbau, V. C-Phycocyanin: A Biliprotein with Antioxidant, Anti-Inflammatory and Neuroprotective Effects. Curr. Protein Pept. Sci. 2003, 4, 207–216. [Google Scholar] [CrossRef]
Eriksen, N.T. Production of phycocyanin—A pigment with applications in biology, biotechnology, foods and medicine. Appl. Microbiol. Biotechnol. 2008, 80, 1–14. [Google Scholar] [CrossRef] [PubMed]
Di Tomo, P.; Canali, R.; Ciavardelli, D.; Di Silvestre, S.; De Marco, A.; Giardinelli, A.; Pipino, C.; Di Pietro, N.; Virgili, F.; Pandolfi, A. β-Carotene and lycopene affect endothelial response to TNF-α reducing nitro-oxidative stress and interaction with monocytes. Mol. Nutr. Food Res. 2012, 56, 217–227. [Google Scholar] [CrossRef] [PubMed]
Jiang, Z.; Hama, Y.; Yamaguchi, K.; Oda, T. Inhibitory effect of sulphated polysaccharide porphyran on nitric oxide production in lipopolysaccharide-stimulated RAW264.7 macrophages. J. Biochem. 2011, 151, 65–74. [Google Scholar] [CrossRef] [Green Version]
Etahiri, S.; Bultel-Poncé, V.; Caux, C.; Guyot, M. New bromoditerpenes from the red alga Sphaerococcus coronopifolius. J. Nat. Prod. 2001, 64, 1024–1027. [Google Scholar] [CrossRef]
Darias, J.; Rovirosa, J.; Martin, A.S.; Díaz, A.-R.; Dorta, A.E.; Cueto, M. Furoplocamioids A–C, Novel Polyhalogenated Furanoid Monoterpenes from Plocamium cartilagineum. J. Nat. Prod. 2001, 64, 1383–1387. [Google Scholar] [CrossRef] [PubMed]
Barreto, M.; Meyer, J. Isolation and antimicrobial activity of a lanosol derivative from Osmundaria serrata (Rhodophyta) and a visual exploration of its biofilm covering. S. Afr. J. Bot. 2006, 72, 521–528. [Google Scholar] [CrossRef] [Green Version]
Kavita, K.; Singh, V.K.; Jha, B. 24-Branched Δ5 sterols from Laurencia papillosa red seaweed with antibacterial activity against human pathogenic bacteria. Microbiol. Res. 2014, 169, 301–306. [Google Scholar] [CrossRef]
Amorim, R.D.N.D.S.; Rodrigues, J.A.G.; Holanda, M.; Quinderé, A.L.G.; de Paula, R.; Melo, V.; Benevides, N.M.B. Antimicrobial effect of a crude sulfated polysaccharide from the red seaweed Gracilaria ornata. Braz. Arch. Biol. Technol. 2012, 55, 171–181. [Google Scholar] [CrossRef]
Stabili, L.; Acquaviva, M.; Biandolino, F.; Cavallo, R.; De Pascali, S.; Fanizzi, F.; Narracci, M.; Petrocelli, A.; Cecere, E. The lipidic extract of the seaweed Gracilariopsis longissima (Rhodophyta, Gracilariales): A potential resource for biotechnological purposes? New Biotechnol. 2012, 29, 443–450. [Google Scholar] [CrossRef]
Thiboutot, D.; Dréno, B.; Sanders, V.; Rueda, M.J.; Gollnick, H. Changes in the management of acne: 2009–2019. J. Am. Acad. Dermatol. 2020, 82, 1268–1269. [Google Scholar] [CrossRef] [PubMed]
Kurokawa, I.; Nakase, K. Recent advances in understanding and managing acne. F1000Research 2020, 9, 792. [Google Scholar] [CrossRef] [PubMed]
Zouboulis, C.C. Endocrinology and immunology of acne: Two sides of the same coin. Exp. Dermatol. 2020, 29, 840–859. [Google Scholar] [CrossRef]
Dawson, A.L.; Dellavalle, R. Acne vulgaris. BMJ 2013, 346, f2634. [Google Scholar] [CrossRef]
Araviiskaia, E.; Dréno, B. The role of topical dermocosmetics in acne vulgaris. J. Eur. Acad. Dermatol. Venereol. 2016, 30, 926–935. [Google Scholar] [CrossRef] [PubMed]
Bhat, Y.; Latief, I.; Hassan, I. Update on etiopathogenesis and treatment of Acne. Indian J. Dermatol. Venereol. Leprol. 2017, 83, 298–306. [Google Scholar] [CrossRef] [PubMed]
Beylot, C.; Auffret, N.; Poli, F.; Claudel, J.-P.; Leccia, M.; Del Giudice, P.; Dreno, B. Propionibacterium acnes: An update on its role in the pathogenesis of acne. J. Eur. Acad. Dermatol. Venereol. 2014, 28, 271–278. [Google Scholar] [CrossRef]
Dréno, B.; Pécastaings, S.; Corvec, S.; Veraldi, S.; Khammari, A.; Roques, C. Cutibacterium acnes(Propionibacterium acnes) and acne vulgaris: A brief look at the latest updates. J. Eur. Acad. Dermatol. Venereol. 2018, 32, 5–14. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Gollnick, H.P.M. From new findings in acne pathogenesis to new approaches in treatment. J. Eur. Acad. Dermatol. Venereol. 2015, 29, 1–7. [Google Scholar] [CrossRef] [PubMed]
Knutsen-Larson, S.; Dawson, A.L.; Dunnick, C.A.; Dellavalle, R. Acne Vulgaris: Pathogenesis, Treatment, and Needs Assessment. Dermatol. Clin. 2012, 30, 99–106. [Google Scholar] [CrossRef] [PubMed]
Li, X.; He, C.; Chen, Z.; Zhou, C.; Gan, Y.; Jia, Y. A review of the role of sebum in the mechanism of acne pathogenesis. J. Cosmet. Dermatol. 2017, 16, 168–173. [Google Scholar] [CrossRef]
Tuchayi, S.M.; Makrantonaki, E.; Ganceviciene, R.; Dessinioti, C.; Feldman, S.R.; Zouboulis, C.P.D. Acne vulgaris. Nat. Rev. Dis. Prim. 2015, 1, 1–20. [Google Scholar] [CrossRef]
Cappel, M. Correlation Between Serum Levels of Insulin-like Growth Factor 1, Dehydroepiandrosterone Sulfate, and Dihydrotestosterone and Acne Lesion Counts in Adult Women. Arch. Dermatol. 2005, 141, 333–338. [Google Scholar] [CrossRef]
Rocha, M.A.; Bagatin, E. Adult-onset acne: Prevalence, impact, and management challenges. Clin. Cosmet. Investig. Dermatol. 2018, 11, 59–69. [Google Scholar] [CrossRef] [Green Version]
Belgorosky, A.; Guercio, G.; Pepe, C.; Saraco, N.; Rivarola, M. Genetic and Clinical Spectrum of Aromatase Deficiency in Infancy, Childhood and Adolescence. Horm. Res. Paediatr. 2009, 72, 321–330. [Google Scholar] [CrossRef] [PubMed]
Makrantonaki, E.; Ganceviciene, R.; Zouboulis, C.C. An update on the role of the sebaceous gland in the pathogenesis of acne. Dermato. Endocrinol. 2011, 3, 41–49. [Google Scholar] [CrossRef] [Green Version]
Gao, W.; Bohl, C.E.; Dalton, J.T. Chemistry and Structural Biology of Androgen Receptor. Chem. Rev. 2005, 105, 3352–3370. [Google Scholar] [CrossRef] [Green Version]
Balachandrudu, B.; Niveditadevi, V.; Rani, T.P. Hormonal Pathogenesis of Acne–Simplified. Int. J. Sci. Study 2015, 3, 183–185. [Google Scholar] [CrossRef]
Hu, T.; Wei, Z.; Ju, Q.; Chen, W. Sex hormones and acne: State of the art. J. der Dtsch. Dermatol. Ges. 2021, 19, 509–515. [Google Scholar] [CrossRef] [PubMed]
Szöllősi, A.G.; Oláh, A.; Bíró, T.; Tóth, B.I. Recent advances in the endocrinology of the sebaceous gland. Dermato-Endocrinology 2017, 9, e1361576. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Melnik, B.C. Acne vulgaris: The metabolic syndrome of the pilosebaceous follicle. Clin. Dermatol. 2018, 36, 29–40. [Google Scholar] [CrossRef] [PubMed]
Bagatin, E.; De Freitas, T.H.P.; Rivitti-Machado, M.C.; Ribeiro, B.M.; Nunes, S.; Da Rocha, M.A.D. Adult female acne: A guide to clinical practice. An. Bras. de Dermatol. 2019, 94, 62–75. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Cole, T.; Ahmed, M.; Preece, M.; Hindmarsh, P.; Dunger, D. The relationship between Insulin-like Growth Factor 1, sex steroids and timing of the pubertal growth spurt. Clin. Endocrinol. 2015, 82, 862–869. [Google Scholar] [CrossRef] [Green Version]
