Funk D, Tamadon S, Coen K, Fletcher P J, Lê A D
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.
Behav Brain Res. 2019 Feb 1;359:258-265. doi: 10.1016/j.bbr.2018.11.006. Epub 2018 Nov 8.
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.
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。