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从头脂肪酸合成对肝脂肪变性和胰岛素抵抗的作用:来自基因工程小鼠的经验教训。

Contribution of de novo fatty acid synthesis to hepatic steatosis and insulin resistance: lessons from genetically engineered mice.

作者信息

Postic Catherine, Girard Jean

机构信息

Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), Paris, France.

出版信息

J Clin Invest. 2008 Mar;118(3):829-38. doi: 10.1172/JCI34275.

Abstract

Nonalcoholic fatty liver disease (NAFLD) is associated with obesity, insulin resistance, and type 2 diabetes. NAFLD represents a large spectrum of diseases ranging from (i) fatty liver (hepatic steatosis); (ii) steatosis with inflammation and necrosis; and (iii) cirrhosis. Although the molecular mechanism leading to the development of hepatic steatosis in the pathogenesis of NAFLD is complex, recent animal models have shown that modulating important enzymes in fatty acid synthesis in liver may be key for the treatment of NAFLD. This review discusses recent advances in the field.

摘要

非酒精性脂肪性肝病(NAFLD)与肥胖、胰岛素抵抗和2型糖尿病相关。NAFLD涵盖了一系列疾病,包括:(i)脂肪肝(肝脂肪变性);(ii)伴有炎症和坏死的脂肪变性;以及(iii)肝硬化。尽管在NAFLD发病机制中导致肝脂肪变性发展的分子机制很复杂,但最近的动物模型表明,调节肝脏中脂肪酸合成的重要酶可能是治疗NAFLD的关键。本文综述了该领域的最新进展。

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