Curcumin protects ANIT-induced cholestasis through signaling pathway of FXR-regulated bile acid and inflammation

胆汁淤积 法尼甾体X受体 姜黄素 医学 肝损伤 胆汁酸 药理学 G蛋白偶联胆汁酸受体 内科学 胃肠病学 核受体 生物化学 化学 转录因子 基因
作者
Fan Yang,Xiaowen Tang,Lili Ding,Yue Zhou,Qiaoling Yang,Junting Gong,Guangyun Wang,Zhengtao Wang,Li Yang
出处
期刊:Scientific Reports [Nature Portfolio]
卷期号:6 (1): 33052-33052 被引量:60
标识
DOI:10.1038/srep33052
摘要

Cholestasis is a clinically significant symptom and widely associated with liver diseases, however, there are very few effective therapies for cholestasis. Danning tablet (DNT, a Chinese patent medicine preparation) has been clinically used to treat human liver and gallbladder diseases for more than 20 years in China. However, which ingredients of DNT contributed to this beneficial effect and their mechanistic underpinnings have been largely unknown. In the present study, we discovered that DNT not only demonstrated greater benefits for cholecystitis patients after cholecystectomy surgery in clinic but also showed protective effect against alpha-naphthylisothiocyanate (ANIT)-induced cholestasis model in rodent. Curcumin, one major compound derived from DNT, exerted the protective effect against cholestasis through farnesoid X receptor (FXR), which has been focused as potential therapeutic targets for treating cholestasis. The underlying mechanism of curcumin against cholestasis was restoring bile acid homeostasis and antagonizing inflammatory responses in a FXR-dependent manner and in turn contributed to overall cholestasis attenuation. Collectively, curcumin can be served as a potential treatment option for liver injury with cholestasis.
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