4.7 Article

Role of GABRD Gene Methylation in the Nucleus Accumbens in Heroin-Seeking Behavior in Rats

Journal

FRONTIERS IN PHARMACOLOGY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2020.612200

Keywords

heroin; nucleus accumbens; GABRD; methylation; reinstatement

Funding

  1. National Key R&D Program of China [2017YFC1310400]
  2. Natural Science Foundation of Zhejiang [LY18H090008]
  3. Natural Science Foundation of China [81671321]
  4. Ningbo Science and Technology Project [2015C110026, 2017A04, 2019A610293, 2019C50076]

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Epigenetic modifications, such as DNA methylation, play a crucial role in regulating gene expression and may influence neuroplasticity and drug-induced aberrant behaviors. The study in Sprague-Dawley rats showed that heroin self-administration led to hypomethylation of the GABRD gene and transcriptional upregulation in the NAc. Manipulations with DNMT inhibitor and MET affected heroin-seeking behavior, possibly through direct repression of DNMT1 and DNMT3A expression to alter the DNA methylation landscape of the GABRD gene.
Epigenetic modifications such as DNA methylation play important roles in regulating gene expression and may mediate neuroplasticity and lead to drug-induced aberrant behaviors. Although several brain regions and neurobiological mechanisms have been suggested to be involved in these processes, there is remarkably little known about the effects of DNA methylation on heroin-seeking behavior. Using a Sprague-Dawley rat model, we show that heroin self-administration resulted in gamma-aminobutyric acid type A receptor subunit delta (GABRD) gene hypomethylation, which was associated with transcriptional upregulation of GABRD in the nucleus accumbens (NAc). Systemic l-methionine (MET) administration significantly strengthened the reinstatement of heroin-seeking behavior induced by heroin priming, whereas intra-NAc injections of the DNA methyltransferase (DNMT) inhibitor 5-aza-2 '-deoxycytidine (5-Aza-dC) had the opposite effect on heroin-seeking. Meanwhile, 5-Aza-dC treatment decreased DNA methylation and upregulated the expression of GABRD in the NAc, whereas MET had the opposite effect. Our results also reveal that 5-Aza-dC might alter the methylation landscape of the GABRD gene by directly repressing DNMT1 and DNMT3A expression. Furthermore, reinstatement of heroin-seeking behavior was significantly inhibited by directly overexpressing GABRD and remarkably reinforced by GABRD gene silencing in the NAc. Collectively, these results suggest that targeting the GABRD gene and its methylation might represent a novel pharmacological strategy for treating heroin addiction and relapse.

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