Department of Biology, Center for Molecular Signaling, Wake Forest University, Winston-Salem, NC 27109, USA.
Department of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Int J Mol Sci. 2022 Oct 5;23(19):11804. doi: 10.3390/ijms231911804.
Chronic exposure to drugs of abuse produces profound changes in gene expression and neural activity associated with drug-seeking and taking behavior. Dysregulation of opioid receptor gene expression is commonly observed across a variety of abused substances including opioids, cocaine, and alcohol. Early studies in cultured cells showed that the spatial and temporal gene expression of opioid receptors are regulated by epigenetic mechanisms including DNA and histone modifications and non-coding RNAs. Accumulating evidence indicate that drugs of abuse can modulate opioid receptor gene expression by targeting various epigenetic regulatory networks. Based on current cellular and animal models of substance use disorder and clinical evidence, this review summarizes how chronic drug exposure alters the gene expression of mu, delta, kappa, and nociceptin receptors via DNA and histone modifications. The influence of drugs of abuse on epigenetic modulators, such as non-coding RNAs and transcription factors, is also presented. Finally, the therapeutic potential of manipulating epigenetic processes as an avenue to treat substance use disorder is discussed.
慢性暴露于成瘾药物会导致与觅药和用药行为相关的基因表达和神经活动发生深刻变化。在包括阿片类药物、可卡因和酒精在内的各种滥用物质中,经常观察到阿片受体基因表达的失调。早期在培养细胞中的研究表明,阿片受体的时空基因表达受表观遗传机制调控,包括 DNA 和组蛋白修饰以及非编码 RNA。越来越多的证据表明,成瘾药物可以通过靶向各种表观遗传调节网络来调节阿片受体基因表达。基于目前的物质使用障碍细胞和动物模型以及临床证据,本综述总结了慢性药物暴露如何通过 DNA 和组蛋白修饰改变μ、δ、κ 和孤啡肽受体的基因表达。还介绍了成瘾药物对表观遗传调节剂(如非编码 RNA 和转录因子)的影响。最后,讨论了操纵表观遗传过程作为治疗物质使用障碍的一种途径的治疗潜力。