Center for Substance Abuse Research, Temple University, Philadelphia, Pennsylvania, USA.
Department of Neural Sciences, Temple University, Philadelphia, PA, USA.
Eur J Neurosci. 2022 Apr;55(7):1742-1755. doi: 10.1111/ejn.15650. Epub 2022 Mar 29.
A powerful motivation to seek opioids remains after drug cessation and intensifies during extended periods of abstinence. Unfortunately, biomarkers associated with continued drug seeking have not been described. Moreover, previous studies have focused on the effects of early abstinence with little exploration into the long-term drug-induced mechanisms that occur after extended abstinence. Here we demonstrated that 30 days (D) of forced abstinence results in a time-dependent increase in morphine seeking in a rat model of morphine self-administration (SA). We measured expression of known drug-responsive microRNAs (miRNAs) in the nucleus accumbens, an area critical for reward-related plasticity, during early or late abstinence in animals that underwent either a cue-induced relapse test or no relapse test. miRNAs are small noncoding RNAs that represent suitable biomarker candidates due to their long-lasting nature. mir-32-5p levels during early abstinence negatively correlated with active lever pressing in both cue-exposed and cue-naïve animals. mir-1298-5p positively correlated with drug SA history after a relapse test during late abstinence. When animals underwent acute abstinence with no relapse test, mir-1298-5p correlated with drug infusions and active lever pressing during SA. In late abstinence with no relapse test, mir-137-3p negatively correlated with drug infusions. Regulation of mir-32-5p target genes and significant correlation of target gene mRNA with mir-32-5p was observed after abstinence. These results indicate that lasting regulation of miRNA expression is associated with drug intake following morphine SA. In addition, we conclude that the miRNA profile undergoes regulation from early to late abstinence and miRNA expression may indicate past drug history.
在戒毒后,寻求阿片类药物的强烈动机仍然存在,并在长时间的禁欲期间加剧。不幸的是,与持续药物寻求相关的生物标志物尚未被描述。此外,以前的研究集中在早期禁欲的影响上,而对延长禁欲后发生的长期药物诱导机制的探索较少。在这里,我们证明在吗啡自我给药(SA)的大鼠模型中,30 天(D)的强制禁欲会导致吗啡寻求的时间依赖性增加。我们在经历线索诱导复发测试或无复发测试的动物中,在早期或晚期禁欲期间测量了已知对药物有反应的 microRNAs(miRNAs)在伏隔核中的表达,伏隔核是与奖励相关的可塑性的关键区域。miRNAs 是小的非编码 RNA,由于其持久的特性,代表合适的生物标志物候选物。在早期禁欲期间,mir-32-5p 的水平与线索暴露和线索-naïve 动物的主动杠杆按压呈负相关。mir-1298-5p 在晚期禁欲期间的复发测试后与药物 SA 史呈正相关。当动物在没有复发测试的情况下进行急性禁欲时,mir-1298-5p 与药物输注和 SA 期间的主动杠杆按压相关。在没有复发测试的晚期禁欲中,mir-137-3p 与药物输注呈负相关。mir-32-5p 靶基因的调节和靶基因 mRNA 与 mir-32-5p 的显著相关性在禁欲后观察到。这些结果表明,miRNA 表达的持久调节与吗啡 SA 后药物摄入有关。此外,我们得出结论,miRNA 谱在早期到晚期禁欲期间发生调节,miRNA 表达可能表明过去的药物史。