Spekker Eleonóra, Laborc Klaudia Flóra, Bohár Zsuzsanna, Nagy-Grócz Gábor, Fejes-Szabó Annamária, Szűcs Mónika, Vécsei László, Párdutz Árpád
Department of Neurology, Interdisciplinary Excellence Center, Faculty of Medicine, Albert Szent-Györgyi Clinical Center, University of Szeged, Semmelweis utca 6, Szeged, H-6725, Hungary.
MTA-SZTE Neuroscience Research Group, Szeged, Hungary.
J Headache Pain. 2021 Mar 31;22(1):17. doi: 10.1186/s10194-021-01229-3.
The topical inflammatory soup can model the inflammation of the dura mater causing hypersensitivity and activation of the trigeminal system, a phenomenon present in migraineurs. Calcitonin gene-related peptide, transient receptor potential vanilloid-1 receptor, and neuronal nitric oxide synthase are important in the sensitization process there. 5-HT receptor agonists, triptans are used as a treatment of migraine. Kynurenic acid an NMDA antagonist can act on structures involved in trigeminal activation.
We investigated the effect of inflammatory soup induced dural inflammation on the calcitonin gene-related peptide, transient receptor potential vanilloid-1 receptor, and neuronal nitric oxide synthase levels in the caudal trigeminal nucleus. We also tested whether pretreatment with a well-known antimigraine drug, such as sumatriptan and kynurenic acid, a compound with a different mechanism of action, can affect these changes and if their modulatory effects are comparable.
After subcutaneous sumatriptan or intraperitoneal kynurenic acid the dura mater of adult male Sprague-Dawley rats (n = 72) was treated with inflammatory soup or its vehicle (synthetic interstitial fluid). Two and a half or four hours later perfusion was performed and the caudal trigeminal nucleus was removed for immunohistochemistry.
Inflammatory soup increased calcitonin gene-related peptide, transient receptor potential vanilloid-1 receptor, and neuronal nitric oxide synthase in the caudal trigeminal nucleus compared to placebo, which was attenuated by sumatriptan and kynurenic acid. This suggests the involvement of 5-HT and NMDA receptors in neurogenic inflammation development of the dura and thus in migraine attacks.
局部炎性汤可模拟硬脑膜炎症,引发超敏反应并激活三叉神经系统,这是偏头痛患者中存在的一种现象。降钙素基因相关肽、瞬时受体电位香草酸受体1和神经元型一氧化氮合酶在该致敏过程中起重要作用。5-羟色胺受体激动剂曲坦类药物被用作偏头痛的治疗药物。犬尿喹啉酸作为一种N-甲基-D-天冬氨酸拮抗剂,可作用于参与三叉神经激活的结构。
我们研究了炎性汤诱导的硬脑膜炎症对三叉神经尾核中降钙素基因相关肽、瞬时受体电位香草酸受体1和神经元型一氧化氮合酶水平的影响。我们还测试了用一种知名的抗偏头痛药物(如舒马曲坦)和一种作用机制不同的化合物犬尿喹啉酸进行预处理是否会影响这些变化,以及它们的调节作用是否相当。
成年雄性Sprague-Dawley大鼠(n = 72)皮下注射舒马曲坦或腹腔注射犬尿喹啉酸后,用炎性汤或其溶媒(合成组织间液)处理硬脑膜。两小时半或四小时后进行灌注,并取出三叉神经尾核进行免疫组织化学检测。
与安慰剂相比,炎性汤使三叉神经尾核中的降钙素基因相关肽、瞬时受体电位香草酸受体1和神经元型一氧化氮合酶增加,而舒马曲坦和犬尿喹啉酸可减弱这种增加。这表明5-羟色胺和N-甲基-D-天冬氨酸受体参与了硬脑膜神经源性炎症的发展,进而参与了偏头痛发作。