Regidor, P.-A. The clinical relevance of progestogens in hormonal contraception: Present status and future developments. Oncotarget 2018, 9, 34628–34638. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Hammes, S.R.; Levin, E.R. Impact of estrogens in males and androgens in females. J. Clin. Investig. 2019, 129, 1818–1826. [Google Scholar] [CrossRef] [Green Version]
Lephart, E.D.; Naftolin, F. Menopause and the Skin: Old Favorites and New Innovations in Cosmeceuticals for Estrogen-Deficient Skin. Dermatol. Ther. 2021, 11, 53–69. [Google Scholar] [CrossRef] [PubMed]
Kanda, N.; Watanabe, S. 17β-estradiol Inhibits the Production of Interferon-induced Protein of 10kDa by Human Keratinocytes. J. Investig. Dermatol. 2003, 120, 411–419. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Shivers, K.-Y.; Amador, N.; Abrams, L.; Hunter, D.; Jenab, S.; Quiñones-Jenab, V. Estrogen alters baseline and inflammatory-induced cytokine levels independent from hypothalamic–pituitary–adrenal axis activity. Cytokine 2015, 72, 121–129. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Murphy, A.J.; Guyre, P.M.; Pioli, P.A. Estradiol Suppresses NF-κB Activation through Coordinated Regulation of let-7a and miR-125b in Primary Human Macrophages. J. Immunol. 2010, 184, 5029–5037. [Google Scholar] [CrossRef]
Rao, A.; Douglas, S.; Hall, J. Endocrine Disrupting Chemicals, Hormone Receptors, and Acne Vulgaris: A Connecting Hypothesis. Cells 2021, 10, 1439. [Google Scholar] [CrossRef]
Straub, R.H. The Complex Role of Estrogens in Inflammation. Endocr. Rev. 2007, 28, 521–574. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Tanghetti, E.A. The Role of Inflammation in the Pathology of Acne. J. Clin. Aesthetic Dermatol. 2013, 6, 27–35. [Google Scholar]
Clayton, R.; Göbel, K.; Niessen, C.; Paus, R.; Van Steensel, M.; Lim, X. Homeostasis of the sebaceous gland and mechanisms of acne pathogenesis. Br. J. Dermatol. 2019, 181, 677–690. [Google Scholar] [CrossRef]
Chen, F.; Hu, X.; Dong, K. Consistency changes of potential lipid markers in acne patients of different ages and their role in acne pathogenesis. J. Cosmet. Dermatol. 2021, 20, 2031–2035. [Google Scholar] [CrossRef]
Zouboulis, C.C.; Picardo, M.; Ju, Q.; Kurokawa, I.; Törőcsik, D.; Bíró, T.; Schneider, M.R. Beyond acne: Current aspects of sebaceous gland biology and function. Rev. Endocr. Metab. Disord. 2016, 17, 319–334. [Google Scholar] [CrossRef]
Zouboulis, C.; Jourdan, E.; Picardo, M. Acne is an inflammatory disease and alterations of sebum composition initiate acne lesions. J. Eur. Acad. Dermatol. Venereol. 2013, 28, 527–532. [Google Scholar] [CrossRef]
Bakry, O.A.; El Farargy, S.M.; Kady, N.N.E.D.E.; Abu Dawy, H.F. Immunohistochemical Expression of Cyclo-oxygenase 2 and Liver X Receptor-α in Acne Vulgaris. J. Clin. Diagn. Res. 2017, 11, WC01–WC07. [Google Scholar] [CrossRef] [PubMed]
Cong, T.-X.; Hao, D.; Wen, X.; Li, X.-H.; He, G.; Jiang, X. From pathogenesis of acne vulgaris to anti-acne agents. Arch. Dermatol. Res. 2019, 311, 337–349. [Google Scholar] [CrossRef] [PubMed]
Dréno, B.; Dagnelie, M.A.; Khammari, A.; Corvec, S. The Skin Microbiome: A New Actor in Inflammatory Acne. Am. J. Clin. Dermatol. 2020, 21, 18–24. [Google Scholar] [CrossRef] [PubMed]
Fournière, M.; Latire, T.; Souak, D.; Feuilloley, M.; Bedoux, G. Staphylococcus epidermidis and Cutibacterium acnes: Two Major Sentinels of Skin Microbiota and the Influence of Cosmetics. Microorg. 2020, 8, 1752. [Google Scholar] [CrossRef] [PubMed]
Claudel, J.-P.; Auffret, N.; Leccia, M.-T.; Poli, F.; Corvec, S.; Dréno, B. Staphylococcus epidermidis: A Potential New Player in the Physiopathology of Acne? Dermatology 2019, 235, 287–294. [Google Scholar] [CrossRef]
Mustarichie, R.; Sulistyaningsih, S.; Runadi, D. Antibacterial Activity Test of Extracts and Fractions of Cassava Leaves (Manihot esculenta Crantz) against Clinical Isolates of Staphylococcus epidermidis and Propionibacterium acnes Causing Acne. Int. J. Microbiol. 2020, 2020, 1975904. [Google Scholar] [CrossRef] [Green Version]
Mayslich, C.; Grange, P.; Dupin, N. Cutibacterium acnes as an Opportunistic Pathogen: An Update of Its Virulence-Associated Factors. Microorganisms 2021, 9, 303. [Google Scholar] [CrossRef]
Leyden, J. How does our increased understanding of the role of inflammation and innate immunity in acne impact treatment approaches? J. Dermatol. Treat. 2016, 27, 1. [Google Scholar] [CrossRef]
Harvey, A.; Huynh, T.T. Inflammation and acne: Putting the pieces together. J. drugs Dermatol. JDD 2014, 13, 459–463. [Google Scholar]
Abdi, F.; Kashani, H.H.; Naeini, F.F.; Narimani, T.; Khorvash, F. Staphylococcus aureus in acne pathogenesis: A case-control study. N. Am. J. Med Sci. 2012, 4, 573–576. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Al-Saif, S.S.A.-L.; Abdel-Raouf, N.; El-Wazanani, H.A.; Aref, I.A. Antibacterial substances from marine algae isolated from Jeddah coast of Red sea, Saudi Arabia. Saudi J. Biol. Sci. 2014, 21, 57–64. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Águila-Ramírez, R.N.; Arenas-gonzález, A.; Hernández-guerrero, C.J.; González-acosta, B.; Borges-souza, J.M.; Véron, B.; Pope, J.; Hellio, C. Antimicrobial and Antifouling Activities Achieved by Extracts of Seaweeds from Gulf of California, Mexico. Actividades Antimicrobiana y Anti-Incrustante Obtenidas de Los Extractos de Algas Marinas Del Golfo de California, México. Hidrobiologica 2012, 22, 8–15. [Google Scholar]
Bianco, É.M.; De Oliveira, S.Q.; Rigotto, C.; Tonini, M.L.; Guimarães, T.D.R.; Bittencourt, F.; Gouvêa, L.P.; Aresi, C.; De Almeida, M.T.R.; Moritz, M.I.G.; et al. Anti-Infective Potential of Marine Invertebrates and Seaweeds from the Brazilian Coast. Molecules 2013, 18, 5761–5778. [Google Scholar] [CrossRef] [Green Version]
Cardoso, I.; Cotas, J.; Rodrigues, A.; Ferreira, D.; Osório, N.; Pereira, L. Extraction and Analysis of Compounds with Antibacterial Potential from the Red Alga Grateloupia turuturu. J. Mar. Sci. Eng. 2019, 7, 220. [Google Scholar] [CrossRef] [Green Version]
Félix, C.; Félix, R.; Carmona, A.; Januário, A.; Dias, P.; Vicente, T.; Silva, J.; Alves, C.; Pedrosa, R.; Novais, S.; et al. Cosmeceutical Potential of Grateloupia turuturu: Using Low-Cost Extraction Methodologies to Obtain Added-Value Extracts. Appl. Sci. 2021, 11, 1650. [Google Scholar] [CrossRef]
Demirel, Z.; Yilmaz-Koz, F.F.; Karabay-Yavasoglu, N.U.; Ozdemir, G.; Sukatar, A. Antimicrobial and Antioxidant Activities of Solvent Extracts and the Essential Oil Composition of Laurencia Obtusa and Laurencia Obtusa Var. Pyramidata. Rom. Biotechnol. Lett. 2011, 16, 5927–5936. [Google Scholar]
