This project will characterize the electrical properties of bullfrog sympathetic neurons, and the modulation of those properties by neurotransmitters. Whole-cell recording from dissociated sympathetic neurons will be used to investigate the voltage- dependent sodium, potassium, and calcium currents that are responsible for generation of the action potential and control of repetitive firing. In addition, the actions upon these voltage- dependent currents by slow synaptic potentials, muscarinic agonists, and neuropeptides will be examined, both on the dissociated cells and on neurons in the intact ganglion. Peptides of particular interest are the luteinizing hormone-releasing hormone of teleost fish, the likely transmitter for the late slow excitatory postsynaptic potential in the ganglion, and substance P. The experiments will use single or dual electrode voltage clamp with patch electrodes in the whole-cell configuration, or single electrode voltage clamp with intracellular microelectrodes. These approaches will increase our understanding of the fundamental mechanisms that generate the electrical activity of nerve cells, and of the ways in which neurotransmitters act to modify the electrical activity of nerve cells, and of the ways in which neurotransmitters act to modify the electrical behavior of neurons.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS024471-03
Application #
3409144
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Project Start
1984-04-01
Project End
1990-03-31
Budget Start
1988-04-01
Budget End
1989-03-31
Support Year
3
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Lopin, Kyle V; Gray, I Patrick; Obejero-Paz, Carlos A et al. (2012) Feýýýýý block and permeation of CaV3.1 (ýý1G) T-type calcium channels: candidate mechanism for non-transferrin-mediated Feýýýýý influx. Mol Pharmacol 82:1194-204
Jones, Stephen W; Friel, David D (2006) The amplitude distribution of release events through a fusion pore. Biophys J 90:L39-41
Obejero-Paz, Carlos A; Gray, I Patrick; Jones, Stephen W (2004) Y3+ block demonstrates an intracellular activation gate for the alpha1G T-type Ca2+ channel. J Gen Physiol 124:631-40
Jones, Stephen W (2003) Calcium channels: unanswered questions. J Bioenerg Biomembr 35:461-75
Frazier, C J; Serrano, J R; George, E G et al. (2001) Gating kinetics of the alpha1I T-type calcium channel. J Gen Physiol 118:457-70
Serrano, J R; Dashti, S R; Perez-Reyes, E et al. (2000) Mg(2+) block unmasks Ca(2+)/Ba(2+) selectivity of alpha1G T-type calcium channels. Biophys J 79:3052-62
Frazier, C J; George, E G; Jones, S W (2000) Apparent change in ion selectivity caused by changes in intracellular K(+) during whole-cell recording. Biophys J 78:1872-80
Serrano, J R; Perez-Reyes, E; Jones, S W (1999) State-dependent inactivation of the alpha1G T-type calcium channel. J Gen Physiol 114:185-201
Kammermeier, P J; Jones, S W (1998) Facilitation of L-type calcium current in thalamic neurons. J Neurophysiol 79:410-7
Block, B M; Stacey, W C; Jones, S W (1998) Surface charge and lanthanum block of calcium current in bullfrog sympathetic neurons. Biophys J 74:2278-84

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