[Urotensin II--a newly discovered modulator of cardiovascular functions in vertebrates].

Ceskoslovenska fysiologie Pub Date : 2013-01-01
A Zemancíková, J Török
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Abstract

Peptide urotensin II was originally isolated from the urophysis of teleost fishes; later it was identified also in higher vertebrates in various organs and tissues, including cardiovascular structures. Since its discovery it has been considered as a highly potent vasoconstrictor inducing contraction of smooth muscle in subnanomolar concentrations. Its wide distribution as well as its high interspecies homology indicates that this peptide is involved in regulation of many important physiological functions in vertebrates. An effort to discover other possible functions of urotensin II was intensified by the identification of its G-protein coupled receptor and its identification in humans. Furthermore, altered levels of expression of urotensin II and its receptor were found in various disease states including hypertension, diabetes, heart and renal failure, in experimental animal models as well as in humans. Therefore, there is widely discussed question regarding the possible role of urotensin II in etiopathogeneses of these diseases, however the exact mechanisms are still unknown. The aim of this review is to summarize the current knowledge about urotensin II with emphasis to its direct and undirect effects in cardiovascular system.

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[Urotensin II——一种新发现的脊椎动物心血管功能调节剂]。
肽尿紧张素II最初是从硬骨鱼的尿体中分离出来的;后来,在高等脊椎动物的各种器官和组织中,包括心血管结构中,也发现了它。自发现以来,它一直被认为是一种高效的血管收缩剂,在亚纳摩尔浓度下诱导平滑肌收缩。其广泛的分布和高度的种间同源性表明,该肽参与了脊椎动物许多重要生理功能的调节。通过鉴定其g蛋白偶联受体及其在人体内的鉴定,加强了发现尿紧张素II其他可能功能的努力。此外,在实验动物模型和人类中,在包括高血压、糖尿病、心脏和肾衰竭在内的各种疾病状态中,尿紧张素II及其受体的表达水平都发生了改变。因此,关于尿紧张素II在这些疾病的发病机制中可能发挥的作用,存在广泛讨论的问题,但其确切机制尚不清楚。这篇综述的目的是总结目前关于尿紧张素II的知识,重点是其在心血管系统中的直接和间接作用。
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