The overall long term objectives of the studies proposed in this application are to identify and to understand the ionic mechanisms that underlie the abnormalities in the transmember potentials of the subepicardial ventricular cells that survive in the epicardial border zone of the infarcted heart. It has been suggested that one or more of these electrophysiologic abnormalities may lead to the serious ventricular arrhythmias known to occur after infarction. Therefore, by more clearly defining and understanding the mechanisms for these electrophysiologic changes, we will provide information that may lead to the development of effective therapeutic interventions needed in this clinical setting. We will use the technique of disaggregated single cells to separate these cells from the epicardial border zone of the infarcted myocardium. Then, by using a variety of electrophysiologic techniques we can determine the underlying basis for the electrical abnormalities. For this proposal, we have focused on clarifying the abnormalities of some of the ionic currents known to be integral to normal cell electrophysiology (iNa, iCaL, iCl(Ca), iK). In addition, upon recognition of the dysfunction of a normal ion channel in cells from the infarcted heart, we will proceed in defining the sensitivity of these altered ion channels to certain pharmacologic agents, e.g. Class I agents, adrenergic amines, Class III antiarrhythmic agents, etc. Finally, we will quantitate and compare resting Cai as well as amplitude of Cai transients in cells dispersed from the epicardial border zone with control cells. In particular, we will focus on rates of relaxation of Cai transients during pharmacologic interventions (e.g. beta adrenergic stimulation) and specific pacing protocols. For these experiments, we will also combine whole cell voltage clamp techniques with the measurement of Cai transients using fura-2 fluorescence microscopy. In this way we can test the hypothesis that alterations in normal cardiac function as well as ion channel function result from or result in measured changes in Cai.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL030557-15
Application #
6109711
Study Section
Project Start
1999-01-01
Project End
2000-07-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
15
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032
Ciaccio, Edward J; Chow, Anthony W; Kaba, Riyaz A et al. (2008) Detection of the diastolic pathway, circuit morphology, and inducibility of human postinfarction ventricular tachycardia from mapping in sinus rhythm. Heart Rhythm 5:981-91
Ciaccio, Edward J; Ashikaga, Hiroshi; Kaba, Riyaz A et al. (2007) Model of reentrant ventricular tachycardia based on infarct border zone geometry predicts reentrant circuit features as determined by activation mapping. Heart Rhythm 4:1034-45
Ciaccio, Edward J; Micheli-Tzanakou, Evangelia (2007) Development of gradient descent adaptive algorithms to remove common mode artifact for improvement of cardiovascular signal quality. Ann Biomed Eng 35:1146-55
Cabo, Candido; Boyden, Penelope A (2006) Heterogeneous gap junction remodeling stabilizes reentrant circuits in the epicardial border zone of the healing canine infarct: a computational study. Am J Physiol Heart Circ Physiol 291:H2606-16
Cabo, Candido; Yao, Jianan; Boyden, Penelope A et al. (2006) Heterogeneous gap junction remodeling in reentrant circuits in the epicardial border zone of the healing canine infarct. Cardiovasc Res 72:241-9
Terrenoire, Cecile; Clancy, Colleen E; Cormier, Joseph W et al. (2005) Autonomic control of cardiac action potentials: role of potassium channel kinetics in response to sympathetic stimulation. Circ Res 96:e25-34
Fishman, Glenn I (2005) Gap junction remodeling and ventricular arrhythmias. Heart Rhythm 2:887-9
Ciaccio, Edward J; Saltman, Adam E; Hernandez, Oscar M et al. (2005) Multichannel data acquisition system for mapping the electrical activity of the heart. Pacing Clin Electrophysiol 28:826-38
Baba, Shigeo; Dun, Wen; Cabo, Candido et al. (2005) Remodeling in cells from different regions of the reentrant circuit during ventricular tachycardia. Circulation 112:2386-96
Ciaccio, Edward J (2005) Ventricular tachycardia duration and form are associated with electrical discontinuities bounding the core of the reentrant circuit. J Cardiovasc Electrophysiol 16:646-54

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