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卡利拉嗪(RGH-188)是一种 D₃ 偏好的多巴胺 D₃/D₂ 受体部分激动剂抗精神病候选药物,在大鼠中显示出抗滥用潜力。

Cariprazine (RGH-188), a D₃-preferring dopamine D₃/D₂ receptor partial agonist antipsychotic candidate demonstrates anti-abuse potential in rats.

机构信息

Pharmacology and Drug Safety Research, Gedeon Richter Plc, Budapest, Hungary.

出版信息

Psychopharmacology (Berl). 2013 Mar;226(2):285-93. doi: 10.1007/s00213-012-2906-7. Epub 2012 Nov 9.

Abstract

RATIONALE

Cariprazine (RGH-188) is a D₃-preferring dopamine D₃/D₂ receptor partial agonist antipsychotic candidate for the treatment of schizophrenia and bipolar mania. Substance abuse is a frequent comorbidity of both disorders and is associated with serious health issues. Based on preclinical efficacy, dopamine D₂ and D₃ receptor partial agonists and antagonists are assumed to have relapse-preventing potential in human cocaine addiction.

OBJECTIVES

We investigated the anti-abuse potential of cariprazine in cocaine self-administration paradigms. Aripiprazole and bifeprunox were used as comparators because of their pharmacological similarity to cariprazine.

METHODS

The effects of compounds on cocaine's rewarding effect were investigated in a continuous self-administration regimen. The relapse-preventing potential of drugs was studied in rats with a history of cocaine self-administration after a period of complete abstinence in a relapse to cocaine-seeking paradigm.

RESULTS

Cariprazine, as well as aripiprazole and bifeprunox, were able to reduce the rewarding effect of cocaine (minimum effective doses were 0.17, 1, and 0.1 mg/kg, respectively) and attenuated relapse to cocaine seeking with half maximal effective dose [ED₅₀] values of 0.2, 4.2, and 0.17 mg/kg, respectively.

CONCLUSIONS

These results may predict a relapse-preventing action for cariprazine in humans in addition to its already established antipsychotic and antimanic efficacy.

摘要

理由

卡利拉嗪(RGH-188)是一种 D₃ 优先的多巴胺 D₃/D₂ 受体部分激动剂抗精神病候选药物,用于治疗精神分裂症和双相躁狂症。物质滥用是这两种疾病的常见共病,与严重的健康问题有关。基于临床前疗效,多巴胺 D₂ 和 D₃ 受体部分激动剂和拮抗剂被认为具有预防可卡因成瘾复发的潜力。

目的

我们研究了卡利拉嗪在可卡因自我给药范式中的抗滥用潜力。阿立哌唑和双氟平诺被用作比较剂,因为它们与卡利拉嗪在药理学上相似。

方法

在连续自我给药方案中研究了化合物对可卡因奖赏效应的影响。在可卡因自我给药史的大鼠中,在完全戒断一段时间后,在可卡因寻求范式中研究药物的复发预防潜力。

结果

卡利拉嗪,以及阿立哌唑和双氟平诺,都能够降低可卡因的奖赏效应(最低有效剂量分别为 0.17、1 和 0.1 毫克/千克),并分别以 0.2、4.2 和 0.17 毫克/千克的半数最大有效剂量[ED₅₀]值减弱可卡因寻求的复发。

结论

这些结果可能预示着卡利拉嗪除了已确立的抗精神病和抗躁狂作用外,还具有预防复发的作用。

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