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Details

Autor(en) / Beteiligte
Titel
Hatakabb, a herbal extract, contains pyrogallol as the novel mediator inhibiting LPS-induced TNF-α production by NF-κB inactivation and HMOX-1 upregulation
Ist Teil von
  • Journal of functional foods, 2022-03, Vol.90, p.104992, Article 104992
Ort / Verlag
Elsevier Ltd
Erscheinungsjahr
2022
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
  • [Display omitted] •Hatakabb inhibits LPS-induced TNF-α, IL-6, COX-2 gene expression in macrophages.•LPS-induced IκB and NF-κB phosphorylation is deviated linking to NF-κB inactivation.•HMOX-1 expression is upregulated in association with increased MAPK phosphorylation.•Pyrogallol acts as the anti-inflammatory mediator inhibiting TNF-α production. Hatakabb is a herbal extract traditionally consumed to ameliorate inflammation from pharynx infections. However, the anti-inflammatory function of Hatakabb was not investigated. This study demonstrated the anti-inflammatory potential, and underlying mechanism of Hatakabb, and its functional ingredient. In LPS-treated macrophages, Hatakabb treatment attenuated TNF-α production. A decrease in TNF-α, IL-6, and COX-2 expression was detected. In regulatory pathway analysis, Hatakabb suppressed IκB-α phosphorylation in accordance with a decrease in IκB-α degradation, and nucleus NF-κB translocation, while enhanced NF-κB phosphorylation. In addition, MAPK phosphorylation was enhanced in association with HMOX-1 upregulation. Our metabolomic analysis showed gallic acid, and pyrogallol contained in the anti-inflammatory subfraction. Compared to gallic acid, pyrogallol strongly diminished TNF-α production. Significant changes in inflammatory gene expression, and regulatory protein phosphorylation were responded to pyrogallol in similar to Hatakabb treatment. Our study, for the first time, reveals the anti-inflammatory effect, and mechanism of Hatakabb in which pyrogallol is the novel mediator inhibiting LPS-induced inflammation.
Sprache
Englisch
Identifikatoren
ISSN: 1756-4646
eISSN: 2214-9414
DOI: 10.1016/j.jff.2022.104992
Titel-ID: cdi_doaj_primary_oai_doaj_org_article_494ed35050e9409399dfa571ed7323b0

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