Ertürk, Ö.; Tas, B. Antibacterial and Antifungal Effects of Some Marine Algae. Kafkas Univ. Vet. Fak. Derg. 2011, 17, 121–124. [Google Scholar]
Ghania, A.; Nabila, B.-B.; Larbi, B.; Elisabeth, M.; Philippe, G.; Mariem, B.; Khadidja, K.-K.; Wacila, B.-R.; Fawzia, A.-B. Antimicrobial and antiparasitic activities of three algae from the northwest coast of Algeria. Nat. Prod. Res. 2017, 33, 742–745. [Google Scholar] [CrossRef]
Pérez, M.J.; Falqué, E.; Domínguez, H. Antimicrobial Action of Compounds from Marine Seaweed. Mar. Drugs 2016, 14, 52. [Google Scholar] [CrossRef] [Green Version]
Ismail, M.M.; Alotaibi, B.S.; El-Sheekh, M.M. Therapeutic Uses of Red Macroalgae. Molecules 2020, 25, 4411. [Google Scholar] [CrossRef]
Choi, J.-S.; Bae, H.-J.; Kim, S.-J.; Choi, I.S. In vitro antibacterial and anti-inflammatory properties of seaweed extracts against acne inducing bacteria, Propionibacterium acnes. J. Environ. Biol. 2011, 32, 313–318. [Google Scholar] [PubMed]
Gribble, G.W. The natural production of organobromine compounds. Environ. Sci. Pollut. Res. 2000, 7, 37–49. [Google Scholar] [CrossRef]
Burreson, B.J.; Moore, R.E.; Roller, P.P. Volatile halogen compounds in the alga Asparagopsis taxiformis (Rhodophyta). J. Agric. Food Chem. 1976, 24, 856–861. [Google Scholar] [CrossRef]
Suzuki, M.; Takahashi, Y.; Nakano, S.; Abe, T.; Masuda, M.; Ohnishi, T.; Noya, Y.; Seki, K.-I. An experimental approach to study the biosynthesis of brominated metabolites by the red algal genus Laurencia. Phytochemistry 2009, 70, 1410–1415. [Google Scholar] [CrossRef] [Green Version]
Liu, M.; Hansen, P.E.; Lin, X. Bromophenols in Marine Algae and Their Bioactivities. Mar. Drugs 2011, 9, 1273–1292. [Google Scholar] [CrossRef] [Green Version]
Lee, K.W.; Heo, S.H.; Lee, J.; Park, S.I.; Kim, M.; Shin, M.S. Antimicrobial, Antioxidative, Elastase and Tyrosinase Inhibitory Effect of Supercritical and Hydrothermal Halopteris scoparia Extract. Turk. J. Comput. Math. Educ. (TURCOMAT) 2021, 12, 407–413. [Google Scholar] [CrossRef]
Blum, R.A.; Rodvold, K.A. Recognition and importance of Staphylococcus epidermidis infections. Clin. Pharm. 1987, 6, 464–475. [Google Scholar] [PubMed]
Lustigman, B.; Brown, C. Antibiotic production by marine algae isolated from the New York/New Jersey coast. Bull. Environ. Contam. Toxicol. 1991, 46, 329–335. [Google Scholar] [CrossRef] [PubMed]
Lever, J.; Curtis, G.; Brkljača, R.; Urban, S. Bromophenolics from the Red Alga Polysiphonia decipiens. Mar. Drugs 2019, 17, 497. [Google Scholar] [CrossRef] [Green Version]
De Rosa, S.; Kamenarska, Z.; Bankova, V.; Stefanov, K.; Dimitrova-Konaklieva, S.; Najdenski, H.; Tzevtkova, I.; Popov, S. Chemical Composition and Biological Activities of the Black Sea Algae Polysiphonia denudata (Dillw.) Kutz. and Polysiphonia denudata f. fragilis (Sperk) Woronich. Z. Nat. C 2001, 56, 1008–1014. [Google Scholar] [CrossRef] [Green Version]
Xu, N.; Fan, X.; Yan, X.; Li, X.; Niu, R.; Tseng, C. Antibacterial bromophenols from the marine red alga Rhodomela confervoides. Phytochemistry 2003, 62, 1221–1224. [Google Scholar] [CrossRef]
Katsui, N.; Suzuki, Y.; Kitamura, S.; Irie, T. 5,6-dibromoprotocatechualdehyde and 2,3-dibromo-4,5-dihydroxybenzyl methyl ether. Tetrahedron 1967, 23, 1185–1188. [Google Scholar] [CrossRef]
Harizani, M.; Ioannou, E.; Roussis, V. The Laurencia Paradox: An Endless Source of Chemodiversity. In Progress in the Chemistry of Organic Natural Products 112; Springer Science and Business Media: Cham, Switzerland, 2016; Volume 102, pp. 91–252. [Google Scholar]
Al-Massarani, S. Phytochemical and Biological Properties of Sesquiterpene Constituents From the Marine Red Seaweed Laurencia: A Review. Nat. Prod. Chem. Res. 2014, 2. [Google Scholar] [CrossRef]
Vairappan, C.S.; Kawamoto, T.; Miwa, H.; Suzuki, M. Potent Antibacterial Activity of Halogenated Compounds against Antibiotic-Resistant Bacteria. Planta Medica 2004, 70, 1087–1090. [Google Scholar] [CrossRef] [Green Version]
Félix, R.; Carmona, A.M.; Félix, C.; Novais, S.C.; Lemos, M.F.L. Industry-Friendly Hydroethanolic Extraction Protocols for Grateloupia turuturu UV-Shielding and Antioxidant Compounds. Appl. Sci. 2020, 10, 5304. [Google Scholar] [CrossRef]
De Alencar, D.B.; De Carvalho, F.C.T.; Rebouças, R.H.; Dos Santos, D.R.; Pires-Cavalcante, K.M.D.S.; De Lima, R.L.; Baracho, B.M.; Bezerra, R.M.; Viana, F.A.; Vieira, R.H.S.D.F.; et al. Bioactive extracts of red seaweeds Pterocladiella capillacea and Osmundaria obtusiloba (Floridophyceae: Rhodophyta) with antioxidant and bacterial agglutination potential. Asian Pac. J. Trop. Med. 2016, 9, 372–379. [Google Scholar] [CrossRef] [PubMed]
Lee, M.S.; Yim, M.; Lee, J.M.; Lee, D.; Kim, M. In Vitro Antimicrobial Activities of Edible Seaweeds Extracts Against Cuti-bacterium Acnes. Korean J. Fish. Aquat. Sci. 2021, 54, 111–117. [Google Scholar]
Bouarab-Chibane, L.; Forquet, V.; Lantéri, P.; Clément, Y.; Léonard-Akkari, L.; Oulahal, N.; Degraeve, P.; Bordes, C. Antibacterial Properties of Polyphenols: Characterization and QSAR (Quantitative Structure–Activity Relationship) Models. Front. Microbiol. 2019, 10, 829. [Google Scholar] [CrossRef]
Karpiński, T.M.; Adamczak, A. Fucoxanthin—An Antibacterial Carotenoid. Antioxidants 2019, 8, 239. [Google Scholar] [CrossRef] [Green Version]
Patra, J.K.; Das, G.; Baek, K.-H. Chemical Composition and Antioxidant and Antibacterial Activities of an Essential Oil Extracted from an Edible Seaweed, Laminaria japonica L. Molecules 2015, 20, 12093–12113. [Google Scholar] [CrossRef] [Green Version]
Gressler, V.; Stein, É.M.; Dorr, F.; Fujii, M.; Colepicolo, P.; Pinto, E. Sesquiterpenes from the essential oil of Laurencia dendroidea (Ceramiales, Rhodophyta): Isolation, biological activities and distribution among seaweeds. Rev. Bras. Farm. 2011, 21, 248–254. [Google Scholar] [CrossRef]
Nafis, A.; Khalloufi, F.E.; Aknaf, A.; Oudra, B.; Marraiki, N.; Al-Rashed, S.; Elgorban, A.M.; Syed, A.; Hassani, L.; Custódio, L. In Vitro Antimicrobial and Synergistic Effect of Essential Oil from the Red Macroalgae Centroceras Clavulatum (C. Agardh) Montagne with Conventional Antibiotics. Asian Pac. J. Trop. Biomed. 2021, 11, 414–420. [Google Scholar]
Pedrosa, R.; Gaudêncio, S.P.; Vasconcelos, V. XVI International Symposium on Marine Natural Products|XI European Conference on Marine Natural Products. Mar. Drugs. 2020, 18, 40. [Google Scholar] [CrossRef] [Green Version]
Kiran, G.S.; Manilal, A.; Sujith, S.; Selvin, J.; Shakir, C.; Lipton, A.P. Antimicrobial potential of marine organisms collected from the southwest coast of India against multiresistant human and shrimp pathogens. Sci. Mar. 2010, 74, 287–296. [Google Scholar] [CrossRef]
