Functional importance of neuronal nitric oxide synthase in the endothelium of rat basilar arteries

被引:24
作者
Benyó, Z
Lacza, Z
Hortobágyi, T
Görlach, C
Wahl, M
机构
[1] Univ Munich, Dept Physiol, D-8000 Munich, Germany
[2] Semmelweis Univ, Inst Physiol 2, Dept Clin Res, H-1446 Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
rat basilar artery; neuronal nitric oxide synthase; cyclic GMP; endothelium; acetylcholine; bradykinin;
D O I
10.1016/S0006-8993(00)02611-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The function of the neuronal isoform of nitric oxide synthase (nNOS) was studied by comparing the effects of the specific nNOS blocker 7-nitro indazole monosodium salt (7-NINA) with that of the general NOS inhibitor N-G-nitro-L-arginine (L-NA) in isolated rat basilar artel ies (BAs). 7-NINA had no significant effect on the resting tone of the vessels, while both L-NA and 1H-[1,2,4]oxadiazolo[4,3-n]quinoxalin-1-one (ODQ), a selective inhibitor of the soluble guanylyl cyclase, induced contraction. The relaxant effect of bradykinin was attenuated in the presence of L-NA but was not changed by 7-NINA. In contrast, 7-NINA markedly reduced the acetylcholine induced, endothelium-dependent relaxation. These results demonstrate that nNOS contributes significantly to the relaxant effect of acetylcholine, indicating the functional importance of this isoenzyme in the cerebrovascular endothelium. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:79 / 84
页数:6
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