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Review

Humulus lupulus L. as a Natural Source of Functional Biomolecules

by
Gonzalo Astray
1,
Patricia Gullón
2,
Beatriz Gullón
3,
Paulo E. S. Munekata
4 and
José M. Lorenzo
4,5,*
1
Department of Physical Chemistry, Faculty of Science, University of Vigo (Campus Ourense), As Lagoas, 32004 Ourense, Spain
2
Nutrition and Bromatology Group, Department of Analytical and Food Chemistry, Faculty of Food Science and Technology, University of Vigo, Ourense Campus, 32004 Ourense, Spain
3
Department of Chemical Engineering, Faculty of Science, University of Vigo (Campus Ourense), As Lagoas, 32004 Ourense, Spain
4
Centro Tecnológico de la Carne de Galicia, Rúa Galicia Nº 4, Parque Tecnológico de Galicia, San Cibrao das Viñas, 32900 Ourense, Spain
5
Área de Tecnología de los Alimentos, Facultad de Ciencias de Ourense, Universidad de Vigo, 32004 Ourense, Spain
*
Author to whom correspondence should be addressed.
Appl. Sci. 2020, 10(15), 5074; https://doi.org/10.3390/app10155074
Submission received: 30 June 2020 / Revised: 20 July 2020 / Accepted: 21 July 2020 / Published: 23 July 2020
(This article belongs to the Special Issue Natural Antimicrobial Preservatives)
Browse Figure
Versions Notes

Abstract

:
Hops (Humulus lupulus L.) are used traditionally in the brewing industry to confer bitterness, aroma, and flavor to beer. However, in recent years, it has been reported that female inflorescences contain a huge variety of bioactive compounds. Due to the growing interest of the consumers by natural ingredients, intense research has been carried out in the last years to find new sources of functional molecules. This review collects the works about the bioactive potential of hops with applications in the food, pharmaceutical, or cosmetic industries. Moreover, an overview of the main extraction technologies to recover biomolecules from hops is shown. Bioactivities of hop extracts such as antibacterial, antifungal, cardioprotective, antioxidant, anti-inflammatory, anticarcinogenic, and antiviral are also summarized. It can be concluded that hops present a high potential of bioactive ingredients with high quality that can be used as preservative agents in fresh foods, extending their shelf life, and they can be incorporated in cosmetic formulation for skincare as well.

1. Introduction

The common hop plant (Humulus lupulus L.) is a hardy and dioecious vine whose aerial part is herbaceous and annual, while the rootstock is perennial, and it can create adventitious roots every year [1]. It is a species of the genus Humulus that belongs to the Cannabaceae family whose genus origin could be China [2]. It can be found principally in European and in Western Asia deciduous forests and thickets, and in other zone areas with a temperate climate [3]. Hops were cultivated in Babylon around 200 A.D. [4], and they have been in ongoing use for centuries (even a millennium) mainly as a beer ingredient [5]. In the European Union, the main producer is Germany, registering for 2018 a production of 41,792 tons for a total of 57,239 tons from the member states [6]. The hop cones are the most utilized portion of this plant [2]; nevertheless, there are parts such as the young shoots or asparagus that can be eaten in different Mediterranean countries [7].
In the last decades, the biological benefits of plants, traditionally used in folk and/or traditional medicine, have been explored by the scientific world [5,8]. In this sense, besides their use in the brewing industry, traditionally hop cones have been applied with medical purposes for the control of the spasms, anxiety, fever, inflammation, activation of the gastric function, and the treatment of sleeping disorders, among others [2,9]. Indeed, hops present numerous benefits for human health due to their antibacterial, antifungal, cardioprotective, antioxidant, anti-inflammatory, anticarcinogenic, and antiviral bioactivities [2,5,9,10,11,12,13].
The female inflorescences (called hop cones or simply hops) as well as other parts of the plant (leaves, stems, and rhizomes) are rich in different biologically active molecules as polyphenolic compounds and acyl phloroglucides, which are responsible for the different health-promoting effects and bioactivities [3,9]. The lupulin glands, which present a yellow-green color, are located on the hop umbel (in the inner and outer bracteoles) and contain bitter resins and aroma substances [1]. The secondary metabolites of the female inflorescences (presented in the lupulin glands) can be divided into three groups: (1) the hop resins, (2) the hop oil, and (3) the hop polyphenols [14]. The levels of the aromatic essential oil and the bitter hop α- and β-acids depend on several factors such as the variety or ripening stage and even on climatological conditions [15]. The main use of hops worldwide, around 97%, is used for brewing purposes [16] to add bitterness, aroma, and taste to the beer.
Taking the above into account, and the current trend of searching natural compounds with novel biological properties, the wealth of the hop in bioactive compounds makes it an excellent source to extract biologically active molecules with multiple applications in the alimentary, pharmaceutical, and nutraceutical industries [12,15,17,18,19,20]. This has promoted intense research in the field of bioactive compounds from hops that allows on the one hand achieving high yields and on the other hand keeping the bioactivities of the extracted compounds. For this, the selection of adequate extraction technology as well as the appropriate solvent is fundamental.
In this context, many publications related to the isolation of the active compounds have been developed over the past decades [5]. Several isolation technologies are well established using conventional (organic) solvents [5,21]; nevertheless, their residual levels must be controlled [21], because they can remain in the final product and have detrimental health effects [5]. According to Marriott [21], EU legislation and organic certification bodies establish the allowed extraction solvents, their maximum residue levels, and further restrictions, respectively. To overcome the shortcomings of the conventional solvents [22], eco-friendly solvents such as natural deep eutectic ones represent a safer alternative, and their use has increased in the last decades [23]. Moreover, the use of emerging technologies such as (1) ultrasound-assisted extraction (UAE), (2) microwave-assisted extraction (MAE), (3) pressurized liquid extraction (PLE), and/or (4) supercritical fluid extraction (SFE) has increased in the last decade [24,25,26,27,28]. These approaches open new alternatives in the design of the extraction process of more efficient of biocompounds from natural biomass within the framework of Green Chemistry [23].
In light of the above and encouraged by the growing interest in hops due to their significant potential as a source of bioactive compounds, this review collects the studies about the use of hops as a natural source of these biocompounds. Aspects related to the different current extraction methods applied in the recovery of phytochemicals from hop as well as the evaluation of their different bioactivities are reviewed. Moreover, the applications of these compounds in different fields such as pharmaceutical, nutraceutical, and cosmetic are also summarized.

2. Main Components

The hop cones have different components, such as (1) resins, (2) essential oils, (3) proteins, and (4) polyphenols, among others [16,29,30]. The classification of hop cone compounds is shown in Figure 1. Some of these phytochemicals are briefly described next.

2.1. Hop Resin

The resins are hop plant secondary metabolites that can be solubilized in cold methanol and diethyl ether [14,16]. The total resins can be divided into two kinds: soft and hard resins [1,14,16,37], and they are characterized by their solubility and insolubility in hexane, respectively [14,16]. According to Almaguer et al. [16], the soft resin content in whole hop cones is high compared to the hard resin; in fact, soft resins range within 10–25%, while the hard resins comprise between 3% and 5% of the total weight of dried hops. The soft resins are formed by two different bitter acids: α-acids (between 3% and 17%) and β-acids (between 2% and 7%) [1]. There is a third group, uncharacterized components, that together with β-acids form the β-fraction [16,38]. The α-acids have five components: humulone, cohumulone, adhumulone, prehumulone, and posthumulone [1,15]. The first three are the majority, and the prehumulone and posthumulone are the minority [15]. In the same way, β-acid has another five homologs (lupulones) [1,15]. Depending on the hop variety, cultivation conditions, and climate, the content of these substances homologs may vary greatly [5]. Moreover, the hop resins could suffer from different changes in the storage with the oxidation start of the α-acids and β-acids; due to this process, these acids would decrease during the storage [16]. It is commonly accepted that hard resins can from the oxidation of the soft resins (although it is not yet well defined) [16]. During the traditional brewing process, raw hops are added to the boiling wort, and α-acids are isomerized to iso-α-acids [15], which are the main compounds responsible for the bitter taste of beer [15,39].

2.2. Hop Oil

Essential oils are secondary metabolites exuded in the lupulin glands [14,16], and they are called essentials because they provide the hops with their distinctive smell and transfer their aroma and flavor to beer [16]. Essential oils account for 0.5–3% of the dried hops, with over 400 different compounds identified in the hop oil fraction [16]. Their components would be divided into three huge groups: (1) hydrocarbons, (2) oxygenated, and (3) sulfur [5,16]. According to the bibliography compiled by Almaguer et al. [16], different families of molecules such as aliphatic, monoterpenes, and sesquiterpenes are present in the first group, the second group contains alcohols, aldehydes, acids, and esters, among others, and finally, the sulfur group is constituted by thioesters and cyclic terpenoid sulfides, among others.
The hydrocarbon fraction is the most abundant (between 50% and 80% of total oil) and the most abundant compounds from this fraction are monoterpenes α- and β-pinene and myrcene, among others [12]. According to the authors [12], the oxygenated fraction represents 30% of the total oil, being a complex mixture of different compounds such as aldehydes or ketones, among others. The main compounds studied from this fraction are linalool or geraniol, among others [12]. The sulfur fraction is present in small quantities in the essential oil of hops (up to 1%). These compounds have potent aromas and low odor thresholds, so they play a key role in the overall flavor of beer [12,16].

