胰岛素抵抗
脂肪肝
2型糖尿病
二酰甘油激酶
糖尿病
胰岛素
医学
疾病
内科学
机制(生物学)
内分泌学
生物
激酶
蛋白激酶C
生物化学
哲学
认识论
作者
Rachel J. Perry,Varman T. Samuel,Kitt Falk Petersen,Gerald I. Shulman
出处
期刊:Nature
[Nature Portfolio]
日期:2014-06-01
卷期号:510 (7503): 84-91
被引量:1091
摘要
Non-alcoholic fatty liver disease and its downstream sequelae, hepatic insulin resistance and type 2 diabetes, are rapidly growing epidemics, which lead to increased morbidity and mortality rates, and soaring health-care costs. Developing interventions requires a comprehensive understanding of the mechanisms by which excess hepatic lipid develops and causes hepatic insulin resistance and type 2 diabetes. Proposed mechanisms implicate various lipid species, inflammatory signalling and other cellular modifications. Studies in mice and humans have elucidated a key role for hepatic diacylglycerol activation of protein kinase Cε in triggering hepatic insulin resistance. Therapeutic approaches based on this mechanism could alleviate the related epidemics of non-alcoholic fatty liver disease and type 2 diabetes.
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