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N-甲基苯丙胺和N,N-二甲基苯丙胺对大鼠和松鼠猴的行为影响。

Behavioral effects of N-methylamphetamine and N,N-dimethylamphetamine in rats and squirrel monkeys.

作者信息

Witkin J M, Ricaurte G A, Katz J L

机构信息

Psychobiology Laboratory, National Institute on Drug Abuse, Addiction Research Center, Baltimore, Maryland.

出版信息

J Pharmacol Exp Ther. 1990 May;253(2):466-74.

PMID:2338643
Abstract

The N-methylated derivative of N-methamphetamine (MA), N,N-dimethylamphetamine (NNDMA), has recently been synthesized for illicit use. The present study compared the psychomotor stimulant, discriminative stimulus, reinforcing and lethal effects of these analogs in rats and squirrel monkeys. NNDMA was 6 to 12 times less potent than MA in decreasing rates of responding in rats or monkeys under fixed interval or fixed ratio schedules of food presentation. Both MA and NNDMA produced dose-dependent increases in the percentage of cocaine-lever responses in rats trained to discriminate 10 mg/kg of cocaine from saline, with NNDMA 12 times less potent than MA. Response-produced i.v. infusions of MA or NNDMA maintained rates of responding that were higher than those maintained by saline infusions in squirrel monkeys trained to self-administer cocaine; NNDMA was 10 times less potent than MA in producing these reinforcing effects. Both drugs increased fixed interval responding in squirrel monkeys; MA was more efficacious than NNDMA. MA also increased rates of responding in rats during time-out periods in which responses had no scheduled consequences, whereas NNDMA did not. Onset and time course data suggested that conversion of NNDMA to MA was probably not necessary for the behavioral effects of NNDMA. In contrast to the relative potencies in behavioral tests, NNDMA was only 3 times less potent than MA in its lethal effects in rats. However, lethality of both drugs was prevented by haloperidol. In general, MA displayed a wider separation in the doses required to produce behavioral vs. lethal effects than did NNDMA.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

N-甲基苯丙胺(MA)的N-甲基化衍生物N,N-二甲基苯丙胺(NNDMA)最近已被合成用于非法用途。本研究比较了这些类似物在大鼠和松鼠猴体内的精神运动兴奋剂、辨别刺激、强化和致死作用。在固定间隔或固定比率的食物呈现时间表下,NNDMA降低大鼠或猴子反应率的效力比MA低6至12倍。在训练用于区分10mg/kg可卡因和生理盐水的大鼠中,MA和NNDMA都能使可卡因杠杆反应的百分比产生剂量依赖性增加,NNDMA的效力比MA低12倍。在训练用于自我给药可卡因的松鼠猴中,静脉注射MA或NNDMA维持的反应率高于生理盐水注射维持的反应率;NNDMA产生这些强化作用的效力比MA低10倍。两种药物都增加了松鼠猴的固定间隔反应;MA比NNDMA更有效。MA还增加了大鼠在无预定后果的超时期间的反应率,而NNDMA则没有。起效和时间进程数据表明,NNDMA的行为效应可能不需要将其转化为MA。与行为测试中的相对效力相反,NNDMA在大鼠中的致死效力仅比MA低3倍。然而,氟哌啶醇可预防两种药物的致死性。一般来说,与NNDMA相比,MA在产生行为效应和致死效应所需的剂量上有更宽的分离度。(摘要截断于250字)

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