The devastating social, medical, and economic effects of alcoholism have intensified the need to understand the neurochemical mechanisms underlying alcohol self administration and dependence. Studies in animals and in vitro systems have produced increasing evidence that the GABA- benzodiazepine receptor complex (GBRC) mediates some of the pharmacological and behavioral effects of ethanol, especially the genetic variability in ethanol response. Furthermore, recent studies from our laboratory in which we have used PET to directly examine regional brain glucose metabolism in the brains of normal male subjects and recently detoxified male alcoholics (Volkow et al. 1993) support the involvement of the GBRC as a neurochemical substrate in alcoholism. Purpose:
Specific aim 1 To investigate the activity of GBRC mediated inhibitory neurotransmission in normal controls and recently detoxified alcoholics;
Specific aim 2 To examine the influence of the time period of alcohol withdrawal on GBRC mediated inhibitory neurotransmission;
Specific aim 3 To examine the influence of the time period of alcohol withdrawal on regional brain glucose metabolism during baseline.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
1M01RR010710-01A1
Application #
6283038
Study Section
Project Start
1998-06-04
Project End
1998-11-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
State University New York Stony Brook
Department
Type
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
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