首页> 外文期刊>Behavioural Brain Research: An International Journal >Kappa opioid receptors mediate yohimbine-induced increases in impulsivity in the 5-choice serial reaction time task
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Kappa opioid receptors mediate yohimbine-induced increases in impulsivity in the 5-choice serial reaction time task

机译:Kappa阿片受体在5选择串行反应时间任务中介导育ohimbine诱导的脉冲增加的增加

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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.
机译:达诺啡因(DYN)及其受体,Kappa阿片受体(kor)参与了药物寻求和复发,但机制明显很差。一个假设是Dyn / Kor激活促进通过增加冲动的毒药,因为诱导Dyn释放的许多刺激增加冲动。在这里,我们系统地比较了在5选择串行反应时间任务(5-CSRTT)上的性能激活Dyn / Kor的药物的影响,持续关注和冲动的测试。在实验1中,确定U50,488(0,2.5,5mg / kg),育亨宾(0,1.25,2.5mg / kg)的效果,尼古丁(0,0.15,0.3mg / kg)在5-- CSRTT性能。在实验2中,我们确定了醇(0,0.5,1.0,1.0,1.5g / kg)在自愿,间歇性酒精暴露之前和之后的5-CSRTT性能的影响。在实验3中,我们确定了Kor在KOR拮抗剂NOR-BNI(10mg / kg)的先前施用中尤其滨(1.25mg / kg)和尼古丁(0.3mg / kg)的潜水作用的潜在作用。早泄,脉冲性的主要措施,由U50,488和酒精减少,但这些药物具有一般抑制作用。育亨宾和尼古丁提高过早响应。 Yohimbine-的,但不是尼古丁诱导的早熟响应的增加因NOR-BNI阻断,表明育亨宾诱导的冲动依赖性。这可能表明KOR介导的延髓诱导的恢复冲动的潜在作用。

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