Negative Inotropic Effect of Insulin in Papillary Muscles From Control and Diabetic Rats

Title:

Negative Inotropic Effect of Insulin in Papillary Muscles From Control and Diabetic Rats

Creator:

Švíglerová, J., Kuncová, J., and Štengl, M.

Identifier:

https://cdk.lib.cas.cz/client/handle/uuid:91a033db-a55b-4caa-bcfa-8b40c348ae24
uuid:91a033db-a55b-4caa-bcfa-8b40c348ae24

Subject:

Insulin, Rat, Heart, Contraction, and Diabetes

Type:

article, model:article, and TEXT

Description:

The inotropic effects of insulin in the rat heart are still incompletely understood. In this study, the effects of insulin on cardiac contraction were studied in right ventricular papillary muscles from both control rats and rats with chronic diabetes (lasting 16 weeks). Diabetes was induced by the application of streptozotocin (STZ) and the development of diabetes was documented by increased levels of blood glucose, by reduction in body weight and by decreased plasma concentrations of insulin. The contraction was significantly smaller in diabetic rats. Insulin (80 IU/l) reduced the contraction force in both control and diabetic groups. The post-rest potentiation of contraction was not influenced by insulin in control rats, but insulin increased it in diabetic rats. The negative inotropic effect of insulin was preserved in the presence of cyclopiazonic acid (3 μmol/l), a blocker of sarcoplasmic reticulum (SR) Ca2+ pump, in both control and diabetic groups. In contrast, the negative inotropic effect of insulin was completely prevented in the presence of nifedipine (3 μmol/l), a blocker of L-type Ca2+ current. We conclude that insulin exerts a significant negative inotropic effect in rat myocardium, both control and diabetic. This effect is probably related to processes of SR Ca2+ release triggering, whereas SR Ca2+ loading is not involved.

Language:

English

Rights:

http://creativecommons.org/licenses/by-nc-sa/4.0/
policy:public

Source:

Physiological research | 2005 Volume:54 | Number:6

Harvested from:

CDK

Metadata only:

false