Comparison of the redox forms of nitrogen monoxide with the nitrergic transmitter in the rat anococcygeus muscle

被引:29
作者
Li, CG [1 ]
Karagiannis, J [1 ]
Rand, MJ [1 ]
机构
[1] Royal Melbourne Inst Technol, Dept Med Lab Sci, Pharmacol Res Unit, Melbourne, Vic 3001, Australia
关键词
Angeli's salt; carboxy-PTIO; hydroxocobalamin; nitrergic transmitter; nitric oxide; nitrosonium cation; nitrosonium tetrafluoroborate; nitroxyl anion; pyrogallol;
D O I
10.1038/sj.bjp.0702540
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 A sustained tone was produced in rat isolated anococcygeus muscles with guanethidine and clonidine and relaxant responses were elicited by electrical stimulation of its nitrergic nerves and by the three redox forms of nitrogen monoxide. 2 The nitroxyl anion (NO-) was donated by dissociation of Angeli's salt; the free radical (NO.) was from an aqueous solution of nitric oxide gas; the nitrosonium cation (NO+) was donated by dissociation of nitrosonium tetrafluoroborate. 3 The concentrations producing approximately 50% relaxations of the anococcygeus muscle were 0.3 mu M for Angeli's salt (nitroxyl), 0.5 mu M for NO. and 100 mu M for nitrosonium tetrafluoroborate. Nitrergic nerve stimulation at 1 Hz for 10 s produced equivalent relaxant responses. 4 The superoxide generator pyrogallol (100 mu M) had no effect on responses to nitrergic nerve stimulation or Angeli's salt but significantly reduced responses to NO. and nitrosonium tetrafluoroborate. 5 The NO. scavenger carboxy-PTIO (100 mu M) had no effect on responses to nitrergic nerve stimulation or Angeli's salt but significantly reduced responses to NO. and nitrosonium tetrafluoroborate. 6 Hydroxocobalamin (30 mu M) had no significant effect on responses to the nitrergic transmitter, enhanced the response to Angeli's salt, and significantly reduced responses to NO. and nitrosonium tetrafluoroborate. 7 The findings suggest that the nitroxyl anion donated by Angeli's salt is a better candidate than NO. to serve as the nitrergic transmitter in the rat anococcygeus muscle, although it still does not behave exactly like the transmitter.
引用
收藏
页码:826 / 834
页数:9
相关论文
共 49 条
[1]   ANTAGONISTIC ACTION OF IMIDAZOLINEOXYL N-OXIDES AGAINST ENDOTHELIUM-DERIVED RELAXING FACTOR .NO THROUGH A RADICAL REACTION [J].
AKAIKE, T ;
YOSHIDA, M ;
MIYAMOTO, Y ;
SATO, K ;
KOHNO, M ;
SASAMOTO, K ;
MIYAZAKI, K ;
UEDA, S ;
MAEDA, H .
BIOCHEMISTRY, 1993, 32 (03) :827-832
[2]   BIOASSAY OF NITRIC-OXIDE RELEASED UPON STIMULATION OF NONADRENERGIC NONCHOLINERGIC NERVES IN THE CANINE ILEOCOLONIC JUNCTION [J].
BOECKXSTAENS, GE ;
PELCKMANS, PA ;
RUYTJENS, IF ;
BULT, H ;
DEMAN, JG ;
HERMAN, AG ;
VANMAERCKE, YM .
BRITISH JOURNAL OF PHARMACOLOGY, 1991, 103 (01) :1085-1091
[3]  
BOECKXSTAENS GE, 1991, J PHARMACOL EXP THER, V256, P441
[4]   NITRIC-OXIDE AS AN INHIBITORY NONADRENERGIC NONCHOLINERGIC NEUROTRANSMITTER [J].
BULT, H ;
BOECKXSTAENS, GE ;
PELCKMANS, PA ;
JORDAENS, FH ;
VANMAERCKE, YM ;
HERMAN, AG .
NATURE, 1990, 345 (6273) :346-347
[5]   S-nitrosothiols and the nitrergic neurotransmitter in the rat gastric fundus: effect of antioxidants and metal chelation [J].
DeMan, JG ;
De Winter, BY ;
Moreels, TG ;
Herman, AG ;
Pelckmans, PA .
BRITISH JOURNAL OF PHARMACOLOGY, 1998, 123 (06) :1039-1046
[6]   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
[7]   UNDERSTANDING THE CONTROVERSY OVER THE IDENTITY OF EDRF [J].
FEELISCH, M ;
POEL, MT ;
ZAMORA, R ;
DEUSSEN, A ;
MONCADA, S .
NATURE, 1994, 368 (6466) :62-65
[8]   CHEMICAL OXIDATION OF N-HYDROXYGUANIDINE COMPOUNDS - RELEASE OF NITRIC-OXIDE, NITROXYL AND POSSIBLE RELATIONSHIP TO THE MECHANISM OF BIOLOGICAL NITRIC-OXIDE GENERATION [J].
FUKUTO, JM ;
WALLACE, GC ;
HSZIEH, R ;
CHAUDHURI, G .
BIOCHEMICAL PHARMACOLOGY, 1992, 43 (03) :607-613
[9]   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
[10]  
FUKUTO JM, 1992, J PHARMACOL EXP THER, V263, P546