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      Quercetin and its role in biological functions: an updated review

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          Abstract

           Dear Editor, Quercetin is an important flavonol among the members of six subclasses of flavonoid compounds. The name quercetin was derived from quercetum (after Quercus, i.e., oak), and has been used since 1857 (Fischer et al., 1997[21]). It has been named as 3,3′,4′,5,7-pentahydroxyflavone by the International Union of Pure and Applied Chemistry (IUPAC). It is also known by its synonym 3,3′,4′,5,7-pentahydroxy-2-phenylchromen-4-one (Li et al., 2016[33]). Quercetin is the most widely distributed and extensively studied flavonoid found in various food sources, including fruits, vegetables, nuts, wine, and seeds (Oboh et al., 2016[44]). Quercetin has various biological properties, including antioxidant, anti-inflammatory, antibacterial, antiviral, radical-scavenging, gastroprotective, and immune-modulatory activities (Anand David et al., 2016[6]; Massi et al., 2017[39]). In addition, in several recently-filed patents the wide therapeutic applications of quercetin and its derivatives have been described in detail (Chen et al., 2016[15]; Eid and Haddad, 2017[19]; Sharma et al., 2018[50]). Quercetin exhibits a wide range of biological activities and therapeutic applications, which are of interest to the pharmaceutical, cosmetic, and food industries (Biler et al., 2017[10]). Here, we summarize the recent studies that have evaluated the biological and pharmacological activities of quercetin (Table 1(Tab. 1); References in Table 1: Abdelhalim et al., 2018[1]; Afifi et al., 2018[2]; Aghapour et al., 2018[3]; Ahmed et al., 2018[4]; Al-Asmari et al., 2018[5]; Ansar et al., 2016[7]; Atef et al., 2017[8]; Beghoul et al., 2017[9]; Calgarotto et al., 2018[11]; Chan et al., 2018[12]; Chang et al., 2017[13]; Chen et al., 2017[14]; Damiano et al., 2018[16]; Dong et al., 2017[17]; Duranti et al., 2018[18]; Esrefoglu et al., 2017[20]; Funakoshi et al., 2017[22]; Guo et al., 2017[23]; He et al., 2016[24]; Huang et al., 2017[25]; Jeon et al., 2017[26]; Ji et al., 2017[27]; Ju et al., 2018[28]; Kee et al., 2016[29]; Lan et al., 2017[30]; Lazo-Gomez and Tapia, 2017[31]; Li et al., 2018[32]; Liu and Zhou, 2017[34]; Liu et al., 2017[35]; Lu et al., 2018[36]; Maciel et al., 2016[37]; Maksymchuk et al., 2017[38]; Mitani et al., 2017[40]; Mkhize et al., 2017[41]; Naseer et al., 2017[42]; Pandya et al., 2017[45]; Patrizio et al., 2018[46]; Qin et al., 2017[47]; Ren et al., 2018[48]; Sameni et al., 2018[49]; Singh et al., 2018[51]; Sohn et al., 2018[52]; Tinay et al., 2017[53]; Veith et al., 2017[54]; Wu et al., 2018[55]; Xingyu et al., 2016[56]; Yang et al., 2017[57]; Yang et al., 2018[58]; Yarahmadi et al., 2017[60]; Yarahmadi et al., 2018[59]; Yazıcı et al., 2018[61]; Yuan et al., 2016[63]; Yuan et al., 2018[62]; Zhang et al., 2018[64]; Zhao et al., 2017[65]; Zhu et al., 2018[66]). Acknowledgements This work was supported by a grant from the Next-Generation BioGreen 21 Program (SSAC, Project #. PJ013328)" Rural Development Administration, Republic of Korea. Conflict of interest The authors declare no conflict of interest.

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          A combination of quercetin and resveratrol reduces obesity in high-fat diet-fed rats by modulation of gut microbiota.