Vasconcelos, M.A.; Arruda, F.V.S.; Carneiro, V.A.; Silva, H.C.; Nascimento, K.S.; Sampaio, A.H.; Cavada, B.; Teixeira, E.H.; Henriques, M.; Pereira, M.O. Effect of Algae and Plant Lectins on Planktonic Growth and Biofilm Formation in Clinically Relevant Bacteria and Yeasts. BioMed Res. Int. 2014, 2014, 365272. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Shanmughapriya, S.; Manilal, A.; Sujith, S.; Selvin, J.; Kiran, G.S.; Natarajaseenivasan, K. Antimicrobial activity of seaweeds extracts against multiresistant pathogens. Ann. Microbiol. 2008, 58, 535–541. [Google Scholar] [CrossRef]
Tuney, I.; Cadirci, B.H.; Unal, D.; Sukatar, A. Locational and Organic Solvent Variation in Antimicrobial Activities of Crude Extracts of Marine Algae from the Coast of Izmir (Turkey). Fresenius Environ. Bull. 2007, 16, 428–434. [Google Scholar]
Karabay-Yavasoglu, N.U.; Sukatar, A.; Ozdemir, G.; Horzum, Z. Antimicrobial activity of volatile components and various extracts of the red algaJania rubens. Phytotherapy Res. 2007, 21, 153–156. [Google Scholar] [CrossRef] [PubMed]
Vairappan, C.S. Potent antibacterial activity of halogenated metabolites from Malaysian red algae, Laurencia majuscula (Rhodomelaceae, Ceramiales). Biomol. Eng. 2003, 20, 255–259. [Google Scholar] [CrossRef]
Bracegirdle, J.; Sohail, Z.; Fairhurst, M.J.; Gerth, M.L.; Zuccarello, G.C.; Hashmi, M.A.; Keyzers, R.A. Costatone C—A New Halogenated Monoterpene from the New Zealand Red Alga Plocamium angustum. Mar. Drugs 2019, 17, 418. [Google Scholar] [CrossRef] [Green Version]
He, X.; Yamauchi, A.; Nakano, T.; Yamaguchi, T.; Ochiai, Y. The composition and anti-inflammatory effect of polysaccharides from the red alga Chondrus verrucosus. Fish. Sci. 2019, 85, 859–865. [Google Scholar] [CrossRef]
Bhatia, S.; Sharma, K.; Sharma, A.; Nagpal, K.; Bers, T. Anti-inflammatory, Analgesic and Antiulcer properties of Porphyra vietnamensis. Avicenna J. Phytomedicine 2015, 5, 69–77. [Google Scholar]
Pereira, J.G.; Mesquita, J.X.; Aragão, K.S.; Franco, Á.X.; Souza, M.H.; Brito, T.V.; Dias, J.M.; Silva, R.O.; Medeiros, J.-V.R.; Oliveira, J.S.; et al. Polysaccharides isolated from Digenea simplex inhibit inflammatory and nociceptive responses. Carbohydr. Polym. 2014, 108, 17–25. [Google Scholar] [CrossRef]
Zou, Y.; Fu, X.; Liu, N.; Duan, D.; Wang, X.; Xu, J.; Gao, X. The synergistic anti-inflammatory activities of agaro-oligosaccharides with different degrees of polymerization. Environ. Boil. Fishes 2019, 31, 2547–2558. [Google Scholar] [CrossRef]
Hamias, R.; Wolak, T.; Huleihel, M.; Paran, E.; Levy-Ontman, O. Red alga polysaccharides attenuate angiotensin II-induced inflammation in coronary endothelial cells. Biochem. Biophys. Res. Commun. 2018, 500, 944–951. [Google Scholar] [CrossRef]
Jang, J.H.; So, B.R.; Yeo, H.J.; Kang, H.J.; Kim, M.J.; Lee, J.J.; Jung, S.K.; Jung, Y.H. Preparation of cellulose microfibril (CMF) from Gelidium amansii and feasibility of CMF as a cosmetic ingredient. Carbohydr. Polym. 2021, 257, 117569. [Google Scholar] [CrossRef] [PubMed]
So, B.R.; Yeo, H.J.; Lee, J.J.; Jung, Y.H.; Jung, S.K. Cellulose nanocrystal preparation from Gelidium amansii and analysis of its anti-inflammatory effect on the skin in vitro and in vivo. Carbohydr. Polym. 2021, 254, 117315. [Google Scholar] [CrossRef]
Batista, J.A.; Dias, E.G.; Brito, T.V.; Prudêncio, R.S.; Silva, R.O.; Ribeiro, R.A.; Souza, M.H.L.; de Paula, R.C.; Feitosa, J.P.; Chaves, L.S.; et al. Polysaccharide isolated from Agardhiella ramosissima: Chemical structure and anti-inflammation activity. Carbohydr. Polym. 2014, 99, 59–67. [Google Scholar] [CrossRef] [Green Version]
Vanderlei, E.D.S.O.; de Araújo, I.W.F.; Quinderé, A.L.G.; Fontes, B.P.; Eloy, Y.R.G.; Rodrigues, J.A.G.; e Silva, A.A.R.; Chaves, H.V.; Jorge, R.J.B.; de Menezes, D.B.; et al. The involvement of the HO-1 pathway in the anti-inflammatory action of a sulfated polysaccharide isolated from the red seaweed Gracilaria birdiae. Inflamm. Res. 2011, 60, 1121–1130. [Google Scholar] [CrossRef]
Chaves, L.D.S.; Nicolau, L.; Silva, R.O.; Barros, F.C.N.; Freitas, A.L.P.; Aragão, K.S.; Ribeiro, R.D.A.; Souza, M.H.L.P.; Barbosa, A.L.R.; Medeiros, J. Antiinflammatory and antinociceptive effects in mice of a sulfated polysaccharide fraction extracted from the marine red algaeGracilaria caudata. Immunopharmacol. Immunotoxicol. 2012, 35, 93–100. [Google Scholar] [CrossRef]
Coura, C.O.; De Araújo, I.W.F.; Vanderlei, E.S.O.; Rodrigues, J.A.G.; Quinderé, A.L.G.; Fontes, B.P.; De Queiroz, I.N.L.; De Menezes, D.B.; Bezerra, M.M.; E Silva, A.A.R.; et al. Antinociceptive and Anti-Inflammatory Activities of Sulphated Polysaccharides from the Red Seaweed Gracilaria cornea. Basic Clin. Pharmacol. Toxicol. 2011, 110, 335–341. [Google Scholar] [CrossRef]
de Brito, T.V.; Prudêncio, R.D.S.; Sales, A.B.; Júnior, F.D.C.V.; Candeira, S.J.N.; Franco, Á.X.; Aragão, K.S.; Ribeiro, R.D.A.; de Souza, M.H.L.P.; Chaves, L.D.S.; et al. Anti-inflammatory effect of a sulphated polysaccharide fraction extracted from the red algae Hypnea musciformis via the suppression of neutrophil migration by the nitric oxide signalling pathway. J. Pharm. Pharmacol. 2013, 65, 724–733. [Google Scholar] [CrossRef]
De Sousa, A.A.; Benevides, N.M.B.; Pires, A.D.F.; Fiuza, F.; Queiroz, M.G.; Morais, T.M.; Pereira, M.G.; Assreuy, A.M. A report of a galactan from marine algaGelidium crinalewith in vivo anti-inflammatory and antinociceptive effects. Fundam. Clin. Pharmacol. 2011, 27, 173–180. [Google Scholar] [CrossRef] [PubMed]
Cui, M.; Wu, J.; Wang, S.; Shu, H.; Zhang, M.; Liu, K.; Liu, K. Characterization and anti-inflammatory effects of sulfated polysaccharide from the red seaweed Gelidium pacificum Okamura. Int. J. Biol. Macromol. 2019, 129, 377–385. [Google Scholar] [CrossRef] [PubMed]
Araújo, I.W.F.; Chaves, H.V.; Pachêco, J.M.; Val, D.R.; Vieira, L.V.; Santos, R.; Freitas, R.S.; Rivanor, R.L.; Monteiro, V.S.; Clemente-Napimoga, J.; et al. Role of central opioid on the antinociceptive effect of sulfated polysaccharide from the red seaweed Solieria filiformis in induced temporomandibular joint pain. Int. Immunopharmacol. 2017, 44, 160–167. [Google Scholar] [CrossRef]
Makkar, F.; Chakraborty, K. Antidiabetic and Anti-inflammatory Potential of Sulphated Polygalactans from Red Seaweeds Kappaphycus Alvarezii and Gracilaria Opuntia. Int. J. Food Prop. 2017, 20, 1326–1337. [Google Scholar] [CrossRef] [Green Version]
Parker, K.H.; Beury, D.W.; Ostrand-Rosenberg, S. Myeloid-Derived Suppressor Cells: Critical Cells Driving Immune Sup-pression in the Tumor Microenvironment. In Advances in Cancer Research; Academic Press Inc.: Cambridge, MA, USA, 2015; Volume 128, pp. 95–139. ISBN 9780128023167. [Google Scholar]
Yang, Y.; Wei, Z.; Teichmann, A.T.; Wieland, F.H.; Wang, A.; Lei, X.; Zhu, Y.; Yin, J.; Fan, T.; Zhou, L.; et al. Development of a novel nitric oxide (NO) production inhibitor with potential therapeutic effect on chronic inflammation. Eur. J. Med. Chem. 2020, 193, 112216. [Google Scholar] [CrossRef] [PubMed]
