Literature DB >> 8777289

Influence of calcium channel blocker treatment on the mechanical properties of diabetic rat myocardium.

R A Brown1, M M Lee, A M Sundareson, D J Woodbury, A O Savage.   

Abstract

The objective of this investigation was to determine whether calcium channel blocker (CCB) treatment effectively restores normal baseline mechanical function in diabetic myocardium and to evaluate its effect on the interval-strength relationship. Wistar rats were made diabetic with streptozotocin (55 mg/kg, IV). Left-ventricular papillary muscles from normal and diabetic (10 weeks) rats were superfused with Tyrode's solution at 30 degrees C. A subgroup of diabetic and normal animals received daily injections of verapamil or nifedipine (10 mg/kg, IP; 8 weeks) to compare the effectiveness of a phenylalkylamine to a dihydropyridine in reversing diabetes-induced contractile dysfunction in vitro. Muscles were electrically stimulated at 0.5 Hz with suprathreshold stimuli, and the following parameters were measured: peak tension developed, time to-peak tension, time-to-90% relaxation, and the maximum velocities of tension development and decay. Experimental diabetes was characterized by: severe hyperglycemia, hepatomegaly, reduced body weight gain, cardiomegaly, and increased plasma phospholipid levels. In addition, baseline values of peak tension developed, time to-peak tension, and time-to-90% relaxation were significantly greater in muscles from diabetic animals. Chronic nifedipine treatment reduced hyperglycemia and plasma phospholipid levels, normalized body weight gain, and reduced both heart and liver sizes in diabetic animals. Nifedipine treatment completely reversed diabetes-induced prolongation in both time-to-peak tension and time-to-90% relaxation. In diabetic myocardium, a slightly positive component was present in the interval-strength relationship between 0.01 and 1 Hz, resulting in a rightward shift in the entire curve across a wide range of stimulation frequencies (0.01-5 Hz). This positive component was absent in muscles from diabetic animals treated with both CCBs, and verapamil produced a leftward shift in the frequency response curve. The results of this study suggest that chronic nifedipine treatment may be more effective than verapamil in restoring normal baseline myocardial mechanical function, reducing hyperglycemia and hyperlipidemia, as well as attenuating both cardiac and liver enlargement in experimental diabetes. In contrast, verapamil treatment tended to normalize more effectively the inotropic response to changes in stimulation frequency in diabetic myocardium.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8777289     DOI: 10.1007/bf00571933

Source DB:  PubMed          Journal:  Acta Diabetol        ISSN: 0940-5429            Impact factor:   4.280


  36 in total

1.  Mechanism of insulin resistance induced by sustained levels of cytosolic free calcium in rat adipocytes.

Authors:  B Draznin; D Lewis; N Houlder; N Sherman; M Adamo; W T Garvey; D LeRoith; K Sussman
Journal:  Endocrinology       Date:  1989-11       Impact factor: 4.736

2.  Mechanism of ion permeation through calcium channels.

Authors:  P Hess; R W Tsien
Journal:  Nature       Date:  1984 May 31-Jun 6       Impact factor: 49.962

3.  Increase in [3H]PN 200-110 binding to cardiac muscle membrane in streptozocin-induced diabetic rats.

Authors:  Y Nishio; A Kashiwagi; T Ogawa; T Asahina; M Ikebuchi; M Kodama; Y Shigeta
Journal:  Diabetes       Date:  1990-09       Impact factor: 9.461

4.  The cardioprotective effect of verapamil.

Authors:  W G Nayler; A M Slade
Journal:  Clin Exp Pharmacol Physiol Suppl       Date:  1982

5.  Altered myocardial response to ouabain in diabetic rats: mechanics and electrophysiology.

Authors:  F S Fein; R S Aronson; C Nordin; B Miller-Green; E H Sonnenblick
Journal:  J Mol Cell Cardiol       Date:  1983-11       Impact factor: 5.000

6.  Altered myocardial mechanics in diabetic rats.

Authors:  F S Fein; L B Kornstein; J E Strobeck; J M Capasso; E H Sonnenblick
Journal:  Circ Res       Date:  1980-12       Impact factor: 17.367

7.  Cardiac function and myosin ATPase in diabetic rats treated with insulin, T3, and T4.

Authors:  D W Garber; A W Everett; J R Neely
Journal:  Am J Physiol       Date:  1983-04

8.  Chronic verapamil treatment attenuates the negative inotropic effect of ethanol in diabetic rat myocardium.

Authors:  R A Brown; P Bhasin; A O Savage; J C Dunbar
Journal:  Can J Physiol Pharmacol       Date:  1994-09       Impact factor: 2.273

9.  Sarcolemmal Ca2+ transport in streptozotocin-induced diabetic cardiomyopathy in rats.

Authors:  N Makino; K S Dhalla; V Elimban; N S Dhalla
Journal:  Am J Physiol       Date:  1987-08

10.  Beneficial effects of verapamil in diabetic cardiomyopathy.

Authors:  N Afzal; P K Ganguly; K S Dhalla; G N Pierce; P K Singal; N S Dhalla
Journal:  Diabetes       Date:  1988-07       Impact factor: 9.461

View more
  2 in total

1.  Effect of successful hypertension control by manidipine or lisinopril on albuminuria and left ventricular mass in diabetic hypertensive patients with microalbuminuria.

Authors:  Roberto Fogari; Amedeo Mugellini; Annalisa Zoppi; Pierangelo Lazzari; Maurizio Destro; Andrea Rinaldi; Paola Preti
Journal:  Eur J Clin Pharmacol       Date:  2005-07-15       Impact factor: 2.953

Review 2.  Cellular Protein Quality Control in Diabetic Cardiomyopathy: From Bench to Bedside.

Authors:  Namrita Kaur; Rida Raja; Andrea Ruiz-Velasco; Wei Liu
Journal:  Front Cardiovasc Med       Date:  2020-10-15
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.