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大鼠冲动性与 MDPV 自身给药的相互作用。

Interactions between impulsivity and MDPV self-administration in rats.

机构信息

Department of Pharmacology, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.

South Texas Veterans Health Care System, San Antonio, Texas, USA.

出版信息

Addict Biol. 2022 May;27(3):e13168. doi: 10.1111/adb.13168.

Abstract

Synthetic cathinones, such as 3,4-methylenedioxypyrovalerone (MDPV), are recreational drugs of abuse often identified in 'bath salts' preparations. Humans report compulsive patterns of bath salts use, and previous work suggests that a subset of rats develop unusually high levels of MDPV self-administration. This study aims to test the hypothesis that high levels of impulsivity (e.g., inability to withhold responding for a sucrose reward) will predispose rats to high levels of MDPV self-administration relative to rats with lower levels of impulsivity. The 1-choice serial reaction time task (1-CSRTT) was used to assess impulsivity (i.e., premature responding) in 10 female and 10 male Sprague Dawley rats. Rats were then allowed to self-administer 0.032 mg/kg/inf MDPV or 0.32 mg/kg/inf cocaine, after which full dose-response curves for MDPV (0.001-0.1 mg/kg/inf) or cocaine (0.01-1 mg/kg/inf) were generated under a FR5 schedule of reinforcement. After a history of self-administering MDPV or cocaine, impulsivity was reassessed under the 1-CSRTT, prior to evaluating the acute effects of MDPV (0.032-0.32 mg/kg) or cocaine (0.1-1 mg/kg) on impulsivity. Level of impulsivity was not correlated with subsequent levels of either MDPV or cocaine self-administration, and level of drug self-administration was also not correlated with subsequent levels of impulsivity, although acute administration of MDPV and cocaine did increase premature responding. In failing to find direct relationships between either impulsivity and subsequent drug-taking behaviour, or drug-taking behaviour and subsequent assessments of impulsivity, these findings highlight the complexity inherent in the associations between impulsive behaviour and drug-taking behaviour in both animal models and humans.

摘要

合成卡西酮,如 3,4-亚甲二氧基吡咯戊酮(MDPV),是常被鉴定为“浴盐”制剂的娱乐性滥用药物。人类报告说有强迫性的使用浴盐的行为,先前的研究表明,一部分大鼠会出现异常高的 MDPV 自我给药水平。本研究旨在验证这样一个假设,即高水平的冲动性(例如,无法为了获得蔗糖奖励而抑制反应)将使大鼠相对于冲动性较低的大鼠更容易产生高水平的 MDPV 自我给药。1 选择序列反应时间任务(1-CSRTT)用于评估 10 只雌性和 10 只雄性 Sprague Dawley 大鼠的冲动性(即过早反应)。然后,让大鼠自行注射 0.032mg/kg/inf 的 MDPV 或 0.32mg/kg/inf 的可卡因,之后在 FR5 强化方案下生成 MDPV(0.001-0.1mg/kg/inf)或可卡因(0.01-1mg/kg/inf)的全剂量反应曲线。在有自行注射 MDPV 或可卡因的历史后,在 1-CSRTT 下重新评估冲动性,然后评估 MDPV(0.032-0.32mg/kg)或可卡因(0.1-1mg/kg)对冲动性的急性影响。冲动性水平与随后的 MDPV 或可卡因自我给药水平均无相关性,药物自我给药水平也与随后的冲动性水平无相关性,尽管 MDPV 和可卡因的急性给药确实增加了过早反应。未能发现冲动性与随后的药物摄取行为之间或药物摄取行为与随后的冲动性评估之间存在直接关系,这些发现强调了动物模型和人类中冲动行为与药物摄取行为之间的关联所固有的复杂性。

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