Our Program focuses on the determinants of cardiac rhythm and arrhythmias in the young. The unifying hypothesis is that the expression of cardiac electrical activity in the young heart is influenced by the autonomic nervous system and determined by ion channels in ways that are unique, and that require our in-depth understanding if we are to advance our capability to prevent and treat disorders of the heart beat. Our previous approach to research was multifaceted, incorporating electrophysiological, pharmacological, biophysical, biochemical and cell culture continues in the renewal to which the perspective of molecular biology has been added and incorporated The research concentrates on mechanisms for normal impulse initiation and the mechanisms whereby abnormal impulse initiation and abnormal repolarization can be facilitated by anomalies of sympathetic innervation, thereby leading to lethal arrhythmias. A key aspect of the work is the relationship of sympathetic innervation to the evolution of ion channel function and signal transduction processes, including both the beta and alpha-adrenergic pathways. The relationship of normal function to that in sympathectomized animals and to that in an inherited model of partial failure of sympathetic innervation and lethal arrhythmias is stressed. The latter model is of particular interest because it appears related to catecholamine-and to exercise-dependent ventricular tachycardias in human subjects. The five Projects in the Program stress the study of electrophysiologic properties and autonomic modulation in intact animals and isolated tissues, ionic and molecular determinants of repolarization studied in single myocytes; ionic and molecular determinants of repolarization studied in single myocytes and in nerves and myocytes in tissue culture; and receptor-effector coupling mechanisms. Two Cores provide administrative and a variety of support services; One Core provides cell disaggregation and tissue culture. The significance of these studies is that while geared to the young age group as a unique population in which rhythm and arrhythmias differ in genesis and autonomic modulation from the adult, the information gained from these studies derives from and is readily referable to advancement of our understanding of rhythm an arrhythmias across all ages. Using the information obtained we will not only advance our understanding of the mechanisms responsible for normal rhythm and arrhythmias, but can design and seek new means for prevention and treatment of arrhythmias.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL028958-19
Application #
6388899
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Program Officer
Lathrop, David A
Project Start
1983-07-01
Project End
2003-06-30
Budget Start
2001-07-01
Budget End
2002-06-30
Support Year
19
Fiscal Year
2001
Total Cost
$2,180,006
Indirect Cost
Name
Columbia University (N.Y.)
Department
Pharmacology
Type
Schools of Medicine
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032
AlmaƧa, Joana; Liang, Tao; Gaisano, Herbert Y et al. (2015) Spatial and temporal coordination of insulin granule exocytosis in intact human pancreatic islets. Diabetologia 58:2810-8
Nawathe, Pooja A; Kryukova, Yelena; Oren, Ronit V et al. (2013) An LQTS6 MiRP1 mutation suppresses pacemaker current and is associated with sinus bradycardia. J Cardiovasc Electrophysiol 24:1021-7
Kryukova, Yelena N; Protas, Lev; Robinson, Richard B (2012) Ca2+-activated adenylyl cyclase 1 introduces Ca2+-dependence to beta-adrenergic stimulation of HCN2 current. J Mol Cell Cardiol 52:1233-9
Yan, Qinghong; Masson, Rajeev; Ren, Yi et al. (2012) Evolution of CpG island promoter function underlies changes in KChIP2 potassium channel subunit gene expression in mammalian heart. Proc Natl Acad Sci U S A 109:1601-6
Guo, Jianfen; Gertsberg, Zoya; Ozgen, Nazira et al. (2011) Protein kinase D isoforms are activated in an agonist-specific manner in cardiomyocytes. J Biol Chem 286:6500-9
Zhang, Hao; Lau, David H; Shlapakova, Iryna N et al. (2011) Implantation of sinoatrial node cells into canine right ventricle: biological pacing appears limited by the substrate. Cell Transplant 20:1907-14
Rosati, Barbara; Yan, Qinghong; Lee, Mi Sun et al. (2011) Robust L-type calcium current expression following heterozygous knockout of the Cav1.2 gene in adult mouse heart. J Physiol 589:3275-88
Kanaporis, G; Brink, P R; Valiunas, V (2011) Gap junction permeability: selectivity for anionic and cationic probes. Am J Physiol Cell Physiol 300:C600-9
Potapova, Irina A; Cohen, Ira S; Doronin, Sergey V (2010) Von willebrand factor increases endothelial cell adhesiveness for human mesenchymal stem cells by activating p38 mitogen-activated protein kinase. Stem Cell Res Ther 1:35
Wang, Wei; Gao, Junyuan; Entcheva, Emilia et al. (2010) A transmural gradient in the cardiac Na/K pump generates a transmural gradient in Na/Ca exchange. J Membr Biol 233:51-62

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