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合成卡西酮 3,4-亚甲二氧基吡咯戊酮增加大鼠的冲动行为。

The synthetic cathinone 3,4-methylenedioxypyrovalerone increases impulsive action in rats.

机构信息

Department of Pharmacology and Toxicology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas.

Department of Pharmaceutical Sciences, College of Pharmacy, Mercer University, Atlanta, Georgia.

出版信息

Behav Pharmacol. 2020 Jun;31(4):309-321. doi: 10.1097/FBP.0000000000000548.

Abstract

A previous study from our laboratory has shown that the selective catecholamine reuptake inhibitor 3,4-methylenedioxypyrovalerone (MDPV) persistently alters impulsive choice as measured by delay discounting. To further understand the proimpulsive effects of MDPV, we examined its capacity to modulate a different impulsive measure - impulsive action - using a differential reinforcement of low rates of responding task with an inter-response time of 20 s. Three groups of male, Sprague-Dawley rats (n = 6) were first tested in daily sessions to understand the acute effects of cocaine (1.0-30.0 mg/kg), MDPV (0.1-3.0 mg/kg), or saline (1.0 ml/kg) on impulsive action. Both cocaine and MDPV increased impulsive action, most notably by decreasing timing error responses and response efficiency, but MDPV was more effective than cocaine. Additionally, MDPV suppressed operant responding in two of six animals at the highest dose tested. Next, the same animals received 10 postsession injections, once every other day, of either 30.0 mg/kg cocaine, 3.0 mg/kg MDPV, or 1.0 ml/kg saline based on their treatment group. An acute dose-effect redetermination was completed following the repeated administration studies, and once again MDPV and cocaine demonstrated proimpulsive effects. Interestingly, timing error responses were decreased in both MDPV and cocaine groups after an acute saline injection, potentially indicating persistent impulsive changes following the repeated administration phase of the experiment. These studies indicate that MDPV increases impulsive action acutely and that this increase may be potentiated following a series of repeated administrations.

摘要

先前,我们实验室的一项研究表明,选择性儿茶酚胺再摄取抑制剂 3,4-亚甲二氧基吡咯戊酮(MDPV)可持续改变延迟折扣测量的冲动选择。为了进一步了解 MDPV 的促冲动作用,我们使用 20 秒间隔的低反应率强化程序,检查了其调制不同冲动测量的能力-冲动行为。三组雄性 Sprague-Dawley 大鼠(n=6)首先在每日试验中进行测试,以了解可卡因(1.0-30.0mg/kg)、MDPV(0.1-3.0mg/kg)或生理盐水(1.0ml/kg)对冲动行为的急性作用。可卡因和 MDPV 均增加冲动行为,最明显的是通过减少时间误差反应和反应效率,但 MDPV 比可卡因更有效。此外,在最高测试剂量下,MDPV 抑制了六个动物中的两个的操作性反应。接下来,相同的动物根据其治疗组接受了 10 次会话后注射,每两天一次,分别为 30.0mg/kg 可卡因、3.0mg/kg MDPV 或 1.0ml/kg 生理盐水。在重复给药研究完成后,进行了急性剂量效应重新测定,结果表明 MDPV 和可卡因再次表现出促冲动作用。有趣的是,在急性生理盐水注射后,MDPV 和可卡因组的时间误差反应均减少,这可能表明在实验的重复给药阶段后,冲动变化持续存在。这些研究表明,MDPV 可急性增加冲动行为,并且这种增加可能在一系列重复给药后增强。

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