CATECHOLAMINE-INDUCED MYOCARDIAL NECROSIS IN EXPERIMENTAL DIABETES-MELLITUS
- 1 January 1983
- journal article
- research article
- Vol. 107 (9), 480-483
Abstract
The pathogenesis of the cardiomyopathy associated with diabetes mellitus is unknown. Among several suggested mechanisms, myocardial necrosis induced by endogenous catecholamines may play a role. The sensitivity of the heart to the effect of varying doses of isoproterenol hydrochloride and norepinephrine bitartrate was examined in diabetic and control rats given streptozotocin. The dose of isoproterenol hydrochloride ranged from 0.008-30 mg/kg body wt. Norepinephrine bitartrate was given in doses from 0.2-1.0 mg/kg body wt. Each dose was given twice, 24 h apart. Animals were killed 48 h after the 1st dose, and their hearts were examined pathologically. Diabetes did not significantly alter the pathological response of the heart to either drug. Evidently diabetic heart is not intrinsically hypersensitive to catecholamines.This publication has 10 references indexed in Scilit:
- Lack of cardiotoxic effect of isoproterenol in streptozotocin diabetic ratsVirchows Archiv, 1982
- The effect of streptozotocin-induced diabetes in rats on cardiac contractile proteins.Circulation Research, 1981
- Depressed cardiac sarcoplasmic reticular function from diabetic ratsJournal of Molecular and Cellular Cardiology, 1981
- Altered myocardial mechanics in diabetic rats.Circulation Research, 1980
- The effect of diabetes on performance and metabolism of rat hearts.Circulation Research, 1980
- Clinical and morphological features of human hypertensive-diabetic cardiomyopathyAmerican Heart Journal, 1980
- Normalization of the Growth Hormone and Catecholamine Response to Exercise in Juvenile-Onset Diabetic Subjects Treated with a Portable Insulin Infusion PumpDiabetes, 1979
- EFFECTS OF INSULIN ON EXPERIMENTAL CATECHOLAMINE CARDIOMYOPATHY1978
- Evidence for Cardiomyopathy in Familial Diabetes MellitusJournal of Clinical Investigation, 1977
- INCREASED SENSITIVITY OF INVIVO PLATELET-AGGREGATION IN RABBITS AFTER ALLOXAN OR STREPTOZOTOCIN1976