Endothelin and endothelin receptors in the renal and cardiovascular systems

被引:79
|
作者
Vignon-Zellweger, Nicolas [2 ]
Heiden, Susi [2 ]
Miyauchi, Takashi [3 ]
Emoto, Noriaki [1 ,2 ]
机构
[1] Kobe Univ, Grad Sch Med, Dept Internal Med, Div Cardiovasc Med,Chuo Ku, Kobe, Hyogo 6500017, Japan
[2] Kobe Pharmaceut Univ, Kobe, Hyogo, Japan
[3] Univ Tsukuba, Fac Med, Div Cardiovasc, Tsukuba, Ibaraki 305, Japan
关键词
Endothelin-1; Endothelin receptor; Molecular biology; Heart; Vasculature; Kidney; DUCT-SPECIFIC KNOCKOUT; MEDULLARY COLLECTING DUCT; KIDNEY BLOOD-FLOW; K-ATP CHANNEL; B-RECEPTOR; ETA-RECEPTOR; ANGIOTENSIN-II; NITRIC-OXIDE; MESSENGER-RNA; CAUSES HYPERTENSION;
D O I
10.1016/j.lfs.2012.03.026
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Endothelin-1 (ET-1) is a multifunctional hormone which regulates the physiology of the cardiovascular and renal systems. ET-1 modulates cardiac contractility, systemic and renal vascular resistance, salt and water renal reabsorption, and glomerular function. ET-1 is responsible for a variety of cellular events: contraction, proliferation, apoptosis, etc. These effects take place after the activation of the two endothelin receptors ETA and ETB, which are present - among others - on cardiomyocytes, fibroblasts, smooth muscle and endothelial cells, glomerular and tubular cells of the kidney. The complex and numerous intracellular pathways, which can be contradictory in term of functional response depending on the receptor type, cell type and physiological situation, are described in this review. Many diseases share an enhanced ET-1 expression as part of the pathophysiology. However, the use of endothelin blockers is currently restricted to pulmonary arterial hypertension, and more recently to digital ulcer. The complexity of the endothelin system does not facilitate the translation of the molecular knowledge to clinical applications. Endothelin antagonists can prevent disease development but secondary undesirable effects limit their usage. Nevertheless, the increasing understanding of the effects of ET-I on the cardiac and renal physiology maintains the endothelin system as a promising therapeutic target. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:490 / 500
页数:11
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