Bourgault Zoe, Matheson Justin, Mann Robert E, Brands Bruna, Wickens Christine M, Tiwari Arun K, Zai Clement C, Kennedy James, Le Foll Bernard
Translational Addiction Research Laboratory, Centre for Addiction and Mental Health, University of Toronto 33 Ursula Franklin Street, Toronto, ON, Canada.
Department of Pharmacology and Toxicology, University of Toronto Toronto, ON, Canada.
Am J Transl Res. 2022 Jan 15;14(1):623-632. eCollection 2022.
The mu-opioid receptor (MOR) mediates the rewarding properties of many psychoactive drugs and is an important target in the treatment of addictions. Functional interactions between the opioid and endocannabinoid systems are established and have been hypothesized to contribute to the effects of cannabis. We investigated associations between three single nucleotide polymorphisms in the MOR gene (rs1799971, rs2281617, and rs510769) and subjective responses to smoked cannabis. Fifty-two regular cannabis users (1-4 days/week) were given a cannabis cigarette (12.5% THC) and rated their subjective responses on visual analog scales at baseline and at multiple time points after smoking. Blood samples were collected for THC quantification. There was a significant impact of the intronic variant rs510769 on subjective cannabis effects and THC blood levels. The influence of this gene variant may thus be mediated by pharmacodynamics and/or pharmacokinetic factors. We provide novel evidence that variability in contributes to individual responses to cannabis and may affect risk of cannabis use disorder. Our findings add to the growing body of literature on the genetic basis of individual responses to cannabis and may have implications for targeting the endogenous opioid system in the treatment of cannabis use disorder.
μ-阿片受体(MOR)介导了许多精神活性药物的奖赏特性,是成瘾治疗的重要靶点。阿片系统和内源性大麻素系统之间已建立起功能相互作用,并且据推测这有助于大麻发挥作用。我们研究了MOR基因中的三个单核苷酸多态性(rs1799971、rs2281617和rs510769)与吸食大麻后的主观反应之间的关联。52名经常吸食大麻的使用者(每周1 - 4天)吸食一支大麻烟(四氢大麻酚含量为12.5%),并在基线以及吸食后的多个时间点通过视觉模拟量表对他们的主观反应进行评分。采集血样用于四氢大麻酚定量分析。内含子变体rs510769对大麻的主观效应和四氢大麻酚血药浓度有显著影响。因此,这种基因变体的影响可能是由药效学和/或药代动力学因素介导的。我们提供了新的证据,表明基因变异性导致个体对大麻的反应不同,并可能影响大麻使用障碍的风险。我们的研究结果增加了关于个体对大麻反应的遗传基础的文献,并且可能对在大麻使用障碍治疗中靶向内源性阿片系统具有启示意义。