The major objectives of this grant proposal are: to assess the effect of acute and chronic diabetes on myocardial intermediary energy metabolism; and to elucidate possible mechanisms responsible for the impairment of substrate utilization and its contribution to diabetic cardiomyopathy. The experimental model will be freshly isolated calcium-tolerant heart myocytes from acutely and chronically streptozotocin-diabetic rats. A secondary objective is to culture these isolated cells in a serum-free, chemically defined medium for the study of hormonal interaction on myocyte metabolism. Freshly isolated cardiac cells represent a fairly new model for studying myocardial metabolism. Despite the fact that they are quiescent, we previously reported that alterations in substrate utilization found in isolated perfused hearts from diabetic rats are also present in isolated myocytes. Preliminary studies from this laboratory have further demonstrated significant differences in substrate utilization patterns in freshly isolated myocytes from acutely and chronically diabetic rats. These may relate to differences in their in vivo diabetic state. In addition, the altered substrate metabolism in chronic diabetes may lead to an energy deficient state. It is therefore important to examine in the isolated myocytes mechanisms that may result in defective energy metabolism. These include determinations of oxidation of selected exogenous substrates, substrate flux through major metabolic pathways, endogenous substrate turnover and availability as energy sources, marker enzyme activities, pertinent intermediary metabolite and energy-rich phosphate levels under conditions resembling those found in normal and diabetic animals. In order to better understand hormonal influences on substrate metabolism, the isolated myocytes will be cultured in a serum-free, hormone-supplemented medium and the metabolic fate of selected substrates will be examined.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL033646-02
Application #
3345745
Study Section
(SRC)
Project Start
1984-09-30
Project End
1987-09-29
Budget Start
1985-09-30
Budget End
1986-09-29
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Yale University
Department
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
Chen, V; Downing, S E (1991) Amelioration of hyperlipidemia by low fat diets in chronically streptozotocin-diabetic rats. Life Sci 49:857-64
Ascuitto, R J; Ross-Ascuitto, N T; Chen, V et al. (1989) Ventricular function and fatty acid metabolism in neonatal piglet heart. Am J Physiol 256:H9-15