Tanaka, T.; Narazaki, M.; Kishimoto, T. IL-6 in Inflammation, Immunity, and Disease. Cold Spring Harb. Perspect. Biol. 2014, 6, a016295. [Google Scholar] [CrossRef] [PubMed]
Zelová, H.; Hošek, J. TNF-α signalling and inflammation: Interactions between old acquaintances. Inflamm. Res. 2013, 62, 641–651. [Google Scholar] [CrossRef]
Wang, Y.; Hwang, J.-Y.; Park, H.-B.; Yadav, D.; Oda, T.; Jin, J.-O. Porphyran isolated from Pyropia yezoensis inhibits lipopolysaccharide-induced activation of dendritic cells in mice. Carbohydr. Polym. 2020, 229, 115457. [Google Scholar] [CrossRef]
Myers, M.J.; Deaver, C.M.; Lewandowski, A.J. Molecular mechanism of action responsible for carrageenan-induced inflammatory response. Mol. Immunol. 2019, 109, 38–42. [Google Scholar] [CrossRef] [PubMed]
Ghorbanzadeh, B.; Mansouri, M.T.; Hemmati, A.A.; Naghizadeh, B.; Mard, S.A.; Rezaie, A. A study of the mechanisms underlying the anti-inflammatory effect of ellagic acid in carrageenan-induced paw edema in rats. Indian J. Pharmacol. 2015, 47, 292–298. [Google Scholar] [CrossRef] [Green Version]
Yermak, I.M.; Sokolova, E.; Davydova, V.N.; Solov’Eva, T.F.; Aminin, D.L.; Reunov, A.V.; Lapshina, L.A. Influence of red algal polysaccharides on biological activities and supramolecular structure of bacterial lipopolysaccharide. Environ. Boil. Fishes 2016, 28, 619–627. [Google Scholar] [CrossRef]
Rocha, C.; Pacheco, D.; Cotas, J.; Marques, J.; Pereira, L.; Gonçalves, A. Seaweeds as Valuable Sources of Essential Fatty Acids for Human Nutrition. Int. J. Environ. Res. Public Health 2021, 18, 4968. [Google Scholar] [CrossRef]
Dang, H.T.; Lee, H.J.; Yoo, E.S.; Shinde, P.B.; Lee, Y.M.; Hong, J.; Kim, D.K.; Jung, J.H. Anti-inflammatory Constituents of the Red Alga Gracilaria verrucosa and Their Synthetic Analogues. J. Nat. Prod. 2008, 71, 232–240. [Google Scholar] [CrossRef] [PubMed]
Taciak, B.; Białasek, M.; Braniewska, A.; Sas, Z.; Sawicka, P.; Kiraga, Łukasz; Rygiel, T.; Król, M. Evaluation of phenotypic and functional stability of RAW 264.7 cell line through serial passages. PLoS ONE 2018, 13, e0198943. [Google Scholar] [CrossRef] [PubMed]
Chatter, R.; Ben Othman, R.; Rabhi, S.; Kladi, M.; Tarhouni, S.; Vagias, C.; Roussis, V.; Guizani-Tabbane, L.; Kharrat, R. In Vivo and in Vitro Anti-Inflammatory Activity of Neorogioltriol, a New Diterpene Extracted from the Red Algae Laurencia glandulifera. Mar. Drugs 2011, 9, 1293–1306. [Google Scholar] [CrossRef] [Green Version]
Chakraborty, K.; Antony, T. Salicornolides A-C from Gracilaria salicornia attenuate pro-inflammatory 5-lipoxygense: Prospective natural anti-inflammatory leads. Phytochemistry 2020, 172, 112259. [Google Scholar] [CrossRef]
Antony†, T.; Chakraborty†, K. First report of antioxidant abeo-labdane type diterpenoid from intertidal red seaweed Gracilaria salicornia with 5-lipoxygenase inhibitory potential. Nat. Prod. Res. 2018, 34, 1409–1416. [Google Scholar] [CrossRef]
Makkar, F.; Chakraborty, K. Highly oxygenated antioxidative 2H-chromen derivative from the red seaweed Gracilaria opuntia with pro-inflammatory cyclooxygenase and lipoxygenase inhibitory properties. Nat. Prod. Res. 2017, 32, 2756–2765. [Google Scholar] [CrossRef] [PubMed]
Makkar, F.; Chakraborty, K. Novel furanyl derivatives from the red seaweed Gracilaria opuntia with pharmacological activities using different in vitro models. Med. Chem. Res. 2018, 27, 1245–1259. [Google Scholar] [CrossRef]
Makkar, F.; Chakraborty, K. Previously undescribed antioxidative azocinyl morpholinone alkaloid from red seaweed Gracilaria opuntia with anti-cyclooxygenase and lipoxygenase properties. Nat. Prod. Res. 2017, 32, 1150–1160. [Google Scholar] [CrossRef]
Zhang, B.; Choi, Y.M.; Lee, J.; An, I.S.; Li, L.; He, C.; Dong, Y.; Bae, S.; Meng, H. Toll-like receptor 2 plays a critical role in pathogenesis of acne vulgaris. Biomed. Dermatol. 2019, 3, 4. [Google Scholar] [CrossRef]
Kim, J.M.; Choo, J.E.; Lee, H.J.; Kim, K.N.; Chang, S.E. Epidermal Growth Factor Attenuated the Expression of Inflammatory Cytokines in Human Epidermal Keratinocyte Exposed to Propionibacterium acnes. Ann. Dermatol. 2018, 30, 54. [Google Scholar] [CrossRef] [Green Version]
Kang, S.; Cho, S.; Chung, J.H.; Hammerberg, C.; Fisher, G.J.; Voorhees, J.J. Inflammation and Extracellular Matrix Degradation Mediated by Activated Transcription Factors Nuclear Factor-κB and Activator Protein-1 in Inflammatory Acne Lesions in Vivo. Am. J. Pathol. 2005, 166, 1691–1699. [Google Scholar] [CrossRef]
Kazłowska, K.; Hsu, T.; Hou, C.-C.; Yang, W.-C.; Tsai, G.-J. Anti-inflammatory properties of phenolic compounds and crude extract from Porphyra dentata. J. Ethnopharmacol. 2010, 128, 123–130. [Google Scholar] [CrossRef]
Becker, K.; Hartmann, A.; Ganzera, M.; Fuchs, D.; Gostner, J.M. Immunomodulatory Effects of the Mycosporine-Like Amino Acids Shinorine and Porphyra-334. Mar. Drugs 2016, 14, 119. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Kim, I.-H.; Kwon, M.-J.; Jung, J.-H.; Nam, T.-J. Protein extracted from Porphyra yezoensis prevents cisplatin-induced nephrotoxicity by downregulating the MAPK and NF-κB pathways. Int. J. Mol. Med. 2017, 41, 511–520. [Google Scholar] [CrossRef]
Ying, R.; Zhang, Z.; Zhu, H.; Li, B.; Hou, H. The Protective Effect of Mycosporine-Like Amino Acids (MAAs) from Porphyra yezoensis in a Mouse Model of UV Irradiation-Induced Photoaging. Mar. Drugs 2019, 17, 470. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Kim, N.H.; Kim, M.E.; Lee, J.S. Inhibitory Effects of Extract from G. lanceolata on LPS-Induced Production of Nitric Oxide and IL-1β via Down-regulation of MAPK in Macrophages. Appl. Biochem. Biotechnol. 2014, 175, 657–665. [Google Scholar] [CrossRef]
Ko, E.-Y.; Heo, S.-J.; Cho, S.-H.; Lee, W.; Kim, S.-Y.; Yang, H.-W.; Ahn, G.; Cha, S.-H.; Kwon, S.-H.; Jeong, M.S.; et al. 3-Bromo-5-(ethoxymethyl)-1,2-benzenediol inhibits LPS-induced pro-inflammatory responses by preventing ROS production and downregulating NF-κB in vitro and in a zebrafish model. Int. Immunopharmacol. 2019, 67, 98–105. [Google Scholar] [CrossRef] [PubMed]
Ha, Y.; Lee, W.-H.; Jeong, J.; Park, M.; Ko, J.-Y.; Kwon, O.W.; Lee, J.; Kim, Y.-J. Pyropia yezoensis Extract Suppresses IFN-Gamma- and TNF-Alpha-Induced Proinflammatory Chemokine Production in HaCaT Cells via the Down-Regulation of NF-κB. Nutrients 2020, 12, 1238. [Google Scholar] [CrossRef] [PubMed]
Lee, D.; Nishizawa, M.; Shimizu, Y.; Saeki, H. Anti-inflammatory effects of dulse (Palmaria palmata) resulting from the simultaneous water-extraction of phycobiliproteins and chlorophyll a. Food Res. Int. 2017, 100, 514–521. [Google Scholar] [CrossRef]
