Hemby S E, Co C, Koves T R, Smith J E, Dworkin S I
Department of Physiology and Pharmacology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, NC 27157-1083, USA.
Psychopharmacology (Berl). 1997 Sep;133(1):7-16. doi: 10.1007/s002130050365.
Studies indicate that nucleus accumbens (NAcc) dopamine neurotransmission is involved in the reinforcing and direct effects of cocaine. The present study was initiated to explore further the relationship of NAcc extracellular dopamine concentrations ([DA]e) and cocaine self-administration using a yoked littermate design. In the first experiment, one rat from each litter was trained to self-administer cocaine i.v. (SA: 0.33 mg/inf) under a fixed ratio 2 schedule, while a second rat received simultaneous infusions of cocaine yoked to the infusions of the SA (YC). NAcc [DA]e and cocaine concentrations ([COC]) were assessed during the test sessions using in vivo microdialysis combined with microbore HPLC procedures. [DA]e and [COC] were significantly elevated in the SA and YC groups during the self-administration session; however, [DA]e were greater in the SA group compared to the YC group in the first hour of the session, even though [COC] were not significantly different. On the following day, the rats previously allowed to self-administer cocaine were administered response-independent cocaine infusions yoked to the infusion pattern from the previous day. [DA]e were significantly elevated above baseline levels during the session but were significantly less than concentrations obtained when cocaine was self-administered by these subjects. [COC] during the sessions were not significantly different between the two days. Baseline [DA]e were not significantly different between the SA and YC groups or between Day 1 and Day 2. Furthermore, there was no significant difference in the in vitro probe recovery between one and two days following probe implantation. These results suggest that the context in which cocaine was administered significantly altered the neurochemical response to equivalent brain concentrations of cocaine. NAcc [DA]e was significantly increased when the delivery of cocaine infusions was contingent on the behavior of the rat, indicative of a role in the neural processes underlying cocaine reinforcement.
研究表明,伏隔核(NAcc)多巴胺神经传递参与了可卡因的强化作用和直接效应。本研究采用同窝对照设计,旨在进一步探讨伏隔核细胞外多巴胺浓度([DA]e)与可卡因自我给药之间的关系。在第一个实验中,从每窝中选取一只大鼠,训练其在固定比率2的给药方案下静脉注射可卡因(SA:0.33mg/次),同时另一只大鼠接受与SA大鼠注射时间同步的可卡因注射(YC)。在测试期间,采用体内微透析结合微径高效液相色谱法评估伏隔核[DA]e和可卡因浓度([COC])。在自我给药期间,SA组和YC组的[DA]e和[COC]均显著升高;然而,在给药的第一个小时内,SA组的[DA]e高于YC组,尽管[COC]无显著差异。次日,先前允许自我给药可卡因的大鼠接受与前一天注射模式同步的非依赖反应性可卡因注射。给药期间[DA]e显著高于基线水平,但显著低于这些大鼠自我给药可卡因时的浓度。两天给药期间的[COC]无显著差异。SA组和YC组之间或第1天和第2天之间的基线[DA]e无显著差异。此外,探针植入后1天和2天的体外探针回收率无显著差异。这些结果表明,可卡因给药的背景显著改变了对同等脑浓度可卡因的神经化学反应。当可卡因注射的给予取决于大鼠的行为时,伏隔核[DA]e显著增加,这表明其在可卡因强化作用的神经过程中发挥作用。