This study was supported by National Institutes of Health grants AA09013 (ALM), AA11605(ALM). DA 09491 (KYL) and AAU7378 (KYL).
GABAA, Receptor α1, α4, and β3 Subunit mRNA and Protein Expression in the Frontal Cortex of Human Alcoholics
Article first published online: 30 MAY 2006
Alcoholism: Clinical and Experimental Research
Volume 22, Issue 4, pages 815–822, June 1998
How to Cite
Mitsuyama, H., Little, K. Y., Sieghart, W., Devaud, L. L. and Morrow, A. L. (1998), GABAA, Receptor α1, α4, and β3 Subunit mRNA and Protein Expression in the Frontal Cortex of Human Alcoholics. Alcoholism: Clinical and Experimental Research, 22: 815–822. doi: 10.1111/j.1530-0277.1998.tb03873.x
- Issue published online: 30 MAY 2006
- Article first published online: 30 MAY 2006
- Received for publication September 16, 1997; accepted January 9, 1998
- GABAA Receptors;
- Ethanol Dependence;
- Postmortem Brain
Animal studies have shown that chronic ethanol consumption produces physical dependence upon ethanol and alters γ-aminobutyric acid-A (GABAA) receptor subunit gene expression in brain. Although extensive investigation has been conducted in animal models, relatively little work has been performed directly on human alcoholic brain tissue to determine if there are alterations in GABAA, receptor gene expression. In this study, GABAA, receptor α1, α4, and β3 subunit mRNA and peptide expression in postmortem frontal cortex from human alcoholics (n= 15) and age- and sex-matched controls (n= 13) were measured by quantitative, competitive reverse transcription polymerase chain reaction and Western blot analysis. GABAA, receptor β3 subunit mRNA expression was 35% greater (p < 0.05) in alcoholics, compared with nonalcoholic controls. We found no significant difference in α1, and α4, subunit mRNA levels between groups. However, there was a trend toward greater (21%) α1 subunit mRNA expression. There was no difference in α1, α4, or β2/3 subunit peptide levels in frontal cortex between controls and alcoholics. Neither the age of the subjects nor the postmortem interval correlated with mRNA or peptide levels. Blood ethanol content also did not correlate with mRNA or peptide expression in alcoholic samples. These data suggest that GABAA, receptor adaptations, resulting from prolonged alcohol consumption in human alcoholics, may differ from animal models of alcohol dependence. These differences may be related to the longevity of alcohol exposure in human alcoholics, as well as variability in the dependence/withdrawal state of the human subjects. Therefore, further studies in human postmortem brain tissue are warranted.