Department of Neurology, Comprehensive Epilepsy Center, New York University School of Medicine, New York, New York, U.S.A.
Epilepsia. 2014 Jun;55(6):791-802. doi: 10.1111/epi.12631. Epub 2014 May 22.
To present a summary of current scientific evidence about the cannabinoid, cannabidiol (CBD) with regard to its relevance to epilepsy and other selected neuropsychiatric disorders. We summarize the presentations from a conference in which invited participants reviewed relevant aspects of the physiology, mechanisms of action, pharmacology, and data from studies with animal models and human subjects. Cannabis has been used to treat disease since ancient times. Δ(9) -Tetrahydrocannabinol (Δ(9) -THC) is the major psychoactive ingredient and CBD is the major nonpsychoactive ingredient in cannabis. Cannabis and Δ(9) -THC are anticonvulsant in most animal models but can be proconvulsant in some healthy animals. The psychotropic effects of Δ(9) -THC limit tolerability. CBD is anticonvulsant in many acute animal models, but there are limited data in chronic models. The antiepileptic mechanisms of CBD are not known, but may include effects on the equilibrative nucleoside transporter; the orphan G-protein-coupled receptor GPR55; the transient receptor potential of vanilloid type-1 channel; the 5-HT1a receptor; and the α3 and α1 glycine receptors. CBD has neuroprotective and antiinflammatory effects, and it appears to be well tolerated in humans, but small and methodologically limited studies of CBD in human epilepsy have been inconclusive. More recent anecdotal reports of high-ratio CBD:Δ(9) -THC medical marijuana have claimed efficacy, but studies were not controlled. CBD bears investigation in epilepsy and other neuropsychiatric disorders, including anxiety, schizophrenia, addiction, and neonatal hypoxic-ischemic encephalopathy. However, we lack data from well-powered double-blind randomized, controlled studies on the efficacy of pure CBD for any disorder. Initial dose-tolerability and double-blind randomized, controlled studies focusing on target intractable epilepsy populations such as patients with Dravet and Lennox-Gastaut syndromes are being planned. Trials in other treatment-resistant epilepsies may also be warranted. A PowerPoint slide summarizing this article is available for download in the Supporting Information section here.
为了就大麻素、大麻二酚(CBD)与癫痫和其他选定神经精神障碍相关的方面呈现当前科学证据的概要,我们总结了一次会议的演示内容,受邀参会者审查了该物质的生理学、作用机制、药理学方面的相关内容,以及来自动物模型和人体研究的数据。自古以来,大麻就被用于治疗疾病。Δ(9)-四氢大麻酚(Δ(9)-THC)是主要的精神活性成分,CBD 是大麻中的主要非精神活性成分。大麻和 Δ(9)-THC 在大多数动物模型中具有抗惊厥作用,但在某些健康动物中可能具有促惊厥作用。Δ(9)-THC 的精神作用限制了其耐受性。CBD 在许多急性动物模型中具有抗惊厥作用,但在慢性模型中数据有限。CBD 的抗癫痫机制尚不清楚,但可能包括对平衡核苷转运蛋白的作用;孤儿 G 蛋白偶联受体 GPR55;香草素型 1 通道的瞬时受体电位;5-HT1a 受体;以及 α3 和 α1 甘氨酸受体。CBD 具有神经保护和抗炎作用,并且在人类中似乎耐受性良好,但在人类癫痫中 CBD 的小型和方法学有限的研究尚无定论。最近关于高比例 CBD:Δ(9)-THC 医用大麻的轶事报道声称其具有疗效,但这些研究未进行对照。CBD 值得在癫痫和其他神经精神障碍中进行研究,包括焦虑、精神分裂症、成瘾和新生儿缺氧缺血性脑病。然而,我们缺乏任何疾病中纯 CBD 疗效的、基于大样本量、双盲、随机、对照研究的数据。目前正在计划针对 Dravet 和 Lennox-Gastaut 综合征等难治性癫痫患者的初始剂量耐受性和双盲随机对照研究,其他治疗抵抗性癫痫的试验也可能是合理的。本文的一个幻灯片总结可在支持信息部分下载。