Department of Psychology, University of North Carolina, Chapel Hill, North Carolina 27599-3270, USA.
Learn Mem. 2011 Oct 17;18(11):693-702. doi: 10.1101/lm.2273111. Print 2011 Nov.
Contextual stimulus control over instrumental drug-seeking behavior relies on the reconsolidation of context-response-drug associative memories into long-term memory storage following retrieval-induced destabilization. According to previous studies, the basolateral amygdala (BLA) and dorsal hippocampus (DH) regulate cocaine-related memory reconsolidation; however, it is not known whether these brain regions interact or independently control this phenomenon. To investigate this question, rats were trained to lever press for cocaine reinforcement in a distinct environmental context followed by extinction training in a different context. Rats were then briefly re-exposed to the cocaine-paired context to destabilize cocaine-related memories, or they were exposed to an unpaired context. Immediately thereafter, the rats received unilateral microinfusions of anisomycin (ANI) into the BLA plus baclofen/muscimol (B/M) into the contralateral (BLA/DH disconnection) or ipsilateral DH, or they received contralateral or ipsilateral microinfusions of vehicle. They then remained in their home cages overnight or for 21 d, followed by additional extinction training and a test of cocaine-seeking behavior (nonreinforced active lever responding). BLA/DH disconnection following re-exposure to the cocaine-paired context, but not the unpaired context, impaired subsequent drug context-induced cocaine-seeking behavior relative to vehicle or ipsilateral ANI + B/M treatment. Prolonged home cage stay elicited a time-dependent increase, or incubation, of drug-context-induced cocaine-seeking behavior, and BLA/DH disconnection inhibited this incubation effect despite some recovery of cocaine-seeking behavior. Thus, the BLA and DH interact to regulate the reconsolidation of cocaine-related associative memories, thereby facilitating the ability of drug-paired contexts to trigger cocaine-seeking behavior and contributing to the incubation of cocaine-seeking behavior.
语境刺激对工具性觅药行为的控制依赖于在提取诱导的不稳定性后,将与上下文相关的反应-药物关联记忆重新巩固到长期记忆存储中。根据之前的研究,基底外侧杏仁核(BLA)和背侧海马(DH)调节可卡因相关记忆的再巩固;然而,尚不清楚这些脑区是相互作用还是独立控制这一现象。为了研究这个问题,大鼠在一个特定的环境背景下接受了按压杠杆以获得可卡因强化的训练,然后在另一个不同的环境中接受了消退训练。然后,大鼠短暂地重新暴露于可卡因配对的环境中,以破坏可卡因相关的记忆,或者暴露于未配对的环境中。之后,立即将大鼠单侧微量注射anisomycin(ANI)到 BLA 中,同时对侧(BLA/DH 断开)或同侧 DH 中注射 baclofen/muscimol(B/M),或者对侧或同侧微量注射 vehicle。然后,它们留在自己的笼子里过夜或 21 天,之后进行额外的消退训练和可卡因寻求行为测试(非强化主动杠杆反应)。与 vehicle 或同侧 ANI + B/M 处理相比,重新暴露于可卡因配对环境后但不暴露于未配对环境中,BLA/DH 断开会损害随后的药物环境诱导的可卡因寻求行为。长时间的笼内停留会引起药物环境诱导的可卡因寻求行为的时间依赖性增加,或潜伏期,BLA/DH 断开会抑制这种潜伏期效应,尽管可卡因寻求行为有一定程度的恢复。因此,BLA 和 DH 相互作用以调节可卡因相关联想记忆的再巩固,从而促进药物配对环境触发可卡因寻求行为的能力,并促进可卡因寻求行为的潜伏期。