The effect of high-dose pentaerythritol tetranitrate on the development of nitrate tolerance in rabbits

被引:18
作者
Müllenheim, J
Müller, S
Laber, U
Thämer, V
Meyer, W
Bassenge, E
Fink, B
Kojda, G
机构
[1] Univ Dusseldorf, Inst Pharmakol & Klin Pharmakol, D-40225 Dusseldorf, Germany
[2] Univ Dusseldorf, Klin Anaesthesiol, D-40225 Dusseldorf, Germany
[3] Univ Dusseldorf, Inst Herz Kreislauf Physiol, D-40225 Dusseldorf, Germany
[4] Tierarztlichen Hsch Hannover, D-30173 Hannover, Germany
[5] Univ Freiburg, Inst Angew Physiol & Balneol, D-79104 Freiburg, Germany
关键词
organic nitrates; pentaerythritol tetranitrate; nitrate tolerance; nitric oxide; rabbit; blood pressure;
D O I
10.1007/s002100100464
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Experimental studies with therapeutic doses of pentaerythritol tetranitrate (PETN) have shown unexpected actions such as a lack of nitrate tolerance and vasoprotective effects in atherosclerosis. We investigated the effect of a 3-week treatment with low- (6 mg kg(-1) day(-1), n=10) and high-dose (100 mg kg(-1) day(-1), n=10) oral PETN given twice daily on the development of nitrate tolerance in rabbits. We measured aortic relaxation in response to acetylcholine, S-nitroso-N-acetyl-D,L-penicillamine and PETN, constriction in response to phenylephrine and production of reactive oxygen species (ROS). Mean aortic pressure (AOPmean) and heart rate were measured after a single oral dose of PETN (50 mg kg(-1), n=6) and after increasing doses of pentaerythritol dinitrate (PEDN, n=5) and pentaerythritol mononitrate (PEMN, n=5) in anaesthetized rabbits. Oral PETN, even at high dosage, was not associated with nitrate tolerance. None of the aortic ring studies showed a difference in the responses to the vasodilators, while the vasoconstriction to phenylephrine was slightly reduced in both PETN groups. The production of vascular ROS was also not different. Oral PETN reduced AOPmean transiently (-19.3 +/-4.4%. P <0.01 vs. controls) and i.v. administration of both PEMN and PEDN reduced AOPmean dose dependently (P <0.05, ANOVA). These results suggest that oral PETN elicits minor nitrate tolerance. This unique feature might be due to the slow onset of vasodilator activity of the predominantly active metabolites PEDN and PEMN and might contribute to the vasoprotective activity of PETN in atherosclerosis.
引用
收藏
页码:269 / 275
页数:7
相关论文
共 27 条
[1]  
AHLNER J, 1991, PHARMACOL REV, V43, P351
[2]  
Benet L., 1996, The pharmacological basis of therapeutics, V9th, P3
[3]  
DAVIDSON IW, 1970, J PHARMACOL EXP THER, V175, P42
[4]  
DEVITA C, 1994, LANCET, V343, P1115
[5]   Spin trapping of superoxide radicals and peroxynitrite by 1-hydroxy-3-carboxy-pyrrolidine and 1-hydroxy-2,2,6,6-tetramethyl-4-oxo-piperidine and the stability of corresponding nitroxyl radicals towards biological reductants [J].
Dikalov, S ;
Skatchkov, M ;
Bassenge, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 231 (03) :701-704
[6]  
Duck K D, 1990, Z Gesamte Inn Med, V45, P736
[7]   UNUSUALLY STABLE THIONITRITE FROM N-ACETYL-D,L-PENICILLAMINE - X-RAY CRYSTAL AND MOLECULAR-STRUCTURE OF 2-(ACETYLAMINO)-2-CARBOXY-1,1-DIMETHYLETHYL THIONITRITE [J].
FIELD, L ;
DILTS, RV ;
RAVICHANDRAN, R ;
LENHERT, PG ;
CARNAHAN, GE .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1978, (06) :249-250
[8]   Unexpected, tolerance-devoid vasomotor and platelet actions of pentaerythrityl tetranitrate [J].
Fink, B ;
Bassenge, E .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1997, 30 (06) :831-836
[9]  
Hacker A, 1999, XXI CONGRESS OF THE EUROPEAN SOCIETY OF CARDIOLOGY, P251
[10]  
HAFNER D, 1977, DRUG RES, V27, P1871