Cordycepin Ameliorates Nonalcoholic Steatohepatitis by Activation of the AMP‐Activated Protein Kinase Signaling Pathway

虫草素 安普克 脂肪变性 代谢综合征 肝移植 脂肪性肝炎 药理学 慢性肝病 医学 AMP活化蛋白激酶 非酒精性脂肪肝 蛋白激酶A 内科学 内分泌学 激酶 脂肪肝 移植 生物 生物化学 糖尿病 肝硬化 疾病
作者
Tian Lan,Yu Yang,Jing Zhang,Haonan Li,Qiqing Weng,Shuo Jiang,Song Tian,Tonghao Xu,Sha Hu,Guizhi Yang,Yan Zhang,Weixuan Wang,Lexun Wang,Qing Zhu,Xianglu Rong,Jiao Guo
出处
期刊:Hepatology [Lippincott Williams & Wilkins]
卷期号:74 (2): 686-703 被引量:175
标识
DOI:10.1002/hep.31749
摘要

BACKGROUND AND AIMS: Nonalcoholic fatty liver disease, especially nonalcoholic steatohepatitis (NASH), has become a major cause of liver transplantation and liver-associated death. NASH is the hepatic manifestation of metabolic syndrome and is characterized by hepatic steatosis, inflammation, hepatocellular injury, and different degrees of fibrosis. However, there is no US Food and Drug Administration-approved medication to treat this devastating disease. Therapeutic activators of the AMP-activated protein kinase (AMPK) have been proposed as a potential treatment for metabolic diseases such as NASH. Cordycepin, a natural product isolated from the traditional Chinese medicine Cordyceps militaris, has recently emerged as a promising drug candidate for metabolic diseases. APPROACH AND RESULTS: We evaluated the effects of cordycepin on lipid storage in hepatocytes, inflammation, and fibrosis development in mice with NASH. Cordycepin attenuated lipid accumulation, inflammation, and lipotoxicity in hepatocytes subjected to metabolic stress. In addition, cordycepin treatment significantly and dose-dependently decreased the elevated levels of serum aminotransferases in mice with diet-induced NASH. Furthermore, cordycepin treatment significantly reduced hepatic triglyceride accumulation, inflammatory cell infiltration, and hepatic fibrosis in mice. In vitro and in vivo mechanistic studies revealed that a key mechanism linking the protective effects of cordycepin were AMPK phosphorylation-dependent, as indicated by the finding that treatment with the AMPK inhibitor Compound C abrogated cordycepin-induced hepatoprotection in hepatocytes and mice with NASH. CONCLUSION: Cordycepin exerts significant protective effects against hepatic steatosis, inflammation, liver injury, and fibrosis in mice under metabolic stress through activation of the AMPK signaling pathway. Cordycepin might be an AMPK activator that can be used for the treatment of NASH.
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