G蛋白偶联胆汁酸受体
内科学
内分泌学
人参皂甙
人参
葡萄糖稳态
甘油三酯
胰岛素抵抗
胆汁酸
肥胖
化学
胰岛素
药理学
医学
胆固醇
生物
替代医学
病理
作者
Linshan Jiang,Li Wei,Tongxi Zhuang,Jie-jing Yu,Shuai Sun,Zhengcai Ju,Zhengtao Wang,Lili Ding,Li Yang
标识
DOI:10.1124/jpet.120.000435
摘要
Obesity, a well known risk factor in multiple metabolic diseases, is dramatically increasing worldwide. Ginsenosides extracted from ginseng have been reported against obesity and the associated metabolic disorders. As a subtype of ginsenoside, ginsenoside Ro is a critical constituent of ginseng. However, its specific effects on obesity remain unknown. G protein-coupled bile acid receptor 5 (TGR5) (also known as GPBAR1) is a bile acid membrane receptor, widely expressed in human tissues contributing to various metabolic processes to confer the regulations of glucose and lipid homeostasis. TGR5 has displayed potential as a therapeutic target for the treatment of metabolic disorders. Here, we explore the antiobesity effect of ginsenoside Ro with TGR5 activation screened by a library of natural products. Our results showed that the ginsenoside Ro (90mg/kg) treatment ameliorated body weight and lipid accumulation in multiple metabolic organs of high-fat diet-induced obese (DIO) mice without affecting food intake and improved oral glucose tolerance tests, intraperitoneal insulin tolerance tests, and fasting serum glucose. We also found that triglyceride and total cholesterol in serum and liver were significantly decreased after ginsenoside Ro treatment. Then we used
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