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Mirtazapine and ketanserin alter preference for gambling-like schedules of reinforcement in rats

机译:米氮平和酮色林改变了大鼠对赌博样强化时间表的偏好

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摘要

Drug and behavioral addictions have overlapping features, e.g., both manifest preference for larger, albeit costlier, reinforcement options in cost/benefit decision-making tasks. Our prior work revealed that the mixed-function serotonergic compound, mirtazapine, attenuates behaviors by rats motivated by abused drugs. To extend this work to behavioral addictions, here we determined if mirtazapine and/or ketanserin, another mixed-function serotonin-acting compound, can alter decision-making in rats that is independent of drug (or food)-motivated reward. Accordingly, we developed a novel variable-ratio task in rats wherein intracranial self-stimulation was used as the positive reinforcer. Using lever pressing for various levels of brain stimulation, the operant task provided choices between a small brain stimulation current delivered on a fixed-ratio schedule (i.e., a predictable reward) and a large brain stimulation delivered following an unpredictable number of responses (i.e., a variable-ratio schedule). This task allowed for demonstration of individualized preference and detection of shifts in motivational influences during a pharmacological treatment. Once baseline preference was established, we determined that pretreatment with mirtazapine or ketanserin significantly decreased preference for the large reinforcer presented after gambling-like schedules of reinforcement. When the rats were tested the next day without drug, preference for the unpredictable large reinforcer option was restored. These data demonstrate that mirtazapine and ketanserin can reduce preference for larger, costlier reinforcement options, and illustrate the potential for these drugs to alter behavior.
机译:毒品和行为上瘾具有重叠的特征,例如,在成本/收益决策任务中,两者都表现出偏好更大,成本更高的强化选择。我们以前的工作表明,多功能的5-羟色胺能化合物米氮平可减弱药物滥用引起的大鼠的行为。为了将这项工作扩展到行为成瘾,我们在这里确定了米氮平和/或酮色林(另一种具有多种功能的5-羟色胺作用化合物)是否可以改变大鼠的决策,而这种决策独立于药物(或食物)激励。因此,我们开发了一种新的大鼠可变比率任务,其中颅内自我刺激被用作正强化剂。通过使用杠杆按压来进行各种级别的脑部刺激,操作任务可以在固定比例的时间表(即可预期的奖励)上传递小脑部刺激电流,以及在响应次数无法预测(例如,可变比率的时间表)。这项任务可以论证个性化的偏爱并在药理学治疗过程中检测动机影响的变化。一旦建立了基线偏好,我们就确定了用米氮平或酮色林预处理可以显着降低对像赌博般的强化时间表后出现的大型强化剂的偏好。第二天在不使用药物的情况下对大鼠进行了测试,恢复了对不可预知的大型增强剂选择的偏好。这些数据表明,米氮平和酮色林可以减少对更大,更昂贵的增强药物选择的偏好,并说明这些药物改变行为的潜力。

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