Pisanu Augusta, Lecca Daniele, Valentini Valentina, Bahi Amine, Dreyer Jean-Luc, Cacciapaglia Fabio, Scifo Andrea, Piras Giovanna, Cadoni Cristina, Di Chiara Gaetano
Institute of Neuroscience, National Research Council of Italy, 09124 Cagliari, Italy.
Neuropharmacology. 2015 Feb;89:398-411. doi: 10.1016/j.neuropharm.2014.10.018.
Microdialysis during i.v. drug self-administration (SA) have implicated nucleus accumbens (NAc) shell DA in cocaine and heroin reinforcement. However, this correlative evidence has not been yet substantiated by experimental evidence obtained by studying the effect of selective manipulation of NAc shell DA transmission on cocaine and heroin SA. In order to investigate this issue, DA D1a receptor (D1aR) expression was impaired in the NAc shell and core by locally infusing lentiviral vectors (LV) expressing specific D1aR-siRNAs (LV-siRNAs). Control rats were infused in the same areas with LV expressing GFP. Fifteen days later, rats were trained to acquire i.v. cocaine or heroin self-administration (SA). At the end of behavioral experiments, in order to evaluate the effect of LV-siRNA on D1aR expression, rats were challenged with amphetamine and the brains were processed for immunohistochemical detection of c-Fos and D1aR. Control rats acquired i.v. cocaine and heroin SA. Infusion of LV-siRNAs in the medial NAc shell reduced D1aR density and the number of c-Fos positive nuclei in the NAc shell, while sparing the core, and prevented the acquisition of cocaine, but not heroin SA. In turn, LV-siRNAs infusion in the core reduced D1aR density and the number of c-Fos positive nuclei in the same area, while sparing the shell, and failed to affect acquisition of cocaine. The differential effect of LV impairment of NAc shell D1aR on cocaine and heroin SA indicates that NAc shell DA acting on D1aR specifically mediates cocaine reinforcement.
静脉注射药物自我给药(SA)期间的微透析研究表明,伏隔核(NAc)壳部多巴胺(DA)参与了可卡因和海洛因的强化作用。然而,通过研究选择性操纵NAc壳部DA传递对可卡因和海洛因SA的影响所获得的实验证据,尚未证实这一相关证据。为了研究这个问题,通过局部注射表达特定D1aR小干扰RNA(LV-siRNAs)的慢病毒载体(LV),使NAc壳部和核心区域的DA D1a受体(D1aR)表达受损。对照组大鼠在相同区域注射表达绿色荧光蛋白(GFP)的LV。15天后,训练大鼠进行静脉注射可卡因或海洛因自我给药(SA)。在行为实验结束时,为了评估LV-siRNA对D1aR表达的影响,用苯丙胺对大鼠进行激发,然后对大脑进行处理,以免疫组织化学方法检测c-Fos和D1aR。对照组大鼠学会了静脉注射可卡因和海洛因SA。向NAc壳部内侧注射LV-siRNAs可降低D1aR密度以及NAc壳部c-Fos阳性细胞核的数量,而对核心区域无影响,并阻止了可卡因SA的习得,但未影响海洛因SA。反过来,向核心区域注射LV-siRNAs可降低同一区域的D1aR密度和c-Fos阳性细胞核的数量,而对壳部无影响,且未影响可卡因的习得。NAc壳部D1aR的LV损伤对可卡因和海洛因SA的不同影响表明,作用于D1aR的NAc壳部DA特异性介导了可卡因的强化作用。