Department of Pharmacology, Kurume University School of Medicine, Kurume, Japan.
Department of Dental Anesthesiology, Tsurumi University School of Dental Medicine, Yokohama, Japan.
Int J Neuropsychopharmacol. 2021 Dec 8;24(12):988-1001. doi: 10.1093/ijnp/pyab067.
Dopamine neurotransmission plays a critical role in reward in drug abuse and drug addiction. However, the role of dopamine in the recognition of drug-associated environmental stimuli, retrieval of drug-associated memory, and drug-seeking behaviors is not fully understood.
Roles of dopamine neurotransmission in the prefrontal cortex (PFC) and nucleus accumbens (NAc) in the cocaine-conditioned place preference (CPP) paradigm were evaluated using in vivo microdialysis.
In mice that had acquired cocaine CPP, dopamine levels in the PFC, but not in the NAc, increased in response to cocaine-associated cues when mice were placed in the cocaine chamber of an apparatus with 2 separated chambers. The induction of the dopamine response and the development of cocaine CPP were mediated through activation of glutamate NMDA (N-methyl-D-aspartate)/AMPA (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid) receptor signaling in the PFC during conditioning. Activation of dopamine D1 or D2 receptor signaling in the PFC was required for cocaine-induced locomotion, but not for the induction of the dopamine response or the development of cocaine CPP. Interestingly, dopamine levels in the NAc increased in response to cocaine-associated cues when mice were placed at the center of an apparatus with 2 connected chambers, which requires motivated exploration associated with cocaine reward.
Dopamine neurotransmission in the PFC is activated by the exposure to the cocaine-associated cues, whereas dopamine neurotransmission in the NAc is activated in a process of motivated exploration of cues associated with cocaine reward. Furthermore, the glutamate signaling cascade in the PFC is suggested to be a potential therapeutic target to prevent the progression of drug addiction.
多巴胺神经传递在药物滥用和成瘾中的奖励中起着关键作用。然而,多巴胺在识别与药物相关的环境刺激、检索与药物相关的记忆以及觅药行为中的作用尚不完全清楚。
使用活体微透析评估多巴胺神经传递在前额叶皮层(PFC)和伏隔核(NAc)中的作用,在可卡因条件性位置偏好(CPP)范式中。
在获得可卡因 CPP 的小鼠中,当小鼠被放置在具有 2 个分离腔室的仪器的可卡因腔室中时,PFC 中的多巴胺水平(而非 NAc 中的多巴胺水平)对可卡因相关线索的反应增加。多巴胺反应的诱导和可卡因 CPP 的发展是通过在条件作用过程中 PFC 中的谷氨酸 NMDA(N-甲基-D-天冬氨酸)/AMPA(α-氨基-3-羟基-5-甲基-4-异恶唑丙酸)受体信号的激活介导的。PFC 中的多巴胺 D1 或 D2 受体信号的激活对于可卡因诱导的运动是必需的,但对于多巴胺反应的诱导或可卡因 CPP 的发展则不是必需的。有趣的是,当小鼠被放置在具有 2 个连接腔室的仪器的中心时,NAc 中的多巴胺水平会对可卡因相关线索做出反应,这需要与可卡因奖励相关的主动探索。
暴露于可卡因相关线索会激活 PFC 中的多巴胺神经传递,而 NAc 中的多巴胺神经传递则会在与可卡因奖励相关的线索的主动探索过程中被激活。此外,PFC 中的谷氨酸信号级联被认为是预防药物成瘾进展的潜在治疗靶点。