2.3. Hop Polyphenols

Polyphenols are a wide group of biologically active secondary metabolites [14,16] whose content and profile depend on the hop variety as well as the different climatic conditions of cultivation [3,16]. The cone bract presents the greatest content of polyphenols in the hop plant, and their content in the cone can fluctuate between 4% and 14% (dry matter) [40]. The hop polyphenols can be grouped into (1) flavonols, (2) flavan-3-ols, (3) phenolic carboxylic acids, and (4) other polyphenolic compounds [16,36]. The most abundant flavonols, according to its content, are quercetin and kaempferol, and among the dominant flavan-3-ols, (+)-catechin, (−)-epicatechin, and (+)-gallocatechin stand out, as well as their polymers proanthocyanidins and condensed tannins [12,16]. Ferulic acid is the most representative compound of the group of phenolic carboxylic acids [12,16]. Other phenolic compounds that are unique to hop inflorescences are multifidol glucosides (phloroglucinol derivatives with prenyl side chains) and prenylflavonoids (xanthohumol, isoxanthohumol, desmethylxanthohumol, and 6- and 8-prenylnaringenin) [5,12]. Numerous efforts have been developed to produce hop extracts with high polyphenolic content due to their possible use as natural additives (antioxidant and/or antimicrobial) in industrial applications [5].

3. Extraction Techniques

The extraction efficiency of the plethora of phytochemicals that can be obtained from hops is highly dependent on the extraction technology applied. These methods must be fast, versatile, easy to use, environmentally friendly, cost-effective, and be able to both extract with high yields and keep the quality of the target compounds [28]. The extraction techniques used for the recovery of bioactive compounds range from (1) the conventional methods to innovative technologies such as (2) ultrasound-assisted extraction, (3) microwave-assisted extraction, (4) pressurized liquid extraction, and (5) supercritical fluid extraction, including the use of green solvents as deep eutectic solvents (DES).

3.1. Conventional Methods

Solid–liquid extraction (SLE) and steam distillation have been applied for extracting bioactive compounds from hops. For this purpose, several organic solvents such as ethanol, methanol, methylene chloride, ethyl acetate, acetone, hexane, and their mixtures with water have been used. The extraction efficiency is greatly affected by the type and polarity of the solvent, the experimental conditions of time and temperature, and the extraction number of cycles [41]. Several phytochemicals have been extracted from hops using conventional methods. For instance, hydrodistillation was applied to extract essential oils from the cone powder, obtaining a yield of 6.3 mL/kg of dry cones [10]. Using gas chromatography coupled to mass spectrometry (GC-MS/MS), the authors identified the presence of 16 compounds, of which myrcene, trans-caryophyllene, and α-humulene were the three main components of hops essential oil [10]. In another study, Jeliazkova et al. [42] evaluated the yield and compound profile of essential oil extracted from whole hop cones via steam distillation using a sequential elution. The results indicated that 83.2% of the oil was extracted during the first hour, in comparison with control performed during 4-h noninterrupted distillation [42]. Furthermore, the profile of eluted compounds was also significantly different, observing that monoterpenes were eluted before sesquiterpenes.
The effect of four organic solvents with different polarities (ethylene chloride, acetone, ethyl acetate, and methanol) on the recovery of flavonoids from spent hops was studied by Bartmańska et al. [43]. According to their results, the increase of polarity of the extractant improved the efficacy of extraction, obtaining the highest yield with methanol (92.95 g/kg). The authors found that the most abundant extract compound was xanthohumol, and they indicated that the highest efficiency and selectivity to recover this compound from spent hops was ethyl acetate (3.51 g/kg) and the solvent, which led to the lowest extraction yield being methylene chloride (1.33 g/kg) [43]. In hydroalcoholic extracts obtained by maceration from hop cones, two main groups of compounds were identified by reverse phase HPLC-UV: prenylated chalcones and acylphloroglucinol derivatives [10].
Prencipe et al. [44] indicated that the dynamic maceration of hops with MeOH–HCOOH (99:1, v/v) led to the best result in terms of hop components recovery, specifically prenylflavonoids and bitter acids, in comparison with other methods including heat-reflux extraction, microwave, or ultrasound.
Although the application of organic solvents is widespread in industrial extraction processes, their employment presents some inconveniences related to health risk and environmental pollution, limiting their use in the recovery of bioactive compounds [27]. Due to this, a new method of solvents generation known as deep eutectic solvents (DESs) has been applied in the last decade as a promising green alternative substitution for conventional organic solvents in the recovery of biomolecules [27]. In this line, Lakka et al. [23] tested the ability of a eutectic mixture composed of glycerol and L-alanine to extract polyphenols from hops. In this study, the authors applied a response surface methodology (RSM) based on a Box–Behnken design for the optimization of process parameters (DES concentration in aqueous mixtures (CDES: 55–85% w/w), liquid-to-solid ratio (LSR: 20–60 mL/g), and speed of stirring (SS: 200–800 rpm)). Under the optimized extraction conditions (CDES = 85% (w/w), LSR = 59 mL/g and SS = 688 rpm), a theoretically optimal yield of total polyphenols of 118.97 mg gallic acid equivalents (GAE)/g dm was obtained [23].

3.2. Emerging Extraction Technologies

The efficient recovery of valuable compounds from different bioresources largely depends on the technology used for their extraction. Conventional extraction methods present various disadvantages associated with the high consumption of solvents, prolonged extraction times, and degradation of thermosensitive biomolecules. To avoid operational hazards and the presence of harmful solvent traces in the extract material, novel alternative extraction techniques have been explored to meet the demand of greener processes to extract and fractionate the different hop valuable components (even to valorize the hop-exhausted solid) [15].

3.2.1. Ultrasound-Assisted Extraction (UAE)

Ultrasound has been identified for its potential use in the phytopharmaceutical extraction industry [45]. The UAE system is an uncomplicated, economical, and efficient alternative to the extraction methods used traditionally that can improve extraction yield, extraction rates, or the recovery of heat-sensitive compounds [46]. This kind of technique uses high-frequency waves that promote the formation of bubbles in the medium, leading to the formation of the cavitation phenomenon [47]. The implosion of these bubbles disrupts the cellular structure and facilitates the diffusion of the solvent into the cellular plant tissue, which increases mass transfer and consequently improves the extraction [47]. The efficiency of the UAE is influenced by various operating parameters such as the type and concentration of the solvent, sonication time, temperature, LSR, ultrasonic power, and frequency, which must be optimized to reach high extraction yields [48]. To give an example, Almeida et al. [49] applied a Central Composite Rotational Design (CCRD) to optimize the recovery of phytochemicals with antioxidant capacity from Brazilian hops. The authors evaluated the effect of three extraction parameters: temperature (33–67 °C), EtOH concentration (43–77%), and LSR (17–33 mL/g) on the total phenolic content (TPC). According to the results of regression analysis, the LSR was the parameter that showed a greater influence on TPC of the extracts, while the temperature and the concentration of ethanol had a lesser effect. Under optimized extraction conditions (52 °C, 49% ethylic alcohol and LSR of 34 mL/g), a TPC of 33.93 mg GAE/g for Brazilian hops was obtained. Moreover, the authors compared Brazilian hop extracts with those obtained with the same variety of hops grown in the USA. The results showed that the Brazilian hops showed a higher content of phenols and flavonoids and better antioxidant potential analyzed by the ABTS (2,2’-azino-di(3-ethylbenzothiazoline-6-suslfonic acid) and DPPH (α,α-Diphenyl-β-picrylhydrazyl) tests compared to the USA hops.
In another study, the UAE has been applied with success for the extraction of diverse types of biocompounds from hops. For example, Muzykiewicz et al. [3] used this technique with different extractants (methyl, ethyl, and isopropyl alcohol) under three different concentrations to assess the total phenolic content and the antioxidant activity. This research was carried out using fresh hop leaves from different harvested years (2017 and 2018). Process parameters were fixed at 40 kHz during different times (15, 30, and 60 min) at room temperature and under different solvent concentrations (40%, 70% and 96–99.5% (v/v)). The authors reported that the extracts (from young hop leaves harvested at the starting vegetation) presented a high antioxidant activity, and this antioxidant potential was influenced by different factors (including the solvent type or extraction time) and concluded that the most effective process was using undiluted methanol during one hour of ultrasound-assisted extraction. The antioxidants content depends on the harvesting time and can be also influenced by climatic conditions, among other environmental elements [3].

3.2.2. Microwave-Assisted Extraction (MAE)

In the last decade, the use of microwave-assisted extraction (MAE) to recover active molecules from several natural sources, including hops, has also been addressed. This extraction technique is based on the application of microwave energy, which is converted into heat mainly through two mechanisms, which are ionic conduction and dipole rotation [48]. This process increases the pressure and temperature inside the cell matrix, which causes the rupture of the cell structure, improving the release of the desired compounds. MAE has been recognized as a promising green technique over conventional extraction methods since it presents various advantages, including (1) shorter extraction time, (2) minor energy input, (3) decreased solvent consumption, (4) ease of operation, and (5) a minimum degradation of bioactive compounds [28,48].
Tyśkiewicz et al. [50] explored the use of microwave-assisted hydrodistillation (MAHD) to extract essential oils from hops scCO2 (sc: supercritical) extract, and the results were compared with those obtained using conventional hydrodistillation (HD). Under optimized conditions (335 W microwave power at LSR of 8:3), MAHD yielded 3.77% of essential oils in an extraction time of 30 min, while with conventional HD, only 1.90% was reached using a longer time (276 min). The results of quantitative analyses of β-myrcene and α-humulene of the obtained oil by MAHD were 77.36% and 9.47%, respectively.

