Membrane alterations resulting from states of myocardial ischemia have been hypothesized as a major factor in the development of irreversible cellular damage. In this proposal, studies will be performed to investigate the mechanism(s) initiating membrane damage as well as a thorough investigation of the functional, structural and biochemical consequences of membrane damage. An isolated perfused heart preparation will be used for these studies. The components of myocardial ischemia that will be tested for their involvement in the development of membrane alterations will include: 1) an evaluation of damage due to the generation of oxygen-derived free radicals resulting in lipid peroxidation of biologial membranes; 2) an examination of membrane phospholipid alterations due to the activation of phospholipases; and 3) an evaluation of cellular and subcellular electrolytes, including documentation of shifts that occur relatively early during ischemia, and evaluation of the role of sodium alterations in producing calcium overloading by sodium-calcium exchange. Specific interventions including free radical scavengers, such as superoxide dismutase, catalase and Alpha-tocopheral, and phospholipase inhibitors, such as chlorpromazine, will be evaluated for their ability to protect against specific alterations thereby providing information on the involvement of various components of ischemia in the damage process. Indices of damage to be evaluated will include: measurements of lipid peroxidation products; phospholipid degradation and alterations in the levels of free fatty acids; electrolyte alterations; structural integrity; function; levels of adenine nucleotides; and enzyme loss. Statistical comparisons will be made between control, ischemic, and reperfused hearts, and hearts treated with various interventions. The proposed studies will provide important insights concerning the significance of membrane lipids in the maintenance of cell survival, the influence of electrolyte alterations in the development of irreversible myocardial injury, and the ability of interventions to protect against specific aspects of the damage process and provide information as to the relative importance of these phenomenon in myocardial injury.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL030570-05
Application #
3341601
Study Section
Cardiovascular and Pulmonary Research B Study Section (CVB)
Project Start
1982-07-01
Project End
1988-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
5
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
Overall Medical
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Burton, K P; Hagler, H K; Nazeran, H (1992) Exposure to free radicals alters ionic calcium transients in isolated adult rat cardiac myocytes. Am J Cardiovasc Pathol 4:235-44