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Review

The Benefits of Anthocyanins against Obesity-Induced Inflammation

by
Chanya Ngamsamer
1,
Jintana Sirivarasai
2 and
Nareerat Sutjarit
2,*
1
Doctor of Philosophy Program in Nutrition, Faculty of Medicine, Ramathibodi Hospital and Institute of Nutrition, Mahidol University, Bangkok, 10400, Thailand
2
Graduate Program in Nutrition, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand
*
Author to whom correspondence should be addressed.
Biomolecules 2022, 12(6), 852; https://doi.org/10.3390/biom12060852
Submission received: 6 June 2022 / Revised: 15 June 2022 / Accepted: 15 June 2022 / Published: 20 June 2022
(This article belongs to the Special Issue The Value of Natural Compounds as Therapeutic Agents)
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Abstract

:
Obesity has become a serious public health epidemic because of its associations with chronic conditions such as type 2 diabetes mellitus, hypertension, cardiovascular disease, and cancer. Obesity triggers inflammation marked by the secretion of low-grade inflammatory cytokines including interleukin-6, C-reactive protein, and tumor necrosis factor-α, leading to a condition known as “meta-inflammation”. Currently, there is great interest in studying the treatment of obesity with food-derived bioactive compounds, which have low toxicity and no severe adverse events compared with pharmacotherapeutic agents. Here, we reviewed the beneficial effects of the bioactive compounds known as anthocyanins on obesity-induced inflammation. Foods rich in anthocyanins include tart cherries, red raspberries, black soybeans, blueberries, sweet cherries, strawberries and Queen Garnet plums. These anthocyanin-rich foods have been evaluated in cell culture, animal, and clinical studies, and found to be beneficial for health, reportedly reducing inflammatory markers. One factor in the development of obesity-related inflammation may be dysbiosis of the gut microbiome. Therefore, we focused this review on the in vitro and in vivo effects of anthocyanins on inflammation and the gut microbiota in obesity.

1. Introduction

Obesity, which has been rising in prevalence worldwide over the past several decades, is now considered a public health epidemic. Obesity for adults is defined as a body mass index of ≥30 kg/m2 in Western populations, while the current Asia-Pacific guidelines recommend using a lower body mass index of ≥25 kg/m2 [1]. Obesity is linked to metabolic conditions such as hyperglycemia and dyslipidemia, which are well-known risk factors for developing chronic noncommunicable diseases, including hypertension, type II diabetes mellitus (T2DM), cancer, and cardiovascular disease (CVD) [2]. Individuals with obesity exhibit chronic low-grade systemic inflammation, which is characterized by increased secretion of pro-inflammatory cytokines from adipose tissue, made dysfunctional by the excessive accumulation of fat into the circulation; these cytokines include interleukin-6 (IL-6), C-reactive protein (CRP) and tumor necrosis factor-α (TNF-α) [3].
Generally, treatments for obesity include lifestyle modification and pharmacotherapy aimed at reducing body weight and alleviating inflammation [4]. Clinical guidelines suggest a combination of lifestyle modification and pharmacotherapy [5]. However, such medicines are associated with severe adverse events such as mental disorders and stroke, and they are quite expensive [6,7]. Currently, there are many studies aimed at treating obesity through dietary lifestyle modifications. Bioactive chemicals, particularly those that are plant or animal-based compounds, have the potential to diminish the prevalence of chronic disorders [8]. Some bioactive compounds are also classified as phytochemicals. Phytochemicals such as polyphenols have antioxidant, anti-inflammatory, anti-obesity, and anti-aging properties [9,10].

2. Human Obesity: Its Causes and Consequences

The World Health Organization reports that “obesity has almost tripled globally since 1975”, highlighting that obesity has become a global epidemic. In 2016, more than 1.9 billion of the world’s population were overweight; of these, over 650 million individuals were classified as obese [11]. More importantly, the obesity epidemic is increasingly affecting children, with an estimated 38.2 million children under the age of 5 years suffering from obesity in 2019 [12]. The cornerstone of the disease of obesity is an energy imbalance that occurs when energy consumption, particularly excessive fat and sugar intake, exceeds energy expenditure. Currently, many individuals with extreme obesity lead a sedentary lifestyle and eventually become bedridden. In fact, the continuous increase in noncommunicable diseases such as T2DM, CVD, hepatic steatosis, neurodegenerative diseases, biliary diseases, and certain cancers are directly linked to the increased prevalence of human obesity [13]. Importantly, these obesity-related diseases also result in a shorter life expectancy and premature death.

3. Obesity-Induced Inflammation

Obesity is associated with inflammation through increased pro-inflammatory cytokine secretion resulting from inflammatory responses and altered metabolic homeostasis. “Meta-inflammation” is a term used to describe chronic low-grade inflammation as a response to obesity [13]. In obesity, excessive accumulation of fat in adipocytes causes adipose tissue dysfunction [14]. Compared with non-obese individuals, the dysfunctional adipose tissues in rodent models of obesity and humans with obesity secrete lower amounts of adiponectin, which exerts an anti-inflammatory effect on the liver, skeletal muscle, and adipose tissue. These dysfunctional tissues simultaneously secrete increased levels of pro-inflammatory cytokines such as CRP, IL-6 and TNF-α [15], which disrupt the metabolic state required to maintain immune homeostasis. Innate immune cells secrete several cytokines and acute-phase proteins to the sites of inflammation [3,16]. In people with obesity, there is a phenotypic switching from M2 macrophages to M1 macrophages in the adipose tissues. M2 macrophages, which are anti-inflammatory, play a role in the maintenance of tissue and are typical in the adipose tissues of lean individuals. By contrast, M1 macrophages produce pro-inflammatory cytokines and thus contribute to the development of insulin resistance [17]. An increase in M1 macrophages, which form a structure around adipocytes and release pro-inflammatory mediators such as IL-1, IL-6, IL-12, TNF-α, and chemokines, is part of the alteration in immune cell profile that is characteristic of obesity (Figure 1). As a result, tissue damage to the liver, colon, and arterial walls may occur. One possible underlying mechanism of obesity-induced inflammation is the activation of toll-like receptors (TLRs) of the innate immune system in obese patients, particularly TLR4, which involves the activation of transcription factors such as nuclear factor kappa B (NF-κB) and the production of pro-inflammatory markers [18,19].
In patients with prolonged obesity, there may be a switch from the innate immune response to the adaptive immune response, leading to the onset of obesity-associated chronic diseases. Thus, obesity-related chronic diseases can be prevented or delayed by preventing long-term obesity [16]. Below we review the nutraceutical and pharmaceutical effects of anthocyanins that might be beneficial for treating obesity-related inflammation.

4. Anthocyanins

Anthocyanins are water-soluble pigments within the phenol class of compounds. They are abundant in nature, and can be found in vegetables, fruits, and flowers. Anthocyanin pigments in plants occur in the form of glycosides. All anthocyanins play a significant role in preventing chronic noncommunicable diseases.

4.1. Chemistry of Anthocyanins

Anthocyanins are considered to be flavonoids, although they have a positive charge at the oxygen atom of the C-ring of the fundamental flavonoid structure. Such a compound is also called the flavylium (2-phenylchromenylium) ion. The general molecular structure of anthocyanins is shown in Figure 2. Anthocyanins are derived from flavanols, but with a flavylium ion lacking a ketone oxygen at the 4-position (Figure 3) [20]. The empirical formula for the flavylium ion of anthocyanin is C15H11O+ with a molecular weight of 207.24724 g/mol [21].

