Spencer Sade, Scofield Michael, Kalivas Peter W
Department of Neuroscience, Medical University of South Carolina, Charleston, SC, USA.
Department of Neuroscience, Medical University of South Carolina, Charleston, SC, USA
J Psychopharmacol. 2016 Nov;30(11):1095-1098. doi: 10.1177/0269881116655248. Epub 2016 Jun 28.
In 1998 we published a perspective review describing how drug-induced neuroadaptations might serve towards understanding drug craving. We proposed experimental perspectives to help discern data relevant to long-lasting brain changes, and to distinguish dopamine-related changes that were largely pharmacological from glutamatergic changes that were based on drug-environment associations. These perspectives are embedded in drug abuse research, and the last 18 years has witnessed marked development in understanding addiction-associated corticostriatal glutamate plasticity. Here we propose three new perspectives on how the field might approach integrating and using the emerging data on glutamatergic adaptations. (1) Consider adaptations produced in kind across drug classes as most useful towards understanding shared characteristics of addiction, such as relapse. (2) Consider how drug-induced changes in glia and the extracellular matrix may contribute to synaptic alterations. (3) Make measurements not only at late withdrawal, but also during drug seeking events to capture transient changes that mediate active drug seeking that are shared across drug classes.
1998年,我们发表了一篇前瞻性综述,描述了药物诱导的神经适应性如何有助于理解药物渴望。我们提出了实验观点,以帮助辨别与持久脑变化相关的数据,并区分主要基于药理学的多巴胺相关变化和基于药物-环境关联的谷氨酸能变化。这些观点已融入药物滥用研究中,在过去18年里,人们对成瘾相关的皮质纹状体谷氨酸可塑性的理解有了显著进展。在此,我们就该领域如何整合和利用有关谷氨酸能适应性的新出现数据提出三个新观点。(1)将各类药物产生的同类适应性视为最有助于理解成瘾共同特征(如复发)的因素。(2)考虑药物诱导的胶质细胞和细胞外基质变化如何导致突触改变。(3)不仅要在戒断后期进行测量,还要在觅药事件期间进行测量,以捕捉介导各类药物共同的主动觅药行为的瞬时变化。