The physiological effects of EtOH appear to be due to its interaction with the cell membrane. Chronic exposure to EtOH induces changes in the membrane which lead to resistance to the effects of EtOH. However, controversy exists about the actual molecular changes occurring in the membrane which result in such tolerance to EtOH. We are studying neuronal cells in culture as a model system to determine the molecular mechanisms underlying the long-term changes after exposure to EtOH. We are using membrane enzymes which we can assay in intact, living cells to determine the time course for development of these changes. Since we use a homogeneous cell line in a defined medium where changes in EtOH concentration are the only variable, we will be able to observe changes in membrane function and lipid composition due to chronic treatment with EtOH. Moreover, since membrane lipid composition can be altered by changing the medium in which the cells grow, we will be able to selectively change membrane lipids and determine the role of individual lipids in the development of tolerance to EtOH. We will also attempt to prevent or reverse the development of tolerance by altering membrane lipid composition. During the period covered by this proposal, we will: characterize the acute and chronic effects of EtOH on adenosine-stimulated adenylate cyclase activity in these intact living cells; determine whether chronic exposure to EtOH also affects fatty acid, phospholipid or cholesterol composition of NG108-15 membranes; determine whether the changes in membrane lipid composition correlate with the observed changes in adenosine-stimulated adenylate cyclase activity; determine how withdrawal of EtOH affects both enzyme activities and lipid composition of NG108-15; determine whether changing the phospholipid and fatty acid composition of the membrane can reverse or prevent the changes produced by chronic treatment with EtOH.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project (R01)
Project #
1R01AA006451-01A1
Application #
3109591
Study Section
(SRC)
Project Start
1985-05-01
Project End
1989-04-30
Budget Start
1985-05-01
Budget End
1986-04-30
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Ernest Gallo Clinic and Research Center
Department
Type
DUNS #
173995366
City
Emeryville
State
CA
Country
United States
Zip Code
94608
Nagy, L E; Diamond, I; Casso, D J et al. (1990) Ethanol increases extracellular adenosine by inhibiting adenosine uptake via the nucleoside transporter. J Biol Chem 265:1946-51