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甲基苯丙胺自我给药后,嗅周皮质至伏隔核回路在新奇显著性中的作用

Perirhinal cortex to the nucleus accumbens circuit in novelty salience following methamphetamine self-administration.

作者信息

Nelson Katharine H, Freels Dylan L, Carter Jordan S, Wood Samuel K, Denton Adam R, Hopkins Jordan L, Goldsmith Sarah T, Lewandowski Stacia I, Scofield Michael D, Reichel Carmela M

机构信息

Department of Neuroscience, Medical University of South Carolina, Basic Science Building 416, MSC 510, 173 Ashley Avenue, Charleston, SC 29425, USA.

Department of Anesthesia and Perioperative Medicine, Medical University of South Carolina, Charleston, SC, USA.

出版信息

Addict Neurosci. 2024 Dec;13. doi: 10.1016/j.addicn.2024.100181. Epub 2024 Oct 14.

Abstract

Methamphetamine (meth) use disorder is part of an overarching use disorder that encompasses continued drug seeking and an increased risk of returning to drug use following periods of abstaining. Chronic meth use results in drug-induced cortical plasticity in the perirhinal cortex (PRC) that mediates responses to novelty. PRH projection targets are numerous and include the nucleus accumbens core (NAc). Whereas the PRH-prefrontal cortex is involved in object recognition; we propose that the PRH-NAc is involved in novelty salience. Rats underwent short-access (ShA, 1 hr) or long-access (LgA, 6 hr) meth self-administration (SA). We then used a dual viral strategy to inhibit or activate PRH-NAc during a novel cue test in which rats were presented with meth-associated and novel levers. Response patterns on these levers differ depending on the meth access protocol: ShA meth SA results in equal responding on both novel- and meth-associated levers, whereas LgA meth results in perseverative responding on the meth-associated lever. Inactivation of the PRH-NAc increased responding on the meth lever relative to the novel lever, resulting in a LgA behavioral phenotype. In contrast, activation in LgA rats was without a behavioral effect. We also report that male LgA sucrose SA animals perseverated on the novel lever rather than the meth-associated lever, which contrast their meth SA counter parts and female specific patterns of behavior. These data open a new line of interest in the role of the PRH-NAc circuit in novelty salience through identification of the behavioral relevance of this circuit.

摘要

甲基苯丙胺(冰毒)使用障碍是一种总体使用障碍的一部分,该障碍包括持续的药物寻求行为以及在戒断一段时间后复吸风险的增加。长期使用冰毒会导致药物诱导的鼻周皮质(PRC)可塑性,该皮质介导对新奇事物的反应。PRH的投射靶点众多,包括伏隔核核心(NAc)。虽然PRH-前额叶皮质参与物体识别;但我们提出PRH-NAc参与新奇显著性。大鼠接受了短时间接触(ShA,1小时)或长时间接触(LgA,6小时)的冰毒自我给药(SA)。然后,我们采用双重病毒策略,在新奇线索测试中抑制或激活PRH-NAc,在此测试中,向大鼠呈现与冰毒相关的杠杆和新奇杠杆。这些杠杆上的反应模式因冰毒接触方案而异:ShA冰毒SA导致对新奇杠杆和与冰毒相关杠杆的反应相同,而LgA冰毒导致对与冰毒相关杠杆的持续反应。PRH-NAc的失活相对于新奇杠杆增加了对冰毒杠杆的反应,导致出现LgA行为表型。相比之下,LgA大鼠中的激活没有行为效应。我们还报告说,雄性LgA蔗糖SA动物在新奇杠杆上持续反应,而不是在与冰毒相关的杠杆上,这与它们的冰毒SA对应物和雌性特定行为模式形成对比。这些数据通过确定该回路的行为相关性,开启了对PRH-NAc回路在新奇显著性中作用的新研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec2/11633022/303885425c58/nihms-2039257-f0001.jpg

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