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甲基甲卡西酮和 3-Cl-甲基甲卡西酮(PAL-434)对恒河猴可卡因辨别或自我给药的影响。

Effects of methcathinone and 3-Cl-methcathinone (PAL-434) in cocaine discrimination or self-administration in rhesus monkeys.

机构信息

Alcohol and Drug Abuse Research Center, McLean Hospital, Harvard Medical School, Belmont, MA, USA.

出版信息

Int J Neuropsychopharmacol. 2013 Oct;16(9):1985-98. doi: 10.1017/S146114571300059X. Epub 2013 Jun 17.

Abstract

Monoamine releasers with varying selectivity for dopamine (DA)/norepinephrine and serotonin (5-HT) release are potential treatment medications for cocaine abuse. Although DA-selective monoamine releasers effectively reduce cocaine abuse, their clinical usefulness is limited by abuse liability. It is hypothesized that increasing 5-HT neurotransmission may reduce the abuse-related effects of DA releasers, but the optimal DA:5-HT release ratio remains to be determined. This study in rhesus monkeys compared the effects of two compounds with differing potency for 5-HT release. Methcathinone and 3-Cl-methcathinone (PAL-434) have equal potency for DA release, but PAL-434 has 10-fold higher potency for 5-HT release. In drug discrimination studies, monkeys were trained to discriminate cocaine (0.4 mg/kg i.m.) from saline in a two-key, food-reinforced procedure. In drug self-administration studies, a separate group of monkeys was trained to respond for cocaine [0.01 mg/kg/injection (inj)] and food (1 g pellets) under a second order schedule of reinforcement [FR2(VR16:S)]. When responding was stable, methcathinone (0.1–0.56 mg/kg.h i.v.) or PAL-434 (0.32–1.8 mg/kg.h i.v.) was administered chronically (one injection every 20 min for 23 h/d) for 7–10 d. In discrimination studies, both compounds dose-dependently increased cocaine-like responding but with different potencies (cocaine=methcathinone >PAL-434). Chronic treatment with methcathinone or PAL-434 dose-dependently and selectively reduced cocaine self-administration. PAL-434 was about 4-fold and methcathinone about 1.6-fold more potent at decreasing cocaine- over food-maintained responding. These data suggest that compounds with moderate selectivity for DA vs. 5-HT release (8–15-fold) may be effective for the treatment of cocaine dependence.

摘要

具有不同多巴胺 (DA)/去甲肾上腺素和 5-羟色胺 (5-HT) 释放选择性的单胺释放剂是可卡因滥用的潜在治疗药物。虽然 DA 选择性单胺释放剂有效地减少了可卡因滥用,但它们的临床用途受到滥用倾向的限制。据推测,增加 5-HT 神经传递可能会降低 DA 释放剂的与滥用相关的作用,但最佳的 DA:5-HT 释放比例仍有待确定。这项在恒河猴中的研究比较了两种具有不同 5-HT 释放能力的化合物的作用。甲卡西酮和 3-Cl-甲卡西酮 (PAL-434) 对 DA 释放的效力相等,但 PAL-434 对 5-HT 释放的效力高 10 倍。在药物辨别研究中,猴子在一个双键、食物强化程序中接受训练,以辨别可卡因(0.4mg/kg 肌内注射)和生理盐水。在药物自我给药研究中,另一组猴子在二级强化程序[FR2(VR16:S)]下接受可卡因[0.01mg/kg/注射(inj)]和食物(1g 丸)的反应训练。当反应稳定时,甲卡西酮(0.1-0.56mg/kg·h 静脉内)或 PAL-434(0.32-1.8mg/kg·h 静脉内)以慢性方式(每天 23 小时内每 20 分钟注射一次)给药 7-10 天。在辨别研究中,两种化合物都剂量依赖性地增加了可卡因样反应,但效力不同(可卡因=甲卡西酮> PAL-434)。慢性给予甲卡西酮或 PAL-434 剂量依赖性地和选择性地减少可卡因自我给药。PAL-434 减少可卡因-而不是食物维持反应的效力约为甲卡西酮的 4 倍,而甲卡西酮减少可卡因-而不是食物维持反应的效力约为 1.6 倍。这些数据表明,对 DA 与 5-HT 释放具有中等选择性的化合物(8-15 倍)可能对可卡因依赖的治疗有效。

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