G蛋白偶联胆汁酸受体
发病机制
胆汁酸
平衡
肠道微生物群
微生物群
法尼甾体X受体
免疫系统
受体
血压
内科学
内分泌学
生物
医学
生物化学
生物信息学
免疫学
核受体
基因
转录因子
作者
Jeanne Ishimwe,Thanvi Dola,Lale A. Ertuğlu,Annet Kirabo
出处
期刊:American Journal of Physiology-heart and Circulatory Physiology
[American Physical Society]
日期:2022-03-04
卷期号:322 (4): H636-H646
被引量:18
标识
DOI:10.1152/ajpheart.00027.2022
摘要
Salt-sensitivity of blood pressure (SSBP) affects 50% of the hypertensive and 25% of the normotensive populations. Importantly, SSBP is associated with increased risk for mortality in both populations independent of blood pressure. Despite its deleterious effects, the pathogenesis of SSBP is not fully understood. Emerging evidence suggests a novel role of bile acids in salt-sensitive hypertension and that they may play a crucial role in regulating inflammation and fluid volume homeostasis. Mechanistic evidence implicates alterations in the gut microbiome, the epithelial sodium channel (ENaC), the farnesoid X receptor, and the G protein-coupled bile acid receptor TGR5 in bile acid-mediated effects on cardiovascular function. The mechanistic interplay between excess dietary sodium-induced alterations in the gut microbiome and immune cell activation, bile acid signaling, and whether such interplay may contribute to the etiology of SSBP is still yet to be defined. The main goal of this review is to discuss the potential role of bile acids in the pathogenesis of cardiovascular disease with a focus on salt-sensitive hypertension.
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