Desensitization is a poorly understood phenomenon characteristic of most or all receptors. We propose an electrophysiological study of neurotransmitter desensitization using two preparations: the isolated nervous system of Aplysia, where the large size of the neuronal cell bodies makes possible a rigorous biophysical analysis of ionic and metabolic mechanisms, and the submerged and perfused rat prepyriform brain slice, in which one can study receptors in a mammalian central nervous system tissue using the techniques of population field potentials, extra- and intracellular recordings from single neurons and voltage clamping of a least those parts of the cell close to the cell body. We propose to study and compare desensitization to several different transmitters, including acetylcholine, dopamine, glutamic acid, serotonin, GABA and several peptides. Since in the Aplysia nervous system there are multiple ionic responses to the same transmitter, we will compare the kinetics and properties of desensitization for different ionic responses to acetylcholine. The overall questions to be asked include whether there are general properties of the process of desensitization which are common to all systems, whether desensitization is a result of a single process or two or more mechanisms and what are the ionic and metabolic dependencies of each of the possible mechanisms. Our preliminary results suggest that at least some Aplysia receptors show two components of desensitization, indicating at least two separate mechanisms as is the case at frog neuromuscular junction. Particular attention will be given to a determination of whether desensitization is a property of the neurotransmitter receptor or the associated channel or ionophore. This is an appropriate question to ask in Aplysia, since the various receptors and ionic responses are known. In addition investigation of the properties of desensitization to conventional neurotransmitters in the mammalian preparation we will investigate the existence of peptide receptors, study desensitization for at least one representative peptide, and investigate any modulatory effects of the various peptides on desensitization to other neurotransmitters. Finally we will attempt to demonstrate that this process has a physiologic role by study of natural synapses in both preparations.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS018435-05
Application #
3398489
Study Section
Physiology Study Section (PHY)
Project Start
1982-04-01
Project End
1988-06-30
Budget Start
1986-04-01
Budget End
1988-06-30
Support Year
5
Fiscal Year
1986
Total Cost
Indirect Cost
Name
New York State Department of Health
Department
Type
DUNS #
002436061
City
Menands
State
NY
Country
United States
Zip Code
12204
Oyama, Y; Hori, N; Allen, C N et al. (1990) Influences of trypsin and collagenase on acetylcholine responses of physically isolated single neurons of Aplysia californica. Cell Mol Neurobiol 10:193-205
Salanki, J; Evans, M L; Carpenter, D O (1989) Desensitization kinetics of a K+ acetylcholine response in Aplysia. Brain Res 495:298-308
Evans, M L; Carpenter, D O (1989) Desensitization kinetics of a chloride acetylcholine response in Aplysia. Brain Res 495:309-18
Busselberg, D; Evans, M L; Carpenter, D O et al. (1989) Effects of exogenous ganglioside and cholesterol application on excitability of Aplysia neurons. Membr Biochem 8:19-26
King, W M; Carpenter, D O (1989) Voltage-clamp characterization of Cl- conductance gated by GABA and L-glutamate in single neurons of Aplysia. J Neurophysiol 61:892-9
Oyama, Y; Hori, N; Evans, M L et al. (1989) Electrophysiological estimation of the actions of acetylcholinesterase inhibitors on acetylcholine receptor and cholinesterase in physically isolated Aplysia neurones. Br J Pharmacol 96:573-82
Oyama, Y; Evans, M L; Akaike, N et al. (1988) Electrophysiological detection of acetylcholinesterase activity using concentration clamp on physically isolated Aplysia neurons. Neurosci Res 6:174-80
Oyama, Y; King, W M; Carpenter, D O (1988) Edrophonium-induced inward membrane current in single neurons physically isolated from Aplysia californica. Brain Res 438:95-100
Oyama, Y; Akaike, N; Carpenter, D O (1988) Strychnine decreases the voltage-dependent Ca2+ current of both Aplysia and frog ganglion neurons. Cell Mol Neurobiol 8:307-14
Hori, N; Carpenter, D O (1988) Excitatory amino acid receptors in piriform cortex do not show receptor desensitization. Brain Res 457:350-4

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