Fishberg Department of Neuroscience and Friedman Brain Institute, Mount Sinai School of Medicine, One Gustave L. Levy Place, BOX 1065, New York, New York 10029, USA.
Nat Rev Neurosci. 2011 Oct 12;12(11):623-37. doi: 10.1038/nrn3111.
Investigations of long-term changes in brain structure and function that accompany chronic exposure to drugs of abuse suggest that alterations in gene regulation contribute substantially to the addictive phenotype. Here, we review multiple mechanisms by which drugs alter the transcriptional potential of genes. These mechanisms range from the mobilization or repression of the transcriptional machinery - including the transcription factors ΔFOSB, cyclic AMP-responsive element binding protein (CREB) and nuclear factor-κB (NF-κB) - to epigenetics - including alterations in the accessibility of genes within their native chromatin structure induced by histone tail modifications and DNA methylation, and the regulation of gene expression by non-coding RNAs. Increasing evidence implicates these various mechanisms of gene regulation in the lasting changes that drugs of abuse induce in the brain, and offers novel inroads for addiction therapy.
长期以来,对滥用药物导致的大脑结构和功能变化的研究表明,基因调控的改变在成瘾表型中起着重要作用。在这里,我们综述了多种药物改变基因转录潜能的机制。这些机制包括转录机器的动员或抑制——包括转录因子 ΔFOSB、环磷酸腺苷反应元件结合蛋白(CREB)和核因子-κB(NF-κB)——以及表观遗传学——包括组蛋白尾部修饰和 DNA 甲基化引起的基因在其天然染色质结构中的可及性改变,以及非编码 RNA 对基因表达的调控。越来越多的证据表明,这些不同的基因调控机制参与了滥用药物在大脑中引起的持久变化,并为成瘾治疗提供了新的途径。