Protective effect of enalapril on vascular reactivity of the rat aorta

被引:13
作者
Baluchnejadmojarad, T
Roghani, M
Imani, A
机构
[1] Iran Univ Med Sci, Dept Physiol, Sch Med, Tehran, Iran
[2] Shahed Univ, Dept Physiol, Sch Med, Tehran, Iran
关键词
aortic reactivity; diabetes mellitus; enalapril; streptozotocin; rat;
D O I
10.1016/j.vph.2004.02.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cardiovascular complications are the major cause of morbidity and mortality in patients with diabetes mellitus (DM). Strategies that interrupt the renin-angiotensin system have been shown to reduce the ensuing threatening risk factors. The present study was carried out to investigate the effect of subchronic administration of enalapril on the aortic reactivity of streptozotocin (STZ)-diabetic rats. For this purpose, STZ-diabetic rats received enalapril (10 and 20 mg/kg ip) daily for 2 months. Contractile responses to phenylephrine (PE) and relaxation responses to acetylcholine (Ach) and isosorbide dinitrate (ISD) were obtained from aortic rings. Concentration-response curves from enalapril-treated diabetic (ED) rats to PE were attenuated as compared to vehicle-treated diabetics (VD), especially at a dose of 20 mg/kg for enalapril. In addition, endothelium-dependent relaxation responses induced by Ach was significantly higher in ED rats as compared to diabetic ones. The endothelium-independent relaxation responses for ISD were also found not to be significantly different among the groups. Therefore, subchronic treatment of diabetic rats with enalapril in a dose-dependent manner could prevent the functional changes in vascular reactivity in diabetic rats. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:301 / 307
页数:7
相关论文
共 34 条
[1]   ENHANCED CONTRACTILE RESPONSES OF ARTERIES FROM DIABETIC RATS TO ALPHA-1-ADRENOCEPTOR STIMULATION IN THE ABSENCE AND PRESENCE OF EXTRACELLULAR CALCIUM [J].
ABEBE, W ;
HARRIS, KH ;
MACLEOD, KM .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1990, 16 (02) :239-248
[2]   ENDOTHELIUM-MEDIATED VASODILATION DURING ACE-INHIBITION [J].
AUCHSCHWELK, W ;
DUSKE, E ;
CLAUS, M ;
GRAF, K ;
GRAFE, M ;
FLECK, E .
EUROPEAN HEART JOURNAL, 1995, 16 :59-65
[3]   ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES [J].
BAYNES, JW .
DIABETES, 1991, 40 (04) :405-412
[4]  
CHANG KC, 1993, J PHARMACOL EXP THER, V266, P992
[5]   ANTIATHEROGENIC EFFECT OF CAPTOPRIL IN THE WATANABE HERITABLE HYPERLIPIDEMIC RABBIT [J].
CHOBANIAN, AV ;
HAUDENSCHILD, CC ;
NICKERSON, C ;
DRAGO, R .
HYPERTENSION, 1990, 15 (03) :327-331
[6]   ANTIOXIDANT EFFECTS OF ANGIOTENSIN-CONVERTING ENZYME (ACE) INHIBITORS - FREE-RADICAL AND OXIDANT SCAVENGING ARE SULFHYDRYL DEPENDENT, BUT LIPID-PEROXIDATION IS INHIBITED BY BOTH SULFHYDRYL-CONTAINING AND NONSULFHYDRYL-CONTAINING ACE INHIBITORS [J].
CHOPRA, M ;
BESWICK, H ;
CLAPPERTON, M ;
DARGIE, HJ ;
SMITH, WE ;
MCMURRAY, J .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1992, 19 (03) :330-340
[7]   Cardiovascular effects of captopril and enalapril in obese Zucker rats [J].
Duarte, J ;
Martinez, A ;
Bermejo, A ;
Vera, B ;
Gámez, MJ ;
Cabo, P ;
Zarzuelo, A .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 365 (2-3) :225-232
[8]   Oxidative stress and diabetic vascular complications [J].
Giugliano, D ;
Ceriello, A ;
Paolisso, G .
DIABETES CARE, 1996, 19 (03) :257-267
[9]  
GOHLKE P, 1995, AM J CARDIOL, V76, pE41
[10]   Angiotensin-converting enzyme inhibition suppresses plasminogen activator inhibitor-1 expression in the neointima of balloon-injured rat aorta [J].
Hamdan, AD ;
Quist, WC ;
Gagne, JB ;
Feener, EP .
CIRCULATION, 1996, 93 (06) :1073-1078