Chang J Y, Sawyer S F, Lee R S, Woodward D J
Department of Physiology and Pharmacology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, North Carolina 27157.
J Neurosci. 1994 Mar;14(3 Pt 1):1224-44. doi: 10.1523/JNEUROSCI.14-03-01224.1994.
The goal of this study was to clarify the role of the nucleus accumbens septi (NAS) in the expression of cocaine self-administration behaviors. Rats were trained in a continuous reinforcement schedule to press a lever to activate a pump that provided an intravenous injection of cocaine. Once the rats were trained, neuronal activity in the NAS was monitored during cocaine self-administration with chronic recording techniques using permanently implanted microwires. In the NAS, 19% of 181 neurons exhibited either increased or decreased firing rates seconds prior to lever pressing (termed "anticipatory responses"), and 48% had altered, predominantly decreased, firing rates for a few minutes after lever pressing ("postcocaine responses"). Two-thirds of the neurons with anticipatory responses had postcocaine responses. Neurons with either of these response patterns were localized histologically to both core and shell regions of the NAS, with no statistically significant differences in the proportion of response types in either area. Analysis of videotaped cocaine self-administration behaviors revealed that anticipatory responses were specifically associated either with the animal orienting toward and pressing the lever or only with movements directly related to pressing the lever. Anticipatory-like phasic spike activity was not observed during similar movements unrelated to lever pressing. In some animals, D1 (SCH 23390) or D2 (pimozide) receptor antagonists were injected systemically prior to or during self-administration sessions to assess the effects of dopamine receptor blockade on anticipatory and postcocaine responses. Each antagonist, given separately, often produced extinction of lever pressing. Both antagonists blocked the post-cocaine inhibitory response of neurons that had anticipatory responses. Neither antagonist modified anticipatory unit responses, nor did they affect postcocaine inhibitory responses in neurons that did not exhibit anticipatory responses. Taken together, these results suggest that the role of the NAS in cocaine self-administration may consist of two different mechanisms: (1) An initiation or trigger mechanism, as represented by the anticipatory neuronal responses, in which the NAS participates in triggering or mediating the goal-directed behaviors (e.g., lever pressing) that lead to the acquisition of the reinforcing agent (e.g., cocaine).(ABSTRACT TRUNCATED AT 400 WORDS)
本研究的目的是阐明伏隔核(NAS)在可卡因自我给药行为表达中的作用。大鼠按照连续强化程序进行训练,按压杠杆以启动一个提供静脉注射可卡因的泵。大鼠训练完成后,在可卡因自我给药期间,使用永久植入的微丝通过慢性记录技术监测NAS中的神经元活动。在NAS中,181个神经元中有19%在杠杆按压前几秒表现出放电率增加或降低(称为“预期反应”),48%在杠杆按压后几分钟内放电率发生改变,主要是降低(“可卡因后反应”)。有预期反应的神经元中有三分之二出现可卡因后反应。具有这两种反应模式之一的神经元在组织学上定位于NAS的核心和壳区域,两个区域中反应类型的比例没有统计学上的显著差异。对录像的可卡因自我给药行为的分析表明,预期反应与动物朝向并按压杠杆的行为或仅与直接与按压杠杆相关的动作特别相关。在与杠杆按压无关的类似动作中未观察到类似预期的相位性尖峰活动。在一些动物中,在自我给药前或给药期间全身注射D1(SCH 23390)或D2(匹莫齐特)受体拮抗剂,以评估多巴胺受体阻断对预期反应和可卡因后反应的影响。单独给予每种拮抗剂通常会导致杠杆按压行为消失。两种拮抗剂均阻断了有预期反应的神经元的可卡因后抑制反应。两种拮抗剂均未改变预期单位反应,也未影响未表现出预期反应的神经元的可卡因后抑制反应。综上所述,这些结果表明,NAS在可卡因自我给药中的作用可能由两种不同机制组成:(1)一种启动或触发机制,由预期神经元反应代表,其中NAS参与触发或介导导致获得强化剂(如可卡因)的目标导向行为(如杠杆按压)。(摘要截短于400字)