Inhibition of NO-mediated responses by 7-ethoxyresorufin, a substrate and competitive inhibitor of cytochrome P-450

被引:14
作者
Li, CG
Rand, MJ
机构
[1] Pharmacology Research Laboratory, Dept. of Medical Laboratory Science, Roy. Melbourne Inst. of Technology, Melbourne, Vic. 3001
关键词
anococcygeus muscle; cytochrome P-450; endothelium-derived relaxing factor (EDRF); 7-ethoxyresorufin; nitrergic nerves; nitric oxide; nitric oxide synthase;
D O I
10.1111/j.1476-5381.1996.tb15366.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 The effects of 7-ethoxyresorufin (7-ER), which is a substrate for and competitive inhibitor of cytochrome P-450, were studied on responses to nitric oxide (NO), the NO donors sodium nitroprusside (SNP) and glyceryl trinitrate (GTN), acetylcholine-induced endothelium-dependent relaxations of rat and rabbit aortic rings and nitrergic nerve stimulation-induced relaxations of rat anococcygeus muscles. 2 In rat and rabbit aortic rings, 7-ER (2 mu M) inhibited the relaxations to acetylcholine in endothelium-intact preparations and the relaxant action of NO in endothelium-denuded preparations. Relaxant responses to SNP and GTN were inhibited by 7-ER in the rat but not rabbit aortic rings. However, the relaxant actions of papaverine and 8-bromo-cyclic GMP were not affected by 7-ER. 3 In rat anococcygeus muscles, 7-ER (2 mu M) inhibited the relaxant action of NO, but relaxations elicited by nitrergic nerve stimulation were only partly inhibited by a higher concentration of 7-ER (10 mu M). 4 After inhibition by 7-ER, superoxide dismutase (100 u ml(-1)) restored NO-induced relaxations of the rat aortic rings, but not acetylcholine-, SNP or GTN-induced relaxations, and restored NO- and nitrergic nerve stimulation-induced relaxations of anococcygeus muscles. 5 Another cytochrome P-450 inhibitor, troleandomycin (10-30 mu M), had no effect on NO- or acetylcholine-induced relaxations of rat aortic rings and NO- or nitrergic nerve stimulation-induced relaxations of anococcygeus muscles. However, resorufin, an analogue of 7-ER, inhibited responses to acetylcholine, NO and GTN in rat aortic rings. 6 The results suggest that 7-ER inhibited responses to NO and nitrergic nerve stimulation through generation of superoxide radicals. However, an additional mechanism may be involved in the reduction in acetylcholine-induced responses in aortic rings. 7 A 7-ER sensitive P-450 system may be involved in the bioactivation of GTN and SNP in rat aortic rings, but not in rabbit aorta or rat anococcygeus muscles.
引用
收藏
页码:57 / 62
页数:6
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