Department of Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA, 52242, USA.
Department of Neurology, University of Iowa, Iowa City, IA, 52242, USA.
J Headache Pain. 2024 Oct 16;25(1):178. doi: 10.1186/s10194-024-01883-3.
Migraine is a common and complex neurological disorder that has a high impact on quality of life. Recent advances with drugs that target the neuropeptide calcitonin gene-related peptide (CGRP) have helped, but treatment options remain insufficient. CGRP is released from trigeminal sensory fibers and contributes to peripheral sensitization, perhaps in part due to actions on immune cells in the trigeminovascular system. In this review, we will discuss the potential of cannabinoid targeting of immune cells as an innovative therapeutic target for migraine treatment. We will cover endogenous endocannabinoids, plant-derived phytocannabinoids and synthetically derived cannabinoids. The focus will be on six types of immune cells known to express multiple cannabinoid receptors: macrophages, monocytes, mast cells, dendritic cells, B cells, and T cells. These cells also contain receptors for CGRP and as such, cannabinoids might potentially modulate the efficacy of current CGRP-targeting drugs. Unfortunately, to date most studies on cannabinoids and immune cells have relied on cell cultures and only a single preclinical study has tested cannabinoid actions on immune cells in a migraine model. Encouragingly, in that study a synthetically created stable chiral analog of an endocannabinoid reduced meningeal mast cell degranulation. Likewise, clinical trials evaluating the safety and efficacy of cannabinoid-based therapies for migraine patients have been limited but are encouraging. Thus, the field is at its infancy and there are significant gaps in our understanding of the impact of cannabinoids on immune cells in migraine. Future research exploring the interactions between cannabinoids and immune cells could lead to more targeted and effective migraine treatments.
偏头痛是一种常见且复杂的神经系统疾病,对生活质量有很大影响。近年来,靶向降钙素基因相关肽(CGRP)的药物取得了进展,但治疗选择仍然不足。CGRP 从三叉神经感觉纤维释放出来,有助于外周致敏,部分原因可能是其对三叉血管系统中的免疫细胞的作用。在这篇综述中,我们将讨论靶向免疫细胞的大麻素作为偏头痛治疗的创新治疗靶点的潜力。我们将涵盖内源性大麻素、植物源性大麻素和合成衍生的大麻素。重点将放在已知表达多种大麻素受体的六种免疫细胞上:巨噬细胞、单核细胞、肥大细胞、树突状细胞、B 细胞和 T 细胞。这些细胞也含有 CGRP 受体,因此大麻素可能潜在地调节当前 CGRP 靶向药物的疗效。不幸的是,迄今为止,大多数关于大麻素和免疫细胞的研究都依赖于细胞培养,只有一项初步临床研究测试了大麻素在偏头痛模型中对免疫细胞的作用。令人鼓舞的是,在该研究中,一种内源性大麻素的合成稳定手性类似物减少了脑膜肥大细胞脱颗粒。同样,评估大麻素类药物治疗偏头痛患者的安全性和疗效的临床试验也很有限,但令人鼓舞。因此,该领域还处于起步阶段,我们对大麻素对偏头痛免疫细胞的影响的理解存在很大差距。未来探索大麻素与免疫细胞之间相互作用的研究可能会导致更有针对性和更有效的偏头痛治疗方法。