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首页> 外文期刊>Neuropsychopharmacology >Aripiprazole Attenuates the Discriminative-Stimulus and Subject-Rated Effects of D-Amphetamine in Humans
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Aripiprazole Attenuates the Discriminative-Stimulus and Subject-Rated Effects of D-Amphetamine in Humans

机译:阿立哌唑减弱人体内D-苯丙胺的鉴别刺激和受试者评级的作用

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摘要

The results of animal research suggest that the use of partial agonists at dopamine (DA) D2 receptors may be an effective strategy for the treatment of stimulant dependence. Aripiprazole is an atypical antipsychotic that has partial agonist activity at D2 receptors. In this experiment, seven human participants with a history of nontherapeutic stimulant use learned to discriminate 15mg oral D-amphetamine. After acquiring the discrimination (ie 80% correct responding on four consecutive sessions), the effects of a range of doses of D-amphetamine (0, 2.5, 5, 10, and 15mg), alone and in combination with aripiprazole (0 and 20mg), were assessed. D-Amphetamine alone functioned as a discriminative stimulus, produced prototypical subject-rated drug effects (eg increased ratings of Active, Alert, Energetic) and elevated cardiovascular indices. These effects were generally a function of dose. Aripiprazole alone did not occasion D-amphetamine-appropriate responding or produce subject-rated effects, but modestly impaired performance. Administration of aripiprazole significantly attenuated the discriminative-stimulus and cardiovascular effects of D-amphetamine, as well as some of the subject-rated drug effects. These data are consistent with previous preclinical findings and suggest that DA partial agonists deserve further evaluation as potential pharmacotherapies in the management of stimulant dependence. Future studies should investigate the ability of aripiprazole or related compounds to attenuate the behavioral effects of stimulants associated with a greater degree of dependence, such as methamphetamine or cocaine, in dependent individuals.
机译:动物研究的结果表明,对多巴胺(DA)D2受体使用部分激动剂可能是治疗兴奋剂依赖性的有效策略。阿立哌唑是一种非典型的抗精神病药,对D2受体具有部分激动剂活性。在该实验中,有七位具有非治疗性兴奋剂使用史的人类受试者学会了区分15mg口服D-苯异丙胺。在获得辨别力(即在连续四个疗程中有80%正确的应答)后,单独或与阿立哌唑(0和20mg),进行评估。单独的D-苯丙胺起到区分性刺激的作用,产生原型评价的受试者药物作用(例如,主动,警觉,精力充沛的等级增加)和心血管指数升高。这些作用通常是剂量的函数。单独使用阿立哌唑不会引起适当的D-苯丙胺反应或产生受试者所评价的效果,但会适度损害其性能。阿立哌唑的给药显着减弱了D-苯异丙胺的歧视性刺激和心血管作用,以及某些受受试者评定的药物作用。这些数据与以前的临床前发现一致,并建议将DA部分激动剂作为刺激物依赖管理中的潜在药物疗法进行进一步评估。未来的研究应研究阿立哌唑或相关化合物减弱依赖人群中与高度依赖相关的兴奋剂(如甲基苯丙胺或可卡因)的行为影响的能力。

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