哌醋甲酯对路易斯大鼠冲动选择和延迟厌恶的影响

IF 1.6 4区 心理学 Q3 BEHAVIORAL SCIENCES Behavioural Pharmacology Pub Date : 2023-04-01 Epub Date: 2023-01-30 DOI:10.1097/FBP.0000000000000719
Kelsey Panfil, Robert Small, Kimberly Kirkpatrick
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引用次数: 0

摘要

注意力缺陷/多动障碍(ADHD)是儿童和青少年常见的一种行为障碍,主要表现为冲动、注意力不集中和多动。本研究的目的是通过测试路易斯大鼠的冲动性选择,评估其作为多动症模型的能力。在冲动性选择任务中,刘易斯大鼠与其源品系 Wistar 大鼠进行了比较。大鼠在服用和停用哌醋甲酯(一种治疗多动症的常用处方药)的情况下完成任务。在停用哌醋甲酯后,刘易斯大鼠比威斯塔大鼠做出了更多的冲动性选择。对选择行为习得的分析表明,两个品系的大鼠都能分辨奖励的大小,但在奖励延迟时间相同的情况下,Lewis大鼠选择较小-较早选项的次数仍然多于选择较大-较晚(LL)选项的次数。这可能是由于LL杠杆与奖励延迟时间最长有关,使大鼠产生了厌恶感。高剂量的哌醋甲酯会增加路易斯大鼠对LL的选择,但会减少Wistar大鼠对LL的选择。总之,这些结果表明,刘易斯大鼠可能是以冲动性选择为症状特征的多动症的可行模型。
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Effects of methylphenidate on impulsive choice and delay aversion in Lewis rats.

Attention-deficit/hyperactivity disorder (ADHD), a common behavioral disorder in children and young adults, is characterized by symptoms of impulsivity, inattention, and hyperactivity. The purpose of this study was to evaluate the Lewis rat strain as a model of ADHD by testing their impulsive choices. Lewis rats were compared to their source strain, the Wistar rat, on an impulsive choice task. Rats completed the tasks on and off methylphenidate, a commonly prescribed medication for ADHD. Off methylphenidate, Lewis rats made more impulsive choices than Wistar rats. Analyses of acquisition of choice behavior suggested that both strains were able to discriminate reward sizes, but Lewis rats still chose the smaller-sooner option more than the larger-later (LL) option when the delays to reward were the same. This may be due to an aversion to the LL lever, which was associated with the longest delays to reward. Higher doses of methylphenidate increased LL choices in Lewis rats but decreased LL choices in Wistar rats. Altogether, these results suggest Lewis rats may be a viable model for ADHD in individuals whose symptoms are characterized by impulsive choices.

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来源期刊
Behavioural Pharmacology
Behavioural Pharmacology 医学-行为科学
CiteScore
3.40
自引率
0.00%
发文量
84
审稿时长
6-12 weeks
期刊介绍: Behavioural Pharmacology accepts original full and short research reports in diverse areas ranging from ethopharmacology to the pharmacology of schedule-controlled operant behaviour, provided that their primary focus is behavioural. Suitable topics include drug, chemical and hormonal effects on behaviour, the neurochemical mechanisms under-lying behaviour, and behavioural methods for the study of drug action. Both animal and human studies are welcome; however, studies reporting neurochemical data should have a predominantly behavioural focus, and human studies should not consist exclusively of clinical trials or case reports. Preference is given to studies that demonstrate and develop the potential of behavioural methods, and to papers reporting findings of direct relevance to clinical problems. Papers making a significant theoretical contribution are particularly welcome and, where possible and merited, space is made available for authors to explore fully the theoretical implications of their findings. Reviews of an area of the literature or at an appropriate stage in the development of an author’s own work are welcome. Commentaries in areas of current interest are also considered for publication, as are Reviews and Commentaries in areas outside behavioural pharmacology, but of importance and interest to behavioural pharmacologists. Behavioural Pharmacology publishes frequent Special Issues on current hot topics. The editors welcome correspondence about whether a paper in preparation might be suitable for inclusion in a Special Issue.
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