Millan-Linares, M.C.; Martín, N.M.R.; Rodriguez, N.M.; Toscano, R.; Claro, C.; Bermudez, B.; Pedroche, J.; Millan, F.; La Paz, S.M.-D. Nutraceutical Extract from Dulse (Palmaria palmata L.) Inhibits Primary Human Neutrophil Activation. Mar. Drugs 2019, 17, 610. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Robertson, R.C.; Guihéneuf, F.; Bahar, B.; Schmid, M.; Stengel, D.B.; Fitzgerald, G.F.; Ross, R.; Stanton, C. The Anti-Inflammatory Effect of Algae-Derived Lipid Extracts on Lipopolysaccharide (LPS)-Stimulated Human THP-1 Macrophages. Mar. Drugs 2015, 13, 5402–5424. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Lee, H.-A.; Kim, I.-H.; Nam, T.-J. Bioactive peptide from Pyropia yezoensis and its anti-inflammatory activities. Int. J. Mol. Med. 2015, 36, 1701–1706. [Google Scholar] [CrossRef] [Green Version]
Yang, E.-J.; Moon, J.-Y.; Kim, M.-J.; Kim, D.S.; Kim, C.-S.; Lee, W.J.; Lee, N.H.; Hyun, C.-G. Inhibitory effect of Jeju endemic seaweeds on the production of pro-inflammatory mediators in mouse macrophage cell line RAW 264.7. J. Zhejiang Univ. Sci. B 2010, 11, 315–322. [Google Scholar] [CrossRef] [Green Version]
Aragao, G.F.; Nonato, D.T.T.; Da Ponta, E.L.; Sales, J.R.; Alencar, D.B.; Sampaio, S.S.; Chaves, E.M.C.; Assreuy, A.M.S. Protective effects of ethanolic extract from the red algae Amansia multifida on experimental inflammation, nociception and seizure experimental models. Acta Sci. Biol. Sci. 2016, 38, 465–471. [Google Scholar] [CrossRef] [Green Version]
Mesquita, J.X.; de Brito, T.V.; Fontenelle, T.P.C.; Damasceno, R.O.S.; de Souza, M.H.L.P.; Lopes, J.L.D.S.; Beltramini, L.M.; Barbosa, A.L.D.R.; Freitas, A.L.P. Lectin from red algae Amansia multifida Lamouroux: Extraction, characterization and anti-inflammatory activity. Int. J. Biol. Macromol. 2021, 170, 532–539. [Google Scholar] [CrossRef]
Yasmeen, A.; Ibrahim, M.; ul Hasan, M.M.; Jilani, T.; Shafique, S.; Rasheed, M. Phycochemical Analyses and Pharmacological Activities of Seven Macroalgae of Arabian Sea (Northern Coast Line). Pak. J. Pharm. Sci. 2021, 34, 963–969. [Google Scholar] [CrossRef]
Abu Bakar, N.A.; Anyanji, V.U.; Mustapha, N.M.; Lim, S.-L.; Mohamed, S. Seaweed (Eucheuma cottonii) reduced inflammation, mucin synthesis, eosinophil infiltration and MMP-9 expressions in asthma-induced rats compared to Loratadine. J. Funct. Foods 2015, 19, 710–722. [Google Scholar] [CrossRef]
Shih, C.-C.; Hwang, H.-R.; Chang, C.-I.; Su, H.-M.; Chen, P.-C.; Kuo, H.-M.; Li, P.-J.; Tsui, K.-H.; Lin, Y.-C.; Huang, S.-Y.; et al. Anti-Inflammatory and Antinociceptive Effects of Ethyl Acetate Fraction of an Edible Red Macroalgae Sarcodia ceylanica. Int. J. Mol. Sci. 2017, 18, 2437. [Google Scholar] [CrossRef] [Green Version]
Abreu, T.M.; Ribeiro, N.A.; Chaves, H.V.; Jorge, R.J.B.; Bezerra, M.M.; Monteiro, H.S.A.; Vasconcelos, I.M.; Mota, É.F.; Benevides, N.M.B. Antinociceptive and Anti-inflammatory Activities of the Lectin from Marine Red Alga Solieria filiformis. Planta Medica 2016, 82, 596–605. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Bringel, P.H.D.S.F.; Marques, G.F.O.; Martins, M.G.D.Q.; Da Silva, M.T.L.; Nobre, C.A.S.; Nascimento, K.S.D.; Cavada, B.S.; Castro, R.R.; Assreuy, A.M.S. The Lectin Isolated from the Alga Hypnea cervicornis Promotes Antinociception in Rats Subjected to Zymosan-Induced Arthritis: Involvement of cGMP Signalization and Cytokine Expression. Inflammation 2020, 43, 1446–1454. [Google Scholar] [CrossRef]
Fontenelle, T.P.C.; Lima, G.C.; Mesquita, J.X.; Lopes, J.; de Brito, T.V.; Júnior, F.D.C.V.; Sales, A.B.; Aragão, K.S.; Souza, M.H.L.P.; Barbosa, A.L.D.R.; et al. Lectin obtained from the red seaweed Bryothamnion triquetrum: Secondary structure and anti-inflammatory activity in mice. Int. J. Biol. Macromol. 2018, 112, 1122–1130. [Google Scholar] [CrossRef] [PubMed]
Silva, L.M.C.M.; Lima, V.; Holanda, M.; Pinheiro, P.G.; Rodrigues, J.A.G.; Lima, M.E.P.; Benevides, N.M.B. Antinociceptive and Anti-inflammatory Activities of Lectin from Marine Red Alga Pterocladiella capillacea. Biol. Pharm. Bull. 2010, 33, 830–835. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Julião, D.R.; Afonso, C.; Gomes-Bispo, A.; Bandarra, N.M.; Cardoso, C. The effect of drying on undervalued brown and red seaweed species: Bioactivity alterations. Phycol. Res. 2021, 69, 246–257. [Google Scholar] [CrossRef]
Regal, A.L.; Alves, V.D.; Gomes, R.; Matos, J.; Bandarra, N.M.; Afonso, C.; Cardoso, C. Drying process, storage conditions, and time alter the biochemical composition and bioactivity of the anti-greenhouse seaweed Asparagopsis taxiformis. Eur. Food Res. Technol. 2020, 246, 781–793. [Google Scholar] [CrossRef]
Grünewald, N.; Groth, I.; Alban, S. Evaluation of Seasonal Variations of the Structure and Anti-inflammatory Activity of Sulfated Polysaccharides Extracted from the Red Alga Delesseria sanguinea (Hudson) Lamouroux (Ceramiales, Delesseriaceae). Biomacromolecules 2009, 10, 1155–1162. [Google Scholar] [CrossRef]
Delgado, N.G.; Vázquez, A.I.F.; Sánchez, H.C.; Del Valle, R.M.S.; Gómez, Y.S.; Alfonso, A.M.S. Anti-inflammatory and antinociceptive activities of methanolic extract from red seaweed Dichotomaria obtusata. Braz. J. Pharm. Sci. 2013, 49, 65–74. [Google Scholar] [CrossRef] [Green Version]
Vázquez, A.I.; Sánchez, C.M.; Delgado, G.; María, A.; Alfonso, S.; Ortega, Y.; Sánchez, H. Anti-Inflammatory and Analgesic Activities of Red Seaweed Dichotomaria Obtusata. Artic. Braz. J. Pharm. Sci. 2011, 47, 111–118. [Google Scholar]
Balasubramaniam, V.; Lee, J.C.; Noh, M.F.M.; Ahmad, S.; Brownlee, I.A.; Ismail, A. Alpha-amylase, antioxidant, and anti-inflammatory activities of Eucheuma denticulatum (N.L. Burman) F.S. Collins and Hervey. Environ. Boil. Fishes 2015, 28, 1965–1974. [Google Scholar] [CrossRef]
Wang, M.-L.; Hou, Y.-Y.; Chiu, Y.-S.; Chen, Y.-H. Immunomodulatory activities of Gelidium amansii gel extracts on murine RAW 264.7 macrophages. J. Food Drug Anal. 2013, 21, 397–403. [Google Scholar] [CrossRef] [Green Version]
Matos, J.; Gomes, A.; Cardoso, C.; Afonso, C.; Campos, A.M.; Gomes, R.; Falé, P.; Delgado, I.; Coelho, I.; Castanheira, I.; et al. Commercial Red Seaweed in Portugal (Gelidium sesquipedale and Pterocladiella capillacea, Florideophyceae): Going beyond a Single-Purpose Product Approach by Valorizing Bioactivity. Thalass. Int. J. Mar. Sci. 2020, 36, 213–224. [Google Scholar] [CrossRef]
Shu, M.-H.; Appleton, D.; Zandi, K.; Abubakar, S. Anti-inflammatory, gastroprotective and anti-ulcerogenic effects of red algae Gracilaria changii (Gracilariales, Rhodophyta) extract. BMC Complement. Altern. Med. 2013, 13, 61. [Google Scholar] [CrossRef] [Green Version]
