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大麻素和内源性大麻素系统在奖励处理和成瘾中的作用:从机制到干预。

Cannabinoids and the endocannabinoid system in reward processing and addiction: from mechanisms to interventions
.

机构信息

Institute of Psychopharmacology, Central Institute of Mental Health, Faculty of Medicine Mannheim, University of Heidelberg, Germany.

出版信息

Dialogues Clin Neurosci. 2020 Sep;22(3):241-250. doi: 10.31887/DCNS.2020.22.3/rspanagel.

DOI:10.31887/DCNS.2020.22.3/rspanagel
PMID:33162767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7605022/
Abstract

The last decades have seen a major gain in understanding the action of cannabinoids and the endocannabinoid system in reward processing and the development of addictive behavior. Cannabis-derived psychoactive compounds such as Δ-tetrahydrocannabinol and synthetic cannabinoids directly interact with the reward system and thereby have addictive properties. Cannabinoids induce their reinforcing properties by an increase in tonic dopamine levels through a cannabinoid type 1 (CB) receptor-dependent mechanism within the ventral tegmental area. Cues that are conditioned to cannabis smoking can induce drug-seeking responses (ie, craving) by eliciting phasic dopamine events. A dopamine-independent mechanism involved in drug-seeking responses involves an endocannabinoid/glutamate interaction within the corticostriatal part of the reward system. In conclusion, pharmacological blockade of endocannabinoid signaling should lead to a reduction in drug craving and subsequently should reduce relapse behavior in addicted individuals. Indeed, there is increasing preclinical evidence that targeting the endocannabinoid system reduces craving and relapse, and allosteric modulators at CB receptors and fatty acid amide hydrolase inhibitors are in clinical development for cannabis use disorder. Cannabidiol, which mainly acts on CB and CB receptors, is currently being tested in patients with alcohol use disorder and opioid use disorder.
.

摘要

在过去的几十年里,人们对大麻素和内源性大麻素系统在奖励处理和成瘾行为发展中的作用有了更深入的了解。大麻衍生的精神活性化合物,如 Δ-四氢大麻酚和合成大麻素,直接与奖励系统相互作用,从而具有成瘾性。大麻素通过大麻素 1 型(CB1)受体依赖性机制增加腹侧被盖区的紧张性多巴胺水平,从而发挥其强化作用。与大麻吸烟相关的线索可以通过引发相位多巴胺事件引起觅药反应(即渴望)。觅药反应涉及奖励系统皮质纹状体部分的内源性大麻素/谷氨酸相互作用,这涉及一种多巴胺非依赖性机制。总之,内源性大麻素信号的药理学阻断应导致对药物的渴望减少,从而减少成瘾个体的复发行为。事实上,越来越多的临床前证据表明,靶向内源性大麻素系统可以减少渴望和复发,CB 受体的别构调节剂和脂肪酸酰胺水解酶抑制剂正在为大麻使用障碍进行临床开发。主要作用于 CB1 和 CB2 受体的大麻二酚目前正在酒精使用障碍和阿片类药物使用障碍患者中进行测试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd88/7605022/06715e923a1f/DCNS_22.3_Spanagel_Figure1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd88/7605022/06715e923a1f/DCNS_22.3_Spanagel_Figure1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd88/7605022/06715e923a1f/DCNS_22.3_Spanagel_Figure1.jpg

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