This proposal addresses the hypothesis that with growth and development there are changes in the normal electrophysiologic, autonomic, metabolic and structural characteristics of the heart, all of which alter the response of the heart to pathological processes and to pharmacologic agents. As a result, we believe that the changes in expression of disease processes as well as the responses of the heart to potentially therapeutic interventions that occur with age are conditioned in part by the developmental stage of the end organ (the heart) as well as by those structures that influence the heart (autonomic nervous system and hormones) and by those processes that control drug interaction with the heart. Hence the theme focuses on a developmental approach to cardiac arrhythmias and their therapy. The approach is multifaceted in that a variety of electrophysiologic, biochemical, pharmacological and ultrastructural techniques will be used. Although the overall approach is to study growth and development throughout the spectrum of life, the most intensive area of investigation is centered on the neonatal, young and adolescent stages. The research is incorporated into 6 Projects and the overall hypothesis tested recurs in the electrophysiological, biochemical, autonomic and clinical studies, as well as in Core C (ultrastructure). Two additional cores provide administrative (A) and tissue culture (B) support. The significance of these studies is that they provide an alternative method to the standard approaches for considering arrhythmias, their genesis and treatment. Using the information obtained about developmental changes in function and structure we can only improve our understanding of the mechanisms responsible for arrhythmias but can design and seek new means for their prevention and treatment.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL028958-03
Application #
3098039
Study Section
Heart, Lung, and Blood Research Review Committee A (HLBA)
Project Start
1983-07-01
Project End
1988-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
Schools of Medicine
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10027
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
Protas, Lev; Oren, Ronit V; Clancy, Colleen E et al. (2010) Age-dependent changes in Na current magnitude and TTX-sensitivity in the canine sinoatrial node. J Mol Cell Cardiol 48:172-80
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

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