Abstract
Chronic alcohol misuse by human subjects leads to neuronal loss in regions such as the superior frontal cortex. Reduced GABA transmission may mediate this. The expression of GABAA receptor β1, β2 and β3 isoform proteins was analyzed by western blotting in vulnerable (superior frontal cortex) and spared (primary motor cortex) cortical tissue obtained at autopsy from Caucasian subjects, and the effect of genotypes of candidate genes for alcoholism assessed. There was a significant regional difference in global isoform expression, but no significant overall group difference in β2 or β3 expression between controls and alcoholics undifferentiated by genotype in either cortical region. There were significant, regionally selective, interactions of DRD2B, SLC1A2 and APOE genotypes with β protein expression when alcoholics were compared with controls. In each instance possession of the alcoholism-associated allele increased the β2:β3 ratio in the pathologically vulnerable region, by two distinct mechanisms. The SFC β2:β3 ratio in DRD2B-B2,B2 alcoholics was 22% higher than that in DRD2B-B1,B1 alcoholics, and 17% higher than that in DRD2B-B2,B2 controls. The SFC β2:β3 ratio in SLC1A2A603 homozygote alcoholics was 25% higher than that in alcoholics with at least one 603G allele, and 75% higher than that in SLC1A2A603 homozygote controls. The SFC β2:β3 ratio in alcoholics lacking an APOE ε3 allele was 73% higher than that in alcoholics with at least one ε3 allele, and 70% higher than that in controls without an ε3 allele. ADH1C genotype also differentiated cases and controls, but the effect was not localized. GABRB2 and GRIN2B genotypes were associated with significant regional differences in the pattern of β subunit expression, but this was not influenced by alcoholism status. DRD2A and SLC6A4 genotypes were without significant effect. A restricted set of genotypes may influence subunit expression in this group of high-consumption alcoholics.
| Original language | English |
|---|---|
| Pages (from-to) | 557-567 |
| Number of pages | 11 |
| Journal | Neurochemistry International |
| Volume | 49 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - Nov 1 2006 |
| Externally published | Yes |
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Keywords
- Brain damage
- Cerebral cortex
- Excitotoxicity
- Pathogenesis
- Phenotype
- Substance misuse and dependence
ASJC Scopus subject areas
- Cellular and Molecular Neuroscience
- Cell Biology
Cite this
GABAA receptor β isoform protein expression in human alcoholic brain : interaction with genotype. / Buckley, S. Tracey; Foley, Philomena F.; Innes, David J.; Loh, El Wui; Shen, Yi; Williams, Susan M.; Harper, Clive G.; Tannenberg, Anthony E.G.; Dodd, Peter R.
In: Neurochemistry International, Vol. 49, No. 6, 01.11.2006, p. 557-567.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - GABAA receptor β isoform protein expression in human alcoholic brain
T2 - interaction with genotype
AU - Buckley, S. Tracey
AU - Foley, Philomena F.
AU - Innes, David J.
AU - Loh, El Wui
AU - Shen, Yi
AU - Williams, Susan M.
AU - Harper, Clive G.
AU - Tannenberg, Anthony E.G.
AU - Dodd, Peter R.
PY - 2006/11/1
Y1 - 2006/11/1
N2 - Chronic alcohol misuse by human subjects leads to neuronal loss in regions such as the superior frontal cortex. Reduced GABA transmission may mediate this. The expression of GABAA receptor β1, β2 and β3 isoform proteins was analyzed by western blotting in vulnerable (superior frontal cortex) and spared (primary motor cortex) cortical tissue obtained at autopsy from Caucasian subjects, and the effect of genotypes of candidate genes for alcoholism assessed. There was a significant regional difference in global isoform expression, but no significant overall group difference in β2 or β3 expression between controls and alcoholics undifferentiated by genotype in either cortical region. There were significant, regionally selective, interactions of DRD2B, SLC1A2 and APOE genotypes with β protein expression when alcoholics were compared with controls. In each instance possession of the alcoholism-associated allele increased the β2:β3 ratio in the pathologically vulnerable region, by two distinct mechanisms. The SFC β2:β3 ratio in DRD2B-B2,B2 alcoholics was 22% higher than that in DRD2B-B1,B1 alcoholics, and 17% higher than that in DRD2B-B2,B2 controls. The SFC β2:β3 ratio in SLC1A2A603 homozygote alcoholics was 25% higher than that in alcoholics with at least one 603G allele, and 75% higher than that in SLC1A2A603 homozygote controls. The SFC β2:β3 ratio in alcoholics lacking an APOE ε3 allele was 73% higher than that in alcoholics with at least one ε3 allele, and 70% higher than that in controls without an ε3 allele. ADH1C genotype also differentiated cases and controls, but the effect was not localized. GABRB2 and GRIN2B genotypes were associated with significant regional differences in the pattern of β subunit expression, but this was not influenced by alcoholism status. DRD2A and SLC6A4 genotypes were without significant effect. A restricted set of genotypes may influence subunit expression in this group of high-consumption alcoholics.
AB - Chronic alcohol misuse by human subjects leads to neuronal loss in regions such as the superior frontal cortex. Reduced GABA transmission may mediate this. The expression of GABAA receptor β1, β2 and β3 isoform proteins was analyzed by western blotting in vulnerable (superior frontal cortex) and spared (primary motor cortex) cortical tissue obtained at autopsy from Caucasian subjects, and the effect of genotypes of candidate genes for alcoholism assessed. There was a significant regional difference in global isoform expression, but no significant overall group difference in β2 or β3 expression between controls and alcoholics undifferentiated by genotype in either cortical region. There were significant, regionally selective, interactions of DRD2B, SLC1A2 and APOE genotypes with β protein expression when alcoholics were compared with controls. In each instance possession of the alcoholism-associated allele increased the β2:β3 ratio in the pathologically vulnerable region, by two distinct mechanisms. The SFC β2:β3 ratio in DRD2B-B2,B2 alcoholics was 22% higher than that in DRD2B-B1,B1 alcoholics, and 17% higher than that in DRD2B-B2,B2 controls. The SFC β2:β3 ratio in SLC1A2A603 homozygote alcoholics was 25% higher than that in alcoholics with at least one 603G allele, and 75% higher than that in SLC1A2A603 homozygote controls. The SFC β2:β3 ratio in alcoholics lacking an APOE ε3 allele was 73% higher than that in alcoholics with at least one ε3 allele, and 70% higher than that in controls without an ε3 allele. ADH1C genotype also differentiated cases and controls, but the effect was not localized. GABRB2 and GRIN2B genotypes were associated with significant regional differences in the pattern of β subunit expression, but this was not influenced by alcoholism status. DRD2A and SLC6A4 genotypes were without significant effect. A restricted set of genotypes may influence subunit expression in this group of high-consumption alcoholics.
KW - Brain damage
KW - Cerebral cortex
KW - Excitotoxicity
KW - Pathogenesis
KW - Phenotype
KW - Substance misuse and dependence
UR - http://www.scopus.com/inward/record.url?scp=33749535686&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33749535686&partnerID=8YFLogxK
U2 - 10.1016/j.neuint.2006.04.008
DO - 10.1016/j.neuint.2006.04.008
M3 - Article
C2 - 16766085
AN - SCOPUS:33749535686
VL - 49
SP - 557
EP - 567
JO - Neurochemistry International
JF - Neurochemistry International
SN - 0197-0186
IS - 6
ER -