LACK OF CROSS-TOLERANCE BETWEEN NITROGLYCERIN AND ENDOTHELIUM-DERIVED RELAXING FACTOR-MEDIATED VASOACTIVE AGENTS IN SPONTANEOUSLY HYPERTENSIVE RATS

被引:14
作者
DEGARAVILLA, L
VOLBERG, ML
PRATT, PF
SILVER, PJ
BUCHHOLZ, RA
机构
[1] Department of Cardiovascular Pharmacology, Sterling Winthrop Pharmaceuticals Research Division, Rensselaer
关键词
NITRATE VASODILATORS; PHOSPHODIESTERASE INHIBITORS; ZAPRINAST; N(OMEGA)-NITRO-L-ARGININE; L-ARGININE; ACETYLCHOLINE; BRADYKININ; BLOOD PRESSURE;
D O I
10.1016/0014-2999(93)90708-P
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to determine whether cross-tolerance develops between nitroglycerin and endothelium-derived relaxing factor (EDRF)-mediated vasoactive agents in vivo. Spontaneously hypertensive rats (SHR) were made tolerant by pretreatment with high doses of nitroglycerin (100 mg/kg s.c., 3 times/day, for 3 consecutive days). The hypotensive effect of challenge doses of nitroglycerin (1, 10, 300, 100 mug/kg i.v.) was completely abolished in nitroglycerin-pretreated SHR. To evaluate cross-tolerance, the effects of the following EDRF-dependent vasoactive agents on blood pressure were determined in groups of nitroglycerin-pretreated and vehicle-pretreated SHR: acetylcholine, bradykinin and L-arginine. In addition, the hypotensive effects of zaprinast (M & B 22,928), a cyclic guanosine monophosphate (cGMP) phosphodiesterase inhibitor, and the hypertensive effects of the nitric oxide-synthase inhibitor N(omega)-nitro-L-arginine were also evaluated. In all cases, there was no difference in the effects of these agents on blood pressure when compared in nitroglycerin-pretreated (tolerant) and vehicle-pretreated (non-tolerant) SHR. The use of a variety of agents which modulate EDRF release or its effects by several different mechanisms suggests that cross-tolerance does not occur between nitroglycerin and EDRF in vivo.
引用
收藏
页码:77 / 82
页数:6
相关论文
共 31 条
[1]  
AHLNER J, 1991, PHARMACOL REV, V43, P353
[2]   L-CYSTEINE AUGMENTS THE VASORELAXATION INDUCED BY SODIUM-NITRITE AND SIN-1 BUT NOT THAT DUE TO ACETYLCHOLINE [J].
ARVOLA, P ;
PORSTI, I ;
VUORINEN, P ;
HUHTALA, H ;
METSAKETELA, T ;
VAPAATALO, H .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 214 (2-3) :289-292
[3]   TOLERANCE TOWARDS NITROGLYCERIN, INDUCED INVIVO, IS CORRELATED TO A REDUCED CGMP RESPONSE AND AN ALTERATION IN CGMP TURNOVER [J].
AXELSSON, KL ;
ANDERSSON, RGG .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1983, 88 (01) :71-79
[4]   NITRATE TOLERANCE FROM A BIOCHEMICAL POINT-OF-VIEW [J].
AXELSSON, KL ;
AHLNER, J .
DRUGS, 1987, 33 :63-68
[5]  
BOESGAARD S, 1991, J PHARMACOL EXP THER, V258, P851
[6]  
BOGAERT M, 1991, J CARDIOVAS PHARM S3, V17, pS313
[7]   N-OMEGA-NITRO-L-ARGININE ATTENUATES THE ACCUMULATION OF AORTIC CYCLIC-GMP AND THE HYPOTENSION PRODUCED BY ZAPRINAST [J].
DUNDORE, RL ;
PRATT, PF ;
OCONNOR, B ;
BUCHHOLZ, RA ;
PAGANI, ED .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1991, 200 (01) :83-87
[8]   SODIUM-NITROPRUSSIDE POTENTIATES THE DEPRESSOR RESPONSE TO THE PHOSPHODIESTERASE INHIBITOR ZAPRINAST IN RATS [J].
DUNDORE, RL ;
PRATT, PF ;
HALLENBECK, WD ;
WASSEY, ML ;
SILVER, PJ ;
BUCHHOLZ, RA .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 185 (01) :91-97
[10]   NITRATE TOLERANCE - A REVIEW OF THE EVIDENCE [J].
FLAHERTY, JT .
DRUGS, 1989, 37 (04) :523-550