Our program addresses the hypothesis that with growth and development there are changes in the normal electrophysiologic, autonomic, biochemical and structural characteristics of the heart, which alter its responses to pathological processes and to pharmacologic agents. We believe that the changes in expression of disease processes and the responses of the heart to potentially therapeutic interventions that occur developmentally are conditioned in part by the developmental stage of the end organ (the heart) as well as by these structures that influence the heart (autonomic nervous system and hormones) and by those processes that control drug interactions 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, biophysical, biochemical, pharmacological, ultrastructural and cell culture techniques are used. The research is incorporated into 5 investigative units (housed in 4 """"""""Projects"""""""") and the overall hypothesis tested recurs in the electrophysiological, biochemical and autonomic studies, as well as in Core C (ultrastructure and immunopathology). Two additional cores provide administrative (A) and tissue culture (B) support. Although the overall approach is to study growth and development through adult life, the most intensive area of investigation is centered on the neonatal and into stages. This is in keeping with our major interest in cardiovascular disease in the young. 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 not only improve our understanding of developmental changes in the mechanisms responsible for normal rhythm and arrhythmias but can design and seek new means for the 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 #
5P01HL028958-10
Application #
3098045
Study Section
Heart, Lung, and Blood Research Review Committee A (HLBA)
Project Start
1983-07-01
Project End
1993-06-30
Budget Start
1992-07-01
Budget End
1993-06-30
Support Year
10
Fiscal Year
1992
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
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

Showing the most recent 10 out of 303 publications