The objective of this project is to ascertain the mechanism(s) for the actions of l-palmitoylcarnitine (l-PC) on the electrophysiological properties of isolated myocytes. In particular, our objective is to learn how l-PC can be arrhythmogenic. Because l-PC accumulates within, and can be released from ischemic heart cells, this amphiphile has been implicated as one of the agents that induces arrhythmias. However, the mechanism(s) by which l-PC induces arrhythmias are not known. Two experimental paradigms will be used, namely, the currently clamp and voltage clamp technique with single ventricular myocytes and the cellular electrophoresis technique with erythrocytes and myocytes. With the former method, experiments will be done to measure the modifications of sarcolemmal ion transport that are induced by l-PC and quantitative reconstructions of altered ionic currents will be used to determine mechanism(s) for the arrhythmogenic effect of this amphiphile. With the cellular electrophoresis method, experiments will be done to evaluate a surface charge hypothesis for the effects of l- PC. From preliminary work, it has been concluded that l-PC acts like elevated extracellular calcium to shift the voltage-dependence of sodium and calcium currents in heart muscle cells by reducing surface negative charge. The validity of the surface charge hypothesis can be tested in electrophoresis experiments and then re-evaluated in isolated myocytes. In this way, the predictions of the surface charge hypothesis will be subjected to careful and systematic evaluations with the quantitative precision available with the voltage clamp method. With these experimental approaches, there will result not only a test of a specific hypothesis for l-PC action, but also a mechanistic description of the altered ion transport processes that are responsible for its arrhythmogenic action. The model for these experiments is one in which a normal (non-ischemic) myocyte is exposed to an abnormally high l-PC concentration arising from a damaged and abnormal (ischemic) heart cell. Eventually, it will be possible to test a myocyte model in which the cell in question is dialyzed with a solution containing l-PC. In this way, one can mimic the condition that obtains in an abnormal cell which is made ischemic and has its intracellular l-PC concentration elevated to an abnormal level.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL042512-03
Application #
2220551
Study Section
Pharmacology A Study Section (PHRA)
Project Start
1991-04-01
Project End
1996-03-31
Budget Start
1993-04-01
Budget End
1996-03-31
Support Year
3
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Connecticut
Department
Pharmacology
Type
Schools of Dentistry
DUNS #
City
Farmington
State
CT
Country
United States
Zip Code
06030