脂肪生成
脂肪肝
脂质代谢
非酒精性脂肪肝
内科学
内分泌学
脂滴
甘油三酯
β氧化
生物
代谢综合征
酒精性肝病
脂肪变性
化学
生物化学
新陈代谢
疾病
医学
胆固醇
肝硬化
糖尿病
作者
Giovanni Musso,R. J. Gambino,M. Cassader
标识
DOI:10.1016/j.plipres.2008.08.001
摘要
Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in Western countries and is considered the hepatic manifestation of metabolic syndrome. The hallmark of NAFLD is hepatic neutral lipid accumulation, mainly triacylglycerol, in the absence of significant ethanol consumption, viral infection or other specific etiologies. Hepatic lipid accumulation results from an imbalance between lipid availability (from circulating lipid uptake or de novo lipogenesis) and lipid disposal (via free fatty acid oxidation or triglyceride-rich lipoprotein secretion) and eventually triggers lipoperoxidative stress and hepatic injury. Each of these steps is altered in NAFLD, although to a different extent. Regulation of these pathways is complex and involves nuclear receptors, membrane transport proteins and cellular enzymes. We will review available data on different steps of hepatic lipid metabolism in NAFLD and recent advances in understanding molecular mechanisms underlying hepatic fat accumulation in these subjects.
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