IMR Press / FBL / Volume 2 / Issue 4 / DOI: 10.2741/A193

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Article

NEUROCHEMICAL BASIS OF DISRUPTION OF HIPPOCAMPAL LONG TERM POTENTIATION BY CHRONIC
ALCOHOL 

Show Less
1 Dept. of Pharmacodynamics, University of Florida, Box 100487, Gainesville FL 32610, USA
2 Depts. of Neuroscience, University of Florida, Box 100487, Gainesville FL 32610, USA
3 Depts. of Physiological Sciences, University of Florida, Box 100487, Gainesville FL 32610, USA
4 Center for Alcohol Research, University of Florida, Box 100487, Gainesville FL 32610, USA
5 University of Florida Brain Institute, University of Florida, Box 100487, Gainesville FL 32610, USA
6 Gainesville Veteran’s Administration Medical Center, Gainesville, USA
Front. Biosci. (Landmark Ed) 1997, 2(4), 309–316; https://doi.org/10.2741/A193
Published: 15 June 1997
Abstract

The aim of this review is to summarize the possible mechanisms underlying the long-term impairment of learning and memory resulting from chronic ethanol treatment (CET) especially that involving decrements in long-term potentiation (LTP) in hippocampus. CET for a 28-week duration affects the rat hippocampal formation in such a way as to decrease the magnitude of LTP; an effect that can last as long as 7 months after ethanol withdrawal. It appears that NMDA receptor number in hippocampus is unchanged after CET whereas the data suggest a more pronounced role for changes in GABAergic and cholinergic synaptic transmission in determining how CET influences the induction of LTP in hippocampus. In particular, changes in presynaptic modulation of neurotransmitter release in hippocampus may be one mechanism by which CET inhibits LTP. Thus, the mechanisms underlying the effect of CET on LTP are a result of changes in a number of neurotransmitter systems in hippocampus (GABAergic and cholinergic) rather than based solely on changes in glutamate transmission.

Share
Back to top