The natural compound, formononetin, extracted from Astragalus membranaceus increases adipocyte thermogenesis by modulating PPARγ activity

芒柄花素 产热 脂肪细胞 内分泌学 内科学 产热素 褐色脂肪组织 生物 脂肪组织 化学 药理学 医学 大豆黄酮 染料木素
作者
Tao Nie,Shiting Zhao,Liufeng Mao,Yiting Yang,Wei Sun,Xiaoliang Lin,Shuo Liu,Kuai Li,Yirong Sun,Peng Li,Zhiguang Zhou,Shaoqiang Lin,Xiaoyan Hui,Aimin Xu,Chung Wah,Yong Xu,Cunchuan Wang,P. Rod Dunbar,Donghai Wu
出处
期刊:British Journal of Pharmacology [Wiley]
卷期号:175 (9): 1439-1450 被引量:60
标识
DOI:10.1111/bph.14139
摘要

Background and Purpose Increasing energy expenditure through adipocyte thermogenesis is generally accepted as a promising strategy to mitigate obesity and its related diseases. However, few clinically effective and safe agents are known to promote adipocyte thermogenesis. In this study, 20 traditional Chinese herbal medicines were screened to examine whether they induced adipocyte thermogenesis. Experimental Approach The effects of Chinese herbal medicines or components isolated from extracts of A. membranaceus, on adipocyte thermogenesis were analysed by assessing expression of uncoupling protein 1 (UCP1) by qPCR. Eight‐week‐old C57BL6/J male mice were fed a high‐fat diet for 8 weeks and then randomized to two groups treated with vehicle or formononetin for another 8 weeks. Glucose tolerance tests and staining of adipose tissue with haematoxylin and eosin were carried out. Whole‐body oxygen consumption was measured with an open‐circuit indirect calorimetry system. Key Results Extracts of A. membranaceus increased expression of Ucp1 in primary cultures of mouse adipocytes. Formononetin was the only known component of A. membranaceus extracts to increase adipocyte Ucp1 expression. Diet‐induced obese mice treated with formononetin gained less weight and showed higher energy expenditure than untreated mice. In addition, formononetin binds directly with PPARγ. Conclusions and Implication Taken together, our study demonstrates that the Chinese herbal medicine from A. membranaceus and its constituent formononetin have the potential to reduce obesity and associated metabolic disorders. Our results suggest that formononetin regulates adipocyte thermogenesis as a non‐classical PPARγ agonist.
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