4.2. Bioavailability of Anthocyanins

The majority of bioactive compounds in functional foods have been linked to lower risks of chronic conditions including CVD and T2DM [8]. Some bioactive compounds, such as polyphenols, are also phytochemicals. Polyphenolic compounds have antioxidant, anti-inflammatory, anti-obesity, and anti-aging properties [9,10]. Apart from the overall content and biological functions of bioactive components, bioavailability is also an important factor. The term “bioavailability” is defined by the US Food and Drug Administration as the rate and extent to which an active ingredient is absorbed from a drug product and becomes available at the site of action, and includes metabolism and excretion [22]. The anthocyanins have exhibited low bioavailability in animal studies, as indicated by low systemic concentrations [23,24,25]. Examinations of plasma after intake of anthocyanin-rich foods such as blackcurrant juice, red wine, and strawberries, have revealed that anthocyanins have limited bioavailability in humans as well [26,27,28]. Previous research in both humans and animals has established that the low bioavailability of anthocyanins is attributable to their limited absorption into the circulation and significant elimination in urine and feces.
In contrast, a study on the phytochemical uptake following human consumption of the Montmorency tart cherry, which is rich in anthocyanins, has shown that anthocyanin metabolites are most bioavailable in the plasma at 1–2 hours post consumption, indicating that anthocyanins might be rapidly absorbed [29]. Moreover, a literature survey on the bioavailability of anthocyanins and anthocyanin-containing foods among humans by Manach et al. (2005), found that the bioavailability of anthocyanins is generally poor, although they may be rapidly absorbed at first. Multiple authors, as cited by Manach, et al. (2005), note that anthocyanins are absorbed rapidly in a manner consistent with stomach absorption, but the absorption efficiencies were very poor with plasma concentrations approximately six orders of magnitude lower than the ingested dose. Furthermore this small absorbed fraction was rapidly eliminated via the urine. [30]. However, there are novel technologies that can be utilized to increase anthocyanin bioavailability, as discussed below.

4.3. Stability of Anthocyanins

The stability of anthocyanin pigments are affected by pH, light, temperature, and structure [20]. Anthocyanins change color in response to different pH levels. Under acidic conditions, anthocyanins may appear as the red-colored flavylium ion, while under alkaline conditions, they change to the blueish color of quinoidal bases [31]. Temperature also affects anthocyanin color. In higher solution temperatures, anthocyanins can become less stable due to coupled oxidation reactions of peroxidase and hydrogen peroxide (H2O2) [32]. The food industry offers many different fruit and vegetable products that are rich in anthocyanins, such as juices and supplements. However, industrial anthocyanin-containing products are often subjected to thermal processing and other common food processing methods that can decrease stability and total anthocyanin content [33]. In the last decade, novel food-processing technologies such as high pressure processing (HPP), high hydrostatic pressure (HHP), and pulsed electric fields (PEF) have been developed that may help prevent the loss of color, total anthocyanin content, and potential health benefits of anthocyanins [34]. To prevent the loss of potential health benefits specifically, we suggest the application of the following novel technologies in food processing: A previous study reported that HPP treatment of blueberry juice led to minor changes in ascorbic acid, total phenolics, anthocyanin stability, and total antioxidant capacity compared with fresh blueberry juice because the pressure–time conditions were maximized at a maximum temperature of 42 °C [35]. Encapsulation technology can also protect a bioactive molecule such as anthocyanin from the effects of oxygen, light, or other factors. Spray-drying is a common technique used for the encapsulation of compounds [36]. An extract of cultivated purple flesh potato (PFPE) was encapsulated by spray-drying with maltodextrin (MD) as the encapsulating agent. The constant degradation rate and bioavailability of anthocyanins within an in vitro gastrointestinal digestion model are significantly higher in PFPE-MD than in non-encapsulated PFPE because powder encapsulation protects the stable colorant and health benefits of anthocyanins [37]. Kanokpanont et al. (2018) demonstrated that anthocyanin-encapsulated alginate/chitosan beads derived from spray-dried mulberries were stable under gastric conditions that simulated gastric fluid conditions or enhanced the bioavailability of anthocyanins [38]. In conclusion, novel technologies such as microencapsulation and HPP treatment are an effective strategy to preserve the biological functions and nutrient content of anthocyanins in food processing.
Anthocyanins comprise a subclass of phenolic phytochemicals. They are water-soluble compounds with orange, red, purple, and blue colors, and are present in fruits and vegetables such as pomegranates, berries, red grapes, purple tomatoes, and red cabbage. The most common types of anthocyanins are pelargonidin, cyanidin, peonidin, petunidin, delphinidin, and malvidin (Table 1) [21,39,40]. Anthocyanins have been investigated as bio-functional molecules possessing anti-inflammatory, antioxidant, and chemoprotective properties, and they play significant preventive roles in chronic diseases [41].

5. Effects of Anthocyanins in Obesity-Associated Inflammation

The abundant natural anthocyanins are well-characterized antioxidants that have been shown to eliminate reactive oxygen species (ROS) in cells, animals, and clinical studies [42,43,44,45,46,47,48].
In cell culture studies, strawberries were found to be rich in anthocyanins and contain a high antioxidant capacity. Heo and Lee (2005) showed that strawberries, as compared with bananas and oranges, dramatically reduced oxidative-stress-induced neurotoxicity in PC12 cells treated with H2O2 [42].
In animal studies, the purple sweet potato color (PSPC) protected against ROS production and restored glutathione content in high-fat diet (HFD)-induced mice [43,44]. Blackberry and blueberry anthocyanin (BLA and BBA) supplementation reduced oxidative stress and inflammation by increasing first-line defense antioxidants such as superoxide dismutase (SOD) and glutathione peroxidase (GPx). Furthermore, supplementation of BLA and BBA for 12 weeks prevented weight gain in HFD-induced obesity in C57BL/6 mice [45]. Mulberry and cherry anthocyanins reduced body weight and improved SOD and GPx activities in HFD-fed mice [46]. In clinical studies, healthy volunteers who supplemented their daily diet with 500 g of strawberries rich in anthocyanins for 1 month lowered their risk for developing CVD, as assessed by improvements in lipid profiles and antioxidant activity [47]. Li et al. (2015) studied participants with T2DM who received purified anthocyanin supplements for 24 weeks and found that anthocyanin improved lipid profiles and enhanced antioxidant capacity, as well as insulin sensitivity [48].
In summary, anthocyanins play a role as antioxidants that can eliminate ROS and help prevent chronic diseases including CVD and T2DM. Additionally, anthocyanins can reduce pro-inflammatory markers associated with obesity, such as CRP, IL-6, and TNF-α (Table 2).

