Palmer R M, Ashton D S, Moncada S
Wellcome Research Laboratories, Beckenham, Kent, UK.
Nature. 1988 Jun 16;333(6174):664-6. doi: 10.1038/333664a0.
Nitric oxide (NO) released by vascular endothelial cells accounts for the relaxation of strips of vascular tissue and for the inhibition of platelet aggregation and platelet adhesion attributed to endothelium-derived relaxing factor. We now demonstrate that NO can be synthesized from L-arginine by porcine aortic endothelial cells in culture. Nitric oxide was detected by bioassay, chemiluminescence or by mass spectrometry. Release of NO from the endothelial cells induced by bradykinin and the calcium ionophore A23187 was reversibly enhanced by infusions of L-arginine and L-citrulline, but not D-arginine or other close structural analogues. Mass spectrometry studies using 15N-labelled L-arginine indicated that this enhancement was due to the formation of NO from the terminal guanidino nitrogen atom(s) of L-arginine. The strict substrate specificity of this reaction suggests that L-arginine is the precursor for NO synthesis in vascular endothelial cells.
血管内皮细胞释放的一氧化氮(NO)可使血管组织条带舒张,并抑制归因于内皮源性舒张因子的血小板聚集和血小板黏附。我们现在证明,培养的猪主动脉内皮细胞可从L-精氨酸合成NO。通过生物测定、化学发光或质谱法检测到了一氧化氮。缓激肽和钙离子载体A23187诱导内皮细胞释放NO,L-精氨酸和L-瓜氨酸的输注可使其释放可逆性增强,但D-精氨酸或其他结构类似物则无此作用。使用15N标记的L-精氨酸进行的质谱研究表明,这种增强是由于L-精氨酸末端胍基氮原子形成了NO。该反应严格的底物特异性表明,L-精氨酸是血管内皮细胞中NO合成的前体。