Role of copper ions and cytochrome P450 in the vasodilator actions of the nitroxyl anion generator, Angeli's salt, on rat aorta

被引:19
作者
Nelli, S [1 ]
McIntosh, L [1 ]
Martin, W [1 ]
机构
[1] Univ Glasgow, Inst Biomed & Life Sci, Div Neurosci & Biomed Syst, Glasgow G12 8QQ, Lanark, Scotland
基金
英国惠康基金;
关键词
cytochrome P450; nitric oxide (NO); nitroxyl anion; S-nitrosothiol; proadifen;
D O I
10.1016/S0014-2999(00)00845-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Since copper ions catalyse the oxidation of nitroxyl anion to nitric oxide, we investigated whether this might explain the vasodilator actions of the nitroxyl generator, Angeli's salt, in rat aorta. Parallel studies were conducted with S-nitroso-N-acetyl-D,L-penicillamine (SNAP), since Cu ions catalyse the liberation of nitric oxide from this compound. Copper sulphate enhanced relaxation to Angeli's salt and SNAP but this resulted from reduced destruction of nitric oxide by superoxide rather than from enhanced generation of nitric oxide, since it was mimicked by superoxide dismutase and by the superoxide dismutase mimetic, MnCl2. Results with the selective Cu2+ chelators, neocuproine and bathocuproine disulfonate, and the Cu2+ chelators, EDTA, cuprizone and diethyldithiocarbamate, confirmed an important role for endogenous copper in mediating relaxation to SNAP but suggested only a minor role for Angeli's salt. Relaxation to Angeli's salt was, however, powerfully blocked by proadifen, suggesting an important role for cytochrome P450. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:281 / 289
页数:9
相关论文
共 37 条
[1]   Neocuproine, a selective Cu(I) chelator, and the relaxation of rat vascular smooth muscle by S-nitrosothiols [J].
AlSadoni, HH ;
Megson, IL ;
Bisland, S ;
Butler, AR ;
Flitney, FW .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 121 (06) :1047-1050
[2]   NO+, NO(CENTER-DOT), AND NO- DONATION BY S-NITROSOTHIOLS - IMPLICATIONS FOR REGULATION OF PHYSIOLOGICAL FUNCTIONS BY S-NITROSYLATION AND ACCELERATION OF DISULFIDE FORMATION [J].
ARNELLE, DR ;
STAMLER, JS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 318 (02) :279-285
[3]  
COCCO D, 1981, J BIOL CHEM, V256, P8983
[4]  
DICKS AP, 1996, J CHEM SOC PERK T, V3, P481
[5]   Nitric oxide (NO center dot), the only nitrogen monoxide redox form capable of activating soluble guanylyl cyclase [J].
Dierks, EA ;
Burstyn, JN .
BIOCHEMICAL PHARMACOLOGY, 1996, 51 (12) :1593-1600
[6]  
ELLIS A, 2000, BRIT J PHARMACOL, V129, P513
[8]   CONVERSION OF NITROXYL (HNO) TO NITRIC-OXIDE (NO) IN BIOLOGICAL-SYSTEMS - THE ROLE OF PHYSIOLOGICAL OXIDANTS AND RELEVANCE TO THE BIOLOGICAL-ACTIVITY OF HNO [J].
FUKUTO, JM ;
HOBBS, AJ ;
IGNARRO, LJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 196 (02) :707-713
[9]  
FUKUTO JM, 1992, J PHARMACOL EXP THER, V263, P546
[10]   N,O-DIACYLATED-N-HYDROXYARYLSULFONAMIDES - NITROXYL PRECURSORS WITH POTENT SMOOTH-MUSCLE RELAXANT PROPERTIES [J].
FUKUTO, JM ;
HSZIEH, R ;
GULATI, P ;
CHIANG, KT ;
NAGASAWA, HT .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 187 (03) :1367-1373