5.1. Anti-Inflammatory Effect

Obesity has been linked to chronic low-grade systemic inflammation. Secretion of inflammatory cytokines such as IL-6 and TNF-α by adipocytes and macrophages in adipose tissue have been shown to activate the inflammatory response [64]. Alleviating inflammation can be achieved by decreasing the release of pro-inflammatory cytokines. Several studies have been conducted using cell cultures and animal models, as well as clinical trials in humans, to examine the impact of anthocyanin-rich foods on obesity-induced inflammation.
In vitro studies have shown that anthocyanin-rich fruit extracts can moderate inflammatory cytokines associated with obesity. Tart cherries rich in anthocyanins significantly reduced the expression of the IL-6 gene in lipopolysaccharide (LPS)-induced adipose stem cells [49]. Consistent with other studies, RAW264.7 mouse macrophage cells that were induced with both Escherichia coli LPS and recombinant interferon-c, and treated with anthocyanin-rich fractions of red raspberries at concentrations of 150 and 200 µg/mL, showed reduced nitric oxide (NO), cyclooxygenase-2 (COX-2), IL-1β, and IL-6 expression, as well as inhibition of the NF-kB inflammatory pathway [50]. Likewise, treatment with black soybean extract decreased TNF-α production, but increased adiponectin secretion and insulin sensitivity, in 3T3-L1 adipocytes [51]. In another study, sweet cherry phenolic-rich extract significantly reduced NO levels and decreased COX-2 and inducible nitric oxide synthase (iNOS) expression in LPS-induced adipose stem cells [52].
Among the animal studies, administration of a blueberry supplement containing phenolics and anthocyanins also decreased the expression of the TNF-α and IL-1β genes in HFD–fed male rats [53]. Anthocyanin-rich tart cherry extract effectively improved the pro-inflammatory cytokine profile by reducing IL-6 and leptin levels in an obese mouse model [54]. Similarly, tart cherry reduced TNF-α, IL-1β, and IL-6 expression and suppressed NF-kB inflammatory expression in HFD-induced obese rats after a 17-week intervention with tart cherry seed powder and tart cherry juice [55]. Therefore, tart cherries have the potential to prevent obesity-induced inflammation. Purified sweet cherry anthocyanins at 200 mg/kg in mice reduced body weight by approximately 11.2% and decreased the expression of the IL-6 and TNF-α genes in white adipose tissue (WAT), slowing down the progression of obesity in these mice [56]. In another study, a pomegranate peel extract (PPE) with high polyphenol content decreased COX-2 and IL-1 mRNA levels in visceral adipose tissue [57].
Anthocyanins have been shown in animal studies and cell cultures to reduce obesity-related inflammation. Therefore, many studies have aimed to evaluate the effect of anthocyanins on inflammation associated with obesity in humans. Strawberry antioxidants containing 81.65 mg anthocyanins/10 g of freeze-dried powder in a beverage significantly attenuated the postprandial inflammatory response by decreasing high-sensitivity CRP and IL-6) in an overweight population, following the consumption of a high-carbohydrate, moderate-fat meal (HCFM) [58]. Black soybean testa (BBT) extracts rich in three major anthocyanins reduced visceral fat, and improved plasma lipid profiles and inflammatory markers including TNF-α and monocyte chemoattractant protein-1 in overweight/obese adults [59]. Bhaswant et al. (2019) discovered that the high anthocyanin content in Queen Garnet plum juice significantly reduced IL-2, IL-6, IL-13, and TNF-α levels in mildly hypertensive overweight or obese people. Queen Garnet plum juice also reduced the levels of low-density lipoprotein, plasma glucose, insulin, C-peptide, leptin, and glucagon-like peptide-1 [60]. Authentic tart cherry juice (TCJ) at 240 mL of 100% TCJ (equivalent to 50 tart cherries) reduced TNF-α and monocyte chemoattractant protein-1 (MCP-1) levels compared to placebo after 4 weeks of consumption in overweight and obese individuals [61].
Both in vitro and in vivo studies have reported that foods rich in anthocyanins reduced inflammation associated with obesity, including tart cherries, PPE, and strawberry beverages. By contrast, some clinical studies found no anti-inflammatory effect of anthocyanins in people with obesity [62,63]. Zunino et al. (2012) showed that people consuming 80 g/serving of freeze-dried strawberry powder mixed with food and drinks for 3 weeks had no effect on inflammatory markers (IL-6, IL-1β, TNF-α) [62]. Similarly, consumption of commercially available red orange juice (250 mg anthocyanins/day) for 12 weeks did not show any effect on body weight or plasma inflammatory markers [63]. Possible reasons for the lack of beneficial effects of anthocyanins on obesity-induced inflammation in these studies are the use of relatively low dosages and the short length of the intervention.

5.2. Regulating the Gut Microbiota

Microbes living in the gut play a role in the onset of obesity [65]. Obesity is associated with changes in the gut microbiota that lead to gut dysbiosis. People with obesity have lower proportions of bacteria from the phylum Bacteroidetes, such as Bacteroides spp., and higher proportions from the phylum Firmicutes, such as Bacillus spp. and Clostridium. Firmicutes bacteria are distinguished by higher endotoxic activity of membrane-bound LPS compared with other gram-negative bacteria, thereby inducing more systemic inflammation. Furthermore, obesity promotes the initiation of numerous pro-inflammatory pathways by causing TLR4-mediated inflammatory responses that involve activation of the transcription factor NF-κB and the production of pro-inflammatory mediators such as IL-6, IL-1, and TNF-α [65,66,67,68]. A previous study reported that pomegranate peel extract (PPE) is rich in anthocyanins. Treatment with a PPE was shown to modulate the gut microbiota in obese mice by lowering COX-2 levels in the colon and visceral adipose tissue, as well as mRNA levels of IL-1 and IL-6 in the colon [57]. Another study in mice demonstrated that cranberry extract at 200 mg/kg reduced the abundance of Firmicutes but enhanced that of Bacteroidetes, and concluded that anthocyanin-rich cranberry extract protects dysbiosis of the microbiota in mice with diet-induced obesity [69].

