Negative allosteric modulation of CB1 cannabinoid receptor signaling suppresses opioid-mediated tolerance and withdrawal without blocking opioid antinociception

• Published in: Neuropharmacology 2024-10, Vol.257, p.110052, Article 110052
• Main Authors: Iyer, Vishakh, Saberi, Shahin A., Pacheco, Romario, Sizemore, Emily Fender, Stockman, Sarah, Kulkarni, Abhijit, Cantwell, Lucas, Thakur, Ganesh A., Hohmann, Andrea G.
• Format: Article
• Language: English
• Subjects: Allosteric modulator; CB1; Endocannabinoid; Opioid; Tolerance; Withdrawal
• ISSN: 0028-3908; 1873-7064; 1873-7064
• DOI: 10.1016/j.neuropharm.2024.110052

The direct blockade of CB1 cannabinoid receptors produces therapeutic effects as well as adverse side-effects that limit their clinical potential. CB1 negative allosteric modulators (NAMs) represent an indirect approach to decrease the affinity and/or efficacy of orthosteric cannabinoid ligands or endocannabinoids at CB1. We recently reported that GAT358, a CB1-NAM, blocked opioid-induced mesocorticolimbic dopamine release and reward via a CB1-allosteric mechanism of action. Whether a CB1-NAM dampens opioid-mediated therapeutic effects such as analgesia or alters other unwanted opioid side-effects remain unknown. Here, we characterized the effects of GAT358 on nociceptive behaviors in the presence and absence of morphine in male rats. We examined the impact of GAT358 on formalin-evoked pain behavior and Fos protein expression, a marker of neuronal activation, in the lumbar spinal cord. We also assessed the impact of GAT358 on morphine-induced slowing of colonic transit, tolerance, and withdrawal behaviors in male mice. GAT358 attenuated morphine antinociceptive tolerance without blocking acute antinociception and reduced morphine-induced slowing of colonic motility without impacting fecal boli production. GAT358 also produced antinociception in the presence and absence of morphine in the formalin model of inflammatory nociception and reduced the number of formalin-evoked Fos protein-like immunoreactive cells in the lumbar spinal cord. Finally, GAT358 mitigated the somatic signs of naloxone-precipitated, but not spontaneous, opioid withdrawal following chronic morphine dosing. Our results support the therapeutic potential of CB1-NAMs as novel drug candidates aimed at preserving opioid-mediated analgesia while preventing their unwanted side-effects. Our studies also uncover previously unrecognized antinociceptive properties associated with an arrestin-biased CB1-NAM. [Display omitted] •CB1 negative allosteric modulator (NAM) GAT358 attenuated morphine tolerance.•GAT358 reduced morphine-induced slowing of colonic motility but not fecal production.•GAT358 was antinociceptive for formalin pain alone and when combined with morphine.•GAT358 reduced formalin-evoked Fos protein expression in the lumbar spinal cord.•GAT358 mitigated naloxone precipitated withdrawal after chronic morphine dosing.