首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Self-administration of the cannabinoid receptor agonist WIN 55,212-2 in drug-naive mice.
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Self-administration of the cannabinoid receptor agonist WIN 55,212-2 in drug-naive mice.

机译:初次使用毒品的小鼠中大麻素受体激动剂WIN 55,212-2的自我给药。

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摘要

Marijuana is one of the most widely used illicit recreational drugs. However, contrary to the majority of drugs abused by humans, there is a general opinion that rewarding effects are not manifested by animals. We studied a synthetic cannabinoid agonist WIN 55,212-2 using an intravenous self-administration model in drug-naive mice. The results of this study show that WIN 55,212-2 was intravenously self-administered by mice in a concentration-dependent manner according to a bell-shaped curve. Thus, self-administration of WIN 55,212-2 significantly increased, with respect to the vehicle self-administration control group, at concentrations of 0.5 and 0.1 mg/kg per injection. However, at WIN 55,212-2 concentration of 0.5 mg/kg per injection, self-administration significantly decreased. The results obtained show how WIN 55,212-2 is able to elicit both rewarding and aversive effects depending on the concentration used. Pretreatment of mice with the cannabinoid CB1 receptor antagonist SR 141716A (0.25 mg/kg, i.p.) completely prevented WIN 55,212-2 (0.1 mg/kg per injection) self-administration, indicating that WIN 55,212-2 rewarding effects are specifically mediated by cannabinoid CB1 receptors.
机译:大麻是使用最广泛的非法娱乐药物之一。但是,与大多数人滥用的药物相反,普遍认为动物没有表现出有益的作用。我们在未吸毒的小鼠中使用静脉内自我给药模型研究了合成的大麻素激动剂WIN 55,212-2。这项研究的结果表明,WIN 55,212-2是由小鼠根据钟形曲线以浓度依赖的方式静脉内自行给药的。因此,相对于媒介物自我给药对照组,WIN 55,212-2的自我给药在每次注射中的浓度分别为0.5和0.1 mg / kg。但是,在每次注射的WIN 55,212-2浓度为0.5 mg / kg时,自我给药明显减少。获得的结果表明,WIN 55,212-2如何能够根据所使用的浓度同时引发奖励和厌恶效果。用大麻素CB1受体拮抗剂SR 141716A(0.25 mg / kg,ip)预处理小鼠完全阻止了WIN 55,212-2(每次注射0.1 mg / kg)的自我给药,这表明WIN 55,212-2的奖励作用是由大麻素特异性介导的CB1受体。

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