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恒河猴中奈法唑酮自我给药的评估。

Evaluation of nefazodone self-administration in rhesus monkeys.

作者信息

Gold L H, Balster R L

机构信息

Department of Pharmacology and Toxicology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0613.

出版信息

Drug Alcohol Depend. 1991 Oct;28(3):241-7. doi: 10.1016/0376-8716(91)90057-6.

Abstract

Intravenous self-administration of nefazodone, a potential new antidepressant medication, was evaluated using a substitution procedure in rhesus monkeys. Subjects had established stable rates of responding for cocaine (0.033 mg/kg per infusion) under a fixed-ratio 10 schedule during 60-min sessions each day. Various does of nefazodone hydrochloride (0.03-0.3 mg/kg per infusion) were substituted for cocaine for four consecutive daily self-administration sessions. Compared to rates of responding obtained during saline substitutions, nefazodone failed to function as a reinforcer when substituted for cocaine. In only one monkey, at one dose, did the rate of responding exceed the range of saline responding; an effect not observed in two subsequent replications in that subject. In all three monkeys, the total number of infusions tended to decrease during the 4-day nefazodone substitution and the majority of nefazodone infusions occurred during the first quarter of each session, with few infusions occurring in the latter three-quarters. Overall intake of nefazodone increased as a function of dose per infusion. Such a result is expected when response rates do not vary with dose, which is more likely to occur when a test drug is not a reinforcer. In summary, the present results provide no evidence of reinforcing effects with nefazodone and suggest that it would possess little or no abuse liability.

摘要

使用替代程序在恒河猴中评估了一种潜在的新型抗抑郁药物奈法唑酮的静脉自我给药情况。实验对象在每天60分钟的实验时段内,按照固定比例10的程序,对可卡因(每次输注0.033毫克/千克)建立了稳定的反应率。将各种剂量的盐酸奈法唑酮(每次输注0.03 - 0.3毫克/千克)连续4天替代可卡因进行自我给药实验。与盐水替代期间获得的反应率相比,奈法唑酮替代可卡因时未能起到强化物的作用。只有一只猴子在一种剂量下的反应率超过了盐水反应的范围;在该实验对象随后的两次重复实验中未观察到这种效应。在所有三只猴子中,在4天的奈法唑酮替代期间,输注总数趋于减少,并且大多数奈法唑酮输注发生在每个实验时段的第一季度,后三个季度的输注很少。奈法唑酮的总体摄入量随每次输注剂量的增加而增加。当反应率不随剂量变化时,会出现这样的结果,当受试药物不是强化物时更可能发生这种情况。总之,目前的结果没有提供奈法唑酮具有强化作用的证据,并表明它几乎没有或没有滥用可能性。

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