Molecular matchmaking between the popular weight-loss herb Hoodia gordonii and GPR119, a potential drug target for metabolic disorder AMERICA
ZHANG SHUYONG1; Ma YY(马玉勇)1; LI JING1; Ma JJ(马君君)1; Yu B(俞飚)1; Xie X(谢欣)1
刊名Proc. Natl. Acad. Sci. U. S. A.
2014
卷号111期号:40页码:14571-14576
其他题名蝴蝶亚仙人掌孕甾皂苷与GPR119受体的相互作用及其在代谢紊乱疾病中的潜在应用
通讯作者俞飚 ; 谢欣
英文摘要African cactiform Hoodia gordonii (Asclepiadaceae) has been used for thousands of years by Xhomani Bushmen as an anorexant during hunting trips and has been proposed as a new agent for the management of body weight. However, its in vivo targets and molecular mechanisms remain elusive. GPR119, a G protein-coupled receptor highly expressed in pancreatic beta cells and intestinal L cells, has been demonstrated to facilitate glucose-stimulated insulin secretion (GSIS) and represents a novel and attractive target for the therapy of metabolic disorders. Here, we disclose that Gordonoside F (a steroid glycoside isolated from H. gordonii), but not the widely known P57, activates specifically GPR119. Successful synthesis of Gordonoside F facilitates further characterization of this compound. Gordonoside F promotes GSIS both in vitro and in vivo and reduces food intake in mice. These effects are mediated by GPR119 because GPR119 knockout prevents the therapeutic effects of Gordonoside F. Interestingly, the appetite-suppressing effect of Hoodia extract was also partially blocked by GPR119 knockout. Our results demonstrate for the first time, to our knowledge, that GPR119 is a direct target and one of the major mechanisms underlying the therapeutic effect of the popular "weight loss" herb H. gordonii. Given the long history of safe application of this herb in weight control, it is foreseeable that the novel scaffold of Gordonoside F provides a promising opportunity to develop new drugs in treating metabolic diseases.
学科主题生命有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1073/pnas.1324130111
语种英语
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/38956]  
专题上海有机化学研究所_生命有机化学国家重点实验室
作者单位1.同济大学
2.中科院上海药物研究所
3.中科院上海有机化学研究所
推荐引用方式
GB/T 7714
ZHANG SHUYONG,Ma YY,LI JING,et al. Molecular matchmaking between the popular weight-loss herb Hoodia gordonii and GPR119, a potential drug target for metabolic disorder AMERICA[J]. Proc. Natl. Acad. Sci. U. S. A.,2014,111(40):14571-14576.
APA ZHANG SHUYONG,马玉勇,LI JING,马君君,俞飚,&谢欣.(2014).Molecular matchmaking between the popular weight-loss herb Hoodia gordonii and GPR119, a potential drug target for metabolic disorder AMERICA.Proc. Natl. Acad. Sci. U. S. A.,111(40),14571-14576.
MLA ZHANG SHUYONG,et al."Molecular matchmaking between the popular weight-loss herb Hoodia gordonii and GPR119, a potential drug target for metabolic disorder AMERICA".Proc. Natl. Acad. Sci. U. S. A. 111.40(2014):14571-14576.
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