Nygard S K, Klambatsen A, Balouch B, Quinones-Jenab V, Jenab S
Department of Psychology, Hunter College, CUNY, 695 Park Avenue, New York, NY 10065, USA; Biopsychology and Behavioral Neuroscience Subprogram, Graduate School and University Center, CUNY, 365 Fifth Avenue, New York, NY 10016, USA.
Department of Psychology, Hunter College, CUNY, 695 Park Avenue, New York, NY 10065, USA.
Neuroscience. 2015 Feb 26;287:1-8. doi: 10.1016/j.neuroscience.2014.12.010. Epub 2014 Dec 15.
The development and maintenance of cocaine addiction depend heavily on learned reward-environment associations that can induce drug-seeking behavior and relapse. Understanding the mechanisms underlying these cue-induced conditioned responses is important for relapse prevention. To test whether intracellular responses measured after cocaine conditioned place preference (CPP) expression are context-dependent, we re-exposed cocaine-treated rats (drug-free) to an environment previously paired with cocaine or saline, 24h after the CPP test. After 8 days of cocaine CPP training with one of two cocaine doses (5mg/kg or 20mg/kg, i.p.), CPP was expressed only after conditioning with the higher cocaine dose. In CPP expressing rats, locomotor responses after re-exposure to the cocaine-chamber were greater than in rats re-exposed to the saline-paired chamber. Nucleus Accumbens (NAc) phosphorylated ERK (pERK) levels were increased after re-exposure to the cocaine-paired, but not the saline-paired chamber, regardless of whether or not CPP behavior was expressed. Caudate Putamen (CPu) pERK and FosB protein levels increased after re-exposure to the cocaine chamber only after conditioning with the higher cocaine dose. Conversely, the higher cocaine dose, independent of environment, resulted in increased NAc FosB, ΔFosB and phosphorylated CREB (pCREB) protein levels compared to those conditioned with 5mg/kg cocaine (non-CPP-expressing). Our results suggest that NAc ERK phosphorylation may be involved with retrieving the contextual information of a cocaine-association, without necessarily motivating the expression of CPP behavior. Additionally, we show distinct patterns of intracellular responses in the NAc and CPu indicating a region-specific role for pERK/pCREB/FosB intracellular signaling in the retrieval of cocaine-context associations.
可卡因成瘾的发展和维持在很大程度上依赖于习得的奖赏 - 环境关联,这种关联可诱发觅药行为和复吸。了解这些线索诱导的条件反应背后的机制对于预防复吸很重要。为了测试在可卡因条件性位置偏爱(CPP)表达后测量的细胞内反应是否依赖于环境,我们在CPP测试后24小时,将经可卡因处理的大鼠(无药物)重新暴露于先前与可卡因或生理盐水配对的环境中。在用两种可卡因剂量(5mg/kg或20mg/kg,腹腔注射)之一进行8天的可卡因CPP训练后,仅在用较高剂量可卡因进行条件化后才出现CPP。在表现出CPP的大鼠中,重新暴露于可卡因室后的运动反应大于重新暴露于生理盐水配对室的大鼠。无论是否表现出CPP行为,重新暴露于与可卡因配对的室后伏隔核(NAc)磷酸化的细胞外信号调节激酶(pERK)水平升高,而重新暴露于与生理盐水配对的室后则没有升高。仅在用较高剂量可卡因进行条件化后,重新暴露于可卡因室后尾壳核(CPu)的pERK和FosB蛋白水平才升高。相反,与用5mg/kg可卡因进行条件化(未表现出CPP)相比,较高剂量的可卡因,无论环境如何,均导致NAc中FosB、ΔFosB和磷酸化的环磷腺苷反应元件结合蛋白(pCREB)蛋白水平升高。我们的结果表明,NAc ERK磷酸化可能参与检索可卡因关联的背景信息,而不一定促使CPP行为的表达。此外,我们显示了NAc和CPu中细胞内反应的不同模式,表明pERK/pCREB/FosB细胞内信号在检索可卡因 - 背景关联中具有区域特异性作用。