TY - JOUR
T1 - Chronic ethanol treatment upregulates the GABA receptor β subunit expression
AU - Mhatre, Molina
AU - Ticku, Maharaj K.
N1 - Funding Information:
We thank P. Binkley and G. Pena for technical assistance and Mrs. Sadie Phillips for excellent secretarial help. We are grateful to Drs. A. Tobin (California) for providing us with the cDNA probes for the /3 t and/33 subunits, and P. Schoch (Basel, Switzerland) for providing us with the BD17 antibody. This work was supported by a grant from the National Institute on Alcohol Abuse and Alcoholism (AA 04090).
PY - 1994/5
Y1 - 1994/5
N2 - The molecular mechanisms associated with ethanol-induced tolerance and physical dependence have yet to be elucidated. In previous studies we have demonstrated that chronic ethanol administration produced a decrease in the GABAA receptor mRNA level of α1, α2, α5 subunits, and a decrease in the polypeptide (α1, α2, and α3) expression in the rat cerebral cortex. In this study we examined the effect of chronic ethanol treatment on the mRNA levels and the expressions of the β-subunits of the GABAA receptors in rat cerebral cortex. The results indicate that chronic ethanol administration produced an upregulation of the β1 subunit mRNA (12 kb) by 29 ± 10%, β2 mRNA (8 kb) by 55 ± 6% and the β3-subunit (6 kb) mRNA 72 ± 9% in cerebral cortex. The levels of the β2 and β3 subunit mRNAs remains elevated at 24 hr withdrawal. We also investigated the effect of chronic ethanol administration on the β-subunit polypeptide expression using monoclonal antibody BD17, which recognizes the β2 (P56) and β3 (P58) polypeptides. Chronic ethanol treatment increased the levels of both of these polypeptides in cerebral cortex. Taken together, chronic ethanol administration produced an upregulation of the β-subunit mRNA and the polypeptide expression of these subunits in rat cerebral cortex. In contrast, chronic ethanol treatment decreased the expression of various α-subunits in the cerebral cortex. Such bidirectional changes in the expression of various subunits could alter the subunit composition of the functional receptors by substitution or altered levels, without changing the density of the receptors. In summary, chronic ethanol treatment has differential effect on various GABAA receptor subunits, which suggests involvement of differential regulatory mechanisms in interaction of ethanol with the GABA receptors.
AB - The molecular mechanisms associated with ethanol-induced tolerance and physical dependence have yet to be elucidated. In previous studies we have demonstrated that chronic ethanol administration produced a decrease in the GABAA receptor mRNA level of α1, α2, α5 subunits, and a decrease in the polypeptide (α1, α2, and α3) expression in the rat cerebral cortex. In this study we examined the effect of chronic ethanol treatment on the mRNA levels and the expressions of the β-subunits of the GABAA receptors in rat cerebral cortex. The results indicate that chronic ethanol administration produced an upregulation of the β1 subunit mRNA (12 kb) by 29 ± 10%, β2 mRNA (8 kb) by 55 ± 6% and the β3-subunit (6 kb) mRNA 72 ± 9% in cerebral cortex. The levels of the β2 and β3 subunit mRNAs remains elevated at 24 hr withdrawal. We also investigated the effect of chronic ethanol administration on the β-subunit polypeptide expression using monoclonal antibody BD17, which recognizes the β2 (P56) and β3 (P58) polypeptides. Chronic ethanol treatment increased the levels of both of these polypeptides in cerebral cortex. Taken together, chronic ethanol administration produced an upregulation of the β-subunit mRNA and the polypeptide expression of these subunits in rat cerebral cortex. In contrast, chronic ethanol treatment decreased the expression of various α-subunits in the cerebral cortex. Such bidirectional changes in the expression of various subunits could alter the subunit composition of the functional receptors by substitution or altered levels, without changing the density of the receptors. In summary, chronic ethanol treatment has differential effect on various GABAA receptor subunits, which suggests involvement of differential regulatory mechanisms in interaction of ethanol with the GABA receptors.
KW - Chronic ethanol treatment
KW - GABA receptor
KW - mRNA level
KW - Polypeptide expression
KW - Upregulation
KW - β-Receptor subunit
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U2 - 10.1016/0169-328X(94)90231-3
DO - 10.1016/0169-328X(94)90231-3
M3 - Article
C2 - 8057781
AN - SCOPUS:0028256367
VL - 23
SP - 246
EP - 252
JO - Brain Research
JF - Brain Research
SN - 0006-8993
IS - 3
ER -