Disrupting Heroin-Associated Memory Reconsolidation through Actin Polymerization Inhibition in the Nucleus Accumbens Core

伏隔核 记忆巩固 海洛因 有条件地点偏好 心理学 消光(光学矿物学) 上瘾 神经科学 药理学 海马体 药品 化学 医学 精神科 多巴胺 矿物学
作者
Haiting Zhao,Haoyu Li,Meng Li,Peng Du,Xin Mo,Mengqi Gong,Jiaxin Chen,Yiwei Liao
出处
期刊:The International Journal of Neuropsychopharmacology [Oxford University Press]
标识
DOI:10.1093/ijnp/pyae065
摘要

Abstract 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 (CPP) 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 ten-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 six hours 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.

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