Cannabinoids: between neuroprotection and neurotoxicity.

Yosef Sarne, Raphael Mechoulam
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引用次数: 110

Abstract

Cannabinoids, such as the delta9-tetrahydrocannabinol (THC), present in the cannabis plant, as well as anandamide and 2-arachidonoyl glycerol, produced by the mammalian body, have been shown to protect the brain from various insults and to improve several neurodegenerative diseases. The current review summarizes the evidence for cannabinoid neuroprotection in vivo, and refers to recent in vitro studies, which help elucidate possible molecular mechanisms underlying this protective effect. Some of these mechanisms involve the activation of CB1 and CB2 cannabinoid receptors, while others are not dependent on them. In some cases, protection is due to a direct effect of the cannabinoids on neuronal cells, while in others, it results from their effects on non-neuronal elements within the brain. In many experimental set-ups, cannabinoid neurotoxicity, particularly by THC, resides side by side with neuroprotection. The current review attempts to shed light on this dual activity, and to dissociate between the two contradictory effects.

大麻素:介于神经保护和神经毒性之间。
大麻素,如存在于大麻植物中的德尔塔9-四氢大麻酚(THC),以及哺乳动物身体产生的阿南达胺和2-花生四烯醇甘油,已被证明可以保护大脑免受各种伤害,并改善几种神经退行性疾病。本综述总结了大麻素在体内神经保护的证据,并参考了最近的体外研究,这些研究有助于阐明这种保护作用的可能分子机制。其中一些机制涉及CB1和CB2大麻素受体的激活,而其他机制则不依赖于它们。在某些情况下,保护是由于大麻素对神经元细胞的直接作用,而在其他情况下,它是由它们对大脑内非神经元元素的作用产生的。在许多实验设置中,大麻素神经毒性,特别是四氢大麻酚,与神经保护作用并存。目前的审查试图阐明这一双重活动,并分离这两种相互矛盾的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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