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κ阿片受体介导育亨宾在5选串行反应时任务中引起的冲动性增加。

Kappa opioid receptors mediate yohimbine-induced increases in impulsivity in the 5-choice serial reaction time task.

作者信息

Funk D, Tamadon S, Coen K, Fletcher P J, Lê A D

机构信息

Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.

Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.

出版信息

Behav Brain Res. 2019 Feb 1;359:258-265. doi: 10.1016/j.bbr.2018.11.006. Epub 2018 Nov 8.

DOI:10.1016/j.bbr.2018.11.006
PMID:30414973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6309760/
Abstract

Dynorphin (DYN), and its receptor, the kappa opioid receptor (KOR) are involved in drug seeking and relapse but the mechanisms are poorly understood. One hypothesis is that DYN/KOR activation promotes drug seeking through increased impulsivity, because many stimuli that induce DYN release increase impulsivity. Here, we systematically compare the effects of drugs that activate DYN/KOR on performance on the 5-choice serial reaction time task (5-CSRTT), a test of sustained attention and impulsivity. In Experiment 1, we determined the effects of U50,488 (0, 2.5, 5 mg/kg), yohimbine (0, 1.25, 2.5 mg/kg), and nicotine (0, 0.15, 0.3 mg/kg) on 5-CSRTT performance. In Experiment 2, we determined the effects of alcohol (0, 0.5, 1.0, 1.5 g/kg) on 5-CSRTT performance before and after voluntary, intermittent alcohol exposure. In Experiment 3, we determined the potential role of KOR in the pro-impulsive effects of yohimbine (1.25 mg/kg) and nicotine (0.3 mg/kg) by the prior administration of the KOR antagonist nor-BNI (10 mg/kg). Premature responding, the primary measure of impulsivity, was reduced by U50,488 and alcohol, but these drugs had a general suppressive effect. Yohimbine and nicotine increased premature responding. Yohimbine-, but not nicotine-induced increases in premature responding were blocked by nor-BNI, suggesting that impulsivity induced by yohimbine is KOR dependent. This may suggests a potential role for KOR-mediated increases in impulsivity in yohimbine-induced reinstatement.

摘要

强啡肽(DYN)及其受体κ-阿片受体(KOR)参与觅药和复发过程,但其机制尚不清楚。一种假说是,DYN/KOR激活通过增加冲动性来促进觅药行为,因为许多诱导DYN释放的刺激都会增加冲动性。在此,我们系统地比较了激活DYN/KOR的药物对5选串行反应时任务(5-CSRTT)表现的影响,该任务是一项持续注意力和冲动性测试。在实验1中,我们确定了U50,488(0、2.5、5mg/kg)、育亨宾(0、1.25、2.5mg/kg)和尼古丁(0、0.15、0.3mg/kg)对5-CSRTT表现的影响。在实验2中,我们确定了酒精(0、0.5、1.0、1.5g/kg)在自愿间歇性酒精暴露前后对5-CSRTT表现的影响。在实验3中,我们通过预先给予KOR拮抗剂nor-BNI(10mg/kg)来确定KOR在育亨宾(1.25mg/kg)和尼古丁(0.3mg/kg)的促冲动效应中的潜在作用。过早反应是冲动性的主要衡量指标,U50,488和酒精可降低过早反应,但这些药物具有普遍的抑制作用。育亨宾和尼古丁增加了过早反应。nor-BNI可阻断育亨宾而非尼古丁引起的过早反应增加,这表明育亨宾诱导的冲动性是KOR依赖性的。这可能暗示KOR介导的冲动性增加在育亨宾诱导的复吸中具有潜在作用。

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κ-Opioid Receptor Activation in Dopamine Neurons Disrupts Behavioral Inhibition.κ-阿片受体在多巴胺神经元中的激活会破坏行为抑制。
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Dissociable effects of systemic and orbitofrontal administration of adrenoceptor antagonists on yohimbine-induced motor impulsivity.全身和眶额部给予肾上腺素能受体拮抗剂对育亨宾诱导的运动冲动性的不同影响。
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Repeated nicotine exposure modulates prodynorphin and pronociceptin levels in the reward pathway.反复接触尼古丁会调节奖赏通路中前强啡肽和前痛敏肽的水平。
Drug Alcohol Depend. 2016 Sep 1;166:150-8. doi: 10.1016/j.drugalcdep.2016.07.002. Epub 2016 Jul 12.
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Dynorphin, Dysphoria, and Dependence: the Stress of Addiction.强啡肽、烦躁不安与成瘾:成瘾的压力
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Dissociating Motivational From Physiological Withdrawal in Alcohol Dependence: Role of Central Amygdala κ-Opioid Receptors.区分酒精依赖中动机性戒断与生理性戒断:中央杏仁核κ-阿片受体的作用
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