雄激素受体
核受体
孕烷X受体
法尼甾体X受体
肝X受体
药物代谢
胆汁酸
G蛋白偶联胆汁酸受体
新陈代谢
脂质代谢
受体
生物化学
非酒精性脂肪肝
生物
化学
内科学
脂肪肝
医学
疾病
基因
转录因子
作者
Tiangang Li,John Y.L. Chiang
标识
DOI:10.3109/03602532.2012.740048
摘要
Bile acids are signaling molecules that activate nuclear receptors, such as farnesoid X receptor, pregnane X receptor, constitutive androstane receptor, and vitamin D receptor, and play a critical role in the regulation of lipid, glucose, energy, and drug metabolism. These xenobiotic/endobiotic-sensing nuclear receptors regulate phase I oxidation, phase II conjugation, and phase III transport in bile acid and drug metabolism in the digestive system. Integration of bile acid metabolism with drug metabolism controls absorption, transport, and metabolism of nutrients and drugs to maintain metabolic homeostasis and also protects against liver injury, inflammation, and related metabolic diseases, such as nonalcoholic fatty liver disease, diabetes, and obesity. Bile-acid–based drugs targeting nuclear receptors are in clinical trials for treating cholestatic liver diseases and fatty liver disease.
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