Hepatic microcirculation and mechanisms of portal hypertension

被引:189
作者
Gracia-Sancho, Jordi [1 ,2 ]
Marrone, Giusi [1 ]
Fernandez-Iglesias, Anabel [1 ]
机构
[1] IDIBAPS Biomed Res Inst, Barcelona Hepat Hemodynam Lab, CIBEREHD, Liver Vasc Biol Res Grp, Barcelona, Spain
[2] Bern Univ, Dept Biomed Res, Inselspital, Hepatol, Bern, Switzerland
关键词
FARNESOID X RECEPTOR; ENDOTHELIAL-CELL PHENOTYPE; KINASE SIGNALING CONTRIBUTES; RECELLULARIZED LIVER GRAFT; OXIDE SYNTHASE ACTIVITY; CIRRHOTIC RAT LIVERS; NITRIC-OXIDE; VASCULAR-TONE; CASPASE INHIBITOR; STELLATE CELLS;
D O I
10.1038/s41575-018-0097-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The liver microcirculatory milieu, mainly composed of liver sinusoidal endothelial cells (LSECs), hepatic stellate cells (HSCs) and hepatic macrophages, has an essential role in liver homeostasis, including in preserving hepatocyte function, regulating the vascular tone and controlling inflammation. Liver microcirculatory dysfunction is one of the key mechanisms that promotes the progression of chronic liver disease (also termed cirrhosis) and the development of its major clinical complication, portal hypertension. In the present Review, we describe the current knowledge of liver microcirculatory dysfunction in cirrhotic portal hypertension and appraise the preclinical models used to study the liver circulation. We also provide a comprehensive summary of the promising therapeutic options to target the liver microvasculature in cirrhosis.
引用
收藏
页码:221 / 234
页数:14
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