The cardiac Purkinje strand is a syncytium. The observed properties of any syncytium depend on both the membrane permeabilities and the interaction of the membrane current flows with the extracellular geometry. The present grant proposal builds on the previous five years of research in which the canine cardiac Purkinje strand was studied by various techniques including morphometric analysis, voltage clamp, extracellular ion selective microelectrodes, and impedance analysis. From these studies we have a characterization of the properties of the cell membrane as distorted by the extracellular space. One major aim of the present grant is to provide similar voltage clamp and impedance analysis of a new preparation, the acutely isolated canine cardiac Purkinje myocyte. It is hoped that a detailed voltage clamp analysis of this building block of the syncytium should provide the necessary missing link to allow us to accurately interpret our data from the intact Purkinje strands. Proposed studies of the dissociated cells include analysis of both plateau and diastolic delayed rectifiers, characterization of the Na/K pump current, and investigation of the effects of various pharmacologic agents on the steady state current-voltage relationship.
A second aim of the present grant proposal is to continue our analysis of various membrane currents in the syncytial preparation. These currents include the Na/K pump current initiated by a period of rapid activity, the slowly inactivating TTX-sensitive """"""""window current"""""""" and both plateau and diastolic delayed rectifiers. Some of the proposed experiments employ simultaneous measurements of both the membrane currents under voltage clamp and the extracellular [K]. This should provide additional insight into the importance of changes in cleft [K] in the interpretation of time dependent membrane currents. It is hoped that these experiments will provide an increase in our understanding of the control of both the action potential duration, and pacemaker activity in normal and pathologic conditions.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL020558-10
Application #
3336152
Study Section
Physiology Study Section (PHY)
Project Start
1977-04-01
Project End
1990-03-31
Budget Start
1986-04-01
Budget End
1987-03-31
Support Year
10
Fiscal Year
1986
Total Cost
Indirect Cost
Name
State University New York Stony Brook
Department
Type
Schools of Medicine
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
Ballou, Lisa M; Lin, Richard Z; Cohen, Ira S (2015) Control of cardiac repolarization by phosphoinositide 3-kinase signaling to ion channels. Circ Res 116:127-37
Potapova, Irina A; Doronin, Sergey V; Kelly, Damon J et al. (2008) Enhanced recovery of mechanical function in the canine heart by seeding an extracellular matrix patch with mesenchymal stem cells committed to a cardiac lineage. Am J Physiol Heart Circ Physiol 295:H2257-63
Potapova, Irina A; Doronin, Sergey V; Kelly, Damon J et al. (2007) Replacing damaged myocardium. J Electrocardiol 40:S199-201
Cohen, Ira S; Rosen, Amy B; Gaudette, Glenn R (2007) A Caveat Emptor for myocardial regeneration: mechanical without electrical recovery will not suffice. J Mol Cell Cardiol 42:285-8
Rosen, Michael R (2005) 15th annual Gordon K. Moe Lecture. Biological pacemaking: in our lifetime? Heart Rhythm 2:418-28
Valiunas, V; Polosina, Y Y; Miller, H et al. (2005) Connexin-specific cell-to-cell transfer of short interfering RNA by gap junctions. J Physiol 568:459-68
Kochupura, Paul V; Azeloglu, Evren U; Kelly, Damon J et al. (2005) Tissue-engineered myocardial patch derived from extracellular matrix provides regional mechanical function. Circulation 112:I144-9
Gao, J; Wang, W; Cohen, I S et al. (2005) Transmural gradients in Na/K pump activity and [Na+]I in canine ventricle. Biophys J 89:1700-9
Doronin, Sergey V; Potapova, Irina A; Lu, Zhongju et al. (2004) Angiotensin receptor type 1 forms a complex with the transient outward potassium channel Kv4.3 and regulates its gating properties and intracellular localization. J Biol Chem 279:48231-7
Yu, Han-Gang; Lu, Zhongju; Pan, Zongming et al. (2004) Tyrosine kinase inhibition differentially regulates heterologously expressed HCN channels. Pflugers Arch 447:392-400

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