3.2.3. Pressurized Methods

Another interesting technique is the pressurized liquid extraction (PLE), which is also named accelerated solvent extraction (ASE) or pressurized hot water extraction (PHWE) when water is used [51]; also, pressurized solvent extraction (PSE) presents important benefits compared to conventional extractions [52].
Formato et al. [53] studied the efficiency of cyclically pressurized solid–liquid extraction using a Naviglio Extractor for the recovery of acidic compounds from hops flowers in comparison with supercritical fluid extraction (SFE). The results showed that the cyclically pressurized solid–liquid extraction was more effective for the extraction of α acids and iso-α-acids, while SFE exhibited a greater potential for the isolation of β acids. The authors concluded that both technologies can be used to obtain high yields of hops extracts, confirming the possibility of adjusting the experimental parameters of both methods to make it selective for specific kinds of compounds.
Gil-Ramírez [51] assessed the suitability of PHWE for the selective extraction of isoxanthohumol (IX) against xanthohumol (XN) from hops. Water extraction was performed using 1500 psi at 150 °C and an extraction time of 30 min (5 min per cycle for 6 cycles). Ethanol extraction at 150 °C during 30 min (5 min per cycle for 6 cycles) was carried out for comparative purposes. Besides, sequential extractions were performed using a solvent in increasing polarity order (hexane, ethanol, and water). Based on the results, PHWE showed high selectivity toward isoxanthohumol against xanthohumol (2.34 mg/g and 0.11 mg/g, respectively, with a ratio IX/XN of 21) in comparison with PLE using EtOH as a solvent, after using hexane (5.15 mg/g and 2.57 mg/g, respectively, with a IX/XN ratio of 2) [51].
PSE has been proposed to extract α-acids and β-acids from hops and hop products [52]. The authors studied the sample preparation method influence and the parameters that affect the extraction efficiency to find an alternative method to the EBC 7.7 extraction method (used for bitter acids determination in hop products) to save time and facilitate the laborious extraction. The most important parameters were optimized (1) temperature, (2) extraction solvent type, (3) process of sample preparation, and (4) number of cycles. The PSE method saved solvent, it was less arduous and time-consuming, and according to the statistical evaluation carried out by the authors, the developed PSE process can be considered comparable to the EBC 7.7 extraction method.

3.2.4. Supercritical Fluid Extraction (SFE)

Another emerging technology that has been advantageously positioned for the green extraction of heat-sensitive biocompounds is supercritical fluid extraction (SFE). CO2 is widely used for SFE due to it being low toxic, non-flammable, inexpensive (compared to organic solvents), and recyclable. According to Hrnčič et al. [5], new opportunities using unconventional supercritical solvents have been appeared such as SF6 or noble gases (or their mixtures), although supercritical CO2 remains as the more used solvent for these operations. However, CO2 is intrinsically non-polar; thus, to improve the extraction of polar compounds such as phenolic compounds, it requires the addition of polar cosolvents (modifiers) such as ethanol or methanol [28]. Formato et al. [53] evaluated the extractive efficiency of SFE-CO2, with or without a cosolvent, to extract the acidic compounds contained in hops flowers. The results revealed that the use of supercritical CO2 with cosolvent improved the performance of α acids (28.3%) compared to pure CO2 (21.5%). In contrast, the highest yield in β acids (46.2%) was found in the extracts obtained with supercritical CO2 versus 37.5% for SFE-CO2 with ethanol.
SFE has been applied successfully for the selective isolation of bitter acids from two hop cultivars (Hallertau Magnum and Herkules) [54]. The authors identified, by HPLC analysis, the presence of two main groups of molecules: α-acids (55.2 w/w and 46.9 w/w in the Herkules and Hallertau Magnum hops, respectively) and β-acids (18.3 w/w and 22.9 w/w, respectively) [54]. Cohumulone accounted 38.7% of α-acids in Herkules hops and 24.9% in Hallertau Magnum hops, and the colupulone was the major component of β-acids, reaching 57.2% and 44.2% in Herkules and Hallertau Magnum, respectively [54].
To valorize the spent hops, Jackowski et al. [55] proposed their use as a raw material for the recovery of xanthohumol. Under 80 °C and 850 bar, a yield of 1.23% of xanthohumol was obtained.
Some studies about the extraction technologies of different phytochemicals from hops are presented in Table 1.

4. Biological Activities of Hop Compounds

As mentioned previously, hop contains several bioactive molecules that exhibit multiple therapeutic properties, such as (1) antioxidant, (2) antimicrobial, (3) antifungal, (4) antiviral, (5) anti-inflammatory, and (6) anticancer, inter alia [5,12,53].

4.1. Antioxidant Activity

Several of the compounds identified in hops and hop products have been investigated for their antioxidant properties. The antioxidant potential of hop extracts depends on various factors including the type of assay used to determine the antioxidant activity, the extraction solvent, as well as the cultivar of hop [43,49,56]. For example, Kobus-Cisowska et al. [56] evaluated the antioxidant potential of hop cone extracts from three different cultivars (Magnum, Lubelski, and Marynka) measured by DPPH and ABTS methods. The aqueous extracts of the three cultivars presented the highest DPPH values; however, the ethanolic extracts exhibited a higher value of antioxidant activity by the ABTS assay.
Alonso-Esteban et al. [2] tested the antioxidant capacity of methanolic extract from hop seeds through different in vitro assays, namely the DPPH, reducing power, β-carotene bleaching inhibition, and thiobarbituric acid reactive substances (TBARS) formation inhibition. This extract had a greater inhibitory effect on the generation of TBARS from the ex vivo decomposition of certain lipid peroxidation products (with an EC50 value of 128 μg/mL), but it exhibited the worst behavior for the β-carotene bleaching inhibition capacity (with an EC50 value of 1330 μg/mL). The latter indicates that the hop extract is less active to neutralize the linoleic hydroperoxyl radicals formed in vitro from the oxidation of linoleic acid. The authors attributed the antioxidant potential mainly to the presence of (+)-catechin and (−)-epicatechin in hop seed extract.
In a previous study, Abram et al. [57] found that ethanolic extracts of hop cones presented up to ca.5-fold more DPPH activity compared to that obtained in the leaf extracts. On the contrary, the best activity measured by the ferric reducing antioxidant power (FRAP) trial was found in the leaf extracts. In another study, Gerhauser et al. reported that the xanthohumol present in the hops showed an antioxidant activity that was 8.9 and 2.9 times higher than the reference compound 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (TROLOX) in scavenging hydroxyl and peroxyl radicals, respectively [58].
In a study carried out by Liu et al. [59], the hydroxyl radical scavenging activity of different hops fractions (hop bitter acids, isomerized hop bitter acids, and others) was evaluated. The results indicated that all the compounds showed antioxidant potential at different levels, of which the α-acids were those that exhibited a lower EC50. Humulone, lupulone, and some terpenes (linalool, β-pinene and γ-terpinene, β-farnesene) from hop essential oils have also been reported for their antioxidant potential [12].

4.2. Antimicrobial Activity

Hops have traditionally been used in beer as a natural preservative because of their high content of bitter acids and polyphenols, which inhibit the growth of a broad spectrum of microorganisms. Pilna et al. [54] studied the antimicrobial potential of extracts of two hop varieties. All extracts showed antimicrobial activity against all pathogenic bacteria tested at minimum inhibitory concentrations (MICs) in the range of 8–512 μg/mL. Gram-positive strains (MICs 8–64 µg/mL) were more sensitive than Gram-negative strains (MICs ≥ 32 µg/mL) and yeast (MIC = 512 µg/mL). The authors identified α- and β-acids as the main substances involved in the inhibitory effects of hop extracts. Humulinic acid (derived from iso-α-acids) has also been reported for their antimicrobial activity against Lactobacillus brevis [60].
Today, there is a global concern to find new active agents to combat microbial resistance to antibiotics [61]. In this sense, methicillin-resistant Staphylococcus aureus (MRSA) strains cause different pathologies that are difficult to treat due to their virulence, resistance to almost all useful antibiotics, as well as the formation of persistent biofilms [61]. Plant-derived natural compounds, characterized by the presence of a wide spectrum of active biomolecules, have been studied as potential antimicrobial agents that are useful to treat several diseases caused by multidrug-resistant microorganisms. According to Bartmánska et al. [43], seven flavonoids, among them two natural (α,β-dihydroxanthohumol and 8-prenylnaringenin) flavonoids identified in spent hops extracts, showed remarkable antimicrobial activity against methicillin-sensitive (MSSA) and resistant Staphylococcus aureus (MRSA) strains. Lupulone, xanthohumol, and desmethylxanthohumol also exhibited strong antimicrobial activity against MRSA as well as the ability to inhibit biofilm formation [61]. Similar findings were also found by Bogdanova et al. [62], who reported that humulone, lupulone, and xanthohumol had strong antimicrobial and antibiofilm activity against MRSA strains. In this research, the authors indicated that lupulone exhibited the strongest effect, which was followed by xanthohumol. Ethanolic extracts of hops also exhibited an antimycobacterial effect on rifampin-sensitive and resistant strains of Mycobacterium tuberculosis [63].
Some authors have also demonstrated the antifungal activity of hop extracts. Bocquet et al. [10] tested crude extracts of different parts of hop (leaves, stems, rhizomes, and female cones) and the essential oil of hops against Zymoseptoria tritici. All extracts and essential oil showed antifungal activity, although only female cones and the essential oil exhibited a visible activity, observing a reduction of 85% and 100% in the growth of Z. tritici at 1.25 g/L, respectively. The authors attributed the antifungal activity of hop cone extracts to the presence of desmethylxanthohumol and co-humulone and concluded that the combination of hops essential oil with synthetic fungicides could be an appropriate strategy to reduce the dose of conventional fungicides in crop protection. Similarly, Alonso-Esteban et al. [2] also reported the antifungal activity of hop seed extract. The results indicated that this extract had a remarkable antifungal effect, which was even better than the positive control, against fungi of the genus Penicillium.