Antony, T.; Chakraborty, K. First report of antioxidative 2H-chromenyl derivatives from the intertidal red seaweed Gracilaria salicornia as potential anti-inflammatory agents. Nat. Prod. Res. 2020, 34, 3470–3482. [Google Scholar] [CrossRef]
Da Costa, E.; Melo, T.; Moreira, A.S.P.; Bernardo, C.; Helguero, L.; Ferreira, I.; Cruz, M.T.; Rego, A.M.; Domingues, P.; Calado, R.; et al. Valorization of Lipids from Gracilaria sp. through Lipidomics and Decoding of Antiproliferative and Anti-Inflammatory Activity. Mar. Drugs 2017, 15, 62. [Google Scholar] [CrossRef] [Green Version]
Ver, M.M.; Wiraw, I.G.P.; Jawi, I.M.; Sritamin, M.; Dewi, N.N.A.; Mirah, A.A.A. Anti-inflammatory Effect of Red Macroalgae Bulung Sangu (Gracilaria sp.) Extract in UVB-Irradiated Mice. Pak. J. Biol. Sci. 2021, 24, 80–89. [Google Scholar] [CrossRef]
da Costa, E.; Melo, T.; Reis, M.; Domingues, P.; Calado, R.; Abreu, M.; Domingues, M. Polar Lipids Composition, Antioxidant and Anti-Inflammatory Activities of the Atlantic Red Seaweed Grateloupia turuturu. Mar. Drugs 2021, 19, 414. [Google Scholar] [CrossRef]
Ferreira, J.; Hartmann, A.; Martins-Gomes, C.; Nunes, F.M.; Souto, E.B.; Santos, D.L.; Abreu, H.; Pereira, R.; Pacheco, M.; Gaivão, I.; et al. Red seaweeds strengthening the nexus between nutrition and health: Phytochemical characterization and bioactive properties of Grateloupia turuturu and Porphyra umbilicalis extracts. Environ. Boil. Fishes 2021, 33, 3365–3381. [Google Scholar] [CrossRef]
Figueiredo, J.G.; Bitencourt, F.S.; Cunha, T.M.; Luz, P.B.; Nascimento, K.S.; Mota, M.R.; Sampaio, A.H.; Cavada, B.S.; Cunha, F.Q.; Alencar, N.M. Agglutinin isolated from the red marine alga Hypnea cervicornis J. Agardh reduces inflammatory hypernociception: Involvement of nitric oxide. Pharmacol. Biochem. Behav. 2010, 96, 371–377. [Google Scholar] [CrossRef]
Makkar, F.; Chakraborty, K. Unprecedented antioxidative cyclic ether from the red seaweed Kappaphycus alvarezii with anti-cyclooxygenase and lipoxidase activities. Nat. Prod. Res. 2017, 31, 1131–1141. [Google Scholar] [CrossRef] [PubMed]
Makkar, F.; Chakraborty, K. Antioxidant and anti-inflammatory oxygenated meroterpenoids from the thalli of red seaweed Kappaphycus alvarezii. Med. Chem. Res. 2018, 27, 2016–2026. [Google Scholar] [CrossRef]
Makkar, F.; Chakraborty, K. First report of dual cyclooxygenase-2 and 5-lipoxygenase inhibitory halogen derivatives from the thallus of intertidal seaweed Kappaphycus alvarezii. Med. Chem. Res. 2018, 27, 2331–2340. [Google Scholar] [CrossRef]
Wijesinghe, W.; Kim, E.-A.; Kang, M.-C.; Lee, W.-W.; Lee, H.-S.; Vairappan, C.S.; Jeon, Y.-J. Assessment of anti-inflammatory effect of 5β-hydroxypalisadin B isolated from red seaweed Laurencia snackeyi in zebrafish embryo in vivo model. Environ. Toxicol. Pharmacol. 2014, 37, 110–117. [Google Scholar] [CrossRef] [PubMed]
Rezende, B.M.; Bernardes, P.T.T.; Resende, C.B.; Arantes, R.M.E.; Souza, D.G.; Braga, F.C.; Castor, M.G.M.; Teixeira, M.M.; Pinho, V. Lithothamnion muelleri Controls Inflammatory Responses, Target Organ Injury and Lethality Associated with Graft-versus-Host Disease in Mice. Mar. Drugs 2013, 11, 2595–2615. [Google Scholar] [CrossRef] [Green Version]
Banskota, A.H.; Stefanova, R.; Sperker, S.; Lall, S.P.; Craigie, J.S.; Hafting, J.T.; Critchley, A. Polar lipids from the marine macroalga Palmaria palmata inhibit lipopolysaccharide-induced nitric oxide production in RAW264.7 macrophage cells. Phytochemistry 2014, 101, 101–108. [Google Scholar] [CrossRef]
Choi, Y.K.; Ye, B.-R.; Kim, E.-A.; Kim, J.; Kim, M.-S.; Lee, W.W.; Ahn, G.-N.; Kang, N.; Jung, W.-K.; Heo, S.-J. Bis (3-bromo-4,5-dihydroxybenzyl) ether, a novel bromophenol from the marine red alga Polysiphonia morrowii that suppresses LPS-induced inflammatory response by inhibiting ROS-mediated ERK signaling pathway in RAW 264.7 macrophages. Biomed. Pharmacother. 2018, 103, 1170–1177. [Google Scholar] [CrossRef]
Cian, R.E.; López-Posadas, R.; Drago, S.R.; de Medina, F.S.; Martínez-Augustin, O. Immunomodulatory Properties of the Protein Fraction from Phorphyra columbina. J. Agric. Food Chem. 2012, 60, 8146–8154. [Google Scholar] [CrossRef]
Senevirathne, M.; Ahn, C.-B.; Je, J.-Y. Enzymatic extracts from edible red algae, Porphyra tenera, and their antioxidant, anti-acetylcholinesterase, and anti-inflammatory activities. Food Sci. Biotechnol. 2010, 19, 1551–1557. [Google Scholar] [CrossRef]
Bergé, J.P.; Debiton, E.; Dumay, J.; Durand, P.; Barthomeuf, C. In Vitro Anti-inflammatory and Anti-proliferative Activity of Sulfolipids from the Red Alga Porphyridium cruentum. J. Agric. Food Chem. 2002, 50, 6227–6232. [Google Scholar] [CrossRef] [PubMed]
Matsui, M.S.; Muizzuddin, N.; Arad, S.; Marenus, K. Sulfated Polysaccharides from Red Microalgae Have Antiinflammatory Properties In Vitro and In Vivo. Appl. Biochem. Biotechnol. 2003, 104, 13–22. [Google Scholar] [CrossRef]
Abreu, T.M.; Silva, L.M.C.M.; Vanderlei, E.S.O.; De Melo, C.M.L.; Pereira, V.R.A.; Benevides, N.M.B. Cytokine production induced by marine algae lectins in BALB/c mice splenocytes. Protein Pept. Lett. 2012, 19, 975–981. [Google Scholar] [CrossRef] [PubMed]
Wiemer, D.F.; Idler, D.D.; Fenical, W. Vidalols A and B, new anti-inflammatory bromophenols from the Caribbean marine red algaVidalia obtusaloba. Cell. Mol. Life Sci. 1991, 47, 851–853. [Google Scholar] [CrossRef] [PubMed]
Gillon, L.-A. WESOURCE—Active Science to Empower Beauty. From the Sea to the Skin—How Algae Adaptations Benefit Skin & Hair? Available online: https://www.flickr.com/photos/fotoosvanrobin/3644416895 (accessed on 27 September 2021).
Sobhan, M.; Rabiei, M.A.S.; Amerifar, M. Correlation Between Lipid Profile and Acne Vulgaris. Clin. Cosmet. Investig. Dermatol. 2020, 13, 67–71. [Google Scholar] [CrossRef]
Jiang, H.; Li, C.Y.; Zhou, L.; Lu, B.; Lin, Y.; Huang, X.; Wei, B.; Wang, Q.; Wang, L.; Lu, J.; et al. Acne patients frequently associated with abnormal plasma lipid profile. J. Dermatol. 2015, 42, 296–299. [Google Scholar] [CrossRef] [Green Version]
Liu, H.-C.; Chang, C.-J.; Yang, T.-H.; Chiang, M.-T. Long-term feeding of red algae (Gelidium amansii) ameliorates glucose and lipid metabolism in a high fructose diet-impaired glucose tolerance rat model. J. Food Drug Anal. 2016, 25, 543–549. [Google Scholar] [CrossRef] [Green Version]
Young, C.N.; Koepke, J.I.; Terlecky, L.J.; Borkin, M.S.; Boyd, S.L.; Terlecky, S.R. Reactive Oxygen Species in Tumor Necrosis Factor-α-Activated Primary Human Keratinocytes: Implications for Psoriasis and Inflammatory Skin Disease. J. Investig. Dermatol. 2008, 128, 2606–2614. [Google Scholar] [CrossRef] [Green Version]
Chen, X.; Andresen, B.; Hill, M.; Zhang, J.; Booth, F.; Zhang, C. Role of Reactive Oxygen Species in Tumor Necrosis Factor-alpha Induced Endothelial Dysfunction. Curr. Hypertens. Rev. 2008, 4, 245–255. [Google Scholar] [CrossRef] [Green Version]

