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即使高剂量口服大麻二酚也不会在人体产生类似四氢大麻酚的效果:对梅里克等人的评论。2016年;1(1):102 - 112;DOI: 10.1089/can.2015.0004

Even High Doses of Oral Cannabidol Do Not Cause THC-Like Effects in Humans: Comment on Merrick et al. 2016;1(1):102-112; DOI: 10.1089/can.2015.0004.

作者信息

Grotenhermen Franjo, Russo Ethan, Zuardi Antonio Waldo

机构信息

nova-Institut GmbH, Chemiepark Knapsack, Hürth, Germany.

PHYTECS, Los Angeles, California.

出版信息

Cannabis Cannabinoid Res. 2017 Jan 1;2(1):1-4. doi: 10.1089/can.2016.0036. eCollection 2017.

DOI:10.1089/can.2016.0036
PMID:28861499
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5531368/
Abstract

This short communication examines the question whether the experimental data presented in a study by Merrick et al. are of clinical relevance. These authors found that cannabidiol (CBD), a major cannabinoid of the cannabis plant devoid of psychotropic effects and of great interest for therapeutic use in several medical conditions, may be converted in gastric fluid into the psychoactive cannabinoids delta-8-THC and delta-9-THC to a relevant degree. They concluded that "the acidic environment during normal gastrointestinal transit can expose orally CBD-treated patients to levels of THC and other psychoactive cannabinoids that may exceed the threshold for a positive physiological response." They issued a warning concerning oral use of CBD and recommend the development of other delivery methods. However, the available clinical data do not support this conclusion and recommendation, since even high doses of oral CBD do not cause psychological, psychomotor, cognitive, or physical effects that are characteristic for THC or cannabis rich in THC. On the contrary, in the past decades and by several groups, high doses of oral CBD were consistently shown to cause opposite effects to those of THC in clinical studies. In addition, administration of CBD did not result in detectable THC blood concentrations. Thus, there is no reason to avoid oral use of CBD, which has been demonstrated to be a safe means of administration of CBD, even at very high doses.

摘要

这篇简短的通讯探讨了Merrick等人的一项研究中所呈现的实验数据是否具有临床相关性这一问题。这些作者发现,大麻二酚(CBD),一种大麻植物中的主要大麻素,没有精神活性作用,并且在多种医疗状况下具有很大的治疗应用价值,它在胃液中可能会在相当程度上转化为具有精神活性的大麻素δ-8-四氢大麻酚(delta-8-THC)和δ-9-四氢大麻酚(delta-9-THC)。他们得出结论:“正常胃肠道转运过程中的酸性环境可能会使口服CBD治疗的患者接触到的THC和其他具有精神活性的大麻素水平超过产生阳性生理反应的阈值。”他们就口服CBD发出了警告,并建议开发其他给药方式。然而,现有的临床数据并不支持这一结论和建议,因为即使是高剂量的口服CBD也不会引起THC或富含THC的大麻所特有的心理、精神运动、认知或身体影响。相反,在过去几十年里,多个研究团队在临床研究中一致表明,高剂量的口服CBD会产生与THC相反的效果。此外,给予CBD并未导致可检测到的THC血药浓度。因此,没有理由避免口服CBD,即使在非常高的剂量下,口服CBD也已被证明是一种安全的给药方式。

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本文引用的文献

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2
Cannabis and epilepsy: An ancient treatment returns to the fore.大麻与癫痫:一种古老的治疗方法再度受到关注。
Epilepsy Behav. 2017 May;70(Pt B):292-297. doi: 10.1016/j.yebeh.2016.09.040. Epub 2016 Dec 15.
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Cannabidiol in patients with treatment-resistant epilepsy: an open-label interventional trial.大麻二酚治疗耐药性癫痫患者:一项开放标签的干预性试验。
Lancet Neurol. 2016 Mar;15(3):270-8. doi: 10.1016/S1474-4422(15)00379-8. Epub 2015 Dec 24.
4
Cannabidiol enhances anandamide signaling and alleviates psychotic symptoms of schizophrenia.大麻二酚增强了内源性大麻素信号传导,并缓解了精神分裂症的精神病症状。
Transl Psychiatry. 2012 Mar 20;2(3):e94. doi: 10.1038/tp.2012.15.
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Acute effects of a single, oral dose of d9-tetrahydrocannabinol (THC) and cannabidiol (CBD) administration in healthy volunteers.健康志愿者单次口服 d9-四氢大麻酚(THC)和大麻二酚(CBD)的急性效应。
Curr Pharm Des. 2012;18(32):4966-79. doi: 10.2174/138161212802884780.
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Cannabidiol reduces the anxiety induced by simulated public speaking in treatment-naïve social phobia patients.大麻二酚可降低治疗初发社交恐惧症患者在模拟公开演讲时的焦虑。
Neuropsychopharmacology. 2011 May;36(6):1219-26. doi: 10.1038/npp.2011.6. Epub 2011 Feb 9.
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[Therapeutical use of the cannabinoids in psychiatry].大麻素在精神病学中的治疗应用
Braz J Psychiatry. 2010 May;32 Suppl 1:S56-66.
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Opposite effects of delta-9-tetrahydrocannabinol and cannabidiol on human brain function and psychopathology.大麻二酚和Δ9-四氢大麻酚对人脑功能和精神病理学的相反影响。
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