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dc.contributor.authorLynds, Randien_US
dc.contributor.authorLyu, Chuangen_US
dc.contributor.authorLyu, Gong-Weien_US
dc.contributor.authorShi, Xie-Qien_US
dc.contributor.authorRosén, Annikaen_US
dc.contributor.authorMustafa, Kamal Babikeir Elnen_US
dc.contributor.authorShi, Tie-Junen_US
dc.PublishedLynds R, Lyu C, Lyu G, Shi XQ, Rosén A, Mustafa KBE, Shi Sten. Neuronal plasticity of trigeminal ganglia in mice following nerve injury. Journal of Pain Research. 2017;10:349-357eng
dc.description.abstractBackground: Nerve injury may induce neuropathic pain. In studying the mechanisms of orofacial neuropathic pain, attention has been paid to the plastic changes that occur in the trigeminal ganglia (TGs) and nucleus in response to an injury of the trigeminal nerve branches. Previous studies have explored the impact of sciatic nerve injury on dorsal root ganglia (DRGs) and it has shown dramatic changes in the expression of multiple biomarkers. In large, the changes in biomarker expression in TGs after trigeminal nerve injury are similar to that in DRGs after sciatic nerve injury. However, important differences exist. Therefore, there is a need to study the plasticity of biomarkers in TGs after nerve injury in the context of the development of neuropathic pain-like behaviors. Aim: The aim of this study was to investigate the plasticity of biomarkers associated with chronic persistent pain in TGs after trigeminal nerve injury. Materials and methods: To mimic the chronic nature of the disorder, we used an intraoral procedure to access the infraorbital nerve (ION) and induced a nerve injury in mice. Immunohistochemistry and quantification were used for revealing the expression level of each biomarker in TGs after nerve injury. Results: Two weeks after partial ION injury, immunohistochemistry results showed strongly upregulated expressions of activating transcription factor 3 and neuropeptide Y (NPY) in the ipsilateral TGs. Microglial cells were also activated after nerve injury. In regard to positive neuronal profile counting, however, no significant difference in expression was observed in galanin, substance P, calcitonin gene-related peptide, neuronal nitric oxide synthase, phosphorylated AKT, or P2X3 in ipsilateral TGs when compared to contralateral TGs. Conclusion: In this study, the expression and regulation of biomarkers in TGs have been observed in response to trigeminal nerve injury. Our results suggest that NPY and Iba1 might play crucial roles in the pathogenesis of orofacial neuropathic pain following this type of injury. Further investigations on the relevance of these changes may help to target suitable treatment possibilities for trigeminal neuralgia.en_US
dc.publisherDove Presseng
dc.rightsAttribution CC BY-NCeng
dc.subjectinfraorbital nerveeng
dc.subjectorofacial paineng
dc.subjectsensory neuronseng
dc.subjectanimal modeleng
dc.titleNeuronal plasticity of trigeminal ganglia in mice following nerve injuryen_US
dc.typePeer reviewed
dc.typeJournal article
dc.rights.holderCopyright 2017 The Author(s)
dc.source.journalJournal of Pain Research

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