Suppr超能文献

苯双甲吗啉和苯甲吗啉在大鼠体内产生类似可卡因的辨别刺激效应。

Cocaine-like discriminative stimulus effects of phendimetrazine and phenmetrazine in rats.

作者信息

Bauer Clayton T, Negus S Stevens, Blough Bruce E, Banks Matthew L

机构信息

aDepartment of Pharmacology and Toxicology bInstitute for Drug and Alcohol Studies, Virginia Commonwealth University, Richmond, Virginia cCenter for Drug Discovery, Research Triangle Institute, Research Triangle Park, North Carolina, USA.

出版信息

Behav Pharmacol. 2016 Apr;27(2-3 Spec Issue):192-5. doi: 10.1097/FBP.0000000000000225.

Abstract

Phendimetrazine is a clinically available anorectic and candidate medication for the treatment of cocaine addiction. Phendimetrazine can be metabolized to the amphetamine-like monoamine releaser phenmetrazine, but it is unclear if phendimetrazine functions as an inactive prodrug or might have activity on its own. As one method to address this issue, the present study compared the potency and time course of phendimetrazine and phenmetrazine to produce cocaine-like discriminative stimulus effects in adult, male rats (N=5) trained to discriminate cocaine (5.6 mg/kg, intraperitoneally) from saline in a two-key food-reinforced discrimination procedure. We hypothesized that, if metabolism to phenmetrazine was required for phendimetrazine effects, then phendimetrazine would be less potent and have a slower onset and offset of effects than phenmetrazine. Both phendimetrazine and phenmetrazine produced dose-dependent cocaine-like discriminative stimulus effects, and phendimetrazine was 7.8-fold less potent than phenmetrazine. However, the time courses of discriminative stimulus effects produced by phendimetrazine and phenmetrazine were similar, with peak effects at 10 min and offset by 100 min. These results show the effectiveness of phendimetrazine to rapidly produce cocaine-like behavioral effects in rats and support other nonhuman primate evidence to suggest that metabolism to phenmetrazine may not be required for phendimetrazine effects.

摘要

苯双甲吗啉是一种临床上可用的食欲抑制剂,也是治疗可卡因成瘾的候选药物。苯双甲吗啉可代谢为苯丙胺样单胺释放剂苯甲吗啉,但尚不清楚苯双甲吗啉是作为无活性前药发挥作用,还是本身可能具有活性。作为解决这一问题的一种方法,本研究比较了苯双甲吗啉和苯甲吗啉在成年雄性大鼠(N = 5)中产生可卡因样辨别刺激效应的效力和时程。这些大鼠通过双键食物强化辨别程序接受训练,以区分可卡因(5.6毫克/千克,腹腔注射)和生理盐水。我们假设,如果苯双甲吗啉的作用需要代谢为苯甲吗啉,那么苯双甲吗啉的效力会更低,起效和作用消失的时间会比苯甲吗啉更慢。苯双甲吗啉和苯甲吗啉均产生剂量依赖性的可卡因样辨别刺激效应,且苯双甲吗啉的效力比苯甲吗啉低7.8倍。然而,苯双甲吗啉和苯甲吗啉产生的辨别刺激效应的时程相似,在10分钟时达到峰值效应,并在100分钟时消失。这些结果表明苯双甲吗啉能在大鼠中迅速产生可卡因样行为效应,并支持其他非人类灵长类动物研究的证据,表明苯双甲吗啉的作用可能不需要代谢为苯甲吗啉。

相似文献

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验