大麻素治疗阿片类药物成瘾

E. McLemon, R. Chesworth
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引用次数: 1

摘要

阿片类药物滥用是一个日益严重的全球性问题。目前阿片类药物滥用的治疗目标是戒断症状,并有一些不良副作用。目前还没有治疗阿片类药物引起的与滥用和成瘾相关的神经适应的方法。临床前研究表明内源性阿片样物质和大麻素系统之间存在相互作用,表明大麻素可用于治疗阿片样物质成瘾和依赖。本综述的目的是评估大麻素如何影响动物模型中阿片类药物依赖和成瘾样行为的行为和分子测量。根据临床前动物模型的证据,大麻二酚和大麻素受体1 (CB1R)拮抗剂似乎具有治疗药物渴望和药物寻求行为的潜力。抑制大麻素降解酶作用的配体在减少啮齿动物阿片戒断症状和阿片自我给药方面也显示出希望。CB1R激动剂可用于治疗阿片类药物戒断症状;然而,这些药物的临床应用受到副作用、大麻素成瘾的可能性和大麻素消耗引起的阿片耐受性增加的限制。大麻素减少阿片类药物成瘾相关行为的机制包括大麻素、血清素和多巴胺受体的调节,以及涉及ERK-CREB-BDNF和过氧化物酶体增殖激活受体-α的信号级联反应。识别相关受体及其作用机制仍是未来研究的关键领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cannabinoid treatment of opiate addiction
Opioid abuse is a growing global problem. Current therapies for opioid abuse target withdrawal symptoms and have several adverse side effects. There are no treatments to address opioid-induced neural adaptations associated with abuse and addiction. Preclinical research demonstrates interactions between the endogenous opioid and cannabinoid systems, suggesting that cannabinoids may be used to treat opioid addiction and dependence. The aim of this review is to assess how cannabinoids affect behavioural and molecular measures of opioid dependence and addiction-like behaviour in animal models. It appears that cannabidiol and cannabinoid receptor 1 (CB1R) antagonists have potential for treating drug-craving and drug-seeking behaviour, based on evidence from preclinical animal models. Ligands which inhibit the action of cannabinoid degradation enzymes also show promise in reducing opioid withdrawal symptoms and opioid self-administration in rodents. Agonists of CB1R could be useful for treating symptoms of opioid withdrawal; however, the clinical utility of these drugs is limited by side effects, the potential for cannabinoid addiction and an increase in opiate tolerance induced by cannabinoid consumption. The mechanisms by which cannabinoids reduce opioid addiction-relevant behaviours include modulation of cannabinoid, serotonin, and dopamine receptors, as well as signalling cascades involving ERK-CREB-BDNF and peroxisome proliferator-activated receptor-α. Identifying the receptors involved and their mechanism of action remains a critical area of future research.
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