4.3. Effects on Specific Diseases

4.3.1. Anti-Inflammatory Activity

Inflammation is a biological response of the organism to injury or infection [12]. However, according to the authors, an excessive inflammatory reaction is associated with certain diseases such as cancer or ischemic heart disease, among others. Bitter acids and polyphenolic compounds from hops have been identified as promising molecules to inhibit inflammatory processes. Both molecules act on the nuclear factor kappa B (NF-kB) that is involved in the expression of pro-inflammatory genes such as tumor necrosis factor alpha (TNF-α), inducible nitric oxide synthase (iNOS), kinases, cyclooxygenases 1 and 2 (COX-1 and COX-2), and an amount interleukins [12,64]. Several in vitro and in vivo studies evidenced that the anti-inflammatory effects of hops are primarily attributed to humulone, xanthohumol, and 8-prenylnaringenin [12,64]. For instance, Lee et al. [65] reported that the topical application of humulone inhibited 12-O-tetradecanoylphorbol-13 acetate (TPA)-induced COX-2 expression through the regulation of nuclear factor-kB. Humulone also reduces the expression of various kinases related to the inflammatory response [66]. Xanthohumol and 8-prenylnaringenin also showed a strong anti-inflammatory effect via the inactivation of NF-kc in microglial cell lines [67]. It has also been studied that the isoxanthohumol reduced inflammatory factors including tumor necrosis factor alpha (TNF-α) and nuclear factor kappa B in human aortic smooth muscle cells and human umbilical vein endothelial cells [68]. In both animal models and human intervention trials, isohumulones have been effective in the treatment of inflammatory arthritis [69].

4.3.2. Cancer-Related Activities

Cancer, an important causes of death in the 21st century, supposes for the health systems an important economic impact, due to the high cost of its treatment [12]. For this reason, it is necessary to develop new substances with anticancer potential that can prevent, stop, or reverse the disease progression, which is the reason why these substances have been the focus of a large number of scientific studies [12]. In this context, it has been reported that some of the bioactive compounds present in hops have anticancer properties. For instance, xanthohumol has been identified as a new agent for the treatment of different types of cancer [12,64]. Yong et al. [11] demonstrated that xanthohumol had an apoptotic effect on the human alveolar adenocarcinoma cell line in a dose- and time-dependent manner. Recently, Roehrer et al. [13] evaluated the antiproliferative effect of xanthohumol, xanthohumol C, and crude hop extract on human breast cancer cells. According to the authors, after 2 days of incubation, xanthohumol C presented the strongest growth inhibition with an IC50 of 4.18 μM, in comparison with crude hop extract (8.84 μM) and xanthohumol (12.25 μM). Lupulone, a β-acid present in hop extracts, displayed anticancer activity on prostate cancer cells via the induction of caspase 8-dependent cell death [70].

4.3.3. Other Biological Activities

Other bioactivities attributed to hop components include neuroprotective, antidiabetic, and cardioprotective effects. Xanthohumol promoted neuronal recovery in rats with intracerebral hemorrhage [71], and it also showed a protective effect on the brain damage induced by aging [72]. This compound also has the ability to inhibit adipogenesis so it can be used in the prevention of obesity. In a study in mice fed with a high-fat diet, the supplementation with 2% or 5% hop extract reduced the increase in body and adipose tissue weight and improved the glucose intolerance [73]. A diet rich in xanthohumol and 8-prenylnaringenin improves metabolic disorders related to type-2 diabetes by modulation of the glucose and lipid pathways [74].
Table 2 summarizes several biological activities of different biocompounds extracted from hop and the main results found.

5. Current Applications of Functional Molecules from Hop

Taking into account the properties of the hop extracts, in the last years, they have been used as preservative agents in different food products. In the case of fresh meat and meat products, plant extracts prevent their oxidative and microbial deterioration, extending their shelf-life and safety as well as conferring functional properties [76,77,78]. For example, Kramer et al. [18] studied the antimicrobial effect in vitro of several hop extracts against L. monocytogenes, Staphylococcus aureus, Salmonella enterica, and Escherichia coli in a model meat marinade and on marinated pork tenderloins. The results obtained by these authors demonstrated that the Gram-positive bacteria were highly inhibited by hop extracts due to its content in β-acid, but in the case of extracts containing α-acid, the inhibition was lower; in contrast, Gram-negative bacteria exhibited a high resistance against all evaluated hop extracts.
In another work, Villalobos-Delgado et al. [79] evaluated the effect of the incorporation of hop infusion or powder in raw and cooked lamb patties, over the oxidative stability of lipids, proteins, and/or color under two scenarios: refrigerated or frozen conditions, as well as in their sensory acceptability. These authors concluded that the use of hop powder showed higher antioxidant activity than hop infusion in lamb patties. Moreover, the lipid and protein oxidation of cooked patties under refrigerated conditions was reduced. However, the sensorial acceptance by the consumers decreased due to changes in flavor when hop powder was added.
Hop extracts find also application as natural ingredients to extend the shelf life of bread due to their antifungal properties. For instance, Nionelli et al. [19] formulated wheat bread with hop extracts and assessed their effects on its shelf life, as well as on its rheological and sensory features. They reported that the hop extract exhibited antifungal properties against Aspergillus parasiticus, Penicillium carneum, Penicillium polonicum, Penicillium paneum, Penicillium chermesinum, Aspergillus niger, and Penicillium roqueforti. Moreover, these authors isolated lactic acid bacteria from hops and selected three for sourdough fermentation for bread making with hop extracts. The authors concluded that the addition of hop extracts increased the antioxidant activity and the concentration of phenols. Moreover, the use of hop-sourdough with or without the incorporation of hop extract to elaborate bread delayed the growth of fungi until 14 days, extending its shelf life. The rheological and sensory properties were not affected.
In cosmetics, hops are used in bath lotions, among others [80]. Vogt et al. [17] used supercritical CO2 extracts of hop cones to formulate shower gels, and the results obtained showed that their addition enhanced their skin-conditioning properties due to their content in bioactive ingredients. Moreover, the formulations containing the extract of hop cones present compounds to treat oil and dandruff in hair. The use of hop extract in hair cosmetics is supported by its antifungal and antiseborrheic properties that decrease its brittleness, nourish it, give it shine, increase its strength, and prevent its loss [17].

6. Conclusions

Traditionally, hops have been used in brewing, but recent studies have revealed their wealth in bioactive molecules with a huge range of therapeutic properties. This has encouraged intense research in the development of a sustainable process that uses eco-friendly solvents combined with intensification technologies that guarantee high yields and extracts with high quality from hops. In fact, in this review, several works based on these technologies demonstrate their suitability to recover extracts that are biologically active. A myriad of properties related to the hop extracts have been evaluated, among them antibacterial, antifungal, cardioprotective, antioxidant, anti-inflammatory, anticarcinogenic, and antiviral. Therefore, hops are shaping up as an excellent and alternative source of bioactive compounds with potential great acceptability by the consumers that increasingly demand natural ingredients with healthy properties. Moreover, the extracts from hops find applications in the alimentary, cosmetic, nutraceutical, and pharmaceutical sector, opening new alternatives in the formulation of different commodities beyond their conventional uses. However, due to the huge variety of biomolecules present in the hop extracts, it is necessary to investigate their interaction with other components of the matrix where they are incorporated, as well as their bioavailability when are ingested as part of a food or used at a topical level when being applied as part of a skin or hair formulation.

Author Contributions

Conceptualization, B.G.; writing—original draft preparation, G.A., P.G., B.G.; writing—review and editing, P.G., G.A., B.G., P.E.S.M., J.M.L. All authors have read and agreed to the published version of the manuscript.

Funding

Thanks to GAIN (Axencia Galega de Innovación) for supporting this research (grant number IN607A2019/01).

