The long-term objective of this project is to determine how ethanol alters neuronal function. Actions of some neurotransmitters involves the membrane-bound enzyme adenylate cyclase, and the activity of this multicomponent system has previously been shown to be increased by ethanol.
The specific aims of this project are: 1) to determine the site of action of ethanol on the adenylate cyclase system; 2) to determine whether chronic administration of ethanol alters the in vitro sensitivity of adenylate cyclase to ethanol, as well as the effect of chronic ethanol treatment on the lipid composition of the plasma membrane; 3) to determine the effect of specific changes in lipid composition of the plasma membrane on the in vitro sensitivity of adenylate cyclase to ethanol. The site of action of ethanol on the adenylate cyclase system will be determined by reconstitution of the purified regulatory subunit of adenylate cyclase into membranes from CYC-cells. The in vitro sensitivity of adenylate cyclase to ethanol will be determined after chronic exposure of both rats and PC12 cells to ethanol. Because tolerance to the effects of ethanol has been suggested to be caused by ethanol-induced changes in membrane lipid composition, changes in the lipid composition of synaptosomal plasma membranes from rat brain and plasma membranes from PC12 cells will also be determined after chronic ethanol administration. Relationship between changes in membrane lipid composition and the sensitivity of adenylate cyclase to ethanol will be further investigated by altering the membrane lipid composition of PC12 cells by incubating cells at different temperatures and by using various dietary supplements. Effect of specific changes in the lipid composition of the plasma membrane on the in vitro sensitivity of adenylate cyclase to ethanol will be determined by reconstituting the solubilized catalytic and regulatory subunits of adenylate cyclase into liposomes of known composition. Experiments in this project will increase our understanding of the mechanism of action and effects of ethanol. This knowledge should lead to the development of better treatment for alcoholism.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project (R01)
Project #
5R01AA006207-03
Application #
3109403
Study Section
Alcohol Biomedical Research Review Committee (ALCB)
Project Start
1984-01-01
Project End
1987-06-30
Budget Start
1986-01-01
Budget End
1987-06-30
Support Year
3
Fiscal Year
1986
Total Cost
Indirect Cost
Name
State University of New York at Buffalo
Department
Type
School of Medicine & Dentistry
DUNS #
038633251
City
Buffalo
State
NY
Country
United States
Zip Code
14260
Oberdoerster, J; Rabin, R A (1999) Enhanced caspase activity during ethanol-induced apoptosis in rat cerebellar granule cells. Eur J Pharmacol 385:273-82
Oberdoerster, J; Rabin, R A (1999) NGF-differentiated and undifferentiated PC12 cells vary in induction of apoptosis by ethanol. Life Sci 64:PL 267-72
Rabin, R A; Winter, J C (1996) Effects of ibogaine and noribogaine on phosphoinositide hydrolysis. Brain Res 731:226-9
Rabin, R A; Winter, J C (1996) Ibogaine and noribogaine potentiate the inhibition of adenylyl cyclase activity by opioid and 5-HT receptors. Eur J Pharmacol 316:343-8
Rabin, R A (1996) Regulation of the stress-like protein adenotin in PC 12 cells by ethanol exposure. Biochem Pharmacol 51:183-6
Zou, J Y; Cohan, C; Rabin, R A et al. (1995) Continuous exposure of cultured rat cerebellar macroneurons to ethanol-depressed NMDA and KCl-stimulated elevations of intracellular calcium. Alcohol Clin Exp Res 19:840-5
Kim, W K; Rabin, R A (1994) Characterization of the purinergic P2 receptors in PC12 cells. Evidence for a novel subtype. J Biol Chem 269:6471-7
Kim, W K; Johnson, R G; Izu, L T et al. (1994) Chronic ethanol exposure inhibits ATP-stimulated but not KCl-stimulated dopamine release in PC 12 cells. J Pharmacol Exp Ther 270:336-41
Rabin, R A (1993) Ethanol-induced desensitization of adenylate cyclase: role of the adenosine receptor and GTP-binding proteins. J Pharmacol Exp Ther 264:977-83
Rabin, R A; Acara, M A (1993) Regulation of Na+, K(+)-ATPase by chronic ethanol exposure of PC 12 cells. Biochem Pharmacol 45:1653-8

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