5.3. Molecular Pathway for Effects of Anthocyanin on Obesity-Associated Inflammation

NF-κB is a family of inducible transcription factors that regulate genes involved in inflammatory responses and includes NF-κB1 (p50), NF-κB2 (p52), RelA, RelB, and c-Rel [70,71]. Under normal conditions, an NF-κB heterodimer (p50-RelA) is retained in an active form through interaction with inhibitory kappa B (IκB). The NF-κB pathway can be activated by extracellular stimuli such as ROS and a HFD. Upon stimulation, IκB is phosphorylated by the IκB kinase complex, then subsequently ubiquitinated and degraded by the 26S proteasome, allowing the p50-RelA heterodimer to translocate into the nucleus, where it promotes the expression of proinflammatory genes including TNF-α, IL-1α, and IL-1β. These genes are pathogenic in a variety of inflammatory disorders, such as obesity, T2DM, and CVD [71,72,73]. Vendramea et al. (2013) reported that an 8-week freeze-dried wild-blueberry-powder-enriched diet containing 1.5% w/w of total anthocyanin content significantly reduced the expression of genes encoding the inflammatory mediators NF-κB, TNF-α, IL-6, and CRP, both in the liver and abdominal adipose tissues, in obese Zucker rats [74]. This study concluded that anthocyanins modulated the molecular pathway of the inflammatory process, i.e., the expression of transcription factor NF-κB.
TLRs are a class of pattern recognition receptors that play a key role in the innate immune system [75]. The binding of LPS to the TLR4 receptor promotes the activation of M1 macrophages, which release pro-inflammatory cytokines [76]. Upon binding of TLR4 ligands, TLR4 recruits the adaptor molecule myeloid differentiation factor 88 (MyD88), which then recruits IL-1 receptor-associated kinase-4 (IRAK-4). Subsequently, IRAK-4 recruits TNF receptor-associated factor 6 (TRNF6) to the receptor complex. When IRAK-4 is phosphorylated, the IRAK-4–TRAF6 complex separates from the receptor complex to conjugate with transforming growth factor-β-activated kinase 1 (TAK1) [77]. Upon activation, TAK1 causes IκB to be phosphorylated and ubiquitinated, leading to degradation of IκB. As a result, the NF-κB signaling pathway is activated and inflammatory mediators are released [78]. Karunarathne et al. (2020) studied anthocyanins isolated from Hibiscus syriacus L. in RAW 264.7 macrophages and found that anthocyanin inhibits TLR4 in LPS-induced cells. Consequently, phosphorylation of MyD88 and IRAK4 is decreased, leading to the inhibition of the NF-κB signaling pathway [79]. Anthocyanins from black soybeans were shown to inhibit IκB phosphorylation, thereby inhibiting NF-κB nuclear translocation and activation in Helicobacter-pylori-induced inflammation in human gastric epithelial cells. As a result, NO and COX-2 gene expression was significantly attenuated [80]. In pro-inflammatory conditions, excess NO is converted to a pro-oxidative role, while COX-2 leads to the formation of pro-inflammatory mediators such as prostaglandin E2 [81]. These mechanisms of NF-κB pathways act as a link between oxidative stress and inflammation. Anthocyanins prevent NF-κB activation, thus suppressing the entire downstream cascade, including proinflammatory cytokines, chemokines, adhesion molecules, NO, and COX-2.
  • SUMMARY POINTS
  • Obesity is associated with meta-inflammation, a newly coined term for chronic low-grade inflammation as a response to obesity.
  • The state of inflammation in obesity is associated with adipose tissue dysfunction, which increases the secretion of pro-inflammatory cytokines such as TNF-α, CRP, and IL-6. Additionally, increased numbers of M1 macrophages in adipose tissue can release pro-inflammatory cytokines.
  • Anthocyanins decrease the production of inflammatory cytokines in obese animal models, in studies conducted both in vitro and in vivo.
  • Anthocyanins might have potential to be a treatment for obesity-related inflammation and chronic diseases.
  • Be aware that the bioavailability, including metabolism and excretion, of anthocyanins is low. Therefore, future research is needed to increase the bioavailability of anthocyanins to improve their beneficial anti-inflammatory effects in people with obesity.

6. Conclusions

We reviewed the benefits of anthocyanin-rich foods such as sweet cherries, black soybeans, and strawberries on obesity prevention, including antioxidant and anti-inflammatory effects, and regulation of the gut microbiota in cell cultures, animal models, and human clinical trials. As shown in Figure 4, dietary anthocyanins may have anti-obesity effects and may reduce the risks of the most common chronic noncommunicable diseases.

