脂肪肝
脂肪性肝炎
二酰甘油激酶
胰岛素抵抗
脂滴
生物
脂质代谢
疾病
磷脂酸
生物化学
医学
内科学
内分泌学
胰岛素
磷脂
信号转导
蛋白激酶C
膜
作者
Yuki Kawano,Shin Nishiumi,Masaya Saito,Yoshihiko Yano,Takeshi Azuma,Masaru Yoshida
出处
期刊:Current Drug Targets
[Bentham Science]
日期:2015-10-14
卷期号:16 (12): 1293-1300
被引量:24
标识
DOI:10.2174/1389450116666150408103318
摘要
Non-alcoholic fatty liver disease (NAFLD) is histologically characterized by the aberrant accumulation of lipid droplets in the liver, which is positively correlated with insulin resistance. Within the spectrum of this disease, patients can develop hepatitis and cirrhosis; i.e., non-alcoholic steatohepatitis (NASH). The mechanisms responsible for the progression of NAFLD are not fully understood. Triacylglycerol (TAG), which is mainly found in lipid droplets, is currently considered to act as a buffer against the accumulation of non-TAG toxic lipid species. In line with this, recent studies have revealed that insulin resistance is driven by the accumulation of phosphatidic acid and diacylglycerol in hepatocytes and that cholesterol-overloaded stellate cells are associated with fibrosis in the liver. Therefore, it is important to identify the toxic lipid species that contribute to NAFLD progression in order to clarify the pathogenesis of NASH and find novel targets for its treatment. In this review, we divided lipids into five classes; i.e., into fatty acyls, glycerophospholipids, glycerolipids, sphingolipids, and sterol lipids, and described their molecular structures, distributions, and metabolism under physiological conditions, as well as the contributions they make to the progression of NAFLD.
科研通智能强力驱动
Strongly Powered by AbleSci AI