The research proposed in this application deals with theoretical and experimental studies toward four major objectives: The first objective is to determine the mechanisms of synchronous firing of pacemaker cells in the sinoatrial (SA) node, and to provide an accurate description of the manner in which local circuit currents control synchronization. Measurements using rabbit SA node tissue will be obtained by superfusion with chemicals that change cell-to-cell coupling, membrane resistance and excitability. Synchronization and intercellular coupling will be studied also using pairs of single SA cells and cell clusters, and in computer simulations using a set of theoretical models of pacemaker activity of the Hodgkin-Huxley type. These studies should help us to predict quantitatively the manner in which thousands of SA node cells initiate the heart beat. The second objective is to expand our studies on the autonomic regulation of heart rate, rhythm and conduction. Specifically, the mechanism of the secondary inhibitory component of the triphasic response of heart rate to brief vagal volleys will be studied in isolated rabbit SA node preparations, and in computer simulations. In addition, we will use isolated SA node preparations, single cells and computer modeling to investigate the cellular basis of the fade in the hyperpolarizing response of SA and AV nodes to continuous vagal stimulation. The third objective is to study the role of passive membrane properties in the conduction of impulses across nonhomogeneous tissues. In sheep and dog Purkinje fibers, we will determine the effects of segmental changes in excitability, membrane resistance and intercellular resistance on propagation velocity, and will estimate the potential arrhythmogenicity of these changes. Finally, we will extend our observations on drug-induced automaticity in ventricular muscle. Specific attention will be given to the spontaneous activity that can be induced at relatively high (-80 to -95 mV) membrane potentials, and to the possible coexistence of this activity with early afterdepolarizations originating at less negative (-40 to -65) levels of potential.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL029439-05
Application #
3340557
Study Section
Cardiovascular Study Section (CVA)
Project Start
1982-08-01
Project End
1990-07-31
Budget Start
1986-08-01
Budget End
1987-07-31
Support Year
5
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Upstate Medical University
Department
Type
Schools of Medicine
DUNS #
058889106
City
Syracuse
State
NY
Country
United States
Zip Code
13210
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