          Resveratrol and quercetin, widely found in foods and vegetables, are plant polyphenols reported to have a wide range of biological activities. Despite their limited bioavailabilities, both resveratrol and quercetin are known to exhibit anti-inflammation and anti-obesity effects. We hypothesized that gut microbiota may be a potential target for resveratrol and quercetin to prevent the development of obesity. The aim of this research was to confirm whether a combination of quercetin and resveratrol (CQR) could restore the gut microbiota dysbiosis induced by a high-fat diet (HFD). In this study, Wistar rats were divided into three groups: a normal diet (ND) group, a HFD group and a CQR group. The CQR group was treated with a HFD and administered with a combination of quercetin [30 mg per kg body weight (BW) per day] and resveratrol [15 mg per kg body weight (BW) per day] by oral gavage. At the end of 10 weeks, CQR reduced the body weight gain and visceral (epididymal, perirenal) adipose tissue weight. Moreover, CQR also reduced serum lipids, attenuated serum inflammatory markers [interleukin (IL)-6, tumor necrosis factor (TNF)-α, monocyte chemotactic protein (MCP)-1] and reversed serum biochemical parameters (adiponectin, insulin, leptin, etc.). Importantly, our results demonstrated that CQR could modulate the gut microbiota composition. 16S rRNA gene sequencing revealed that CQR had an impact on gut microbiota, decreasing Firmicutes (P < 0.05) and the proportion of Firmicutes to Bacteroidetes (P = 0.052). CQR also significantly inhibited the relative abundance of Desulfovibrionaceae (P < 0.01), Acidaminococcaceae (P < 0.05), Coriobacteriaceae (P < 0.05), Bilophila (P < 0.05), Lachnospiraceae (P < 0.05) and its genus Lachnoclostridium (P < 0.001), which were reported to be potentially related to diet-induced obesity. Moreover, compared with the HFD group, the relative abundance of Bacteroidales_S24-7_group (P < 0.01), Christensenellaceae (P < 0.001), Akkermansia (P < 0.01), Ruminococcaceae (P < 0.01) and its genera Ruminococcaceae_UCG-014 (P < 0.01), and Ruminococcaceae_UCG-005 (P < 0.01), which were reported to have an effect of relieving HFD-induced obesity, was markedly increased in the CQR group. Overall, these results indicated that administration of CQR may have beneficial effects on ameliorating HFD-induced obesity and reducing HFD-induced gut microbiota dysbiosis.
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            Therapeutic Effects of Quercetin on Inflammation, Obesity, and Type 2 Diabetes

            In previous studies, abdominal obesity has been related to total low-grade inflammation and in some cases has resulted in insulin resistance and other metabolism related disorders such as diabetes. Quercetin is a polyphenol, which is a derivative of plants, and has been shown in vitro as well as in a few animal models to have several potential anti-inflammatory as well as anticarcinogenic applications. The substance has also been shown to aid in the attenuation of lipid peroxidation, platelet aggregation, and capillary permeability. However, further research is called for to gain a better understanding of how quercetin is able to provide these beneficial effects. This manuscript reviewed quercetin's anti-inflammatory properties in relation to obesity and type 2 diabetes.
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              Quercetin ameliorates kidney injury and fibrosis by modulating M1/M2 macrophage polarization

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                Author and article information

                Journal
                EXCLI J
                EXCLI J
                EXCLI J
                EXCLI Journal
                Leibniz Research Centre for Working Environment and Human Factors
                1611-2156
                27 August 2018
                2018
                : 17
                : 856-863
                Affiliations
                [1 ]Division of Life Sciences and Convergence Research Center for Insect Vectors, Incheon National University, Incheon 22012, Korea
                [2 ]Department of Crop Science, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon, 34134, Korea
                Author notes
                *To whom correspondence should be addressed: Sang Un Park, Department of Crop Science, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon, 34134, Korea; Tel.: +82-42-821-5730, Fax: +82-42-822-2631, E-mail: supark@ 123456cnu.ac.kr
                Article
                2018-1538 Doc856
                10.17179/excli2018-1538
                6141818
                30233284
                64cfdfb9-0fa6-44b6-92ed-1960300d11a2
                Copyright © 2018 Kim et al.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence ( http://creativecommons.org/licenses/by/4.0/) You are free to copy, distribute and transmit the work, provided the original author and source are credited.

                History
                : 15 July 2018
                : 18 August 2018
                Categories
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