Interactions of captopril and verapamil on glucose tolerance and insulin action in an animal model of insulin resistance

被引:44
作者
Dal Ponte, DB
Fogt, DL
Jacob, S
Henriksen, EJ
机构
[1] Univ Arizona, Coll Med, Dept Physiol, Muscle Metab Lab, Tucson, AZ 85721 USA
[2] Univ Tubingen, Dept Endocrinol, Tubingen, Germany
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 1998年 / 47卷 / 08期
关键词
D O I
10.1016/S0026-0495(98)90355-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have shown previously that the combination of a long-acting, non-sulfhydryl-containing angiotensin-converting enzyme (ACE) inhibitor (trandolapril) and the Ca2+ channel blocker verapamil improve insulin-stimulated glucose transport in skeletal muscle of the obese Zucker rat, a model of insulin resistance, hyperinsulinemia, and dyslipidemia. In the present study, we investigated the interactions of chronic treatment (28 days) with verapamil (20 mg/kg) and a short-acting, sulfhydryl-containing ACE inhibitor (captopril, 50 mg/kg) in combination on insulinemia, lipidemia, glucose tolerance, and insulin action on skeletal muscle glucose transport (2-deoxyglucose uptake in epitrochlearis) in lean and obese Zucker rats. In lean animals, verapamil alone and in combination with captopril actually increased (P <.05) plasma insulin, whereas in obese animals, verapamil alone worsened the hyperinsulinemia already present, and this effect was abolished by cotreatment with captopril. Captopril alone or in combination with verapamil reduced plasma free fatty acid (FFA) levels in obese rats, but not in lean rats. Captopril alone reduced the glucose-insulin index in obese animals given an oral glucose load, and this was associated with a significant increase in insulin-mediated muscle glucose transport. The greatest improvement in these responses was elicited in obese animals receiving combined captopril and verapamil treatment, and was associated with increases in muscle GLUT-4 glucose transporter protein and hexokinase and citrate synthase activities. In conclusion, these findings indicate that the short-acting, sulfhydryl-containing ACE inhibitor captopril can elicit beneficial metabolic effects on the hyperinsulinemia, dyslipidemia, glucose intolerance, and insulin resistance of muscle glucose transport of the obese Zucker rat. Moreover, there is a positive interactive effect on these pathophysiological parameters between captopril and verapamil in this animal model of insulin resistance. Copyright (C) 1998 by W.B. Saunders Company.
引用
收藏
页码:982 / 987
页数:6
相关论文
共 40 条
[1]  
Alberti KGMM, 1996, DIABETIC MED, V13, P927, DOI 10.1002/(SICI)1096-9136(199611)13:11<927::AID-DIA279>3.0.CO
[2]  
2-E
[3]   Role of fatty acids in the pathogenesis of insulin resistance and NIDDM [J].
Boden, G .
DIABETES, 1997, 46 (01) :3-10
[4]   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
[5]  
CORTEZ MY, 1991, AM J PHYSIOL, V261, pE613
[6]  
Decarie A, 1996, PEPTIDES, V17, P1009
[7]   Enalapril and captopril enhance antioxidant defenses in mouse tissues [J].
deCavanagh, EMV ;
Fraga, CG ;
Ferder, L ;
Inserra, F .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1997, 272 (02) :R514-R518
[8]   INSULIN RESISTANCE - A MULTIFACETED SYNDROME RESPONSIBLE FOR NIDDM, OBESITY, HYPERTENSION, DYSLIPIDEMIA, AND ATHEROSCLEROTIC CARDIOVASCULAR-DISEASE [J].
DEFRONZO, RA ;
FERRANNINI, E .
DIABETES CARE, 1991, 14 (03) :173-194
[9]   Potential role of bradykinin in forearm muscle metabolism in humans [J].
Dietze, GJ ;
Wicklmayr, M ;
Rett, K ;
Jacob, S ;
Henriksen, EJ .
DIABETES, 1996, 45 :S110-S114
[10]   Glucose transport and cell surface GLUT-4 protein in skeletal muscle of the obese Zucker rat [J].
Etgen, GJ ;
Wilson, CM ;
Jensen, J ;
Cushman, SW ;
Ivy, JL .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1996, 271 (02) :E294-E301