Department of Clinical Experimental Research, Glostrup Research Institute, Copenhagen University Hospital, Rigshospitalet Glostrup, 2600 Glostrup, Denmark.
Department of Biology, Section of Cell Biology and Physiology, University of Copenhagen, 1017 Copenhagen, Denmark.
Cells. 2022 Aug 6;11(15):2444. doi: 10.3390/cells11152444.
Migraines constitute a common neurological and headache disorder affecting around 15% of the world's population. In addition to other mechanisms, neurogenic neuroinflammation has been proposed to play a part in migraine chronification, which includes peripheral and central sensitization. There is therefore considerable evidence suggesting that inflammation in the intracranial meninges could be a key element in addition to calcitonin gene-related peptide (CGRP), leading to sensitization of trigeminal meningeal nociceptors in migraines. There are several studies that have utilized this approach, with a strong focus on using inflammatory animal models. Data from these studies show that the inflammatory process involves sensitization of trigeminovascular afferent nerve terminals. Further, by applying a wide range of different pharmacological interventions, insight has been gained on the pathways involved. Importantly, we discuss how animal models should be used with care and that it is important to evaluate outcomes in the light of migraine pathology.
偏头痛是一种常见的神经和头痛疾病,影响全球约 15%的人口。除了其他机制外,神经源性神经炎症被认为在偏头痛慢性化中起作用,包括外周和中枢敏化。因此,有相当多的证据表明,颅内脑膜中的炎症可能是除降钙素基因相关肽(CGRP)之外的一个关键因素,导致偏头痛中三叉神经脑膜伤害感受器的敏化。有几项研究采用了这种方法,重点是使用炎症动物模型。这些研究的数据表明,炎症过程涉及三叉血管传入神经末梢的敏化。此外,通过应用广泛的不同药理学干预措施,我们对涉及的途径有了更深入的了解。重要的是,我们讨论了应该如何谨慎使用动物模型,以及根据偏头痛病理来评估结果的重要性。