Freeman Willard M, Patel Kruti M, Brucklacher Robert M, Lull Malinda E, Erwin Mandi, Morgan Drake, Roberts David C S, Vrana Kent E
Department of Pharmacology, Penn State College of Medicine, Hershey, PA 17033, USA.
Neuropsychopharmacology. 2008 Jul;33(8):1807-17. doi: 10.1038/sj.npp.1301577. Epub 2007 Sep 12.
Cocaine-responsive gene expression changes have been described after either no drug abstinence or short periods of abstinence. Little data exist on the persistence of these changes after long-term abstinence. Previously, we reported that after discrete-trial cocaine self-administration and 10 days of forced abstinence, incubation of cocaine reinforcement was observable by a progressive ratio schedule. The present study used rat discrete-trial cocaine self-administration and long-term forced abstinence to examine extinction responding, mRNA abundance of known cocaine-responsive genes, and chromatin remodeling. At 30 and 100 days of abstinence, extinction responding increased compared to 3-day abstinent rats. Decreases in both medial prefrontal cortex (mPFC) and nucleus accumbens c-fos, Nr4a1, Arc, and EGR1 mRNA were observed, and in most cases persisted, for 100 days of abstinence. The signaling peptides CART and neuropeptide Y (NPY) transiently increased in the mPFC, but returned to baseline levels following 10 days of abstinence. To investigate a potential regulatory mechanism for these persistent mRNA changes, levels of histone H3 acetylation at promoters for genes with altered mRNA expression were examined. In the mPFC, histone H3 acetylation decreased after 1 and 10 days of abstinence at the promoter for EGR1. H3 acetylation increased for NPY after 1 day of abstinence and returned to control levels by 10 days of abstinence. Behaviorally, these results demonstrate incubation after discrete-trial cocaine self-administration and prolonged forced abstinence. This incubation is accompanied by changes in gene expression that persist long after cessation of drug administration and may be regulated by chromatin remodeling.
在未戒断或短期戒断可卡因后,已观察到可卡因反应性基因表达的变化。关于长期戒断后这些变化的持续性,现有数据很少。此前,我们报道,在离散式可卡因自我给药和10天强制戒断后,通过渐进比率程序可观察到可卡因强化作用的潜伏期。本研究采用大鼠离散式可卡因自我给药和长期强制戒断,以检测消退反应、已知可卡因反应性基因的mRNA丰度以及染色质重塑。在戒断30天和100天时,与戒断3天的大鼠相比,消退反应增强。内侧前额叶皮质(mPFC)和伏隔核中的c-fos、Nr4a1、Arc和EGR1 mRNA均减少,且在大多数情况下,在戒断100天时仍持续存在。信号肽可卡因-安非他明调节转录肽(CART)和神经肽Y(NPY)在mPFC中短暂增加,但在戒断10天后恢复到基线水平。为了研究这些持续性mRNA变化的潜在调节机制,我们检测了mRNA表达改变的基因启动子处组蛋白H3乙酰化水平。在mPFC中,戒断1天和10天后,EGR1启动子处的组蛋白H3乙酰化减少。戒断1天后,NPY的H3乙酰化增加,到戒断10天时恢复到对照水平。行为学上,这些结果表明在离散式可卡因自我给药和长期强制戒断后出现了潜伏期。这种潜伏期伴随着药物停用后长期持续的基因表达变化,并且可能受染色质重塑的调节。