Author Contributions

Conceptualization: C.N. and N.S.; writing—original draft preparation: C.N.; writing—review and editing, C.N., N.S. and J.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. WHO Expert Consultation. Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. Lancet. 2004, 363, 157–163. [Google Scholar] [CrossRef]
  2. Finucane, M.M.; Stevens, G.A.; Cowan, M.J.; Danaei, G.; Lin, J.K.; Paciorek, C.J.; Singh, G.M.; Gutierrez, H.R.; Lu, Y.; Bahalim, A.N.; et al. National, regional, and global trends in body-mass index since 1980: Systematic analysis of health examination surveys and epidemiological studies with 960 country-years and 91 million participants. Lancet 2011, 377, 557–567. [Google Scholar] [CrossRef] [Green Version]
  3. Gregor, M.F.; Hotamisligil, G.S. Inflammatory mechanisms in obesity. Annu. Rev. Immunol. 2011, 29, 415–445. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Forsythe, L.K.; Wallace, J.M.; Livingstone, M.B. Obesity and inflammation: The effects of weight loss. Nutr. Res. Rev. 2008, 21, 117–133. [Google Scholar] [CrossRef] [PubMed]
  5. Garvey, W.T.; Mechanick, J.I.; Brett, E.M.; Garber, A.J.; Hurley, D.L.; Jastreboff, A.M.; Nadolsky, K.; Pessah-Pollack, R.; Plodkowski, R.; Reviewers of the AACE/ACE Obesity Clinical Practice Guidelines. American Association of Clinical Endocrinologists and American College of Endocrinology Comprehensive Clinical Practice Guidelines for Medical Care of Patients with Obesity. Endocr Pract. 2016, 22 (Suppl. S3), 1–203. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Bessesen, D.H.; Van Gaal, L.F. Progress and challenges in anti-obesity pharmacotherapy. Lancet Diabetes Endocrinol. 2018, 6, 237–248. [Google Scholar] [CrossRef]
  7. Kang, J.G.; Park, C.Y. Anti-obesity drugs: A review about their effects and safety. Diabetes Metab. J. 2012, 36, 13–25. [Google Scholar] [CrossRef] [Green Version]
  8. Konstantinidi, M.; Koutelidakis, A.E. Functional foods and bioactive compounds: A review of its possible role on weight management and obesity’s metabolic consequences. Medicines 2019, 6, 94. [Google Scholar] [CrossRef] [Green Version]
  9. Wang, S.; Moustaid-Moussa, N.; Chen, L.; Mo, H.; Shastri, A.; Su, R.; Bapat, P.; Kwun, I.; Shen, C.-L. Novel insights of dietary polyphenols and obesity. J. Nutr. Biochem. 2014, 25, 1–18. [Google Scholar] [CrossRef] [Green Version]
  10. Joseph, S.V.; Edirisinghe, I.; Burton-Freeman, B.M. Fruit polyphenols: A review of anti-inflammatory effects in humans. Crit. Rev. Food Sci. Nutr. 2016, 56, 419–444. [Google Scholar] [CrossRef]
  11. WHO. WHO Fact Files: Obesity and overweight. Geneva: WHO 2020. Available online: https://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight (accessed on 12 December 2021).
  12. Ogden, C.L.; Carroll, M.D.; Curtin, L.R.; Lamb, M.M.; Flegal, K.M. Prevalence of high body mass index in US children and adolescents, 2007–2008. JAMA. 2010, 303, 242–249. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Hotamisligil, G.S. Inflammation and metabolic disorders. Nature 2006, 444, 860–867. [Google Scholar] [CrossRef] [PubMed]
  14. Longo, M.; Zatterale, F.; Naderi, J.; Parrillo, L.; Formisano, P.; Raciti, G.A.; Beguinot, F.; Miele, C. Adipose tissue dysfunction as determinant of obesity-associated metabolic complications. Int. J. Mol. Sci. 2019, 20, 2358. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Shoelson, S.E.; Lee, J.; Goldfine, A.B. Inflammation and insulin resistance. J. Clin. Investig. 2006, 116, 1793–1801. [Google Scholar] [CrossRef]
  16. Lee, B.C.; Lee, J. Cellular and molecular players in adipose tissue inflammation in the development of obesity-induced insulin resistance. Biochim. Biophys. Acta 2014, 1842, 446–462. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Schipper, H.S.; Prakken, B.; Kalkhoven, E.; Boes, M. Adipose tissue-resident immune cells: Key players in immunometabolism. Trends Endocrinol. Metab. 2012, 23, 407–415. [Google Scholar] [CrossRef]
  18. Odegaard, J.I.; Chawla, A. The immune system as a sensor of the metabolic state. Immunity 2013, 38, 644–654. [Google Scholar] [CrossRef] [Green Version]
  19. Li, C.; Xu, M.M.; Wang, K.; Adler, A.J.; Vella, A.T.; Zhou, B. Macrophage polarization and meta-inflammation. Transl. Res. 2018, 191, 29–44. [Google Scholar] [CrossRef]
  20. Lahleh, G.H.; Frydoonfar, H.; Heidary, R.; Jamei, R.; Zare, S. The effect of light, temperature, pH and species on stability of anthocyanin pigments in four berberis species. Pak. J. Nutr. 2006, 5, 90–92. [Google Scholar]
  21. Khoo, H.E.; Azlan, A.; Tang, S.T.; Lim, S.M. Anthocyanidins and anthocyanins: Colored pigments as food, pharmaceutical ingredients, and the potential health benefits. Food Nutr. Res. 2017, 61, 1361779. [Google Scholar] [CrossRef] [Green Version]
  22. Fang, J. Bioavailability of anthocyanins. Drug Metab. Rev. 2014, 46, 508–520. [Google Scholar] [CrossRef] [PubMed]
  23. Borges, G.; Roowi, S.; Rouanet, J.M.; Duthie, G.G.; Lean, M.E.; Crozier, A. The bioavailability of raspberry anthocyanins and ellagitannins in rats. Mol. Nutr. Food Res. 2007, 51, 714–725. [Google Scholar] [CrossRef] [PubMed]
  24. Felgines, C.; Texier, O.; Besson, C.; Fraisse, D.; Lamaison, J.L.; Rémésy, C. Blackberry anthocyanins are slightly bioavailable in rats. J. Nutr. 2002, 132, 1249–1253. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Ichiyanagi, T.; Shida, Y.; Rahman, M.M.; Hatano, Y.; Konishi, T. Bioavailability and tissue distribution of anthocyanins in bilberry (Vaccinium myrtillus L.) extract in rats. J. Agric. Food Chem. 2006, 54, 6578–6587. [Google Scholar] [CrossRef]
  26. Rechner, A.R.; Kuhnle, G.; Hu, H.; Roedig-Penman, A.; van den Braak, M.H.; Moore, K.P.; Rice-Evans, C.A. The metabolism of dietary polyphenols and the relevance to circulating levels of conjugated metabolites. Free Radic. Res. 2002, 36, 1229–1241. [Google Scholar] [CrossRef]
  27. Bub, A.; Watzl, B.; Heeb, D.; Rechkemmer, G.; Briviba, K. Malvidin-3-glucoside bioavailability in humans after ingestion of red wine, dealcoholized red wine and red grape juice. Eur. J. Nutr. 2001, 40, 113–120. [Google Scholar] [CrossRef]
  28. Felgines, C.; Talavéra, S.; Gonthier, M.P.; Texier, O.; Scalbert, A.; Lamaison, J.L.; Rémésy, C. Strawberry anthocyanins are recovered in urine as glucuro- and sulfoconjugates in humans. J. Nutr. 2003, 133, 1296–1301. [Google Scholar] [CrossRef] [Green Version]
  29. Keane, K.M.; Bell, P.G.; Lodge, J.K.; Constantinou, C.L.; Jenkinson, S.E.; Bass, R.; Howatson, G. Phytochemical uptake following human consumption of Montmorency tart cherry (L. Prunus cerasus) and influence of phenolic acids on vascular smooth muscle cells in vitro. Eur. J. Nutr. 2016, 55, 1695–1705. [Google Scholar]
  30. Manach, C.; Williamson, G.; Morand, C.; Scalbert, A.; Rémésy, C. Bioavailability and bioefficacy of polyphenols in humans. I. Review of 97 bioavailability studies. Am. J. Clin. Nutr. 2005, 81, 230s–242s. [Google Scholar] [CrossRef] [Green Version]
