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高选择性多巴胺D3激动剂PF-592,379在大鼠药物自我给药和药物辨别实验中无滥用潜力。

Lack of abuse potential in a highly selective dopamine D3 agonist, PF-592,379, in drug self-administration and drug discrimination in rats.

作者信息

Collins Gregory T, Butler Paul, Wayman Chris, Ratcliffe Sian, Gupta Paul, Oberhofer Geoffrey, Caine S Barak

机构信息

Alcohol & Drug Abuse Research Center, Division of Neuroscience, McLean Hospital, Harvard Medical School, Belmont, Massachusetts 02478, USA.

出版信息

Behav Pharmacol. 2012 Jun;23(3):280-91. doi: 10.1097/FBP.0b013e3283536d21.

Abstract

Dopamine D3-preferring agonists are commonly used to treat Parkinson's disease and restless leg syndrome; however, laboratory animal studies suggest that they may possess a moderate abuse potential. These studies aimed to compare the highly selective, full D3 agonist PF-592,379 to the less selective D3 agonist 7-OH-DPAT, and the indirect dopamine agonist cocaine in drug self-administration and discrimination assays. Although rats readily acquired high rates of fixed ratio (FR)1 responding for cocaine, experimentally naive rats failed to acquire responding when 7-OH-DPAT or PF-592,379 was made available during an 18-session acquisition period. Cocaine also maintained dose-dependent levels of responding when available under a FR5 or a progressive ratio (PR) schedule of reinforcement. Although 7-OH-DPAT maintained modest levels of responding when substituted under a FR5, it failed to maintain significant levels of PR responding. PF-592,379 maintained saline-like rates of responding when substituted under FR5 or PR schedules of reinforcement. Similar behavioral profiles were observed in cocaine discrimination assays, with 7-OH-DPAT partially substituting for cocaine, and PF-592,379 producing saline-like effects over a wide range of doses. Together, the results of these studies predict that highly selective D3 agonists, such as PF-592,379, will have low abuse potential in humans.

摘要

偏爱多巴胺D3的激动剂常用于治疗帕金森病和不宁腿综合征;然而,实验动物研究表明它们可能具有一定程度的滥用潜力。这些研究旨在在药物自我给药和辨别试验中,将高选择性的、完全D3激动剂PF-592,379与选择性较低的D3激动剂7-羟基-DPAT以及间接多巴胺激动剂可卡因进行比较。虽然大鼠很容易学会为可卡因按固定比率(FR)-1快速做出反应,但未经实验的大鼠在18节的习得期内可获得7-羟基-DPAT或PF-592,379时却未能学会做出反应。当可卡因在FR-5或累进比率(PR)强化程序下可用时,也能维持剂量依赖性的反应水平。虽然7-羟基-DPAT在FR-5替代时能维持适度的反应水平,但它未能维持显著水平的PR反应。当PF-592,379在FR-5或PR强化程序下替代时,维持类似生理盐水的反应率。在可卡因辨别试验中观察到类似的行为特征,7-羟基-DPAT部分替代可卡因,而PF-592,379在很宽的剂量范围内产生类似生理盐水的效应。总之,这些研究结果预测,高选择性的D3激动剂,如PF-592,379,在人类中的滥用潜力较低。

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