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Cannabidiol: Pharmacology and potential therapeutic role in epilepsy and other neuropsychiatric disorders

期刊

EPILEPSIA
卷 55, 期 6, 页码 791-802

出版社

WILEY
DOI: 10.1111/epi.12631

关键词

Cannabidiol; Cannabis; Tetrahydroacannabinol; Dravet syndrome; GPR55; Medical marijuana

资金

  1. GW Pharmaceuticals
  2. Epilepsy Therapy Project for human trials of CBD
  3. UCB
  4. Eisai
  5. Action Medical Research
  6. Epilepsy Research UK
  7. Great Ormond Street Hospital Children's Charity
  8. Bristol-Myers Squibb
  9. Mylan
  10. Pfizer
  11. Reckitt Benckiser Pharmaceuticals
  12. Merck
  13. CHUM Department of Psychiatry
  14. Universite de Montreal Department of Psychiatry
  15. CHUM Research Center
  16. National Institutes of Health (National Center for the Advancement of Translational Science) [UL1 TR000038]

向作者/读者索取更多资源

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. 9-Tetrahydrocannabinol (9-THC) is the major psychoactive ingredient and CBD is the major nonpsychoactive ingredient in cannabis. Cannabis and 9-THC are anticonvulsant in most animal models but can be proconvulsant in some healthy animals. The psychotropic effects of 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 3 and 1 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: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.

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