Moncada S
Wellcome Research Laboratories, Beckenham, Kent, United Kingdom.
Schweiz Rundsch Med Prax. 1993 Oct 19;82(42):1154-60.
The endothelial relaxation factor postulated by Furchgott has been identified as the endogenous nitro-vasodilatator nitric oxide (nitrogen monoxide, NO). NO is derived from L-arginine and plays an important role in the regulation of circulation. In man, too, inhibitors of NO synthesis like L-NG monomethylarginine (L-NMMA) led to hypertension as well as to reduction of local blood flow. In vivo inhibition of NO synthesis leads to amplification of the effect and of the duration of the effect of nitrates. L-arginine/NO metabolism has also been detected in nonvascular tissues, i.e. from lungs, gastrointestinal tract and urogenital tract. The discovery of inducible nitric-oxide synthase activity in vascular smooth muscle cells, able to produce a great amount of NO, represents another important recent development. Important stimuli for the induction of this NO-synthase are cytokines that play possibly an important clinical role in the context of endotoxemic shock. Research over the last ten years has demonstrated that the L-arginine/NO system represents a central biological regulatory mechanism that plays an important role under physiologic and pathophysiologic conditions not only for the circulation but also in other organs.
弗奇戈特提出的内皮舒张因子已被确认为内源性硝基血管扩张剂一氧化氮(NO)。NO由L-精氨酸衍生而来,在循环调节中起重要作用。在人类中,NO合成抑制剂如L-NG单甲基精氨酸(L-NMMA)也会导致高血压以及局部血流减少。体内抑制NO合成会导致硝酸盐作用的增强和作用持续时间的延长。在非血管组织中,即肺、胃肠道和泌尿生殖道中也检测到了L-精氨酸/NO代谢。血管平滑肌细胞中可诱导产生大量NO的一氧化氮合酶活性的发现是近期的另一项重要进展。诱导这种NO合酶的重要刺激因素是细胞因子,它们在内毒素性休克的情况下可能发挥重要的临床作用。过去十年的研究表明,L-精氨酸/NO系统是一种核心的生物调节机制,不仅在生理和病理生理条件下对循环,而且在其他器官中都起着重要作用。