非酒精性脂肪肝
脂肪变性
医学
慢性肝病
代谢综合征
疾病
非酒精性脂肪性肝炎
药理学
肝病
脂肪性肝炎
药品
发病机制
药物开发
生物信息学
脂肪肝
纤维化
内科学
生物
肝硬化
肥胖
作者
Henrik H. Hansen,Michael Feigh,Sanne Skovgård Veidal,Kristoffer T.G. Rigbolt,Niels Vrang,Keld Fosgerau
标识
DOI:10.1016/j.drudis.2017.06.007
摘要
Nonalcoholic fatty liver disease (NAFLD) has become the most common cause of chronic liver disease in the Western world. NAFLD is a complex spectrum of liver diseases ranging from benign hepatic steatosis to its more aggressive necroinflammatory manifestation, nonalcoholic steatohepatitis (NASH). NASH pathogenesis is multifactorial and risk factors are almost identical to those of the metabolic syndrome. This has prompted substantial efforts to identify novel drug therapies for correcting underlying metabolic deficits, and to prevent or alleviate hepatic fibrosis in NASH. Available mouse models of NASH address different aspects of the disease, have varying clinical translatability, and, therefore, also show different utility in drug discovery.
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