首页> 外文期刊>Behavioural Brain Research: An International Journal >Cannabinoid CB1 receptor knockout mice fail to self-administer morphine but not other drugs of abuse.
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Cannabinoid CB1 receptor knockout mice fail to self-administer morphine but not other drugs of abuse.

机译:大麻素CB1受体敲除小鼠不能自我施用吗啡,但不能自我施用其他滥用药物。

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摘要

The rewarding effects of morphine, cocaine, amphetamine and nicotine were evaluated in CB1 receptor knockout mice by means of an intravenous self-administration model. Experiments were carried out on drug-naive animals using a nose-poking response (NPR)-like as operandum. The results of the present study indicate that morphine did not induce intravenous self-administration in mutant CB1 receptor knockout mice, whereas it was significantly self-administered by the corresponding wild type mice. On the contrary, cocaine, amphetamine and nicotine were self-administered to the same extent by both wild type and CB1 receptor knockout mice. These data clearly indicate that the CB1 cannabinoid receptor is essential not only for the expression of cannabinoid reinforcing effects but also for the modulation of morphine rewarding effects. The specificity of such interaction is supported by the finding that contrary to morphine, cocaine, d-amphetamine and nicotine were self-administered by mice at the same extent either in presence or in absence of the CB1 receptor.
机译:通过静脉内自我给药模型评价了吗啡,可卡因,苯丙胺和尼古丁对CB1受体敲除小鼠的奖励作用。实验针对未使用过毒品的动物,使用类似鼻戳的反应(NPR)作为操作数。本研究的结果表明吗啡在突变的CB1受体基因敲除小鼠中并未诱导静脉内自我给药,而相应的野生型小鼠却明显地自我给药。相反,可卡因,苯丙胺和尼古丁是由野生型和CB1受体敲除小鼠以相同的程度自我给药的。这些数据清楚地表明,CB1大麻素受体不仅对于表达大麻素增强作用至关重要,而且对于调节吗啡奖励作用也必不可少。这种相互作用的特异性得到了以下发现的支持:与吗啡相反,可卡因,d-苯异丙胺和尼古丁在存在或不存在CB1受体的情况下都以相同的程度由小鼠自行施用。

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