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脑大麻素受体2:表达、功能及调节

Brain cannabinoid receptor 2: expression, function and modulation.

作者信息

Chen De-Jie, Gao Ming, Gao Fen-Fei, Su Quan-Xi, Wu Jie

机构信息

Department of Neurology, Yunfu People's Hospital, Yunfu 527300, China.

Department of Neurobiology, Barrow Neurological Institute, St Joseph's Hospital and Medical Center, Phoenix, AZ 85013-4409, USA.

出版信息

Acta Pharmacol Sin. 2017 Mar;38(3):312-316. doi: 10.1038/aps.2016.149. Epub 2017 Jan 9.

Abstract

Cannabis sativa (marijuana) is a fibrous flowering plant that produces an abundant variety of molecules, some with psychoactive effects. At least 4% of the world's adult population uses cannabis annually, making it one of the most frequently used illicit drugs in the world. The psychoactive effects of cannabis are mediated primarily through cannabinoid receptor (CBR) subtypes. The prevailing view is that CB1Rs are mainly expressed in the central neurons, whereas CBRs are predominantly expressed in peripheral immune cells. However, this traditional view has been challenged by emerging strong evidence that shows CBRs are moderately expressed and function in specific brain areas. New evidence has demonstrated that brain CBRs modulate animal drug-seeking behaviors, suggesting that these receptors may exist in brain regions that regulate drug addiction. Recently, we further confirmed that functional CBRs are expressed in mouse ventral tegmental area (VTA) dopamine (DA) neurons and that the activation of VTA CBRs reduces neuronal excitability and cocaine-seeking behavior. In addition, CBR-mediated modulation of hippocampal CA3 neuronal excitability and network synchronization has been reported. Here, we briefly summarize recent lines of evidence showing how CBRs modulate function and pathophysiology in the CNS.

摘要

大麻( Cannabis sativa )是一种纤维状开花植物,能产生多种分子,其中一些具有精神活性作用。全球至少4%的成年人口每年使用大麻,使其成为世界上最常用的非法药物之一。大麻的精神活性作用主要通过大麻素受体(CBR)亚型介导。普遍观点认为,CB1Rs主要在中枢神经元中表达,而CBRs主要在外周免疫细胞中表达。然而,这一传统观点受到了新出现的有力证据的挑战,这些证据表明CBRs在特定脑区有中度表达并发挥功能。新证据表明,脑内CBRs调节动物的觅药行为,提示这些受体可能存在于调节药物成瘾的脑区。最近,我们进一步证实功能性CBRs在小鼠腹侧被盖区(VTA)多巴胺(DA)神经元中表达,并且VTA CBRs的激活降低神经元兴奋性和可卡因觅求行为。此外,已有报道称CBR介导对海马CA3神经元兴奋性和网络同步性的调节。在此,我们简要总结最近一系列证据,展示CBRs如何调节中枢神经系统的功能和病理生理。

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