Trigeminal nerve stimulation triggers oral mast cell activation and vascular permeability

外渗 辣椒素 医学 P物质 刺激 脱颗粒 埃文斯蓝 神经源性炎症 血管通透性 内科学 内分泌学 三叉神经节 炎症 肥大细胞 组胺 麻醉 病理 神经肽 免疫学 受体 生物 神经科学 感觉系统
作者
Mohammed A. Alhelal,Iro Palaska,Smaro Panagiotidou,Richard Létourneau,Theoharis C. Theoharides
出处
期刊:Annals of Allergy Asthma & Immunology [Elsevier BV]
卷期号:112 (1): 40-45 被引量:11
标识
DOI:10.1016/j.anai.2013.10.011
摘要

The nervous system contributes to the pathophysiology of allergic and inflammatory diseases, including oral inflammation. Mast cells (MCs) are involved in their pathogenesis through proinflammatory mediator release.To investigate the effect of trigeminal nerve (TN) stimulation compared with sham operation on MC activation and oral vascular permeability in the gingiva, palate, buccal mucosa, and tongue of the rat and to examine the possible role of substance P using rats treated with capsaicin as neonates to deplete substance P.Six male Sprague-Dawley rats (250 g) were anesthetized and injected intravenously with Evans Blue (EB). Six other rats were injected neonatally with capsaicin (n = 3) or solvent (n = 3) and then injected with EB when they reached 250 g. The mandibular branch of the TN was stimulated for 1 minute (n = 3), and the remaining rats (n = 3) were subjected to sham operation. The ipsilateral and contralateral sides of the mouth were examined for EB extravasation, and tissue sections were removed for light and electron microscopy.TN stimulation resulted in EB extravasation in the ipsilateral side compared with the contralateral side or the ipsilateral side of sham-operated rats. Significant degranulation of MCs also was evident only on the ipsilateral side (P < .0001). There was no difference in MC degranulation between the vehicle- and capsaicin-treated rats, implying that neuropeptides other than substance P may be involved.This is the first time that TN stimulation has been shown to result in MC activation and oral vascular permeability, suggesting that MC inhibitors may be used for the treatment of oral inflammatory diseases.
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