肝硬化
胆汁淤积
受体
发病机制
法尼甾体X受体
医学
胆汁酸
G蛋白偶联胆汁酸受体
病态的
生物信息学
内科学
生物
核受体
生物化学
转录因子
基因
作者
Andrei Mihai Voiosu,Signe Skovgaard Wiese,Theodor Alexandru Voiosu,Flemming Bendtsen,Søren Møller
摘要
Cirrhotic cardiomyopathy and the hyperdynamic syndrome are clinically important complications of cirrhosis, but their exact pathogenesis is still partly unknown. Experimental models have proven the cardiotoxic effects of bile acids and recent studies of their varied receptor-mediated functions offer new insight into their involvement in cardiovascular dysfunction in cirrhosis. Bile acid receptors such as farnesoid X-activated receptor and TGR5 are currently under investigation as potential therapeutic targets in a variety of pathological conditions. These receptors have also recently been identified in cardiomyocytes, vascular endothelial cells and smooth muscle cells where they seem to play an important role in cellular metabolism. Chronic cholestasis leading to abnormal levels of circulating bile acids alters the normal signalling pathways and contributes to the development of profound cardiovascular disturbances. This review summarizes the evidence regarding the role of bile acids and their receptors in the generation of cardiovascular dysfunction in cirrhosis.
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