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大麻素受体在大脑中与药物奖赏相关的作用。

Role of cannabinoid receptor in the brain as it relates to drug reward.

作者信息

Yamamoto T, Takada K

机构信息

Department of Pharmacology, Graduate school of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Jpn J Pharmacol. 2000 Nov;84(3):229-36. doi: 10.1254/jjp.84.229.

Abstract

Understanding of cannabinoid (CB) actions has been remarkably advanced during the last decade, due mainly to the identification of the G-protein-coupled cannabinoid receptors, namely, CB1 receptors that are predominantly found in the brain and CB2 receptors that are exclusively found in peripheral tissues. Endogenous ligands for these receptors have also been identified. Research to date suggests that the analgesic effect of cannabinoids and the enhancement of opioid analgesia by cannabinoids are both CB1 receptor-mediated via the activation of opioid receptors. The involvement of the CB1 receptor in mediating reinforcing and physical dependence-producing effects of opioids has also been suggested, with the former being considered the result of interaction with the dopaminergic neurotransmission in the midbrain dopamine system. However, the discriminative stimulus effects of cannabinoids have been reported to be highly specific in that the effects were not substituted by other classes of compounds including opioidergic and dopaminergic agents nor were they antagonized by antagonists of various neurotransmission systems, suggesting that the discriminative stimulus effects only involve the cannabinoid system. Thus the cannabinoid actions appear to be classifiable into at least two kinds: 1) those mediated directly through cannabinoid receptors and 2) those mediated indirectly through other systems such as opioidergic systems. Detailed research into these actions may help to elucidate not only the mechanisms of action of exogenous cannabinoids but also the role of endogenous cannabinoids, especially in the brain reward system.

摘要

在过去十年中,对大麻素(CB)作用的理解取得了显著进展,这主要归功于G蛋白偶联大麻素受体的鉴定,即主要存在于大脑中的CB1受体和仅存在于外周组织中的CB2受体。这些受体的内源性配体也已被鉴定出来。迄今为止的研究表明,大麻素的镇痛作用以及大麻素对阿片类镇痛的增强作用均由CB1受体介导,通过激活阿片受体实现。也有研究表明CB1受体参与介导阿片类药物的强化作用和产生身体依赖性的作用,前者被认为是与中脑多巴胺系统中的多巴胺能神经传递相互作用的结果。然而,据报道,大麻素的辨别性刺激作用具有高度特异性,即这些作用不会被包括阿片类和多巴胺能药物在内的其他类化合物所替代,也不会被各种神经传递系统的拮抗剂所拮抗,这表明辨别性刺激作用仅涉及大麻素系统。因此,大麻素的作用似乎至少可分为两类:1)直接通过大麻素受体介导的作用;2)间接通过其他系统(如阿片类系统)介导的作用。对这些作用的详细研究不仅有助于阐明外源性大麻素的作用机制,还有助于阐明内源性大麻素的作用,尤其是在大脑奖赏系统中的作用。

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