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1.
Int J Mol Sci ; 21(7)2020 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-32244806

RESUMEN

Periodontal diseases are caused by bacterial infection and may progress to chronic dental disease; severe inflammation may result in bone loss. Therefore, it is necessary to prevent bacterial infection or control inflammation. Periodontal ligament fibroblasts (PDLFs) are responsible for the maintenance of tissue integrity and immune and inflammatory events in periodontal diseases. The formation of bacterial complexes by Fusobacterium nucleatum and Porphyromonas gingivalis is crucial in the pathogenesis of periodontal disease. F. nucleatum is a facultative anaerobic species, considered to be a key mediator of dental plaque maturation and aggregation of other oral bacteria. P. gingivalis is an obligate anaerobic species that induces gingival inflammation by secreting virulence factors. In this study, we investigated whether Osmunda japonica extract exerted anti-inflammatory effects in primary PDLFs stimulated by oral pathogens. PDLFs were stimulated with F. nucleatum or P. gingivalis. We showed that pro-inflammatory cytokine (IL-6 and IL-8) expression was induced by LPS or bacterial infection but decreased by treatment with O. japonica extract following bacterial infection. We found that the activation of NF-κB, a transcription factor for pro-inflammatory cytokines, was modulated by O. japonica extract. Thus, O. japonica extract has immunomodulatory activity that can be harnessed to control inflammation.


Asunto(s)
Infecciones Bacterianas/prevención & control , Citocinas/antagonistas & inhibidores , Fibroblastos/efectos de los fármacos , Mediadores de Inflamación/antagonistas & inhibidores , FN-kappa B/metabolismo , Extractos Vegetales/farmacología , Adulto , Infecciones Bacterianas/metabolismo , Infecciones Bacterianas/microbiología , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Citocinas/genética , Citocinas/metabolismo , Regulación hacia Abajo/efectos de los fármacos , Helechos/química , Fibroblastos/metabolismo , Fibroblastos/microbiología , Regulación de la Expresión Génica/efectos de los fármacos , Humanos , Mediadores de Inflamación/metabolismo , Ligamento Periodontal/citología , Porphyromonas gingivalis/efectos de los fármacos , Porphyromonas gingivalis/fisiología
2.
Int J Mol Sci ; 19(9)2018 Aug 23.
Artículo en Inglés | MEDLINE | ID: mdl-30142971

RESUMEN

Periodontal disease, a chronic disease caused by bacterial infection, eventually progresses to severe inflammation and bone loss. Regulating excessive inflammation of inflamed periodontal tissues is critical in treating periodontal diseases. The periodontal ligament (PDL) is primarily a connective tissue attachment between the root and alveolar bone. PDL fibroblasts (PDLFs) produce pro-inflammatory cytokines in response to bacterial infection, which could further adversely affect the tissue and cause bone loss. In this study, we determined the ability of Litsea japonica leaf extract (LJLE) to inhibit pro-inflammatory cytokine production in PDLFs in response to various stimulants. First, we found that LJLE treatment reduced lipopolysaccharide (LPS)-induced pro-inflammatory cytokine (interleukin-6 and interleukin-8) mRNA and protein expression in PDLFs without cytotoxicity. Next, we observed the anti-inflammatory effect of LJLE in PDLFs after infection with various oral bacteria, including Fusobacterium nucleatum, Porphyromonas gingivalis, Treponema denticola, and Tannerella forsythia. These anti-inflammatory effects of LJLE were dose-dependent, and the extract was effective following both pretreatment and posttreatment. Moreover, we found that LJLE suppressed the effect of interleukin-1 beta-induced pro-inflammatory cytokine production in PDLFs. Taken together, these results indicate that LJLE has anti-inflammatory activity that could be exploited to prevent and treat human periodontitis by controlling inflammation.


Asunto(s)
Antiinflamatorios/farmacología , Fibroblastos/efectos de los fármacos , Interleucina-1beta/antagonistas & inhibidores , Lipopolisacáridos/antagonistas & inhibidores , Litsea/química , Extractos Vegetales/farmacología , Adulto , Antiinflamatorios/química , Diente Premolar/citología , Diente Premolar/cirugía , Supervivencia Celular/efectos de los fármacos , Técnicas de Cocultivo , Fibroblastos/citología , Fibroblastos/inmunología , Fibroblastos/microbiología , Fusobacterium nucleatum/química , Fusobacterium nucleatum/crecimiento & desarrollo , Fusobacterium nucleatum/patogenicidad , Voluntarios Sanos , Humanos , Interleucina-1beta/farmacología , Interleucina-6/antagonistas & inhibidores , Interleucina-6/biosíntesis , Interleucina-6/inmunología , Interleucina-8/antagonistas & inhibidores , Interleucina-8/biosíntesis , Interleucina-8/inmunología , Lipopolisacáridos/farmacología , Diente Molar/citología , Diente Molar/cirugía , Ligamento Periodontal/citología , Ligamento Periodontal/cirugía , Extractos Vegetales/química , Hojas de la Planta/química , Porphyromonas gingivalis/química , Porphyromonas gingivalis/crecimiento & desarrollo , Porphyromonas gingivalis/patogenicidad , Cultivo Primario de Células , Tannerella forsythia/química , Tannerella forsythia/crecimiento & desarrollo , Tannerella forsythia/patogenicidad , Treponema denticola/química , Treponema denticola/crecimiento & desarrollo , Treponema denticola/patogenicidad
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