Acknowledgments

Gonzalo Astray thanks to the University of Vigo for his contract supported by “Programa de retención de talento investigador da Universidade de Vigo para o 2018” budget application 0000 131H TAL 641. B.G. acknowledges postdoctoral fellowship support from the Ministry of Economy and Competitiveness (MINECO, Spain) “Ramón y Cajal” program (Grant reference RYC2018-026177-I). Paulo E.S. Munekata acknowledges postdoctoral fellowship support from the Ministry of Economy and Competitiveness (MINECO, Spain) “Juan de la Cierva” program (FJCI-2016-29486). Jose M. Lorenzo is member of the HealthyMeat network, funded by CYTED (ref. 119RT0568).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Krottenthaler, M. Hops. In Handbook of Brewing: Processes, Technology, Markets; Eßlinger, H.M., Ed.; WILEY-VCH: Weinheim, Germany, 2009; pp. 85–104. [Google Scholar]
  2. Alonso-Esteban, J.I.; Pinela, J.; Barros, L.; Ćirić, A.; Soković, M.; Calhelha, R.C.; Torija-Isasa, E.; de Cortes Sánchez-Mata, M.; Ferreira, I.C.F.R. Phenolic composition and antioxidant, antimicrobial and cytotoxic properties of hop (Humulus lupulus L.) Seeds. Ind. Crops Prod. 2019, 134, 154–159. [Google Scholar] [CrossRef]
  3. Muzykiewicz, A.; Nowak, A.; Zielonka-Brzezicka, J.; Florkowska, K.; Duchnik, W.; Klimowicz, A. Comparison of antioxidant activity of extracts of hop leaves harvested in different years. Herba Pol. 2019, 65, 1–9. [Google Scholar] [CrossRef] [Green Version]
  4. Moir, M. Hops—A millennium review. J. Am. Soc. Brew. Chem. 2000, 58, 131–146. [Google Scholar] [CrossRef]
  5. Hrnčič, M.K.; Španinger, E.; Košir, I.J.; Knez, Ž.; Bren, U. Hop compounds: Extraction techniques, chemical analyses, antioxidative, antimicrobial, and anticarcinogenic effects. Nutrients 2019, 11, 257. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. European Commission. Hop Report for the Harvest Year 2018; European Commission: Brussels, Belgium, 2018. [Google Scholar]
  7. Tardío, J.; De Cortes Sánchez-Mata, M.; Morales, R.; Molina, M.; García-Herrera, P.; Morales, P.; Díez-Marqués, C.; Fernández-Ruiz, V.; Cámara, M.; Pardo-De-Santayana, M.; et al. Ethnobotanical and food composition monographs of selected mediterranean wild edible plants. In Mediterranean Wild Edible Plants: Ethnobotany and Food Composition Tables; De Cortes Sánchez-Mata, M., Tardío, J., Eds.; Springer: New York, NY, USA, 2016; pp. 273–470. [Google Scholar]
  8. Lorenzo, J.M.; Mousavi Khaneghah, A.; Gavahian, M.; Marszałek, K.; Eş, I.; Munekata, P.E.S.; Ferreira, I.C.F.R.; Barba, F.J. Understanding the potential benefits of thyme and its derived products for food industry and consumer health: From extraction of value-added compounds to the evaluation of bioaccessibility, bioavailability, anti-inflammatory, and antimicrobial activities. Crit. Rev. Food Sci. Nutr. 2019, 59, 2879–2895. [Google Scholar] [CrossRef]
  9. Zanoli, P.; Zavatti, M. Pharmacognostic and pharmacological profile of Humulus lupulus L. J. Ethnopharmacol. 2008, 116, 383–396. [Google Scholar] [CrossRef]
  10. Bocquet, L.; Rivière, C.; Dermont, C.; Samaillie, J.; Hilbert, J.-L.; Halama, P.; Siah, A.; Sahpaz, S. Antifungal activity of hop extracts and compounds against the wheat pathogen Zymoseptoria tritici. Ind. Crops Prod. 2018, 122, 290–297. [Google Scholar] [CrossRef]
  11. Yong, W.K.; Ho, Y.F.; Malek, S.N.A. Xanthohumol induces apoptosis and S phase cell cycle arrest in A549 non-small cell lung cancer cells. Pharmacogn. Mag. 2015, 11, S275–S283. [Google Scholar]
  12. Karabín, M.; Hudcová, T.; Jelínek, L.; Dostálek, P. Biologically Active Compounds from Hops and Prospects for Their Use. Compr. Rev. Food Sci. Food Saf. 2016, 15, 542–567. [Google Scholar] [CrossRef] [Green Version]
  13. Roehrer, S.; Stork, V.; Ludwig, C.; Minceva, M.; Behr, J. Analyzing bioactive effects of the minor hop compound xanthohumol C on human breast cancer cells using quantitative proteomics. PLoS ONE 2019, 14, e0213469. [Google Scholar] [CrossRef]
  14. Steenackers, B.; De Cooman, L.; De Vos, D. Chemical transformations of characteristic hop secondary metabolites in relation to beer properties and the brewing process: A review. Food Chem. 2015, 172, 742–756. [Google Scholar] [CrossRef] [PubMed]
  15. Sanz, V.; Torres, M.D.; López Vilariño, J.M.; Domínguez, H. What is new on the hop extraction? Trends Food Sci. Technol. 2019, 93, 12–22. [Google Scholar] [CrossRef]
  16. Almaguer, C.; Schönberger, C.; Gastl, M.; Arendt, E.K.; Becker, T. Humulus lupulus—A story that begs to be told. A review. J. Inst. Brew. 2014, 120, 289–314. [Google Scholar] [CrossRef]
  17. Vogt, O.; Sikora, E.; Ogonowski, J. The effect of selected supercritical CO2 plant extract addition on user properties of shower gels. Polish J. Chem. Technol. 2014, 16, 51–54. [Google Scholar] [CrossRef] [Green Version]
  18. Kramer, B.; Thielmann, J.; Hickisch, A.; Muranyi, P.; Wunderlich, J.; Hauser, C. Antimicrobial activity of hop extracts against foodborne pathogens for meat applications. J. Appl. Microbiol. 2015, 118, 648–657. [Google Scholar] [CrossRef] [PubMed]
  19. Nionelli, L.; Pontonio, E.; Gobbetti, M.; Rizzello, C.G. Use of hop extract as antifungal ingredient for bread making and selection of autochthonous resistant starters for sourdough fermentation. Int. J. Food Microbiol. 2018, 266, 173–182. [Google Scholar] [CrossRef] [PubMed]
  20. Jelínek, L.; Karabín, M.; Kotlíková, B.; Hudcová, T.; Dostálek, P. Application of a hop by-product in brewing: Reduction in the level of haze-active prolamines and improved antioxidant properties of the beer. J. Inst. Brew. 2014, 120, 99–104. [Google Scholar] [CrossRef]
  21. Marriott, R.J. Greener chemistry preparation of traditional: Lavour extracts and molecules. Agro Food Ind. Hi-Tech 2010, 21, 46–48. [Google Scholar]
  22. Barba, F.J.; Putnik, P.; Bursać Kovačević, D.; Poojary, M.M.; Roohinejad, S.; Lorenzo, J.M.; Koubaa, M. Impact of conventional and non-conventional processing on prickly pear (Opuntia spp.) and their derived products: From preservation of beverages to valorization of by-products. Trends Food Sci. Technol. 2017, 67, 260–270. [Google Scholar] [CrossRef]
  23. Lakka, A.; Karageorgou, I.; Kaltsa, O.; Batra, G.; Bozinou, E.; Lalas, S.; Makris, D. Polyphenol Extraction from Humulus lupulus (Hop) Using a Neoteric Glycerol/L-Alanine Deep Eutectic Solvent: Optimisation, Kinetics and the E ect of Ultrasound-Assisted Pretreatment. AgriEngineering 2019, 1, 30. [Google Scholar] [CrossRef] [Green Version]
  24. Putnik, P.; Lorenzo, J.; Barba, F.; Roohinejad, S.; Režek Jambrak, A.; Granato, D.; Montesano, D.; Bursać Kovačević, D. Novel food processing and extraction technologies of high-added value compounds from plant materials. Foods 2018, 7, 106. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Bursać Kovačević, D.; Maras, M.; Barba, F.J.; Granato, D.; Roohinejad, S.; Mallikarjunan, K.; Montesano, D.; Lorenzo, J.M.; Putnik, P. Innovative technologies for the recovery of phytochemicals from Stevia rebaudiana Bertoni leaves: A review. Food Chem. 2018, 268, 513–521. [Google Scholar] [CrossRef] [PubMed]
  26. Chemat, F.; Abert Vian, M.; Fabiano-Tixier, A.-S.; Nutrizio, M.; Režek Jambrak, A.; Munekata, P.E.S.; Lorenzo, J.M.; Barba, F.J.; Binello, A.; Cravotto, G. A review of sustainable and intensified techniques for extraction of food and natural products. Green Chem. 2020, 22, 2325–2353. [Google Scholar] [CrossRef] [Green Version]
  27. Gullón, P.; Gullón, B.; Romaní, A.; Rocchetti, G.; Lorenzo, J.M. Smart advanced solvents for bioactive compounds recovery from agri-food by-products: A review. Trends Food Sci. Technol. 2020, 101, 182–197. [Google Scholar] [CrossRef]
  28. Gullón, B.; Lú-Chau, T.A.; Moreira, M.T.; Lema, J.M.; Eibes, G. Rutin: A review on extraction, identification and purification methods, biological activities and approaches to enhance its bioavailability. Trends Food Sci. Technol. 2017, 67, 220–235. [Google Scholar] [CrossRef]
  29. Stevens, R. The Chemistry of Hop Constituents. Chem. Rev. 1967, 67, 19–71. [Google Scholar] [CrossRef]
