Department of Psychological and Brain Sciences, Indiana University Bloomington, Bloomington, Indiana, USA.
Department of Pharmaceutical Sciences, Northeastern University, Boston, Massachusetts, USA.
Addict Biol. 2024 Aug;29(8):e13429. doi: 10.1111/adb.13429.
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 negative allosteric modulation of CB1R signalling would reduce the reinforcing properties of morphine and decrease behaviours associated with opioid misuse. By employing intravenous self-administration in mice, we studied the effects of GAT358, a functionally-biased CB1R negative allosteric modulator (NAM), on morphine intake, relapse-like behaviour and motivation to work for morphine infusions. GAT358 reduced morphine infusion intake during the maintenance phase of morphine self-administration under a fixed ratio 1 schedule of reinforcement. GAT358 also decreased morphine-seeking behaviour after forced abstinence. Moreover, GAT358 dose dependently decreased the motivation to obtain morphine infusions under 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 was reward specific. Furthermore, GAT58 did not produce motor ataxia in the rotarod test. Our results suggest that CB1R NAMs reduced the reinforcing properties of morphine and could represent a viable therapeutic route to safely decrease misuse of opioids.
内源性大麻素系统与奖励系统相互作用,调节对自然强化物以及滥用药物的反应。先前的临床前研究表明,直接阻断 CB1 大麻素受体 (CB1R) 可能成为治疗药物使用障碍的潜在药物治疗方法,但由于严重的精神副作用,该策略在临床试验中失败。已经出现了替代策略,通过开发变构调节剂来规避直接 CB1 结合的副作用。我们假设 CB1R 信号的负变构调节将降低吗啡的强化作用,并减少与阿片类药物滥用相关的行为。通过在小鼠中进行静脉内自我给药,我们研究了 GAT358(一种具有功能偏向的 CB1R 负变构调节剂 (NAM))对吗啡摄入、类复发行为和获得吗啡输注的动机的影响。在固定比率 1 强化方案下,GAT358 减少了吗啡自我给药维持阶段的吗啡输注摄入量。GAT358 还减少了强制戒断后的吗啡寻求行为。此外,GAT358 剂量依赖性地降低了在递增比率强化方案下获得吗啡输注的动机。引人注目的是,GAT358 并未在相同的递增比率任务中影响获得食物奖励的动机,这表明 GAT358 降低阿片类自我给药的作用是特定于奖励的。此外,GAT58 在旋转棒测试中不会引起运动共济失调。我们的结果表明,CB1R NAMs 降低了吗啡的强化作用,可能代表一种安全减少阿片类药物滥用的可行治疗途径。