  31. Andersen, O.M.J. Basic Anthocyanin Chemistry and Dietary Sources; CRC Press: Boca Raton, FL, USA, 2014. [Google Scholar]
  32. Rehman, R.N.U.; You, Y.; Zhang, L.; Goudia, B.D.; Khan, A.R.; Li, P.; Ma, F. High temperature induced anthocyanin inhibition and active degradation in Malus profusion. Front. Plant Sci. 2017, 8, 1401. [Google Scholar] [CrossRef]
  33. Patras, A.; Brunton, N.P.; O’Donnell, C.; Tiwari, B.K. Effect of thermal processing on anthocyanin stability in foods, mechanisms and kinetics of degradation. Trends Food Sci. Technol. 2010, 21, 3–11. [Google Scholar] [CrossRef]
  34. Tiwari, B.K.; O’Donnell, C.P.; Cullen, P.J. Effect of non-thermal processing technologies on the anthocyanin content of fruit juices. Trends Food Sci. Technol. 2009, 20, 137–145. [Google Scholar] [CrossRef]
  35. Barba, F.J.; Esteve, M.J.; Frigola, A. Physicochemical and nutritional characteristics of blueberry juice after high pressure processing. Food Res. Int. 2013, 50, 545–549. [Google Scholar] [CrossRef]
  36. Akhavan Mahdavi, S.; Jafari, S.M.; Assadpoor, E.; Dehnad, D. Microencapsulation optimization of natural anthocyanins with maltodextrin, gum arabic and gelatin. Int. J. Biol. Macromol. 2016, 85, 379–385. [Google Scholar] [CrossRef] [PubMed]
  37. Vergara, C.; Pino, M.T.; Zamora, O.; Parada, J.; Pérez, R.; Uribe, M.; Kalazich, J. Microencapsulation of anthocyanin extracted from purple flesh cultivated potatoes by spray drying and its effects on in vitro gastrointestinal digestion. Molecules 2020, 25, 722. [Google Scholar] [CrossRef] [Green Version]
  38. Kanokpanont, S.; Yamdech, R.; Aramwit, P. Stability enhancement of mulberry-extracted anthocyanin using alginate/chitosan microencapsulation for food supplement application. Artif. Cells Nanomed. Biotechnol. 2018, 46, 773–782. [Google Scholar] [CrossRef] [Green Version]
  39. Castañeda-Ovando, A.; Pacheco-Hernández, M.D.L.; Páez-Hernández, M.E.; Rodríguez, J.A.; Galán-Vidal, C.A. Chemical studies of anthocyanins: A review. Food Chem. 2009, 113, 859–871. [Google Scholar] [CrossRef]
  40. He, J.; Giusti, M.M. Anthocyanins: Natural colorants with health-promoting properties. Annu Rev Food Sci Technol. 2010, 1, 163–187. [Google Scholar] [CrossRef]
  41. Cianciosi, D.; Varela-Lopez, A.; Forbes-Hernandez, T.Y.; Gasparrini, M.; Afrin, S.; Reboredo-Rodriguez, P.; Zhang, J.; Quiles, J.L.; Nabavi, S.F.; Battino, M.; et al. Targeting molecular pathways in cancer stem cells by natural bioactive compounds. Pharmacol. Res. 2018, 135, 150–165. [Google Scholar] [CrossRef]
  42. Heo, H.J.; Lee, C.Y. Strawberry and its anthocyanins reduce oxidative stress-induced apoptosis in PC12 cells. J. Agric. Food Chem. 2005, 53, 1984–1989. [Google Scholar] [CrossRef]
  43. Zhang, Z.F.; Lu, J.; Zheng, Y.L.; Wu, D.M.; Hu, B.; Shan, Q.; Cheng, W.; Li, M.-Q.; Sun, Y.-Y. Purple sweet potato color attenuates hepatic insulin resistance via blocking oxidative stress and endoplasmic reticulum stress in high-fat-diet-treated mice. J. Nutr. Biochem. 2013, 24, 1008–1018. [Google Scholar] [CrossRef]
  44. Esatbeyoglu, T.; Rodríguez-Werner, M.; Schlösser, A.; Winterhalter, P.; Rimbach, G. Fractionation, enzyme inhibitory and cellular antioxidant activity of bioactives from purple sweet potato (Ipomoea batatas). Food Chem. 2017, 221, 447–456. [Google Scholar] [CrossRef] [PubMed]
  45. Wu, T.; Gao, Y.; Guo, X.; Zhang, M.; Gong, L. Blackberry and blueberry anthocyanin supplementation counteract high-fat-diet-induced obesity by alleviating oxidative stress and inflammation and accelerating energy expenditure. Oxid. Med. Cell Longev. 2018, 2018, 4051232. [Google Scholar] [CrossRef] [PubMed]
  46. Wu, T.; Yin, J.; Zhang, G.; Long, H.; Zheng, X. Mulberry and cherry anthocyanin consumption prevents oxidative stress and inflammation in diet-induced obese mice. Mol. Nutr. Food Res. 2016, 60, 687–694. [Google Scholar] [CrossRef] [PubMed]
  47. Alvarez-Suarez, J.M.; Giampieri, F.; Tulipani, S.; Casoli, T.; Di Stefano, G.; González-Paramás, A.M.; Santos-Buelga, C.; Busco, F.; Quiles, J.L.; Cordero, M.D.; et al. One-month strawberry-rich anthocyanin supplementation ameliorates cardiovascular risk, oxidative stress markers and platelet activation in humans. J. Nutr. Biochem. 2014, 25, 289–294. [Google Scholar] [CrossRef] [PubMed]
  48. Li, D.; Zhang, Y.; Liu, Y.; Sun, R.; Xia, M. Purified anthocyanin supplementation reduces dyslipidemia, enhances antioxidant capacity, and prevents insulin resistance in diabetic patients. J. Nutr. 2015, 145, 742–748. [Google Scholar] [CrossRef] [PubMed]
  49. Zhou, Z.; Nair, M.G.; Claycombe, K.J. Synergistic inhibition of interleukin-6 production in adipose stem cells by tart cherry anthocyanins and atorvastatin. Phytomedicine 2012, 19, 878–881. [Google Scholar] [CrossRef]
  50. Li, L.; Wang, L.; Wu, Z.; Yao, L.; Wu, Y.; Huang, L.; Liu, K.; Zhou, X.; Gou, D. Anthocyanin-rich fractions from red raspberries attenuate inflammation in both RAW264.7 macrophages and a mouse model of colitis. Sci. Rep. 2014, 4, 6234. [Google Scholar] [CrossRef] [Green Version]
  51. Matsukawa, T.; Inaguma, T.; Han, J.; Villareal, M.O.; Isoda, H. Cyanidin-3-glucoside derived from black soybeans ameliorate type 2 diabetes through the induction of differentiation of preadipocytes into smaller and insulin-sensitive adipocytes. J. Nutr. Biochem. 2015, 26, 860–867. [Google Scholar] [CrossRef]
  52. Gonçalves, A.C.; Costa, A.R.; Flores-Félix, J.D.; Falcão, A.; Alves, G.; Silva, L.R. Anti-inflammatory and antiproliferative properties of sweet cherry phenolic-rich extracts. Molecules 2022, 27, 268. [Google Scholar] [CrossRef]
  53. Lee, S.; Keirsey, K.I.; Kirkland, R.; Grunewald, Z.I.; Fischer, J.G.; de La Serre, C.B. Blueberry supplementation influences the gut microbiota, inflammation, and insulin resistance in high-fat-diet-fed rats. J. Nutr. 2018, 148, 209–219. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Nemes, A.; Homoki, J.R.; Kiss, R.; Hegedűs, C.; Kovács, D.; Peitl, B.; Gál, F.; Stündl, L.; Szilvássy, Z.; Remenyik, J. Effect of anthocyanin-rich tart cherry extract on inflammatory mediators and adipokines involved in type 2 diabetes in a high fat diet induced obesity mouse model. Nutrients 2019, 11, 1966. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Martinelli, I.; Tomassoni, D.; Bellitto, V.; Roy, P.; Di Bonaventura, M.V.M.; Amenta, F.; Amantini, C.; Cifani, C.; Tayebati, S.K. Anti-inflammatory and antioxidant properties of tart cherry consumption in the heart of obese rats. Biology 2022, 11, 646. [Google Scholar] [CrossRef] [PubMed]
  56. Wu, T.; Tang, Q.; Yu, Z.; Gao, Z.; Hu, H.; Chen, W.; Zheng, X.; Yu, T. Inhibitory effects of sweet cherry anthocyanins on the obesity development in C57BL/6 mice. Int. J. Food Sci. Nutr. 2014, 65, 351–359. [Google Scholar] [CrossRef] [PubMed]