  30. Verzele, M. 100 years of hop chemistry and its relevance to brewing. J. Inst. Brew. 1986, 92, 32–48. [Google Scholar] [CrossRef]
  31. Palamand, S.R.; Aldenhoff, J.M. Bitter tasting compounds of beer. Chemistry and taste properties of some hop resin compounds. J. Agric. Food Chem. 1973, 21, 535–543. [Google Scholar] [CrossRef]
  32. Hough, J.S.; Briggs, D.E.; Stevens, R.; Young, T.W. Malting and Brewing Science. Volume II Hopped Wort and Beer; Springer Science + Business Media: New York, NY, USA, 1982. [Google Scholar]
  33. Roberts, T.R.; Wilson, R.J.H. Hops. In Handbook of Brewing; Priest, F.G., Stewart, G.G., Eds.; Taylor & Francis: Boca Raton, FL, USA, 2006; pp. 177–280. [Google Scholar]
  34. Sharpe, F.R.; Laws, D.R.J. The essential oil of hops a review. J. Inst. Brew. 1981, 87, 96–107. [Google Scholar] [CrossRef]
  35. Jahnsen, V.J. Complexity of Hop Oil. Nature 1962, 196, 474–475. [Google Scholar] [CrossRef]
  36. Biendl, M. Hops and Health. Tech. Q. Master Brew. Assoc. Am. 2009, 46, 1–7. [Google Scholar] [CrossRef]
  37. Taniguchi, Y.; Taniguchi, H.; Yamada, M.; Matsukura, Y.; Koizumi, H.; Furihata, K.; Shindo, K. Analysis of the components of hard resin in hops (Humulus lupulus L.) and structural elucidation of their transformation products formed during the brewing process. J. Agric. Food Chem. 2014, 62, 11602–11612. [Google Scholar] [CrossRef] [PubMed]
  38. Biendl, M.; Engelhard, B.; Forster, A.; Gahr, A.; Lutz, A.; Mitter, W.; Schmidt, R.; Schönberger, C. Hops: Their Cultivation, Composition and Usage; Fachverlag Hans Carl: Nürnberg, Germany, 2014. [Google Scholar]
  39. Spreng, S.; Hofmann, T. Activity-Guided Identification of in Vitro Antioxidants in Beer. J. Agric. Food Chem. 2018, 66, 720–731. [Google Scholar] [CrossRef] [PubMed]
  40. Gresser, A. Properties and Quality. In Handbook of Brewing: Processes, Technology, Markets; Eßlinger, H.M., Ed.; WILEY-VCH: Weinheim, Germany, 2009; pp. 359–397. ISBN 9783527316748. [Google Scholar]
  41. Alirezalu, K.; Pateiro, M.; Yaghoubi, M.; Alirezalu, A.; Peighambardoust, S.H.; Lorenzo, J.M. Phytochemical constituents, advanced extraction technologies and techno-functional properties of selected Mediterranean plants for use in meat products. A comprehensive review. Trends Food Sci. Technol. 2020, 100, 292–306. [Google Scholar] [CrossRef]
  42. Jeliazkova, E.; Zheljazkov, V.D.; Kačániova, M.; Astatkie, T.; Tekwani, B.L. Sequential elution of essential oil constituents during steam distillation of hops (Humulus lupulus L.) and influence on oil yield and antimicrobial activity. J. Oleo Sci. 2018, 67, 871–883. [Google Scholar] [CrossRef] [Green Version]
  43. Bartmańska, A.; Wałecka-Zacharska, E.; Tronina, T.; Popłoński, J.; Sordon, S.; Brzezowska, E.; Bania, J.; Huszcza, E. Antimicrobial properties of spent hops extracts, flavonoids isolated therefrom, and their derivatives. Molecules 2018, 23, 2059. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Prencipe, F.P.; Brighenti, V.; Rodolfi, M.; Mongelli, A.; dall’Asta, C.; Ganino, T.; Bruni, R.; Pellati, F. Development of a new high-performance liquid chromatography method with diode array and electrospray ionization-mass spectrometry detection for the metabolite fingerprinting of bioactive compounds in Humulus lupulus L. J. Chromatogr. A 2014, 1349, 50–59. [Google Scholar] [CrossRef]
  45. Vilkhu, K.; Mawson, R.; Simons, L.; Bates, D. Applications and opportunities for ultrasound assisted extraction in the food industry—A review. Innov. Food Sci. Emerg. Technol. 2008, 9, 161–169. [Google Scholar] [CrossRef]
  46. Tiwari, B.K. Ultrasound: A clean, green extraction technology. TrAC Trends Anal. Chem. 2015, 71, 100–109. [Google Scholar] [CrossRef]
  47. Martínez-Patiño, J.C.; Gullón, B.; Romero, I.; Ruiz, E.; Brnčić, M.; Žlabur, J.Š.; Castro, E. Optimization of ultrasound-assisted extraction of biomass from olive trees using response surface methodology. Ultrason. Sonochem. 2019, 51, 487–495. [Google Scholar] [CrossRef]
  48. Gullón, B.; Gagaoua, M.; Barba, F.J.; Gullón, P.; Zhang, W.; Lorenzo, J.M. Seaweeds as promising resource of bioactive compounds: Overview of novel extraction strategies and design of tailored meat products. Trends Food Sci. Technol. 2020, 100, 1–18. [Google Scholar] [CrossRef]
  49. Almeida, A.D.R.; Maciel, M.V.D.O.B.; Machado, M.H.; Bazzo, G.C.; de Armas, R.D.; Vitorino, V.B.; Vitali, L.; Block, J.M.; Barreto, P.L.M. Bioactive compounds and antioxidant activities of Brazilian hop (Humulus lupulus L.) extracts. Int. J. Food Sci. Technol. 2020, 55, 340–347. [Google Scholar] [CrossRef]
  50. Tyśkiewicz, K.; Gieysztor, R.; Konkol, M.; Szałas, J.; Rój, E. Essential oils from Humulus lupulus scCO2 extract by hydrodistillation and microwave-assisted hydrodistillation. Molecules 2018, 23, 2866. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  51. Gil-Ramírez, A.; Mendiola, J.A.; Arranz, E.; Ruíz-Rodríguez, A.; Reglero, G.; Ibáñez, E.; Marín, F.R. Highly isoxanthohumol enriched hop extract obtained by pressurized hot water extraction (PHWE). Chemical and functional characterization. Innov. Food Sci. Emerg. Technol. 2012, 16, 54–60. [Google Scholar] [CrossRef] [Green Version]
  52. Čulík, J.; Jurková, M.; Horák, T.; Čejka, P.; Kellner, V.; Dvořák, J.; Karásek, P.; Roth, M. Extraction of bitter acids from hops and hop products using Pressurized Solvent Extraction (PSE). J. Inst. Brew. 2009, 115, 220–225. [Google Scholar] [CrossRef]
  53. Formato, A.; Gallo, M.; Ianniello, D.; Montesano, D.; Naviglio, D. Supercritical fluid extraction of α- and β-acids from hops compared to cyclically pressurized solid-liquid extraction. J. Supercrit. Fluids 2013, 84, 113–120. [Google Scholar] [CrossRef]
  54. Pilna, J.; Vlkova, E.; Krofta, K.; Nesvadba, V.; Rada, V.; Kokoska, L. In vitro growth-inhibitory effect of ethanol GRAS plant and supercritical CO2 hop extracts on planktonic cultures of oral pathogenic microorganisms. Fitoterapia 2015, 105, 260–268. [Google Scholar] [CrossRef]
  55. Jackowski, J.; Hurej, M.; Rój, E.; Popłoński, J.; Kośny, L.; Huszcza, E. Antifeedant activity of xanthohumol and supercritical carbon dioxide extract of spent hops against stored product pests. Bull. Entomol. Res. 2015, 105, 456–461. [Google Scholar] [CrossRef]
  56. Kobus-Cisowska, J.; Szymanowska-Powałowska, D.; Szczepaniak, O.; Kmiecik, D.; Przeor, M.; Gramza-Michałowska, A.; Cielecka-Piontek, J.; Smuga-Kogut, M.; Szulc, P. Composition and in vitro effects of cultivars of humulus lupulus L. Hops on cholinesterase activity and microbial growth. Nutrients 2019, 11, 1377. [Google Scholar] [CrossRef] [Green Version]
  57. Abram, V.; Čeh, B.; Vidmar, M.; Hercezi, M.; Lazić, N.; Bucik, V.; Možina, S.S.; Košir, I.J.; Kač, M.; Demšar, L.; et al. A comparison of antioxidant and antimicrobial activity between hop leaves and hop cones. Ind. Crops Prod. 2015, 64, 124–134. [Google Scholar] [CrossRef]
  58. Gerhauser, C.; Alt, A.; Heiss, E.; Gamal-Eldeen, A.; Klimo, K.; Knauft, J.; Neumann, I.; Scherf, H.-R.; Frank, N.; Bartsch, H.; et al. Cancer chemopreventive activity of xanthohumol, a natural product derived from hop. Mol. Cancer Ther. 2002, 1, 959–969. [Google Scholar] [PubMed]
  59. Liu, Y.; Gu, X.-H.; Tang, J.; Liu, K. Antioxidant activities of hops (Humulus lupulus) and their products. J. Am. Soc. Brew. Chem. 2007, 65, 116–121. [Google Scholar] [CrossRef]
  60. Schurr, B.C.; Hahne, H.; Kuster, B.; Behr, J.; Vogel, R.F. Molecular mechanisms behind the antimicrobial activity of hop iso-α-acids in Lactobacillus brevis. Food Microbiol. 2015, 46, 553–563. [Google Scholar] [CrossRef] [PubMed]
  61. Bocquet, L.; Sahpaz, S.; Bonneau, N.; Beaufay, C.; Mahieux, S.; Samaillie, J.; Roumy, V.; Jacquin, J.; Bordage, S.; Hennebelle, T.; et al. Phenolic compounds from humulus lupulus as natural antimicrobial products: New weapons in the fight against methicillin resistant staphylococcus aureus, leishmania mexicana and trypanosoma brucei strains. Molecules 2019, 24, 1024. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  62. Bogdanova, K.; Röderova, M.; Kolar, M.; Langova, K.; Dusek, M.; Jost, P.; Kubelkova, K.; Bostik, P.; Olsovska, J. Antibiofilm activity of bioactive hop compounds humulone, lupulone and xanthohumol toward susceptible and resistant staphylococci. Res. Microbiol. 2018, 169, 127–134. [Google Scholar] [CrossRef]
