Considerable attention has been directed toward both gestational and senescent-related cardiovascular changes; however, little information is currently available with respect to the perinatal period. It is clear that the perinatal period encompassing weaning to early adulthood represents a time of rapid increase in cardiac hemodynamic function. Cellular and subcellular correlates of cardiac hemodynamic function have been investigated, but conclusions to date have failed to consider the heterogeneous cellular composition of cardiac tissue. Therefore, the overall objective of the proposed work is to define the characteristic cellular adaptations which occur during rat heart development from the time of weaning until early adulthood. Within the overall objective the specific aims are: 1. To determine the relative cellular, i.e. cardiac muscle cell and nonmuscle cell, composition. Total cell numbers and relative fractional cell composition will be considered. 2. To define the cellular characteristics of both cardiac muscle and non-muscle cells. Cell size, protein synthetic capacity, and indices of aerobic metabolic capability will be considered. 3. To define myocyte specific characteristics including enzymatic activity (ATPase) of contractile proteins and contractile performance determined in isolated, single cardiac myocytes.
The specific aims outlined above will characterize cardiac muscle and nonmuscle cells prepared from hearts during the process of normal cell growth. From this characterization, factors which influence contractile properties of heart myocytes can be identified through complementary research areas including biochemistry and physiology. Identification of factors influencing contractile properties of normally developing heart muscle cells will serve as a useful reference for studies of altered cellular properties in various cardiac disease entities.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL033677-02
Application #
3345771
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
University of Kansas
Department
Type
Schools of Medicine
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
Nyquist-Battie, C; Dowell, R T; Fernandez, H (1989) Acetylcholinesterase molecular forms in muscle and non-muscle cells of rat heart. J Mol Cell Cardiol 21:987-94
Dowell, R T (1987) Phosphorylcreatine shuttle enzymes during perinatal heart development. Biochem Med Metab Biol 37:374-84
Dowell, R T (1986) Mitochondrial component of the phosphorylcreatine shuttle is enhanced during rat heart perinatal development. Biochem Biophys Res Commun 141:319-25
Dowell, R T; Atkins, F L; Love, S (1986) Integrative nature and time course of cardiovascular alterations in the diabetic rat. J Cardiovasc Pharmacol 8:406-13
Dowell, R T; Martin, A F (1985) Cardiac myofibrillar creatine kinase is not influenced by hypothyroidism. Can J Physiol Pharmacol 63:627-9