Oliva Idaira, Kazi Fezaan, Cantwell Lucas N, Thakur Ganesh A, Crystal Jonathon D, Hohmann Andrea G
bioRxiv. 2024 Jan 19:2024.01.16.575900. doi: 10.1101/2024.01.16.575900.
The endocannabinoid system interacts with the reward system to modulate responsiveness to natural reinforcers, as well as drugs of abuse. Previous preclinical studies suggested that direct blockade of CB1 cannabinoid receptors (CB1R) could be leveraged as a potential pharmacological approach to treat substance use disorder, but this strategy failed during clinical trials due to severe psychiatric side effects. Alternative strategies have emerged to circumvent the side effects of direct CB1 binding through the development of allosteric modulators. We hypothesized that pharmacological inhibition of CB1R signaling through negative allosteric modulation (NAM) would reduce the reinforcing properties of morphine and decrease opioid addictive behaviors. By employing i.v. self-administration in mice, we studied the effects of the CB1-biased NAM GAT358 on morphine intake, relapse-like behavior, and motivation to work for morphine infusions. Our data revealed that GAT358 reduced morphine infusion intake during the maintenance phase of morphine self-administration under fixed ratio 1 schedule of reinforcement. GAT358 decreased morphine-seeking behavior after forced abstinence. Moreover, GAT358 dose-dependently decreased the motivation to obtain morphine infusions in a progressive ratio schedule of reinforcement. Strikingly, GAT358 did not affect the motivation to work for food rewards in an identical progressive ratio task, suggesting that the effect of GAT358 in decreasing opioid self-administration is reward specific. Furthermore, GAT58 did not produce motor ataxia in the rota-rod test. Our results suggest that CB1R NAMs reduced the reinforcing properties of morphine and could represent a viable therapeutic route to safely decrease opioid-addicted behaviors.
内源性大麻素系统与奖赏系统相互作用,以调节对天然强化物以及滥用药物的反应性。先前的临床前研究表明,直接阻断CB1大麻素受体(CB1R)可作为治疗物质使用障碍的一种潜在药理学方法,但由于严重的精神副作用,该策略在临床试验中失败了。通过开发变构调节剂,出现了替代策略来规避直接结合CB1的副作用。我们假设,通过负性变构调节(NAM)对CB1R信号进行药理学抑制将降低吗啡的强化特性,并减少阿片类药物成瘾行为。通过在小鼠中采用静脉自我给药,我们研究了CB1偏向性NAM GAT358对吗啡摄入量、复发样行为以及为获得吗啡输注而工作的动机的影响。我们的数据显示,在固定比率1强化方案下,GAT358在吗啡自我给药的维持阶段减少了吗啡输注摄入量。GAT358减少了强制戒断后的觅药行为。此外,在累进比率强化方案中,GAT358剂量依赖性地降低了获得吗啡输注的动机。令人惊讶的是,在相同的累进比率任务中,GAT358并不影响为获得食物奖励而工作的动机,这表明GAT358降低阿片类药物自我给药的作用具有奖赏特异性。此外,GAT58在转棒试验中未产生运动共济失调。我们的结果表明,CB1R NAMs降低了吗啡的强化特性,可能代表了一种安全减少阿片类药物成瘾行为的可行治疗途径。