Department of Behavioral Science, University of Kentucky, 845 Angliana Avenue, Lexington, KY 40508, United States; Department of the Center on Drug and Alcohol Research, University of Kentucky, Lexington, KY 40508, United States.
Department of Behavioral Science, University of Kentucky, 845 Angliana Avenue, Lexington, KY 40508, United States; Department of Pharmacology, University of Kentucky, Lexington, KY 40508, United States; Department of Pharmaceutical Sciences, University of Kentucky, Lexington, KY 40508, United States; Department of Psychiatry, University of Kentucky, Lexington, KY 40508, United States; Department of the Center on Drug and Alcohol Research, University of Kentucky, Lexington, KY 40508, United States.
Eur Neuropsychopharmacol. 2020 Jul;36:206-216. doi: 10.1016/j.euroneuro.2020.03.002. Epub 2020 Apr 6.
The endogenous opioid and cannabinoid receptor systems are widely distributed and co-localized throughout central and peripheral nervous system regions. A large body of preclinical evidence suggests that there are functional interactions between these two systems that may be leveraged to address various health conditions. Numerous animal studies have shown that cannabinoid agonists (e.g., delta-9-tetrahydrocannabinol [Δ-THC]) enhance the analgesic effects of µ-opioid analgesics as evidenced by decreasing the opioid dose required for analgesia (i.e., opioid sparing) and extending the duration of the opioid analgesia. In contrast, controlled human laboratory studies and clinical trials have not demonstrated robust analgesic or opioid-sparing effects from opioid-cannabinoid combinations. Meta-analyses of the literature (clinical trials, controlled laboratory studies; some non-controlled studies/case reports) have examined the effects of cannabis/cannabinoids for pain relief in those taking a wide variety of analgesics, including prescription opioid medications. These data do not strongly support the use of cannabinoids for chronic pain nor do prospective studies demonstrate significant cannabinoid-mediated opioid-sparing effects. Preclinical studies have also suggested a role for cannabinoids for the treatment of opioid withdrawal. Controlled laboratory and clinical studies suggest that there may be a modest signal for Δ-THC to suppress some opioid signs and symptoms but they are not completely ameliorated and there may also be concerns around safety of Δ-THC administration in a state of heightened autonomic arousal as occurs with opioid withdrawal. Despite anecdotal and correlational reports suggesting a benefit of cannabis on reducing opioid overdose, there is no strong data supporting this contention and emerging reports have conflicting results. In summary, there is a groundswell of public advocacy supporting the use of cannabis and cannabinoids to replace opioid analgesics or to reduce opioid use; however, the extant controlled clinical data do not support the role of cannabinoids for opioid replacement or opioid-sparing effects when treating opioid use disorder or chronic pain.
内源性阿片和大麻素受体系统广泛分布于中枢和外周神经系统区域。大量临床前证据表明,这两个系统之间存在功能相互作用,可用于治疗各种健康状况。许多动物研究表明,大麻素激动剂(例如,Δ-9-四氢大麻酚 [Δ-THC])增强了 μ-阿片类镇痛药的镇痛作用,表现为减少了镇痛所需的阿片类药物剂量(即阿片类药物节省)并延长了阿片类镇痛药的作用持续时间。相比之下,对照人体实验室研究和临床试验并未显示出阿片类药物 - 大麻素联合使用具有明显的镇痛或阿片类药物节省作用。对文献(临床试验、对照实验室研究;一些非对照研究/病例报告)的荟萃分析检查了大麻/大麻素对服用各种镇痛药(包括处方阿片类药物)的人的疼痛缓解作用。这些数据并不强烈支持使用大麻素治疗慢性疼痛,也没有前瞻性研究表明大麻素具有显著的阿片类药物节省作用。临床前研究还表明大麻素在治疗阿片类药物戒断方面具有作用。对照实验室和临床研究表明,Δ-THC 可能抑制一些阿片类药物的迹象和症状,但不能完全缓解,并且在出现阿片类药物戒断时自主神经兴奋的情况下,Δ-THC 给药的安全性也可能存在问题。尽管有轶事和相关性报告表明大麻可减少阿片类药物过量,但没有强有力的数据支持这一说法,并且新出现的报告结果相互矛盾。总之,公众强烈支持使用大麻和大麻素替代阿片类镇痛药或减少阿片类药物使用;然而,现有的对照临床数据不支持大麻素在治疗阿片类药物使用障碍或慢性疼痛时作为阿片类药物替代品或节省阿片类药物的作用。