Nic Dhonnchadha Bríd A, Cunningham Kathryn A
Center for Addiction Research, Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Behav Brain Res. 2008 Dec 16;195(1):39-53. doi: 10.1016/j.bbr.2008.06.026. Epub 2008 Jul 1.
Drug-associated memories are a hallmark of addiction and a contributing factor in the continued use and relapse to drugs of abuse. Repeated association of drugs of abuse with conditioned stimuli leads to long-lasting behavioral responses that reflect reward-controlled learning and participate in the establishment of addiction. A greater understanding of the mechanisms underlying the formation and retrieval of drug-associated memories may shed light on potential therapeutic approaches to effectively intervene with drug use-associated memory. There is evidence to support the involvement of serotonin (5-HT) neurotransmission in learning and memory formation through the families of the 5-HT(1) receptor (5-HT(1)R) and 5-HT(2)R which have also been shown to play a modulatory role in the behavioral effects induced by many psychostimulants. While there is a paucity of studies examining the effects of selective 5-HT(1A)R ligands, the available dataset suggests that 5-HT(1B)R agonists may inhibit retrieval of cocaine-associated memories. The 5-HT(2A)R and 5-HT(2C)R appear to be integral in the strong conditioned associations made between cocaine and environmental cues with 5-HT(2A)R antagonists and 5-HT(2C)R agonists possessing potency in blocking retrieval of cocaine-associated memories following cocaine self-administration procedures. The complex anatomical connectivity between 5-HT neurons and other neuronal phenotypes in limbic-corticostriatal brain structures, the heterogeneity of 5-HT receptors (5-HT(X)R) and the conflicting results of behavioral experiments which employ non-specific 5-HT(X)R ligands contribute to the complexity of interpreting the involvement of 5-HT systems in addictive-related memory processes. This review briefly traces the history of 5-HT involvement in retrieval of drug-cue associations and future targets of serotonergic manipulation that may reduce the impact that drug cues have on addictive behavior and relapse.
与药物相关的记忆是成瘾的一个标志,也是药物滥用持续使用和复发的一个促成因素。滥用药物与条件刺激的反复关联会导致持久的行为反应,这些反应反映了奖赏控制学习,并参与成瘾的形成。对药物相关记忆形成和提取背后机制的更深入理解,可能会为有效干预与药物使用相关记忆的潜在治疗方法提供线索。有证据支持血清素(5-HT)神经传递通过5-HT(1)受体(5-HT(1)R)和5-HT(2)R家族参与学习和记忆形成,这两个家族在许多精神兴奋剂诱导的行为效应中也发挥调节作用。虽然研究选择性5-HT(1A)R配体作用的研究较少,但现有数据集表明5-HT(1B)R激动剂可能会抑制可卡因相关记忆的提取。5-HT(2A)R和5-HT(2C)R似乎在可卡因与环境线索之间形成的强烈条件关联中不可或缺,5-HT(2A)R拮抗剂和5-HT(2C)R激动剂在可卡因自我给药程序后具有阻断可卡因相关记忆提取的效力。5-HT神经元与边缘-皮质-纹状体脑结构中其他神经元表型之间复杂的解剖连接、5-HT受体(5-HT(X)R)的异质性以及使用非特异性5-HT(X)R配体的行为实验的矛盾结果,都导致了解释5-HT系统在成瘾相关记忆过程中的参与情况变得复杂。本综述简要追溯了5-HT参与药物线索关联提取的历史,以及可能减少药物线索对成瘾行为和复发影响的5-羟色胺能操纵的未来靶点。