Rees D D, Palmer R M, Moncada S
Wellcome Research Laboratories, Beckenham, Kent, United Kingdom.
Proc Natl Acad Sci U S A. 1989 May;86(9):3375-8. doi: 10.1073/pnas.86.9.3375.
The role of endothelium-derived nitric oxide in the regulation of blood pressure in the anesthetized rabbit was studied with N omega-monomethyl-L-arginine (L-NMMA), a specific inhibitor of its formation from L-arginine. L-NMMA (3-100 mg.kg-1), but not its D-enantiomer, induced a dose-dependent long-lasting (15-90 min) increase in mean systemic arterial blood pressure. L-NMMA (100 mg.kg-1) also inhibited significantly the hypotensive action of acetylcholine, without affecting that of glyceryl trinitrate. Both these actions of L-NMMA were reversed by L-arginine (300 mg.kg-1), but not by D-arginine (300 mg.kg-1), indomethacin (1 mg.kg-1), prazosin (0.3 mg.kg-1), or by vagotomy. The effects of L-NMMA in vivo were associated with a significant inhibition of the release of nitric oxide from perfused aortic segments ex vivo. This inhibition was reversed by infusing L-arginine through the aortic segments. These results indicate that nitric oxide formation from L-arginine by the vascular endothelium plays a role in the regulation of blood pressure and in the hypotensive actions of acetylcholine.
用Nω-单甲基-L-精氨酸(L-NMMA),一种从L-精氨酸形成一氧化氮的特异性抑制剂,研究了内皮衍生的一氧化氮在麻醉兔血压调节中的作用。L-NMMA(3-100mg·kg-1),但不是其D-对映体,引起平均体循环动脉血压的剂量依赖性持久(15-90分钟)升高。L-NMMA(100mg·kg-1)也显著抑制乙酰胆碱的降压作用,而不影响硝酸甘油的降压作用。L-NMMA的这两种作用都被L-精氨酸(300mg·kg-1)逆转,但不被D-精氨酸(300mg·kg-1)、吲哚美辛(1mg·kg-1)、哌唑嗪(0.3mg·kg-1)或迷走神经切断术逆转。L-NMMA在体内的作用与离体灌注主动脉段一氧化氮释放的显著抑制有关。通过主动脉段输注L-精氨酸可逆转这种抑制作用。这些结果表明,血管内皮从L-精氨酸形成一氧化氮在血压调节和乙酰胆碱的降压作用中起作用。