Imperio Caesar G, McFalls Ashley J, Colechio Elizabeth M, Masser Dustin R, Vrana Kent E, Grigson Patricia S, Freeman Willard M
Department of Neural and Behavioral Sciences, Penn State College of Medicine, Hershey, PA, United States.
Department of Pharmacology, Penn State College of Medicine, Hershey, Pennsylvania, United States.
Brain Res Bull. 2016 May;123:71-80. doi: 10.1016/j.brainresbull.2015.12.005. Epub 2015 Dec 28.
Heroin addiction is a disease of chronic relapse that harms the individual through devaluation of personal responsibilities in favor of finding and using drugs. Only some recreational heroin users devolve into addiction but the basis of these individual differences is not known. We have shown in rats that avoidance of a heroin-paired taste cue reliably identifies individual animals with greater addiction-like behavior for heroin. Here rats received 5min access to a 0.15% saccharin solution followed by the opportunity to self-administer either saline or heroin for 6h. Large Suppressors of the heroin-paired taste cue displayed increased drug escalation, motivation for drug, and drug loading behavior compared with Small Suppressors. Little is known about the molecular mechanisms of these individual differences in addiction-like behavior. We examined the individual differences in mRNA expression in the nucleus accumbens (NAc) of rats that were behaviorally stratified by addiction-like behavior using next-generation sequencing. We hypothesized that based on the avoidance of the drug-paired cue there will be a unique mRNA profile in the NAc. Analysis of strand-specific whole genome RNA-Seq data revealed a number of genes differentially regulated in NAc based on the suppression of the natural saccharine reward. Large Suppressors exhibited a unique mRNA prolife compared to Saline controls and Small Suppressors. Genes related to immunity, neuronal activity, and behavior were differentially expressed among the 3 groups. In total, individual differences in avoidance of a heroin-paired taste cue are associated with addiction-like behavior along with differential NAc gene expression.
海洛因成瘾是一种慢性复发性疾病,它通过贬低个人责任以利于寻找和使用毒品来伤害个体。只有一些吸食海洛因的娱乐使用者会发展成成瘾者,但这些个体差异的基础尚不清楚。我们在大鼠身上已经表明,回避与海洛因配对的味觉线索能够可靠地识别出对海洛因具有更强成瘾样行为的个体动物。在此,大鼠先有5分钟接触0.15%糖精溶液的机会,然后有6小时自行注射生理盐水或海洛因的机会。与小抑制者相比,对与海洛因配对的味觉线索有大抑制反应的大鼠表现出更高的药物升级、对药物的动机以及药物加载行为。关于这些成瘾样行为个体差异的分子机制知之甚少。我们使用下一代测序技术,研究了根据成瘾样行为进行行为分层的大鼠伏隔核(NAc)中mRNA表达的个体差异。我们假设,基于对与药物配对线索的回避,NAc中会有独特的mRNA谱。对链特异性全基因组RNA-Seq数据的分析显示,基于对天然糖精奖励的抑制,NAc中有许多基因受到差异调节。与生理盐水对照组和小抑制者相比,大抑制者表现出独特的mRNA谱。与免疫、神经元活动和行为相关基因在这三组中差异表达。总的来说,回避与海洛因配对的味觉线索的个体差异与成瘾样行为以及NAc基因表达差异有关。