  57. Neyrinck, A.M.; Van Hée, V.F.; Bindels, L.B.; De Backer, F.; Cani, P.D.; Delzenne, N.M. Polyphenol-rich extract of pomegranate peel alleviates tissue inflammation and hypercholesterolaemia in high-fat diet-induced obese mice: Potential implication of the gut microbiota. Br. J. Nutr. 2013, 109, 802–809. [Google Scholar] [CrossRef] [Green Version]
  58. Edirisinghe, I.; Banaszewski, K.; Cappozzo, J.; Sandhya, K.; Ellis, C.L.; Tadapaneni, R.; Kappagoda, C.T.; Burton-Freeman, B.M. Strawberry anthocyanin and its association with postprandial inflammation and insulin. Br. J. Nutr. 2011, 106, 913–922. [Google Scholar] [CrossRef]
  59. Lee, M.; Sorn, S.R.; Park, Y.; Park, H.K. Anthocyanin rich-black soybean testa improved visceral fat and plasma lipid profiles in overweight/obese Korean adults: A randomized controlled trial. J. Med. Food 2016, 19, 995–1003. [Google Scholar] [CrossRef]
  60. Bhaswant, M.; Brown, L.; Mathai, M.L. Queen garnet plum juice and raspberry cordial in mildly hypertensive obese or overweight subjects: A randomized, double-blind study. J. Funct. Foods 2019, 56, 119–126. [Google Scholar] [CrossRef]
  61. Martin, K.R.; Burrell, L.; Bopp, J. Authentic tart cherry juice reduces markers of inflammation in overweight and obese subjects: A randomized, crossover pilot study. Food Funct. 2018, 9, 5290–5300. [Google Scholar] [CrossRef]
  62. Zunino, S.J.; Parelman, M.A.; Freytag, T.L.; Stephensen, C.B.; Kelley, D.S.; Mackey, B.E.; Woodhouse, L.R.; Bonnel, E.L. Effects of dietary strawberry powder on blood lipids and inflammatory markers in obese human subjects. Br. J. Nutr. 2012, 108, 900–909. [Google Scholar] [CrossRef] [Green Version]
  63. Azzini, E.; Venneria, E.; Ciarapica, D.; Foddai, M.S.; Intorre, F.; Zaccaria, M.; Maiani, F.; Palomba, L.; Barnaba, L.; Tubili, C.; et al. Effect of red orange juice consumption on body composition and nutritional status in overweight/obese female: A pilot study. Oxid. Med. Cell Longev. 2017, 2017, 1672567. [Google Scholar] [CrossRef] [PubMed]
  64. Bastard, J.P.; Maachi, M.; Lagathu, C.; Kim, M.J.; Caron, M.; Vidal, H.; Capeau, J.; Feve, B. Recent advances in the relationship between obesity, inflammation, and insulin resistance. Eur. Cytokine Netw. 2006, 17, 4–12. [Google Scholar] [PubMed]
  65. John, G.K.; Mullin, G.E. The gut microbiome and obesity. Curr. Oncol. Rep. 2016, 18, 45. [Google Scholar] [CrossRef] [PubMed]
  66. Ley, R.E.; Bäckhed, F.; Turnbaugh, P.; Lozupone, C.A.; Knight, R.D.; Gordon, J.I. Obesity alters gut microbial ecology. Proc. Natl. Acad. Sci. USA 2005, 102, 11070–11075. [Google Scholar] [CrossRef] [Green Version]
  67. Green, M.; Arora, K.; Prakash, S. Microbial medicine: Prebiotic and probiotic functional foods to target obesity and metabolic syndrome. Int. J. Mol. Sci. 2020, 21, 2890. [Google Scholar] [CrossRef]
  68. Lu, Y.C.; Yeh, W.C.; Ohashi, P.S. LPS/TLR4 signal transduction pathway. Cytokine 2008, 42, 145–151. [Google Scholar] [CrossRef]
  69. Anhê, F.F.; Roy, D.; Pilon, G.; Dudonné, S.; Matamoros, S.; Varin, T.V.; Garofalo, C.; Moine, Q.; Desjardins, Y.; Levy, E.; et al. A polyphenol-rich cranberry extract protects from diet-induced obesity, insulin resistance and intestinal inflammation in association with increased Akkermansia spp. population in the gut microbiota of mice. Gut 2015, 64, 872–883. [Google Scholar] [CrossRef] [Green Version]
  70. Sun, S.C.; Chang, J.H.; Jin, J. Regulation of nuclear factor-κB in autoimmunity. Trends Immunol. 2013, 34, 282–289. [Google Scholar] [CrossRef] [Green Version]
  71. Liu, T.; Zhang, L.; Joo, D.; Sun, S.-C. NF-κB signaling in inflammation. Signal Transduct. Target Ther. 2017, 2, 17023. [Google Scholar] [CrossRef] [Green Version]
  72. Hayden, M.S.; Ghosh, S. Shared principles in NF-kappaB signaling. Cell 2008, 132, 344–362. [Google Scholar] [CrossRef] [Green Version]
  73. Singh, A.; Kumar, D.S.; Vinayak, M. Recent development in antihyperalgesic effect of phytochemicals: Anti-inflammatory and neuro-modulatory actions. Inflamm. Res. 2018, 67, 633–654. [Google Scholar] [CrossRef] [PubMed]
  74. Vendrame, S.; Daugherty, A.; Kristo, A.S.; Riso, P.; Klimis-Zacas, D. Wild blueberry (Vaccinium angustifolium) consumption improves inflammatory status in the obese Zucker rat model of the metabolic syndrome. J. Nutr. Biochem. 2013, 24, 1508–1512. [Google Scholar] [CrossRef] [PubMed]
  75. Vidya, M.K.; Kumar, V.G.; Sejian, V.; Bagath, M.; Krishnan, G.; Bhatta, R. Toll-like receptors: Significance, ligands, signaling pathways, and functions in mammals. Int. Rev. Immunol. 2018, 37, 20–36. [Google Scholar] [CrossRef] [PubMed]
  76. Stephens, M.; Liao, S.; von der Weid, P.-Y. Ultra-purification of lipopolysaccharides reveals species-specific signalling bias of TLR4: Importance in macrophage function. Sci. Rep. 2021, 11, 1335. [Google Scholar] [CrossRef]
  77. Kim, T.W.; Staschke, K.; Bulek, K.; Yao, J.; Peters, K.; Oh, K.H.; Vandenburg, Y.; Xiao, H.; Qian, W.; Hamilton, T.; et al. A critical role for IRAK4 kinase activity in Toll-like receptor-mediated innate immunity. J. Exp. Med. 2007, 204, 1025–1036. [Google Scholar] [CrossRef] [Green Version]
  78. Sato, S.; Sanjo, H.; Takeda, K.; Ninomiya-Tsuji, J.; Yamamoto, M.; Kawai, T.; Matsumoto, K.; Takeuchi, O.; Akira, S. Essential function for the kinase TAK1 in innate and adaptive immune responses. Nat. Immunol. 2005, 6, 1087–1095. [Google Scholar] [CrossRef]
  79. Karunarathne, W.; Lee, K.T.; Choi, Y.H.; Jin, C.Y.; Kim, G.Y. Anthocyanins isolated from Hibiscus syriacus L. attenuate lipopolysaccharide-induced inflammation and endotoxic shock by inhibiting the TLR4/MD2-mediated NF-κB signaling pathway. Phytomedicine. 2020, 76, 153237. [Google Scholar] [CrossRef]
  80. Kim, J.-M.; Kim, K.-M.; Park, E.-H.; Seo, J.-H.; Song, J.-Y.; Shin, S.-C.; Kang, H.-Y.; Lee, W.-K.; Cho, M.-J.; Rhee, K.-H.; et al. Anthocyanins from black soybean inhibit Helicobacter pylori-induced inflammation in human gastric epithelial AGS cells. Microbiol. Immunol. 2013, 57, 366–373. [Google Scholar] [CrossRef]
  81. Vendrame, S.; Klimis-Zacas, D. Anti-inflammatory effect of anthocyanins via modulation of nuclear factor-κB and mitogen-activated protein kinase signaling cascades. Nutr. Rev. 2015, 73, 348–358. [Google Scholar] [CrossRef]
Biomolecules 12 00852 g001 550
Figure 1. Hallmark of meta-inflammation. The major cause of obesity is a positive energy balance between energy intake and energy expenditure leading to meta-inflammation, a chronic low-grade inflammatory condition.
Figure 1. Hallmark of meta-inflammation. The major cause of obesity is a positive energy balance between energy intake and energy expenditure leading to meta-inflammation, a chronic low-grade inflammatory condition.
Biomolecules 12 00852 g001
Biomolecules 12 00852 g002 550
Figure 2. Fundamental structure of anthocyanin. (Drawn using the tool ACD/ChemSketch, version 2021.2.1, Advanced Chemistry Development, Inc., Toronto, ON, Canada).
