Soluble epoxide hydrolase inhibitory activity of anthraquinone components from Aloe

被引:16
|
作者
Sun, Ya Nan [1 ]
Kim, Jang Hoon [2 ]
Li, Wei [3 ]
Jo, A. Reum [1 ]
Yan, Xi Tao [4 ]
Yang, Seo Young [1 ]
Kim, Young Ho [1 ]
机构
[1] Chungnam Natl Univ, Coll Pharm, Taejon 305764, South Korea
[2] RDA, Natl Inst Hort & Herbal Sci, Dept Hort Environm, Virol Unit, Wanju Gun 440310, South Korea
[3] Yeungnam Univ, Sch Biotechnol, Kyongsan 712749, Gyeongbuk, South Korea
[4] Northwest A&F Univ, Coll Sci, Shaanxi Key Lab Nat Prod & Chem Biol, Yangling 712100, Shaanxi, Peoples R China
基金
新加坡国家研究基金会;
关键词
Aloe; Anthraquinone derivatives; Soluble epoxide hydrolase (sEH); Molecular simulation; BARBADENSIS MILLER; CARDIOVASCULAR-DISEASES; THERAPEUTIC TARGET; VERA; RECEPTOR; INFLAMMATION; ANTIOXIDANT; METABOLISM; CHROMONE; ALPHA;
D O I
10.1016/j.bmc.2015.09.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aloe is a short-stemmed succulent herb widely used in traditional medicine to treat various diseases and as raw material in cosmetics and heath foods. In this study, we isolated and identified two new anthraquinone derivatives, aloinoside C (6) and aloinoside D (7), together with six known compounds from an aqueous dissolved Aloe exudate. Their structures were identified by spectroscopic analysis. The inhibitory effects of the isolated compounds on soluble epoxide hydrolase (sEH) were evaluated. Compounds 1-8 inhibited sEH activity potently, with IC50 values ranging from 4.1 +/- 0.6 to 41.1 +/- 4.2 mu M. A kinetic analysis of compounds 1-8 revealed that the inhibitory actions of compounds 1, 6 and 8 were non-competitive, whereas those of compounds 2-5 and 7 were the mixed-type. Molecular docking increases our understanding of receptor-ligand binding of all compounds. These results demonstrate that compounds 1-8 from Aloe are potential sEH inhibitors. (c) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6659 / 6665
页数:7
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