Halbrügge T, Lütsch K, Thyen A, Graefe K H
Department of Pharmacology, University of Würzburg, Federal Republic of Germany.
J Neural Transm Suppl. 1991;34:113-9. doi: 10.1007/978-3-7091-9175-0_15.
In the anaesthetized rabbit, L-NG-monomethyl-arginine (L-NMMA), a specific inhibitor of nitric oxide (NO) formation, was used to assess the role of endothelium-derived NO in the regulation of haemodynamics and noradrenaline release (RNA). L-NMMA dose-dependently increased mean arterial pressure and total peripheral resistance (TPR), but decreased heart rate, cardiac output and RNA. The curvilinear relationship between RNA and TPR obtained for L-NMMA was virtually identical with that produced by phenylephrine, indicating that L-NMMA-induced decreases in RNA are mediated by the baroreflex. Since the maximum RNA inhibition by L-NMMA was 69%, the counterregulation against peripheral vasodilatation by endothelium-derived NO accounts for 69% of basal RNA.
在麻醉兔中,使用一氧化氮(NO)生成的特异性抑制剂L-NG-单甲基精氨酸(L-NMMA)来评估内皮源性NO在血流动力学调节和去甲肾上腺素释放(RNA)中的作用。L-NMMA剂量依赖性地增加平均动脉压和总外周阻力(TPR),但降低心率、心输出量和RNA。L-NMMA产生的RNA与TPR之间的曲线关系与去氧肾上腺素产生的曲线关系几乎相同,表明L-NMMA诱导的RNA降低是由压力反射介导的。由于L-NMMA对RNA的最大抑制率为69%,内皮源性NO对外周血管舒张的反调节占基础RNA的69%。