Figure 2. Fundamental structure of anthocyanin. (Drawn using the tool ACD/ChemSketch, version 2021.2.1, Advanced Chemistry Development, Inc., Toronto, ON, Canada).
Biomolecules 12 00852 g002
Biomolecules 12 00852 g003 550
Figure 3. Two-dimensional structure of a flavylium ion. (Drawn using the tool ACD/ChemSketch, version 2021.2.1, Advanced Chemistry Development, Inc., Toronto, ON, Canada).
Figure 3. Two-dimensional structure of a flavylium ion. (Drawn using the tool ACD/ChemSketch, version 2021.2.1, Advanced Chemistry Development, Inc., Toronto, ON, Canada).
Biomolecules 12 00852 g003
Biomolecules 12 00852 g004 550
Figure 4. The anti-obesity effects of anthocyanins. (a) Anthocyanins are antioxidants that eliminate reactive oxygen species (ROS) by increasing antioxidant enzymes such as superoxide dismutase (SOD) and glutathione peroxidase (GPx). (b) Anthocyanins prevent nuclear factor kappa B (NF-κB) activation, thus decreasing the entire downstream cascade of pro-inflammatory mediators such as C-reactive protein (CRP), interleukin (IL)-6, and tumor necrosis factor (TNF)-α. (c) Anthocyanins also improve gut dysbiosis, restoring a balanced gut microbiota.
Figure 4. The anti-obesity effects of anthocyanins. (a) Anthocyanins are antioxidants that eliminate reactive oxygen species (ROS) by increasing antioxidant enzymes such as superoxide dismutase (SOD) and glutathione peroxidase (GPx). (b) Anthocyanins prevent nuclear factor kappa B (NF-κB) activation, thus decreasing the entire downstream cascade of pro-inflammatory mediators such as C-reactive protein (CRP), interleukin (IL)-6, and tumor necrosis factor (TNF)-α. (c) Anthocyanins also improve gut dysbiosis, restoring a balanced gut microbiota.
Biomolecules 12 00852 g004
Table
Table 1. Colors and sources of the six most well-studied anthocyanins [21,39,40].
Table 1. Colors and sources of the six most well-studied anthocyanins [21,39,40].
Main AnthocyaninsColorpH RangesSources
PelargonidinRed, orange
Biomolecules 12 00852 i001		Low pH
(pH < 3)		Radish, pomegranate, red potato, ripe raspberry
CyanidinRed, reddish-purple
Biomolecules 12 00852 i002		Low to neutral pH (pH 3–7)Blackberry, red sweet potato, purple corn, tart and sweet cherry
PeonidinPurplish-red
Biomolecules 12 00852 i003		Neutral pH
(pH 6–7)		Sweet potato, cranberry, grape, purple corn
PetunidinPurple, dark red
Biomolecules 12 00852 i004		Low to high pH (pH 3–8)Blackcurrant, black bean, red berry
DelphinidinPurple, blue-reddish
Biomolecules 12 00852 i005		Neutral to high pH
(pH 7–11)		Pomegranate, black bean, purple tomato
MalvidinPurple
Biomolecules 12 00852 i006		Neutral pH
(pH 7–8)		Blueberry, red wine, bilberry, mulberry
Table
Table 2. Effects of anthocyanins on obesity-associated inflammation [49,50,51,52,53,54,55,56,57,58,59,60,61,62,63].
Table 2. Effects of anthocyanins on obesity-associated inflammation [49,50,51,52,53,54,55,56,57,58,59,60,61,62,63].
Food SourceBioactive of AnthocyaninsEffectsStudy GroupReference
Tart cherries
  • Cyanidin-3-O-glucoside
  • Cyanidin-3-O-glucosyl-rutinoside
  • Cyanidin-3-O-rutinoside
Reduced IL-6 levelAdipose stem cells[49]
Red raspberriesIdentified anthocyanins N/A
  • Reduced NO, COX-2, IL-1β, IL-6 expression
  • Suppressed NF-kB pathway
RAW264.7
macrophages		[50]
Black soybeans
  • Cyanidin-3-O-glucoside
  • Pelargonidin 3-glucoside
  • Delphinidin-3-glucoside
  • Reduced TNF-α secretion
  • Increased adiponectin and insulin sensitivity
3T3-L1 cells[51]
Sweet cherry
  • Cyanidin 3-O-rutinoside
  • Reduced NO level
  • Decreased COX-2 and iNOS expression
RAW 264.7
macrophages		[52]
Blueberry supplementationPhenolics and anthocyanin
  • Improved TNF-α and IL-1β gene expression
  • Improved gut microbiota
Male Wistar rats
fed HFD		[53]
Tart cherry extract
  • Cyanidin-3-O-glucoside
  • Cyanidin-3-O-glucosyl-rutinoside
  • Cyanidin-3-O-rutinoside
Decreased IL-6 andleptin levelsObese mice[54]
Tart cherry seed powder and tart cherry juiceIdentified anthocyanins N/A
  • Reduced TNF-α, IL-1β and IL-6 expression
  • Suppressed NF-kB pathway
Male Wistar rats
fed HFD		[55]
Sweet cherry
  • Cyanidin-3-O-glucosyl-rutinoside
  • Cyanidin-3-O-rutinoside
  • Pelargonidin 3-rutinoside
  • Decreased body weight
  • Decreased IL-6 and TNF-α gene expression in WAT
Male C57BL/6 mice
fed HFD		[56]
Pomegranate peel extractEllagitannins and anthocyanins
  • Reduced COX-2 in the colon and visceral adipose tissue
  • Reduced mRNA levels of IL-1β in the visceral adipose tissue
  • Reduced IL-6 in the colon
Balb/c obese mice[57]
Strawberrybeverage
  • Pelargonidin 3-glucoside
  • Pelargonidin 3-malonylglucoside
  • Pelargonidin 3-rutinoside
Improved hs-CRPand IL-6Overweight adults[58]
Black soybean testa extracts
  • Cyanidin-3-glucoside
  • Delphinidin-3-glucoside
  • Petunidin-3-glucoside
  • Improved visceral fat
  • Improved plasma
  • Lipid profiles
  • Reduced TNF-α and MCP-1
Overweight and
obese adults		[59]
Queen garnet plumCyanidin 3-O-β-D-glucosideReduced LDL level, plasma glucose, insulin, C-peptide, leptin and GLP-1 concentrationsMildly hypertensive obese/overweight adults[60]
Authentic tart cherry juice
  • Cyanidin-3-2G-glucosylrutinoside
  • Cyanidin-3-glucoside
  • Cyanidin-3-rutinoside
  • Peonidin-3-rutinoside
Reduced TNF-α and MCP-1Overweight and
obese adults		[61]
StrawberryIdentified anthocyanins N/ANo effect on inflammatory markers (e.g., IL-6, IL-1β, TNF-α)Obese healthy males
and females		[62]
Commercially available red orange juiceIdentified anthocyanins N/ANo effect on body weight and plasma inflammatory markersOverweight
or obese
females		[63]
NO = nitric oxide; iNOS = inducible nitric oxide synthase; COX-2 = cyclooxygenase-2; IL = interleukin; NF-kB = nuclear factor-kB; TNF = tumor necrosis factor; HFD = high-fat diet; N/A = not applicable; hs-CRP = high-sensitivity C-reactive protein; MCP-1 = monocyte chemoattractant protein-1; LDL = low-density lipoprotein; GLP-1 = glucagon-like peptide 1.
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Ngamsamer, C.; Sirivarasai, J.; Sutjarit, N. The Benefits of Anthocyanins against Obesity-Induced Inflammation. Biomolecules 2022, 12, 852. https://doi.org/10.3390/biom12060852

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Ngamsamer C, Sirivarasai J, Sutjarit N. The Benefits of Anthocyanins against Obesity-Induced Inflammation. Biomolecules. 2022; 12(6):852. https://doi.org/10.3390/biom12060852

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Ngamsamer, Chanya, Jintana Sirivarasai, and Nareerat Sutjarit. 2022. "The Benefits of Anthocyanins against Obesity-Induced Inflammation" Biomolecules 12, no. 6: 852. https://doi.org/10.3390/biom12060852

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Ngamsamer, C., Sirivarasai, J., & Sutjarit, N. (2022). The Benefits of Anthocyanins against Obesity-Induced Inflammation. Biomolecules, 12(6), 852. https://doi.org/10.3390/biom12060852

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