Tölle Markus, van der Giet Markus
Med. Klinik IV-Nephrology, Charite-Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, Germany.
Peptides. 2008 May;29(5):743-63. doi: 10.1016/j.peptides.2007.08.029. Epub 2007 Sep 6.
Urotensin II (U-II) is a vasoactive peptide with many potent effects in the cardiorenovascular system. U-II activates a G-protein-coupled receptor termed UT. UT and U-II are highly expressed in the cardiovascular and renal system. Patients with various cardiovascular diseases show high U-II plasma levels. It was demonstrated that elevated U-II plasma levels and increased UT expression seem to play a role in heart failure, end-stage renal disease and atherosclerosis. U-II induces potent changes in vascular tone regulation. In addition, U-II stimulates vascular smooth muscle cell proliferation and cardiomyocyte hypertrophy. Currently several pharmaceutical companies are developing compounds to control the U-II/UT system. There are preclinical and some clinical studies showing potential benefits of inhibiting U-II function in renal disease, heart failure, and diabetes. This article will review both pre- and clinical data concerning cardiorenovascular effects of U-II.
尾加压素II(U-II)是一种血管活性肽,在心血管系统中具有多种强效作用。U-II激活一种名为UT的G蛋白偶联受体。UT和U-II在心血管系统和肾脏系统中高度表达。患有各种心血管疾病的患者血浆中U-II水平较高。已证实,血浆U-II水平升高和UT表达增加似乎在心力衰竭、终末期肾病和动脉粥样硬化中起作用。U-II可引起血管张力调节的显著变化。此外,U-II刺激血管平滑肌细胞增殖和心肌细胞肥大。目前,几家制药公司正在研发控制U-II/UT系统的化合物。临床前和一些临床研究表明,抑制U-II功能对肾病、心力衰竭和糖尿病具有潜在益处。本文将综述关于U-II心血管效应的临床前和临床数据。