Choi K-H, Whisler K, Graham D L, Self D W
Department of Psychiatry, Seay Center for Basic and Applied Research in Psychiatric Illness, University of Texas Southwestern Medical Center, Dallas, 75390-9070, USA.
Neuroscience. 2006;137(2):373-83. doi: 10.1016/j.neuroscience.2005.10.049. Epub 2005 Dec 15.
Repeated cocaine exposure up-regulates cyclic AMP signaling and increases the transcriptional activity of cyclic AMP response element binding protein (CREB) in the nucleus accumbens. To study the possibility that nucleus accumbens CREB activity regulates self-administration behavior, we tested the effects of a single, bilateral infusion of CREB antisense oligonucleotide into nucleus accumbens core and shell sub-regions on cocaine self-administration in rats. Nucleus accumbens core infusions of CREB antisense reduced CREB and the CREB-regulated immediate early gene brain-derived neurotrophic factor by 31 and 27%, respectively, but failed to alter levels of the homologous CREB family proteins cyclic AMP response element modulator and activating transcription factor 1, and had no effect on CREB levels in adjacent nucleus accumbens shell tissue. Similar infusions of CREB antisense in either core or shell produced a transient downward shift in cocaine self-administration dose-response curves on a fixed ratio 5 (five responses/injection) reinforcement schedule, indicating a reduction in cocaine reinforcement that fully recovered 3 days after treatment. CREB antisense also increased the threshold dose of cocaine required for reinstating cocaine self-administration, indicating that nucleus accumbens CREB levels regulate the incentive properties of cocaine. When access to cocaine was less restricted on a fixed ratio 1 schedule, infusion of CREB antisense in the core, but not shell, caused a transient (1-2 days) reduction in stabilized cocaine self-administration, but had no effect on responding maintained by sucrose pellets, indicating that basal CREB levels in the nucleus accumbens core regulate drug intake. None of these effects were produced by nucleus accumbens infusions of complementary sense oligonucleotide. These results suggest a necessary role for nucleus accumbens CREB activity in cocaine reinforcement, and, by converse analogy, up-regulation in CREB activity after chronic cocaine use could contribute to addiction-related increases in cocaine self-administration.
反复接触可卡因会上调环磷酸腺苷(cAMP)信号,并增加伏隔核中cAMP反应元件结合蛋白(CREB)的转录活性。为了研究伏隔核CREB活性调节自我给药行为的可能性,我们测试了向大鼠伏隔核核心和壳亚区单次双侧注射CREB反义寡核苷酸对可卡因自我给药的影响。向伏隔核核心注射CREB反义寡核苷酸分别使CREB和CREB调节的即刻早期基因脑源性神经营养因子减少了31%和27%,但未能改变同源CREB家族蛋白cAMP反应元件调节剂和激活转录因子1的水平,且对相邻伏隔核壳组织中的CREB水平没有影响。在核心或壳中类似地注射CREB反义寡核苷酸,在固定比率5(每注射5次反应)强化方案下,可卡因自我给药剂量反应曲线出现短暂的向下移动,表明可卡因强化作用降低,治疗3天后完全恢复。CREB反义寡核苷酸还增加了恢复可卡因自我给药所需的可卡因阈值剂量,表明伏隔核CREB水平调节可卡因的激励特性。当在固定比率1方案下对可卡因的获取限制较少时,向核心而非壳中注射CREB反义寡核苷酸会导致稳定的可卡因自我给药出现短暂(1 - 2天)减少,但对蔗糖颗粒维持的反应没有影响,表明伏隔核核心中的基础CREB水平调节药物摄入。向伏隔核注射互补义寡核苷酸不会产生这些效应。这些结果表明伏隔核CREB活性在可卡因强化中起必要作用,并且通过相反的类推,长期使用可卡因后CREB活性的上调可能导致与成瘾相关的可卡因自我给药增加。