Fagergren P, Smith H R, Daunais J B, Nader M A, Porrino L J, Hurd Y L
Karolinska Institute, Department of Clinical Neuroscience, Karolinska Hospital, S-171 76 Stockholm, Sweden.
Eur J Neurosci. 2003 May;17(10):2212-8. doi: 10.1046/j.1460-9568.2003.02636.x.
Several human and rat studies suggest that the striatal dynorphin system is important for neuroadaptation following cocaine exposure. In the current study, prodynorphin (PDYN) mRNA expression was examined in monkeys at initial and chronic phases of cocaine self-administration. Adult Rhesus monkeys were trained to self-administer food (banana flavoured pellets) or cocaine (0.03 or 0.3 mg/kg per injection) on a fixed interval 3-min schedule for 5 or 100 sessions. Each session ended after 30 reinforcers were delivered. The PDYN mRNA expression was analysed in the precommissural striatum using in situ hybridization histochemistry. We found a specific activation of PDYN mRNA expression in the limbic-innervated patch/striosome compartment of the dorsal caudate and dorsal putamen during the initial (i.e. 5 day) phase of the high dose cocaine self-administration. After 100 days of the high dose exposure, the patch/striosome compartment remained activated, but an increase in PDYN mRNA levels was also evident in the sensorimotor-connected matrix compartment of the caudate. Neither self-administration phase resulted in significant changes in the corresponding striatal regions of the low dose cocaine-exposed primates. Moreover, cocaine self-administration failed to alter the PDYN mRNA expression in high- or low-expressing PDYN cell populations in the nucleus accumbens during any condition studied. These results demonstrate the vulnerability of the dorsal striatum (in particular the caudate) to neuroadaptations following long-term high dose cocaine self-administration. In addition, the temporal nature of the changes in PDYN gene expression within the striatal compartments could reflect a change in drug responsivity that occurs during the transition to drug dependence.
多项人体和大鼠研究表明,纹状体强啡肽系统对可卡因暴露后的神经适应很重要。在本研究中,检测了猴子在可卡因自我给药初始阶段和慢性阶段前强啡肽(PDYN)mRNA的表达。成年恒河猴被训练在固定间隔3分钟的时间表上自我给药食物(香蕉味颗粒)或可卡因(每次注射0.03或0.3mg/kg),持续5或100次给药。每次给药在给予30次强化刺激后结束。使用原位杂交组织化学分析前连合纹状体中PDYN mRNA的表达。我们发现在高剂量可卡因自我给药的初始阶段(即5天),背侧尾状核和背侧壳核的边缘神经支配的斑块/纹状体区室中PDYN mRNA表达有特异性激活。在高剂量暴露100天后,斑块/纹状体区室仍然被激活,但尾状核的感觉运动连接基质区室中PDYN mRNA水平也明显增加。低剂量可卡因暴露的灵长类动物的相应纹状体区域在两个自我给药阶段均未发生显著变化。此外,在任何研究条件下,可卡因自我给药均未能改变伏隔核中高表达或低表达PDYN细胞群体中的PDYN mRNA表达。这些结果表明,长期高剂量可卡因自我给药后,背侧纹状体(特别是尾状核)易发生神经适应。此外,纹状体区室中PDYN基因表达变化的时间特性可能反映了在向药物依赖转变过程中发生的药物反应性变化。