微粒体甘油三酯转移蛋白
单酰甘油脂肪酶
高脂血症
PCSK9
药理学
酰基转移酶
脂质代谢
前蛋白转化酶
可欣
化学
内科学
胆固醇
低密度脂蛋白受体
内分泌学
脂蛋白
生物化学
生物
极低密度脂蛋白
医学
受体
内大麻素系统
糖尿病
酶
生物合成
作者
Hui Li,Jing Xian,Xiaolan Deng,Dongsheng Ouyang
出处
期刊:PubMed
日期:2013-01-01
卷期号:38 (1): 101-8
被引量:2
标识
DOI:10.3969/j.issn.1672-7347.2013.01.019
摘要
Hyperlipidemia is one of the most important risk factors for atherosclerosis, coronary heart disease and other cardiovascular diseases. It is the main effect of lipid-lowering drugs to reduce the plasma low-density lipoprotein or to enhance high-density lipoprotein. Niemann-Pick C1 like 1 protein (NPC1L1), acyl-coenzyme A: cholesterol acyltransferases (ACAT), ATP binding cassette transporter G member 5 and member 8 (ABCG5/G8), microsomal triglyceride transfer protein (MTP), monoacylglycerol acyltransferase, diacylglycerol acyltransferases (MAGT), peroxisome proliferator-activated receptor (PPAR), farnesoid X receptor (FXR), and proprotein convertase subtilisin/kexin type 9 (PCSK9) play key roles in the metabolism of lipid, which are regarded as the targets of anti-hyperlipidemia drugs and evidence for clinic choice of lipid-lowering drugs. These proteins are considered as breakthrough points for new lipid-lowering drug development.
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