  63. Esmi Serkani, J.; Nasr Isfahani, B.; Safaei, H.G.; Kasra Kermanshahi, R.; Asghari, G. Evaluation of the effect of humulus lupulus alcoholic extract on rifampin-sensitive and resistant isolates of mycobacterium tuberculosis. Res. Pharm. Sci. 2012, 7, 235–242. [Google Scholar]
  64. Bocquet, L.; Sahpaz, S.; Hilbert, J.L.; Rambaud, C.; Rivière, C. Humulus lupulus L., a very popular beer ingredient and medicinal plant: Overview of its phytochemistry, its bioactivity, and its biotechnology. Phytochem. Rev. 2018, 17, 1047–1090. [Google Scholar] [CrossRef]
  65. Lee, J.-C.; Kundu, J.K.; Hwang, D.-M.; Na, H.-K.; Surh, Y.-J. Humulone inhibits phorbol ester-induced COX-2 expression in mouse skin by blocking activation of NF-κB and AP-1: IκB kinase and c-Jun-N-terminal kinase as respective potential upstream targets. Carcinogenesis 2007, 28, 1491–1498. [Google Scholar] [CrossRef] [Green Version]
  66. Van Cleemput, M.; Cattoor, K.; De Bosscher, K.; Haegeman, G.; De Keukeleire, D.; Heyerick, A. Hop (Humulus lupulus)-derived bitter acids as multipotent bioactive compounds. J. Nat. Prod. 2009, 72, 1220–1230. [Google Scholar] [CrossRef]
  67. Bartmańska, A.; Tronina, T.; Popłoński, J.; Huszcza, E. Biotransformations of prenylated hop flavonoids for drug discovery and production. Curr. Drug Metab. 2013, 14, 1083–1097. [Google Scholar] [CrossRef]
  68. Negrão, R.; Duarte, D.; Costa, R.; Soares, R. Isoxanthohumol modulates angiogenesis and inflammation via vascular endothelial growth factor receptor, tumor necrosis factor alpha and nuclear factor kappa B pathways. BioFactors 2013, 39, 608–622. [Google Scholar] [CrossRef] [PubMed]
  69. Bland, J.S.; Minich, D.; Lerman, R.; Darland, G.; Lamb, J.; Tripp, M.; Grayson, N. Isohumulones from hops (Humulus lupulus) and their potential role in medical nutrition therapy. PharmaNutrition 2015, 3, 46–52. [Google Scholar] [CrossRef] [Green Version]
  70. Mouratidis, P.X.E.; Colston, K.W.; Tucknott, M.L.; Tyrrell, E.; Pirianov, G. An investigation into the anticancer effects and mechanism of action of hop β-acid lupulone and its natural and synthetic derivatives in prostate cancer cells. Nutr. Cancer 2013, 65, 1086–1092. [Google Scholar] [CrossRef] [PubMed]
  71. Wang, Y.; Zhang, Y.; Ming, W.; Jin, X.; Zhai, K.; Liu, B.; Bai, H.; Liu, X. Xanthohumol promotes neuronal and behavioral recovery by suppressing inflammatory response and apoptosis in a rat model of intracerebral hemorrhage. Int. J. Clin. Exp. Med. 2017, 10, 7843–7850. [Google Scholar]
  72. Rancán, L.; Paredes, S.D.; García, I.; Muñoz, P.; García, C.; López de Hontanar, G.; de la Fuente, M.; Vara, E.; Tresguerres, J.A.F. Protective effect of xanthohumol against age-related brain damage. J. Nutr. Biochem. 2017, 49, 133–140. [Google Scholar] [CrossRef] [PubMed]
  73. Sumiyoshi, M.; Kimura, Y. Hop (Humulus lupulus L.) extract inhibits obesity in mice fed a high-fat diet over the long term. Br. J. Nutr. 2013, 109, 162–172. [Google Scholar] [CrossRef] [Green Version]
  74. Costa, R.; Rodrigues, I.; Guardão, L.; Rocha-Rodrigues, S.; Silva, C.; Magalhães, J.; Ferreira-de-Almeida, M.; Negrão, R.; Soares, R. Xanthohumol and 8-prenylnaringenin ameliorate diabetic-related metabolic dysfunctions in mice. J. Nutr. Biochem. 2017, 45, 39–47. [Google Scholar] [CrossRef]
  75. Cömert Önder, F.; Ay, M.; Aydoğan Türkoğlu, S.; Tura Köçkar, F.; Çelik, A. Antiproliferative activity of Humulus lupulus extracts on human hepatoma (Hep3B), colon (HT-29) cancer cells and proteases, tyrosinase, β-lactamase enzyme inhibition studies. J. Enzyme Inhib. Med. Chem. 2016, 31, 90–98. [Google Scholar] [CrossRef] [Green Version]
  76. Nikmaram, N.; Budaraju, S.; Barba, F.J.; Lorenzo, J.M.; Cox, R.B.; Mallikarjunan, K.; Roohinejad, S. Application of plant extracts to improve the shelf-life, nutritional and health-related properties of ready-to-eat meat products. Meat Sci. 2018, 145, 245–255. [Google Scholar] [CrossRef]
  77. Fernandes, R.P.P.; Trindade, M.A.; Lorenzo, J.M.; de Melo, M.P. Assessment of the stability of sheep sausages with the addition of different concentrations of Origanum vulgare extract during storage. Meat Sci. 2018, 137, 244–257. [Google Scholar] [CrossRef]
  78. Domínguez, R.; Pateiro, M.; Gagaoua, M.; Barba, F.J.; Zhang, W.; Lorenzo, J.M. A comprehensive review on lipid oxidation in meat and meat products. Antioxidants 2019, 8, 429. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  79. Villalobos-Delgado, L.H.; Caro, I.; Blanco, C.; Bodas, R.; Andrés, S.; Giráldez, F.J.; Mateo, J. Effect of the addition of hop (infusion or powder) on the oxidative stability of lean lamb patties during storage. Small Rumin. Res. 2015, 125, 73–80. [Google Scholar] [CrossRef]
  80. Cieśliński, M.; Idowski, P. Application of common hop in medicine and cosmetology. Pol. J. Cosmetol. 2003, 6, 188–192. [Google Scholar]
Applsci 10 05074 g001 550
Figure 1. A brief classification of hops cone compounds based on the reviewed literature [16,29,31,32,33,34,35,36].
Figure 1. A brief classification of hops cone compounds based on the reviewed literature [16,29,31,32,33,34,35,36].
Applsci 10 05074 g001
Table
Table 1. Extraction technologies for obtaining active molecules from hops.
Table 1. Extraction technologies for obtaining active molecules from hops.
MatrixTarget CompoundMethodExtraction ConditionsOutcomesReference
HopsEssential oil (desmethylxanthohumol, xanthohumol, co-humulone, lupulone, co-lupulone, and lupulone)MacerationExtraction with ethanol:H2O (9:1) with 3 cycles of 2 h and a full night in stirring in the dark
Fractionation of the active fraction was carried out using a liquid/liquid extraction with methylene chloride in proportion CH2Cl2/H2O (5:5)		Essential oil yield: 6.3 mL/kg of dry cones
Identification of 16 compounds, the three major compounds being myrcene, trans-caryophyllene, and α-humulene 		[10]
Whole hop conesEssential oil (monoterpenes and sequiterpenes) Steam distillationSequential elution at 8 distillation timeEssential oil yield: 83.2% (the first hour), 9.6% (the second hour), and 7.2% (second half of the distillation)
Chemical profile: Monoterpenes are the first to be eluted and sequiterpenes were later eluted		[42]
Spent hopsFlavonoids (xanthohumol)SLEExtraction with methylene chloride, acetone, ethyl acetate, and methanol for 24 h on a rotary shaker and LSR 4:1 (mL/g)Yield: 92.95 g/kg (methanol); 38.57 g/kg (ethyl acetate); 29.82 g/kg (acetone); 26.01 g/kg (methylene chloride)
Xanthohumol: 3.51 g/kg (ethyl acetate); 2.97 g/kg (acetone), 2.94 g/kg (methanol); 1.33 g/kg (methylene chloride)		[43]
HopsPrenylflavonoids and bitter acids (prenylphloroglucinols)Dynamic macerationExtraction with MeOH–HCOOH (99:1, v/v), at room temperature for 30 min under magnetic stirring using an LSR of 20 mL/g ≈17.5 mg/g bitter acids and ≈1.4 mg/g prenylflavonoids[44]
HopsPolyphenolsSLEExtraction with DES based on glycerol and L-alanine for 150 min, at 50 °C in an oil bath. Optimal conditions of extraction: CDES = 85% (w/w), LSR = 59 mL/g, and SS = 688 rpmYield: 118.97 mg GAE/of dry mass[23]
Hop leavesPolyphenolsUAEExtraction with methyl, ethyl, and isopropyl alcohol at different concentrations (40%, 70%, and 96–99.5% (v/v)) using a frequency of 40 kHz for 15, 30, and 60 min at room temperatureTPC: 0.51–6.60 mg GA/g raw material (collected in 2017) and 0.02–6.22 GA/g raw material (collected in 2018)[3]
Hop extractsEssential oils (β-myrcene and α-humulene)MAHD335 W microwave power for 30 min using an LSR of 8:3 (using water as solvent)Yield: 3.77%; β-myrcene: 77.36%; α-humulene: 9.47%[50]
Hop flowersAcidic compounds (α acids, iso α acids, β acids)PLE with a Naviglio ExtractorSample weight: 21 g; solvent: ethyl alcohol; static phase: 2 min; dynamic phase: 5 cycles with 12 sec of stop piston; total cycles: 360 (24 h)α acids: 50.2%; iso α acids: 9.3%; β acids: 16.3%[53]
Hops (pellets)Isoxanthohumol and xanthohumolPHWE/PLEPHWE: 1500 psi at 150 °C and extraction time of 30 min (5 min by cycle -6 cycles-)
