Gordon-Fennell L, Farero R D, Burgeno L M, Murray N L, Abraham A D, Soden M E, Stuber G D, Chavkin C, Zweifel L S, Phillips P E M
Graduate Program in Neuroscience, University of Washington, Seattle, WA 98195.
Center for Neurobiology of Addiction, Pain & Emotion, University of Washington, Seattle, WA 98195.
bioRxiv. 2023 Dec 23:2023.12.21.572842. doi: 10.1101/2023.12.21.572842.
Increases in drug consumption over time, also known as escalation, is a key behavioral component of substance use disorder (SUD) that is related to potential harm to users, such as overdose. Studying escalation also allows researchers to investigate the transition from casual drug use to more SUD-like drug use. Understanding the neurobiological systems that drive this transition will inform therapeutic treatments in the aim to prevent increases in drug use and the development of SUD. The kappa opioid receptor (KOR) system is typically known for its role in negative affect, which is commonly found in SUD as well. Furthermore, the KOR system has also been implicated in drug use and importantly, modulating the negative effects of drug use. However, the specific neuronal subpopulation expressing KOR involved has not been identified. Here, we first demonstrated that pharmacologically inhibiting KOR in the nucleus accumbens core (NAcC), as a whole, blocks cocaine escalation under long-access self-administration conditions. We then demonstrated that KOR expressed on ventral tegmental area (VTA) neurons but not NAcC neurons is sufficient for blocking cocaine escalation by utilizing a novel virally-mediated CRISPR-SaCas9 knock-out of the gene. Together, this suggests that activation of KOR on VTA terminals in the NAcC drives the transition to the SUD-like phenotype of escalation of cocaine consumption.
随着时间的推移,药物消费量的增加,也称为剂量递增,是物质使用障碍(SUD)的一个关键行为组成部分,与对使用者的潜在危害有关,如过量用药。研究剂量递增还使研究人员能够调查从偶尔吸毒到更类似物质使用障碍的吸毒行为的转变。了解驱动这种转变的神经生物学系统将为治疗方法提供依据,以防止药物使用量增加和物质使用障碍的发展。κ阿片受体(KOR)系统通常因其在负面影响中的作用而为人所知,这种负面影响在物质使用障碍中也很常见。此外,KOR系统也与药物使用有关,重要的是,它能调节药物使用的负面影响。然而,尚未确定表达KOR的具体神经元亚群。在这里,我们首先证明,在长期获取自我给药条件下,整体上药理抑制伏隔核核心(NAcC)中的KOR可阻断可卡因剂量递增。然后,我们利用一种新型病毒介导的基因CRISPR-SaCas9敲除技术,证明腹侧被盖区(VTA)神经元而非NAcC神经元上表达的KOR足以阻断可卡因剂量递增。总之,这表明激活NAcC中VTA终末上的KOR会驱动向可卡因消费剂量递增的类似物质使用障碍表型的转变。