Pharmacology and Therapeutics, School of Medicine, Centre for Pain Research and Galway Neuroscience Centre, National University of Ireland, Galway, Ireland.
Drug Science, St. Peters House, Wood Street, London, UK; Faculty of Medicine, Department of Brain Sciences, Imperial College London, UK.
Pharmacol Ther. 2022 Dec;240:108216. doi: 10.1016/j.pharmthera.2022.108216. Epub 2022 May 21.
Characterised by chronic widespread musculoskeletal pain, generalised hyperalgesia, and psychological distress, fibromyalgia (FM) is a significant unmet clinical need. The endogenous cannabinoid system plays an important role in modulating both pain and the stress response. Here, we appraise the evidence, from preclinical and clinical studies, for a role of the endocannabinoid system in FM and the therapeutic potential of targeting the endocannabinoid system. While many animal models have been used to study FM, the reserpine-induced myalgia model has emerged as perhaps the most translatable to the clinical phenotype. Inhibition of fatty acid amide hydrolase (FAAH) has shown promise in preclinical studies, ameliorating pain- and anxiety-related behaviour . Clinically, there is evidence for alterations in the endocannabinoid system in patients with FM, including single nucleotide polymorphisms and increased levels of circulating endocannabinoids and related N-acylethanolamines. Single entity cannabinoids, cannabis, and cannabis-based medicines in patients with FM show promise therapeutically but limitations in methodology and lack of longitudinal studies to assess efficacy and tolerability preclude the current recommendation for their use in patients with FM. Gaps in the literature that warrant further investigation are discussed, particularly the need for further development of animal models with high validity for the multifaceted nature of FM, balanced studies to eliminate sex-bias in preclinical research, and ultimately, better translation between preclinical and clinical research.
纤维肌痛(FM)的特征是慢性广泛的肌肉骨骼疼痛、全身性痛觉过敏和心理困扰,是未满足的重要临床需求。内源性大麻素系统在调节疼痛和应激反应方面起着重要作用。在这里,我们评估了来自临床前和临床研究的内源性大麻素系统在 FM 中的作用以及靶向内源性大麻素系统的治疗潜力的证据。虽然已经使用了许多动物模型来研究 FM,但育亨宾诱导的肌痛模型已被证明最能转化为临床表型。在临床前研究中,抑制脂肪酸酰胺水解酶(FAAH)显示出有希望的结果,可改善疼痛和焦虑相关行为。临床证据表明 FM 患者的内源性大麻素系统发生了改变,包括单核苷酸多态性以及循环内源性大麻素和相关 N-酰基乙醇胺水平升高。单一实体大麻素、大麻和大麻基药物在 FM 患者中显示出治疗潜力,但方法学的局限性以及缺乏评估疗效和耐受性的纵向研究,排除了目前建议将其用于 FM 患者的使用。讨论了需要进一步研究的文献中的空白,特别是需要进一步开发具有高有效性的动物模型,以研究 FM 的多方面性质,平衡研究以消除临床前研究中的性别偏见,以及最终在临床前和临床研究之间更好地转化。