Cellular Neurobiology Research Branch, Behavioral Neurophysiology Research Section, National Institute on Drug Abuse Intramural Research Program, Baltimore, Maryland 21224.
Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, Oregon 97239.
J Neurosci. 2021 Jan 13;41(2):342-353. doi: 10.1523/JNEUROSCI.1755-20.2020. Epub 2020 Nov 20.
Substance use disorders (SUDs) are characterized by maladaptive behavior. The ability to properly adjust behavior according to changes in environmental contingencies necessitates the interlacing of existing memories with updated information. This can be achieved by assigning learning in different contexts to compartmentalized "states." Though not often framed this way, the maladaptive behavior observed in individuals with SUDs may result from a failure to properly encode states because of drug-induced neural alterations. Previous studies found that the dorsomedial striatum (DMS) is important for behavioral flexibility and state encoding, suggesting the DMS may be an important substrate for these effects. Here, we recorded DMS neural activity in cocaine-experienced male rats during a decision-making task where blocks of trials represented distinct states to probe whether the encoding of state and state-related information is affected by prior drug exposure. We found that DMS medium spiny neurons (MSNs) and fast-spiking interneurons (FSIs) encoded such information and that prior cocaine experience disrupted the evolution of representations both within trials and across recording sessions. Specifically, DMS MSNs and FSIs from cocaine-experienced rats demonstrated higher classification accuracy of trial-specific rules, defined by response direction and value, compared with those drawn from sucrose-experienced rats, and these overly strengthened trial-type representations were related to slower switching behavior and reaction times. These data show that prior cocaine experience paradoxically increases the encoding of state-specific information and rules in the DMS and suggest a model in which abnormally specific and persistent representation of rules throughout trials in DMS slows value-based decision-making in well trained subjects. Substance use disorders (SUDs) may result from a failure to properly encode rules guiding situationally appropriate behavior. The dorsomedial striatum (DMS) is thought to be important for such behavioral flexibility and encoding that defines the situation or "state." This suggests that the DMS may be an important substrate for the maladaptive behavior observed in SUDs. In the current study, we show that prior cocaine experience results in over-encoding of state-specific information and rules in the DMS, which may impair normal adaptive decision-making in the task, akin to what is observed in SUDs.
物质使用障碍(SUD)的特征是适应不良的行为。根据环境变化适当调整行为的能力需要将现有记忆与更新的信息交织在一起。这可以通过将学习分配到不同的环境中,将其分配到“状态”来实现。尽管人们通常不会以这种方式表达,但 SUD 患者中观察到的适应不良行为可能是由于药物引起的神经改变而导致无法正确编码状态所致。先前的研究发现,背内侧纹状体(DMS)对于行为灵活性和状态编码很重要,这表明 DMS 可能是这些影响的重要基础。在这里,我们在决策任务中记录了可卡因经验丰富的雄性大鼠的 DMS 神经活动,其中,试验块代表了不同的状态,以探究先前的药物暴露是否会影响状态和状态相关信息的编码。我们发现,DMS 中的中间神经元(MSNs)和快速放电中间神经元(FSIs)编码了这种信息,并且可卡因的先前经历破坏了试验内和整个记录会话中的表示的演变。具体来说,与来自蔗糖经验丰富的大鼠相比,可卡因经验丰富的大鼠的 DMS MSNs 和 FSIs 对通过反应方向和价值定义的特定于试验的规则具有更高的分类准确性,而这些过度增强的试验类型表示与较慢的转换行为和反应时间有关。这些数据表明,先前的可卡因经验会增加 DMS 中状态特异性信息和规则的编码,这表明了一种模型,即在 DMS 中,整个试验中规则的异常具体和持久表示会减慢经过良好训练的对象的基于价值的决策。物质使用障碍(SUD)可能是由于无法正确编码指导情境适当行为的规则所致。背内侧纹状体(DMS)被认为对于这种行为灵活性和定义情况或“状态”的编码很重要。这表明 DMS 可能是 SUD 中观察到的适应不良行为的重要基础。在当前的研究中,我们表明,可卡因的先前经验会导致 DMS 中状态特定信息和规则的过度编码,这可能会损害任务中的正常适应性决策,类似于 SUD 中观察到的情况。