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Role of acid-sensing ion channel 3 in sub-acute-phase inflammation

BACKGROUND: Inflammation-mediated hyperalgesia involves tissue acidosis and sensitization of nociceptors. Many studies have reported increased expression of acid-sensing ion channel 3 (ASIC3) in inflammation and enhanced ASIC3 channel activity with pro-inflammatory mediators. However, the role of AS...

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Detalles Bibliográficos
Autores principales: Yen, Yi-Tin, Tu, Pan-Hsien, Chen, Chien-Ju, Lin, Yi-Wen, Hsieh, Sung-Tsang, Chen, Chih-Cheng
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2632618/
https://www.ncbi.nlm.nih.gov/pubmed/19126241
http://dx.doi.org/10.1186/1744-8069-5-1
Descripción
Sumario:BACKGROUND: Inflammation-mediated hyperalgesia involves tissue acidosis and sensitization of nociceptors. Many studies have reported increased expression of acid-sensing ion channel 3 (ASIC3) in inflammation and enhanced ASIC3 channel activity with pro-inflammatory mediators. However, the role of ASIC3 in inflammation remains inconclusive because of conflicting results generated from studies of ASIC3 knockout (ASIC3(-/-)) or dominant-negative mutant mice, which have shown normal, decreased or increased hyperalgesia during inflammation. RESULTS: Here, we tested whether ASIC3 plays an important role in inflammation of subcutaneous tissue of paw and muscle in ASIC3(-/- )mice induced by complete Freund's adjuvant (CFA) or carrageenan by investigating behavioral and pathological responses, as well as the expression profile of ion channels. Compared with the ASIC3(+/+ )controls, ASIC3(-/- )mice showed normal thermal and mechanical hyperalgesia with acute (4-h) intraplantar CFA- or carrageenan-induced inflammation, but the hyperalgesic effects in the sub-acute phase (1–2 days) were milder in all paradigms except for thermal hyperalgesia with CFA-induced inflammation. Interestingly, carrageenan-induced primary hyperalgesia was accompanied by an ASIC3-dependent Nav1.9 up-regulation and increase of tetrodotoxin (TTX)-resistant sodium currents. CFA-inflamed muscle did not evoke hyperalgesia in ASIC3(-/- )or ASIC3(+/+ )mice, whereas carrageenan-induced inflammation in muscle abolished mechanical hyperalgesia in ASIC3(-/- )mice, as previously described. However, ASIC3(-/- )mice showed attenuated pathological features such as less CFA-induced granulomas and milder carrageenan-evoked vasculitis as compared with ASIC3(+/+ )mice. CONCLUSION: We provide a novel finding that ASIC3 participates in the maintenance of sub-acute-phase primary hyperalgesia in subcutaneous inflammation and mediates the process of granuloma formation and vasculitis in intramuscular inflammation.