胆固醇
孤儿受体
医学
平衡
心肌梗塞
生物信息学
低密度脂蛋白受体
受体
内科学
脂蛋白
内分泌学
生物
遗传学
基因
转录因子
作者
Brendan P. Wilkins,Angela M. Finch,Yan Wang,Nicola J. Smith
标识
DOI:10.1016/j.tem.2022.04.008
摘要
Atherosclerosis predisposes to myriad cardiovascular complications, including myocardial infarction and stroke. Statins have revolutionised cholesterol management but they do not work for all patients, particularly those with familial hypercholesterolaemia (FH). Genome-wide association studies have linked SNPs at orphan G protein-coupled receptor 146 (GPR146) to human atherosclerosis but how GPR146 influences serum cholesterol homeostasis was only recently described. Gpr146 deletion in mice reduces serum cholesterol and atherosclerotic plaque burden, confirming GPR146 as a potential therapeutic target for managing circulating cholesterol. Critically, this effect was independent of the low-density lipoprotein receptor. While still an orphan, the activation of GPR146 by serum suggests identification of its endogenous ligand is tantalisingly close. Herein, we discuss the evidence for GPR146 inhibition as a treatment for atherosclerosis.
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