安普克
化学
胆固醇7α羟化酶
蛋白激酶A
低密度脂蛋白受体
甾醇调节元件结合蛋白
甾醇
胆固醇
还原酶
AMP活化蛋白激酶
HMG-CoA还原酶
磷酸化
生物化学
乙酰辅酶A羧化酶
脂蛋白
丙酮酸羧化酶
酶
作者
Xin Liu,Jiejie Hao,Lijuan Zhang,Xia Zhao,Xiaoxi He,Miaomiao Li,Xiaoliang Zhao,Jiandong Wu,Peiju Qiu,Guangli Yu
标识
DOI:10.1016/j.ejmech.2014.07.107
摘要
Low molecular weight and sulfated low molecular weight guluronate (LMG and SLMG) were prepared and hypolipidemic effects were studied in a human hepatocellular carcinoma HepG2 cell line. Both compounds decreased total cholesterol (TC) and triglycerides (TG) and inhibited 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR) activity in HepG2 cells. In general, SLMG had greater effects than LMG. Activation of sterol regulatory element-binding protein 2 (SREBP-2), low density lipoprotein receptor (LDLR), AMP-activated protein kinase (AMPK), and AMPK's downstream targets were evidenced by increased phosphorylation of AMPK, HMGCR, and acetyl-CoA-carboxylase (ACC), which decreased HMGRC and ACC activity. We further demonstrated that activated AMPK was linked to down-regulated SREBP-1 and up-regulated cholesterol 7α-hydroxylase (CYP7A1).
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