Peoples Laura L, Kravitz Alexxai V, Lynch Kevin G, Cavanaugh Daniel J
Department of Psychology, University of Pennsylvania, Philadelphia, PA 19106, USA.
Neuropsychopharmacology. 2007 May;32(5):1141-58. doi: 10.1038/sj.npp.1301203. Epub 2006 Oct 4.
Hypoactivity of the accumbens is induced by repeated cocaine exposure and is hypothesized to play a role in cocaine addiction. However, it is difficult to understand how a general hypoactivity of the accumbens, which facilitates multiple types of motivated behaviors, could contribute to the selective increase in drug-directed behavior that defines addiction. Electrophysiological recordings, made during sessions in which rats self-administer cocaine, show that most accumbal neurons that encode events related to drug-directed behavior achieve and maintain higher firing rates during the period of cocaine exposure (Task-Activated neurons) than do other accumbal neurons (Task-Non-Activated neurons). We have hypothesized that this difference in activity makes the neurons that facilitate drug-directed behavior less susceptible than other neurons to the chronic inhibitory effects of cocaine. A sparing of neurons that facilitate drug-directed behavior from chronic hypoactivity might lead to a relative increase in the transmission of neuronal signals that facilitate drug-directed behavior through accumbal circuits and thereby contribute to changes in behavior that characterize addiction (ie differential inhibition hypothesis). A prediction of the hypothesis is that neurons that are activated in relation to task events during cocaine self-administration sessions will show less of a decrease in firing across repeated self-administration sessions than will other neurons. To test this prediction, rats were exposed to 30 daily (6 h/day) cocaine self-administration sessions. Chronic extracellular recordings of single accumbal neurons were made during the second to third session and the 30th session. Between-session comparisons showed that decreases in firing were exhibited by Task-Non-Activated, but not by Task-Activated, neurons. During the day 30 session, the magnitude of the difference in firing rate between the two groups of neurons was positively related to the propensity of animals to seek and take cocaine. The findings of the present study are consistent with a basic prediction of the differential inhibition hypothesis and may be relevant to understanding cocaine addiction.
反复接触可卡因会导致伏隔核活动减退,据推测这在可卡因成瘾中起作用。然而,很难理解伏隔核的普遍活动减退(这种减退促进多种类型的动机行为)如何能导致定义成瘾的药物导向行为的选择性增加。在大鼠自我给药可卡因的过程中进行的电生理记录显示,与药物导向行为相关事件编码的大多数伏隔核神经元在可卡因暴露期间(任务激活神经元)比其他伏隔核神经元(任务非激活神经元)达到并维持更高的放电率。我们推测,这种活动差异使得促进药物导向行为的神经元比其他神经元对可卡因的慢性抑制作用更不敏感。促进药物导向行为的神经元免受慢性活动减退的影响,可能会导致通过伏隔核回路促进药物导向行为的神经元信号传递相对增加,从而导致成瘾特征性行为的改变(即差异抑制假说)。该假说的一个预测是,在可卡因自我给药过程中与任务事件相关被激活的神经元,与其他神经元相比,在反复自我给药过程中放电减少的程度会更小。为了验证这一预测,将大鼠每天暴露于30次(6小时/天)的可卡因自我给药过程中。在第二次至第三次以及第30次过程中对单个伏隔核神经元进行慢性细胞外记录。过程间比较显示,任务非激活神经元表现出放电减少,而任务激活神经元则没有。在第30天的过程中,两组神经元放电率差异的大小与动物寻求和摄取可卡因的倾向呈正相关。本研究结果与差异抑制假说的基本预测一致,可能与理解可卡因成瘾有关。