Methylation of glucocorticoid receptor gene promoter modulates morphine dependence and accompanied hypothalamus–pituitary–adrenal axis dysfunction

Abstract

Previous studies demonstrated that dysfunction of the hypothalamus-pituitary-adrenal (HPA) axis played an important role in morphine dependence. Nonetheless, the molecular mechanism underlying morphine-induced HPA axis dysfunction and morphine dependence remains unclear. In the current study, 5'-aza-2'-deoxycytidine (5-aza), an inhibitor of DNA methyltransferases (DNMTs), was used to examine the effects of glucocorticoid receptor (GR) promoter 1 methylation on chronic morphine-induced HPA axis dysfunction and behavioral changes in rats and the underlying mechanism. Our results showed that chronic but not acute morphine downregulated the expression of nuclear GR protein and GR exon 1 variant mRNA, and upregulated the methylation of GR 1 exon promoter in the hippocampus of rats. Meanwhile, 5-aza per se had no effect on observed molecular and behavior change. In contrast, pretreatment of 5-aza into rat hippocampus reversed chronic morphine-induced hypermethylation of GR 1 promoter and decrease in GR expression. Moreover, pretreatment of 5-aza attenuated chronic morphine-enhanced HPA axis reactivity and the naloxone-precipitated somatic signs in morphine-dependent rats. Our results suggest that chronic morphine induced hypermethylation of GR 1 promoter, which then downregulated the expression of hippocampal GR, and was thus involved in chronic morphine-induced dysfunction of the HPA axis and the modulation of morphine dependence. Moreover, chronic morphine-induced hypermethylation of GR 1 promoter may be at least partially due to the increase in hippocampal DNMT 1 expression and its binding at GR 1 promoter in the rat hippocampus. © 2016 Wiley Periodicals, Inc.

Clinical and Imaging Study of Repetitive Transcranial Magnetic Stimulation in the Treatment of Morphine Dependence Through mGluR5/TDP43/NR2B Pathway

“…Although the position of morphine in the NMDA receptor has not been determined, it has been found that the effect of morphine on the central nervous system is related to the tolerance of the receptor, their phosphorylation position, and location, especially NR2B. Morphine treatment of mice with less than 25 mM can significantly inhibit NR2B, and a slightly higher concentration can inhibit NR2A, but even if the concentration reaches 100 mm, it has no inhibitory effect on NR2C and NR2D [ 21 ].…”

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

“…Moreover, methamphetamine induced Tet methylcytosine dioxygenase gene-dependent DNA hypomethylation (Jayanthi et al, 2018). Furthermore, Zhu et al (2017b) noted that chronic morphine administration induced hypermethylation of the glucocorticoid receptor (GR) promoter and then downregulated the expression of hippocampal GR. Research also suggested that chronic, heavy alcohol consumption led to changes in DNA methylation patterns.…”