MECHANISM OF ETHANOL INHIBITION OF NMDA RECEPTOR FUNCTION IN PRIMARY CULTURES OF CEREBRAL CORTICAL-CELLS

Citation
Sv. Bhave et al., MECHANISM OF ETHANOL INHIBITION OF NMDA RECEPTOR FUNCTION IN PRIMARY CULTURES OF CEREBRAL CORTICAL-CELLS, Alcoholism, clinical and experimental research, 20(5), 1996, pp. 934-941
Citations number
47
Categorie Soggetti
Substance Abuse
ISSN journal
01456008
Volume
20
Issue
5
Year of publication
1996
Pages
934 - 941
Database
ISI
SICI code
0145-6008(1996)20:5<934:MOEION>2.0.ZU;2-7
Abstract
Ethanol is a potent inhibitor of the function of the N-methyl-D-aspart ate (NMDA) subtype of glutamate receptor in various neuronal preparati ons. in primary cultures of cerebellar granule cells, ethanol was sugg ested to interact with the glycine co-agonist site of the receptor by a mechanism involving protein kinase C. In the present study, the inte raction of ethanol with various sites on the NMDA receptor was examine d in primary cultures of cerebral cortical cells from embryonic rats. NMDA receptor function was determined by measuring increases in intrac ellular Ca2+ with fura-2 fluorescence. Ethanol inhibited the function of the NMDA receptor in cerebral cortical cells, but in contrast to th e results in cerebellar granule cells, phorbol ester treatment did not inhibit the NMDA response, and ethanol did not alter the effect of gl ycine on NMDA receptor function. Ethanol also did not affect inhibitio n of the NMDA response by Mg2+ or dizocilpine. The results support the hypothesis that the mechanism of ethanol inhibition of NMDA receptor function can vary in neurons from different brain regions.