Expression of ASIC3 in the Trigeminal Nucleus Caudalis Plays a Role in a Rat Model of Recurrent Migraine
Autor: | Guangcheng Qin, Sha Wang, Wen-Hui Yan, Lixue Chen, Jiying Zhou, Chaoyang Liu, Baixue Wu |
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Rok vydání: | 2018 |
Předmět: |
Male
Pain Threshold 0301 basic medicine Nervous system medicine.medical_specialty Calcitonin Gene-Related Peptide Migraine Disorders Stimulation Calcitonin gene-related peptide Receptor Activity-Modifying Protein 1 Rats Sprague-Dawley Pathogenesis 03 medical and health sciences Cellular and Molecular Neuroscience Trigeminal Caudal Nucleus 0302 clinical medicine Internal medicine medicine Animals Receptor business.industry General Medicine medicine.disease Rats Acid Sensing Ion Channels 030104 developmental biology Endocrinology medicine.anatomical_structure Migraine RAMP1 business 030217 neurology & neurosurgery |
Zdroj: | Journal of Molecular Neuroscience. 66:44-52 |
ISSN: | 1559-1166 0895-8696 |
DOI: | 10.1007/s12031-018-1113-3 |
Popis: | Acid-sensing ion channel 3 (ASIC3) is abundant in the trigeminal nervous system and is most sensitive to a slight pH decrease. Recent studies have indicated that ASIC3 in the peripheral trigeminal ganglia is likely involved in the pathogenesis of migraine pain. However, it is unclear whether this receptor plays a role in recurrent migraine, namely, migraine chronicity. Here, we aimed to investigate the role of ASIC3 in an animal model of recurrent migraine (RM). In this study, we established a rat model of RM through repeated administration of inflammatory soup (IS) onto the dura. Then, we tested the mechanical pain thresholds of the face and hindpaws by von Frey filaments. qRT-PCR, Western blot and immunofluorescence labelling were used to detect the expression and localization of ASIC3 in the trigeminal nucleus caudalis (TNC). The protein levels of calcitonin gene-related peptide (CGRP), its receptor component receptor activity modifying protein 1 (RAMP1) and c-Fos were analysed following treatment with the ASIC3 inhibitor APETx2 and activator 2-guanidine-4-methylquinazoline (GMQ). We found decreased pain thresholds after repeated dural inflammatory stimulation, which suggested the establishment of an RM model. Based on this model, we observed elevated expression of ASIC3 in the TNC group compared to that in the Sham group. ASIC3 was primarily expressed in neurons but not in astrocytes of the TNC. Moreover, APETx2 attenuated tactile allodynia and significantly decreased the expression of c-Fos, CGRP and RAMP1, while GMQ aggravated these effects compared to those observed in the IS + vehicle group. These findings indicate a critical role of ASIC3 channels in the pathophysiology of RM, and ASIC3 might represent a potential therapeutic target to prevent the progression of migraine. |
Databáze: | OpenAIRE |
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