This renewal application of our Program Project consists of 8 projects which explore ionic, electrical and mechanical factors contributing to the pathophysiology of sudden cardiac death. These projects utilize membrane vessicles and lipid bilayers of sarcoplasmic reticulum, guinea pig papillary muscles, in situ and in vivo pig hearts and man. They employ microelectrodes, ion- selective electrodes and programmed electrical stimulation and are supported by an animal/electrode core, a computer/biostatistics core, an electronics core and an administrative core. The projects are united by one or more of 4 common themes: the pathogenesis of sudden cardiac death, the correlation between the ionic, electrical and mechanical changes resulting from ischemia, the effects of drugs on the ischemic process and of ischemia on the effects of the drugs, and the effects of increasing rate on the ischemia induced changes. These projects are divided into 3 groups. The three in group A explore the ionic, electrical and mechanical correlations during low flow and no flow ischemia in the in situ and in vivo pig heart. They use multiple ion-specific electrodes and extensive computer technology. The three projects in group B use membrane vessicles, isolated superfused papillary muscles and microelectrode techniques in order to gain a more fundamental understanding of the ionic, electrical and mechanical alterations induced by ischemia, the factors causing slow conduction and the mechanism of action of cardio-active drugs. The two projects in group C seek a greater understanding of factors predisposing to sudden cardiac death in man. They attempt to identify prospectively those at highest risk for this ultimate event and to prevent its occurrence. The program involves investigators from the Department of Biochemistry, Physiology, Medicine, Biostatistics, and Biomedical Mathematics and Engineering and includes collaborations with Dr. Michiel Janse and his co workers at the University of Amsterdam, Holland and Dr. Bernard Gersch and co workers at the Mayo Clinic/medical School in Rochester, MN. The eight projects in this renewal application are the direct outgrowth of studies conducted in the 5 projects comprising our current Program. They reflect the maturation of our concepts and ideas resulting from the integrated, multidiscipline approach made possible by the Program Project mechanism.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
2P01HL027430-06
Application #
3097975
Study Section
(SRC)
Project Start
1982-07-01
Project End
1992-06-30
Budget Start
1987-07-01
Budget End
1988-06-30
Support Year
6
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Medicine
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Cole, R T; Lucas, C L; Cascio, W E et al. (2005) A LabVIEW model incorporating an open-loop arterial impedance and a closed-loop circulatory system. Ann Biomed Eng 33:1555-73
Cascio, Wayne E; Yang, Hua; Muller-Borer, Barbara J et al. (2005) Ischemia-induced arrhythmia: the role of connexins, gap junctions, and attendant changes in impulse propagation. J Electrocardiol 38:55-9
Xu, Le; Meissner, Gerhard (2004) Mechanism of calmodulin inhibition of cardiac sarcoplasmic reticulum Ca2+ release channel (ryanodine receptor). Biophys J 86:797-804
Kim, Chang-Soo; Ufer, Stefan; Seagle, Christopher M et al. (2004) Use of micromachined probes for the recording of cardiac electrograms in isolated heart tissues. Biosens Bioelectron 19:1109-16
Graff, Ronald D; Kelley, Scott S; Lee, Greta M (2003) Role of pericellular matrix in development of a mechanically functional neocartilage. Biotechnol Bioeng 82:457-64
Stange, Mirko; Xu, Le; Balshaw, David et al. (2003) Characterization of recombinant skeletal muscle (Ser-2843) and cardiac muscle (Ser-2809) ryanodine receptor phosphorylation mutants. J Biol Chem 278:51693-702
Bidasee, Keshore R; Xu, Le; Meissner, Gerhard et al. (2003) Diketopyridylryanodine has three concentration-dependent effects on the cardiac calcium-release channel/ryanodine receptor. J Biol Chem 278:14237-48
Sun, Junhui; Xu, Le; Eu, Jerry P et al. (2003) Nitric oxide, NOC-12, and S-nitrosoglutathione modulate the skeletal muscle calcium release channel/ryanodine receptor by different mechanisms. An allosteric function for O2 in S-nitrosylation of the channel. J Biol Chem 278:8184-9
Yamaguchi, Naohiro; Xu, Le; Pasek, Daniel A et al. (2003) Molecular basis of calmodulin binding to cardiac muscle Ca(2+) release channel (ryanodine receptor). J Biol Chem 278:23480-6
Lemasters, John J; Qian, Ting; He, Lihua et al. (2002) Role of mitochondrial inner membrane permeabilization in necrotic cell death, apoptosis, and autophagy. Antioxid Redox Signal 4:769-81

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