Effects of Chitosan Particles in Periodontal Pathogens and Gingival Fibroblasts
Author
dc.contributor.author
Arancibia R., Elizabeth
Author
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Maturana Salgado, Cristian
es_CL
Author
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Silva, D.
es_CL
Author
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Tobar, N.
es_CL
Author
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Tapia Villanueva, Cristián
es_CL
Author
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Salazar, J.C.
es_CL
Author
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Martínez, J.
es_CL
Author
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Smith, P.C.
es_CL
Admission date
dc.date.accessioned
2014-01-24T13:28:28Z
Available date
dc.date.available
2014-01-24T13:28:28Z
Publication date
dc.date.issued
2013
Cita de ítem
dc.identifier.citation
J Dent Res 92(8):740-745, 2013
en_US
Identifier
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DOI: 10.1177/0022034513494816
Identifier
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https://repositorio.uchile.cl/handle/2250/129163
General note
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Artículo de publicación ISI
en_US
Abstract
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Chitosan is a naturally derived polymer with antimicrobial and anti-inflammatory properties. However, studies evaluating the role of chitosan in the control of periodontal pathogens and the responses of fibroblasts to inflammatory stimuli are lacking. In the present study, we analyzed whether chitosan particles may inhibit the growth of periodontal pathogens and modulate the inflammatory response in human gingival fibroblasts. Chitosan particles were generated through ionic gelation. They inhibited the growth of Porphyromonas gingivalis and Aggregatibacter actinomycetemcomitans at 5 mg/mL. Conversely, IL-1β strongly stimulated PGE2 protein levels in gingival fibroblasts, and chitosan inhibited this response at
50 μg/mL. IL-1β–stimulated PGE2 production was dependent on the JNK pathway, and chitosan strongly inhibited this response. IL-1β stimulated NF-κB activation, another signaling pathway involved in PGE2 production. However, chitosan particles were unable to modify NF-κB signaling. The present study shows that chitosan exerts a predominantly anti-inflammatory activity by modulating PGE2 levels through the JNK pathway, which may be useful in the prevention or treatment of periodontal inflammation.
en_US
Lenguage
dc.language.iso
en
en_US
Publisher
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International & American Associations for Dental Research