Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN, 37232, USA.
Vanderbilt Center for Addiction Research, Vanderbilt University School of Medicine, Nashville, TN, 37232, USA.
Neuropsychopharmacology. 2019 Jun;44(7):1189-1197. doi: 10.1038/s41386-019-0320-0. Epub 2019 Jan 23.
While preclinical work has aimed to outline the neural mechanisms of drug addiction, it has overwhelmingly focused on male subjects. There has been a push in recent years to incorporate females into existing addiction models; however, males and females often have different behavioral strategies, making it important to not only include females, but to develop models that assess the factors that comprise female drug addiction. Traditional self-administration models often include light or tone cues that serve as discriminative stimuli and/or consequent stimuli, making it nearly impossible to disentangle the effects of cue learning, the cues themselves, and acute effects of psychostimulant drugs. To disentangle the interaction between drug-associated cues and the consummatory and appetitive responding driven by cocaine, we have developed a new behavioral procedure that combines Pavlovian-instrumental transfer with behavioral economic analysis. This task can be completed within a single session, allowing for studies looking at estrous cycle stage-dependent effects in intact cycling females, something that has been difficult in the past. In this study, we found no differences in self-administration across the estrous cycle in the absence of cues; however, when cues were introduced, the cues that acquired value during estrus-but not during diestrus or in males-increased motivation. Cues paired during estrus also increased c-fos expression to a greater extent in striatal regions, an effect that may underlie the observed increases in seeking induced by these cues, even weeks later. Together, these data suggest that fundamental differences in the motivational properties of psychostimulant drugs between males and females are complex and are driven primarily by the interaction between drug-associated stimuli and drug effects.
虽然临床前工作旨在概述药物成瘾的神经机制,但它主要集中在男性受试者身上。近年来,人们一直在推动将女性纳入现有的成瘾模型中;然而,男性和女性通常具有不同的行为策略,因此不仅要纳入女性,还要开发评估构成女性药物成瘾的因素的模型非常重要。传统的自我给药模型通常包括作为辨别刺激和/或后继刺激的光或音调线索,这使得很难区分线索学习、线索本身以及精神兴奋剂药物的急性效应的影响。为了理清与药物相关的线索与可卡因驱动的消费和欲望反应之间的相互作用,我们开发了一种新的行为程序,该程序将条件反射与行为经济学分析结合起来。该任务可以在单个会话中完成,允许研究在完整的循环女性中研究发情周期阶段依赖性效应,这在过去是很难的。在这项研究中,我们发现在没有线索的情况下,发情周期对自我给药没有影响;然而,当引入线索时,在发情期而不是在发情期或在雄性动物中获得价值的线索会增加动机。在发情期配对的线索也会更大程度地增加纹状体区域中的 c-fos 表达,这种效应可能是这些线索引起的寻求行为增加的基础,即使是在几周后。总之,这些数据表明,雄性和雌性之间精神兴奋剂药物的动机特性存在根本差异,这种差异是复杂的,主要是由与药物相关的刺激和药物作用之间的相互作用驱动的。