PLE: EtOH as a solvent, after using hexane at 150 °C for 20 min each extraction		PHWE: 2.34 mg/g of isoxanthohumol and 0.11 mg/g of xanthohumol
PLE: 5.15 mg/g of isoxanthohumol and 2.57 mg/g of xanthohumol		[51]
Hop and hop productsα- and β-acidsPSEPSE optimal conditions: number of cycles 3 (5 min each), static mode, 80 °C, 15 MPa, solvent: methanol-diethylether (1:1), inert matrix: sea sand (50 to 70 μm), solvent rinsing: 20 sec, nitrogen blowdown: 2 min, amount of sample: 1.5 g of ground hop cones or pellets or 0.3 g of hop extractYields between 96.8% and 102.7%[52]
Hop flowersAcidic compounds (α acids, β acids)SFESFE-CO2 (SFE-I) and SFE-CO2 with ethanol (SFE-II): 350 bar at 35 °C, a static period of 10 min, and a dynamic phase of 260 minSFE-I: 21.5% α acids; 46.2% β acids
SFE-II: 28.3% α acids; 37.5% β acids		[53]
Hop pellets (Herkules and Hallertau Magnum)Acidic compounds (α-acids (cohumulone), β-acids (colupulone))SFESFE-CO2 was carried out at a pressure of 29 MPa, 50 °C during 4 hH. lupulus ‘Herkules’: 55.2% of α-acids (38.7% of cohumulone); 18.3% of β-acids (57.2% colupulone)
H. lupulus ‘Hallertau Magnum’: 46.9% of α-acids (24.9% of cohumulone); 22.9% of β-acids (44.2% colupulone)		[54]
Spent hopsXanthohumolSFESFE-CO2 was carried out at a pressure of 850 bar at 80 °C1.23% of yield of xanthohumol [55]
DES: deep eutectic solvents; LSR: liquid-to-solid ratio; SFE: supercritical fluid extraction; SLE: solid–liquid extraction; UAE: ultrasound-assisted extraction; MAHD: microwave-assisted hydrodistillation; PSE: pressurized solvent extraction; GAE: gallic acid equivalents; IX: isoxanthohumol; XN: xanthohumol; PLE: pressurized liquid extraction; PHWE: pressurized hot water extraction; SS: speed of stirring; CDES: concentration.
Table
Table 2. Biological activities of compounds extracted from hops.
Table 2. Biological activities of compounds extracted from hops.
Responsible Compound MethodologyOutcomesReference
Antioxidant Activity
Phenolic Acids and flavonolsDPPH and ABTSDPPH ranged from 3.50 mmol Trolox/g dw for Marynka variety ethanol extract to 4.75 mmol Trolox/g dw for Magnum variety water extract. ABTS varied from 1.32 mmol Trolox/g dw for Magnum variety water extract to 2.43 mmol Trolox/g dw for Marynka variety ethanol extract[56]
(+)-catechin and (−)-epicatechinDPPH, reduction power, β-carotene bleaching inhibition capacity, TBARSEC50 values: DPPH: 505 µg/mL; Reduction power: 530 µg/mL; β-Carotene bleaching inhibition capacity: 1330 µg/mL; TBARS: 128 µg/mL[2]
Phenolic compoundsDPPH and FRAPDPPH EC50: 0.070 mg/mL; FRAP: reduction of 0.117 mL/µg of ferric ions in 25 min[57]
XanthohumolORACThe antioxidant activity determined by the ORAC assay was higher than the reference compound TROLOX[58]
Quercetin and isoquercetinDPPH and ABTSDPPH EC50: 3.91 µL/mL; ABTS EC50: 21.29 µL/mL[49]
Bitter acids, isomerized hop bitter acids, hop oil, and hexahydro-β-acidsHydroxyl radical scavenging activityEC50: α-acid: 0.21 mg/mL; β-acid: 0.96 mg/mL; Dihydro-iso-α-acid: 1.36 mg/mL; tetrahydro-iso-α-acid 1.77 mg/mL; hexahydro-iso-α-acid 1.40 mg/mL; hexahydro-β-acid 0.50 mg/mL; oil 0.18 mg/mL[59]
Antimicrobial Activity
α- and β-acidsMicrodilution methodGram-positive bacteria: MICs 8–64 µg/mL; Gram-negative bacteria: MICs ≥ 32 µg/mL; yeast: MIC = 512 µg/mL[54]
Flavonoids among them two natural (α, β-dihydroxanthohumol and 8-prenylnaringenin)Microdilution methodGrowth inhibition of MSSA and MRSA at MIC80 values of 5–50 µg/mL[43]
Humulinic acidMicrodilution methodInhibition of Lactobacillus brevis at MIC < 10 µM[60]
Lupulone, xanthohumol, and desmethylxanthohumolMicrodilution methodAntimicrobial effect against MSSA and MRSA with MICs values of 0.6–1.2 µg/mL for lupulone, 9.8–19.5 µg/mL for xanthohumol and 19.5–39 µg/mL for desmethylxanthohumol
Xanthohumol totally inhibited the biofilm formation at the MIC value. Desmethylxanthohumol and lupulone inhibited the biofilm formation at sub-inhibitory concentrations		[61]
Humulone, lupulone, and xanthohumolMicrodilution methodMICs values: 7.5–30 µg/mL for humulone, 0.5–4 µg/mL for lupulone, 2–4 µg/mL for xanthohumol
MBCs values: 30–125 µg/mL for humulone, 1–15 µg/mL for lupulone, 2–7.5 µg/mL for xanthohumol
90% reduction in biofilm formation using 2–7.5 µg/mL of lupulone, 15–30 µg/mL of xanthohumol and 30–250 µg/mL of humulone		[62]
Desmethylxanthohumol and co-humuloneSpotting methodAntifungal activity against Zymoseptoria tritici.
IC50 values: 0.36 g/L for essential oil and 0.73 g/L for cone extracts		[10]
(+)-catechin and (−)-epicatechinMicrodilution methodMIC: 0.15 mg/mL for Penicillium ochrochloron, 0.075 mg/mL for Penicillium funiculosum, 0.15 mg/mL for Penicillium verrucosum var. cyclopium
MBC: 0.30 mg/mL for Penicillium ochrochloron, 0.15 mg/mL for Penicillium funiculosum, 0.30 mg/mL for Penicillium verrucosum var. cyclopium		[2]
Anti-Inflammatory Activity
HumuloneMouse skin stimulated with the tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA)Humulone at 10 µmol inhibited TPA-induced COX-2 expression through the regulation of nuclear factor-kB[65]
IsoxanthohumolHuman umbilical vein endothelial cells (HUVEC) and human aortic smooth muscle cells (HASMC)Isoxanthohumol at a dose of 10 µmol reduced in HASMC the TNF-α by 26% and nuclear factor kappa B by 24%; in HUVEC, the decrease was 40% for TNF-α and 42% for nuclear factor kappa B[68]
Anticancer Activity
XanthohumolSulforhodamine B assayInduced cell death in human alveolar adenocarcinoma cell line[11]
Xanthohumol, xanthohumol C, and crude hop extractCellTiter 96 Aqueous Non-Radioactive Cell Proliferation Assay from PromegaAntiproliferative effects on breast cancer cells[13]
LupuloneMTT AssayAnticancer potential on 2 prostate cancer cell lines (PC3 and DU145 cells). IC50 was 5 μM for both cell lines after 3 days of treatment[70]
Hop extractMTT AssayAntiproliferative effects on human hepatoma carcinoma at doses of 0.6–1 mg/mL[75]
Other Bioactivities
XanthohumolIntracerebral hemorrhage model was induced by intrastriatal injection of bacterial collagenaseReduced the hemorrhagic injury and promote the neuronal recovery[71]
XanthohumolSenescence-accelerated prone male mice
(SAMP8)		Prevents the expression of brain damage induced by aging[72]
Hop extractMale C57BL/6J mice (4 weeks old) fed a
high-fat diet		Inhibited the increasing body and adipose tissue weight, adipose cell diameter, and liver lipids, and improved glucose tolerance induced by a high-fat diet[73]
Xanthohumol or 8-prenylnaringeninType 2 diabetes mellitus (T2DM) mice modelImproves metabolic dysfunctions associated with diabetes: body weight gain; decreased glycemia, triglyceride, cholesterol and alkaline phosphatase levels; and improved insulin sensitivity[74]
ORAC: oxygen radical absorbance capacity; TBARS: thiobarbituric acid reactive substances; MIC: minimum inhibitory concentration; MBC: minimum bactericidal concentration; MSSA: methicillin sensitive strains Staphylococcus; MRSA: methicillin resistant strains Staphylococcus; TPA: 12-O-tetradecanoylphorbol-13-acetate; MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide.

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Astray, G.; Gullón, P.; Gullón, B.; Munekata, P.E.S.; Lorenzo, J.M. Humulus lupulus L. as a Natural Source of Functional Biomolecules. Appl. Sci. 2020, 10, 5074. https://doi.org/10.3390/app10155074

AMA Style

Astray G, Gullón P, Gullón B, Munekata PES, Lorenzo JM. Humulus lupulus L. as a Natural Source of Functional Biomolecules. Applied Sciences. 2020; 10(15):5074. https://doi.org/10.3390/app10155074

Chicago/Turabian Style

Astray, Gonzalo, Patricia Gullón, Beatriz Gullón, Paulo E. S. Munekata, and José M. Lorenzo. 2020. "Humulus lupulus L. as a Natural Source of Functional Biomolecules" Applied Sciences 10, no. 15: 5074. https://doi.org/10.3390/app10155074

APA Style

Astray, G., Gullón, P., Gullón, B., Munekata, P. E. S., & Lorenzo, J. M. (2020). Humulus lupulus L. as a Natural Source of Functional Biomolecules. Applied Sciences, 10(15), 5074. https://doi.org/10.3390/app10155074

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