Figure 1. Acne vulgaris pathophysiology process schematics. (I) Pilosebaceous unit in normal conditions; (II) hormonal imbalance triggers seborrhea; (III) comedogenesis; (IV) microbial proliferation and inflammatory mediators’ release; (V) immune response followed by inflammation. The arrows represent the interplay between triggers.

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

Share and Cite

MDPI and ACS Style

Januário, A.P.; Félix, R.; Félix, C.; Reboleira, J.; Valentão, P.; Lemos, M.F.L. Red Seaweed-Derived Compounds as a Potential New Approach for Acne Vulgaris Care. Pharmaceutics 2021, 13, 1930. https://doi.org/10.3390/pharmaceutics13111930

AMA Style

Januário AP, Félix R, Félix C, Reboleira J, Valentão P, Lemos MFL. Red Seaweed-Derived Compounds as a Potential New Approach for Acne Vulgaris Care. Pharmaceutics. 2021; 13(11):1930. https://doi.org/10.3390/pharmaceutics13111930

Chicago/Turabian Style

Januário, Adriana P., Rafael Félix, Carina Félix, João Reboleira, Patrícia Valentão, and Marco F. L. Lemos. 2021. "Red Seaweed-Derived Compounds as a Potential New Approach for Acne Vulgaris Care" Pharmaceutics 13, no. 11: 1930. https://doi.org/10.3390/pharmaceutics13111930

APA Style

Januário, A. P., Félix, R., Félix, C., Reboleira, J., Valentão, P., & Lemos, M. F. L. (2021). Red Seaweed-Derived Compounds as a Potential New Approach for Acne Vulgaris Care. Pharmaceutics, 13(11), 1930. https://doi.org/10.3390/pharmaceutics13111930

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Menu

Red Seaweed-Derived Compounds as a Potential New Approach for Acne Vulgaris Care

Abstract

1. Introduction

2. Research Methodology

3. Pathophysiological Targets for the Management of Acne Vulgaris

3.1. Hormonal Influence

3.2. Seborrhoea

3.3. Comedogenesis

3.4. Microbial Proliferation

3.5. Inflammatory Response

4. Seaweed Extracts and Compounds to Address AV Disease

4.1. Antibacterials from Red Macroalgae

4.2. Anti-Inflammatory Extracts and Compounds from Red Macroalgae

4.3. Extracts and Compounds from Red Macroalgae Targeting Other Mechanisms of AV

5. Conclusions

Author Contributions

Funding

Conflicts of Interest

References

Share and Cite

Article Metrics

Article Access Statistics

Further Information

Guidelines

MDPI Initiatives

Follow MDPI