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伏隔核壳转录组学揭示了与吗啡和蔗糖渴望相关的性别和强化物特异性特征。

Transcriptomics in the nucleus accumbens shell reveal sex- and reinforcer-specific signatures associated with morphine and sucrose craving.

机构信息

Department of Psychology and Neuroscience, Temple University, Philadelphia, PA, USA.

出版信息

Neuropsychopharmacology. 2022 Sep;47(10):1764-1775. doi: 10.1038/s41386-022-01289-2. Epub 2022 Feb 21.

Abstract

Incubation of craving is a well-documented phenomenon referring to the intensification of drug craving over extended abstinence. The neural adaptations that occur during forced abstinence following chronic drug taking have been a topic of intense study. However, little is known about the transcriptomic changes occurring throughout this window of time. To define gene expression changes associated with morphine consumption and extended abstinence, male and female rats underwent 10 days of morphine self-administration. Separate drug-naive rats self-administered sucrose in order to compare opioid-induced changes from those associated with natural, non-drug rewards. After one or 30 days of forced abstinence, rats were tested for craving, or nucleus accumbens shell tissue was dissected for RNA sequencing. Morphine consumption was predictive of drug seeking after extended (30 days) but not brief (1 day) abstinence in both sexes. Extended abstinence was also associated with robust sex- and reinforcer-specific changes in gene expression, suggesting sex differences underlying incubation of morphine and sucrose seeking respectively. Importantly, these changes in gene expression occurred without re-exposure to drug-paired cues, indicating that chronic morphine causes long-lasting changes in gene expression that prime the system for increased craving. These findings lay the groundwork for identifying specific therapeutic targets for curbing opioid craving without impacting the natural reward system in males and females.

摘要

译文

渴望潜伏期是一种有充分文献记录的现象,指的是在长时间的禁欲后,对药物的渴望加剧。在慢性药物使用后强制禁欲期间发生的神经适应一直是一个激烈研究的课题。然而,对于在此时间段内发生的转录组变化,人们知之甚少。为了确定与吗啡消耗和长期禁欲相关的基因表达变化,雄性和雌性大鼠接受了 10 天的吗啡自我给药。单独的无药物经验的大鼠自行给予蔗糖,以便将阿片类药物引起的变化与与天然非药物奖励相关的变化进行比较。在 1 天或 30 天的强制禁欲后,对大鼠进行渴望测试,或分离伏隔核壳组织进行 RNA 测序。吗啡消耗可预测雄性和雌性大鼠在长期(30 天)而非短暂(1 天)禁欲后的觅药行为。长期禁欲还与性别和强化物特异性的基因表达的强烈变化相关,这表明分别存在与吗啡和蔗糖觅药的潜伏期相关的性别差异。重要的是,这些基因表达的变化发生在没有重新暴露于药物配对线索的情况下,表明慢性吗啡会导致基因表达的持久变化,从而使系统对增强的渴望做好准备。这些发现为确定具体的治疗靶点奠定了基础,以抑制阿片类药物的渴望,而不会影响雄性和雌性的自然奖励系统。

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