EFFECT OF N(G)-MONOMETHYL-L-ARGININE ON THE BETA-ADRENOCEPTOR-MEDIATED RELAXATION OF RAT MESENTERIC RESISTANCE ARTERIES

被引:18
作者
BLANKESTEIJN, WM
THIEN, T
机构
[1] Dept. of Medicine, Div. of General Internal Medicine, University Hospital Nijmegen, Nijmegen, 6500 HB Nijmegen
关键词
D O I
10.1016/0024-3205(93)90178-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Beta-adrenoceptors are present on vascular smooth muscle and on endothelium. We investigated whether the endothelial beta-adrenoceptors induce relaxation of rat mesenteric resistance arteries by stimulation of endothelium-derived relaxing factor (EDRF) release. To this end, the relaxation was studied in the presence and absence of 100 muM N(G)-monomethyl-L-arginine (L-NMMA), a specific inhibitor of the production of EDRF. The maximal relaxation with isoprenaline, expressed as a percentage of the precontraction, was 44.0 +/- 4.0 % (n = 12) in the L-NMMA treated group and 58.0 +/- 2.6 % (n = 13) in the untreated group, a statistically significant difference (P = 0.008). However, the precontraction with 40 mM K+ tended to be higher in the presence of L-NMMA. The pD2-value for isoprenaline was not significantly changed by the L-NMMA treatment. We conclude that the isoprenaline-mediated relaxation of mesenteric resistance arteries is inhibited by L-NMMA, but that this effect can at least in part be ascribed to an inhibition of baseline EDRF-release.
引用
收藏
页码:PL135 / PL139
页数:5
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