Haiting Zhao, Haoyu Li, Li Meng, Peng Du, Xin Mo, Mengqi Gong, Jiaxin Chen, Yiwei Liao
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Rats underwent ten days of intravenous heroin self-administration paired with conditioned cues. Subsequently, a 10-day extinction phase aimed to reduce heroin-seeking behaviors. Following this, rats participated in a 15-minute retrieval trial with or without cues. Immediately post-retrieval, rats received bilateral injections of the actin polymerization inhibitor Latrunculin A (Lat A) into the nucleus accumbens core (NACc), a critical brain region for memory reconsolidation.</p><p><strong>Results: </strong>Immediate administration of Lat A into the NACc post-retrieval significantly reduced cue-induced and heroin-primed reinstatement of heroin-seeking behavior for at least 28 days. However, administering Lat A 6-hour post-retrieval or without a retrieval trial, as well as administering Jasplakionlide prior to memory reactivation did not affect heroin-seeking behaviors.</p><p><strong>Conclusions: </strong>Inhibiting actin polymerization during the reconsolidation window disrupts heroin-associated memory reconsolidation, leading to decreased heroin-seeking behavior and prevention of relapse. 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引用次数: 0
摘要
背景:了解药物成瘾是一种适应不良的学习障碍,其中药物相关或环境线索引发药物渴望和寻求,对于开发有效的治疗方法至关重要。肌动蛋白聚合是一种生物化学过程,在药物相关记忆的形成中起着至关重要的作用,特别是在涉及吗啡和甲基苯丙胺等药物的条件位置偏好(CPP)范式中。然而,肌动蛋白聚合在海洛因相关记忆再巩固中的作用仍未得到充分研究。方法:采用自用海洛因啮齿动物模型,研究肌动蛋白聚合在海洛因相关记忆再巩固中的作用。大鼠接受为期10天的静脉注射海洛因自我管理,并辅以条件提示。随后,一个为期十天的戒毒阶段旨在减少寻求海洛因的行为。在此之后,大鼠参加了一个有或没有线索的15分钟的检索试验。检索后立即将肌动蛋白聚合抑制剂Latrunculin A (Lat A)注射到大脑中记忆再巩固的关键区域伏隔核(NACc)。结果:检索后立即给药Lat A可显著减少线索诱导和海洛因引发的海洛因寻求行为恢复至少28天。然而,在检索后6小时或没有检索试验时给予Lat A,以及在记忆再激活前给予Jasplakionlide,对海洛因寻求行为没有影响。结论:抑制再巩固窗口期肌动蛋白聚合破坏海洛因相关记忆再巩固,导致海洛因寻求行为减少,预防复发。这些影响取决于检索试验的存在,并表现出时间特异性,揭示了成瘾机制和潜在的治疗干预措施。
Disrupting heroin-associated memory reconsolidation through actin polymerization inhibition in the nucleus accumbens core.
Background: Understanding drug addiction as a disorder of maladaptive learning, where drug-associated or environmental cues trigger drug cravings and seeking, is crucial for developing effective treatments. Actin polymerization, a biochemical process, plays a crucial role in drug-related memory formation, particularly evident in conditioned place preference paradigms involving drugs like morphine and methamphetamine. However, the role of actin polymerization in the reconsolidation of heroin-associated memories remains understudied.
Methods: This study employed a rodent model of self-administered heroin to investigate the involvement of actin polymerization in the reconsolidation of heroin-associated memories. Rats underwent ten days of intravenous heroin self-administration paired with conditioned cues. Subsequently, a 10-day extinction phase aimed to reduce heroin-seeking behaviors. Following this, rats participated in a 15-minute retrieval trial with or without cues. Immediately post-retrieval, rats received bilateral injections of the actin polymerization inhibitor Latrunculin A (Lat A) into the nucleus accumbens core (NACc), a critical brain region for memory reconsolidation.
Results: Immediate administration of Lat A into the NACc post-retrieval significantly reduced cue-induced and heroin-primed reinstatement of heroin-seeking behavior for at least 28 days. However, administering Lat A 6-hour post-retrieval or without a retrieval trial, as well as administering Jasplakionlide prior to memory reactivation did not affect heroin-seeking behaviors.
Conclusions: Inhibiting actin polymerization during the reconsolidation window disrupts heroin-associated memory reconsolidation, leading to decreased heroin-seeking behavior and prevention of relapse. These effects are contingent upon the presence of a retrieval trial and exhibit temporal specificity, shedding light on addiction mechanisms and potential therapeutic interventions.
期刊介绍:
The central focus of the journal is on research that advances understanding of existing and new neuropsychopharmacological agents including their mode of action and clinical application or provides insights into the biological basis of psychiatric disorders and thereby advances their pharmacological treatment. Such research may derive from the full spectrum of biological and psychological fields of inquiry encompassing classical and novel techniques in neuropsychopharmacology as well as strategies such as neuroimaging, genetics, psychoneuroendocrinology and neuropsychology.