Publication | Open Access
Chronic Alcohol Treatment-Induced GABA-Aα5 Histone H3K4 Trimethylation Upregulation Leads to Increased GABA-Aα5 Expression and Susceptibility to Alcohol Addiction in the Offspring of Wistar Rats
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Citations
13
References
2018
Year
GeneticsAlcohol-induced Memory DeficitsPrefrontal Cortex Gaba-aα5PsychologySocial SciencesAlcohol MisuseWistar RatsAddiction MedicineLong-term AlcoholismAlcohol AddictionAddiction GeneticsPsychiatryBehavioral PharmacologyNeuropharmacologyAlcohol AbuseAddiction PsychologyPharmacologyEpigenetic RegulationAlcohol DependenceGaba-aα5 ExpressionSubstance AbuseAddictionNeuroscienceMedicine
Gamma-aminobutyric acid (GABA)-Aα5 is considered to be associated with alcohol-induced memory deficits. However, whether it participates in the formation of alcohol addiction or in the regulation of its susceptibility is unknown. Here, we used a chronic alcohol treatment model to obtain alcohol-addicted Wistar rats. Long-term alcoholism increased the expression of prefrontal cortex GABA-Aα5 by inducing its histone H3K4 trimethylation, and these changes could be hereditary and lead to increased vulnerability to alcohol addiction in offspring. This study indicates the risk of long-term alcoholism in future generations, emphasizes the importance of GABA-Aα5 in the formation of alcohol addiction and the regulation of its susceptibility, and provides new evidence regarding the mechanisms underlying alcohol addiction.
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