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首届罗伯特·弗奇戈特讲座:从内皮依赖性舒张到L-精氨酸:一氧化氮途径。

The first Robert Furchgott lecture: from endothelium-dependent relaxation to the L-arginine:NO pathway.

作者信息

Moncada S

机构信息

Wellcome Research Laboratories, Beckenham, UK.

出版信息

Blood Vessels. 1990;27(2-5):208-17. doi: 10.1159/000158812.

Abstract

Nitric oxide (NO) is released from vascular endothelial cells and fresh vascular tissue in amounts sufficient to account for the biological actions of endothelium-derived relaxing factor. It is synthesized from the terminal guanidino nitrogen atom(s) of L-arginine, a process that is inhibited by NG-monomethyl-L-arginine (L-NMMA). Studies using L-NMMA have shown that NO is constantly generated by the vessel wall to maintain vasodilator tone. The L-arginine:NO pathway has now been identified in a number of other cells and tissues, in many of which it acts as the transduction mechanism for stimulation of the soluble guanylate cyclase.

摘要

一氧化氮(NO)从血管内皮细胞和新鲜血管组织中释放出来,其释放量足以解释内皮源性舒张因子的生物学作用。它由L-精氨酸的末端胍基氮原子合成,该过程受到NG-单甲基-L-精氨酸(L-NMMA)的抑制。使用L-NMMA的研究表明,血管壁持续产生NO以维持血管舒张张力。现在已经在许多其他细胞和组织中发现了L-精氨酸:NO途径,其中许多细胞和组织中它作为刺激可溶性鸟苷酸环化酶的转导机制。

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