Histone deacetylases mediate GABA A receptor expression, physiology, and behavioral maladaptations in rat models of alcohol dependence
Alcohol use disorders are chronic debilitating diseases characterized by severe withdrawal symptoms that contribute to morbidity and relapse. GABA receptor (GABA R) adaptations have long been implicated in the chronic effects of alcohol and contribute to many withdrawal symptoms associated with alco...
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Published in | Neuropsychopharmacology (New York, N.Y.) Vol. 43; no. 7; p. 1518 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
01.06.2018
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Subjects | |
Online Access | Get full text |
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Summary: | Alcohol use disorders are chronic debilitating diseases characterized by severe withdrawal symptoms that contribute to morbidity and relapse. GABA
receptor (GABA
R) adaptations have long been implicated in the chronic effects of alcohol and contribute to many withdrawal symptoms associated with alcohol dependence. In rodents, GABA
R hypofunction results from decreases in Gabra1 expression, although the underlying mechanism controlling Gabra1 expression after chronic ethanol exposure is still unknown. We found that chronic ethanol exposure using either ethanol gavage or two-bottle choice voluntary access paradigms decreased Gabra1 expression and increased Hdac2 and Hdac3 expression. Administration of the HDAC inhibitor trichostatin A (TSA) after chronic ethanol exposure prevents the decrease in Gabra1 expression and function as well as the increase in Hdac2 and Hdac3 expression in both the cortex and the medial prefrontal cortex (mPFC). Chronic ethanol exposure and withdrawal, but not acute ethanol exposure or acute withdrawal, cause a selective upregulation of HDAC2 and HDAC3 associated with the Gabra1 promoter that accompanies a decrease in H3 acetylation of the Gabra1 promoter and the reduction in GABA
R α1 subunit expression. TSA administration prevented each of these molecular events as well as behavioral manifestations of ethanol dependence, including tolerance to zolpidem-induced loss of righting reflex, reduced open-arm time in the elevated plus maze, reduced center-time and locomotor activity in the open-field assay, and TSA reduced voluntary ethanol consumption. The results show how chronic ethanol exposure regulates the highly prominent GABA
R α1 subunit by an epigenetic mechanism that represents a potential treatment modality for alcohol dependence. |
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ISSN: | 1740-634X |
DOI: | 10.1038/s41386-018-0034-8 |