4.7 Article

A Comparative In Vitro Evaluation of the Anti-Inflammatory Effects of a Tisochrysis lutea Extract and Fucoxanthin

期刊

MARINE DRUGS
卷 19, 期 6, 页码 -

出版社

MDPI
DOI: 10.3390/md19060334

关键词

microalgae; Tisochrysis lutea; fucoxanthin; inflammation; RAW 264; 7; microRNA

资金

  1. Ente Cassa di Risparmio Firenze [2015.0919, 2018.1002]
  2. Regione Toscana (Italy) under Par-FAS 2007-2013 Projects (Centro di Competenza VALORE)
  3. POR FSE 2014-2020-Progetto Strategico STREAMING sottoprogetto PhotoWING (Regione Toscana, Italy) [UNIFI_FSE2017]

向作者/读者索取更多资源

The study compared the effects of T. lutea F&M-M36 methanolic extract with fucoxanthin (FX) on LPS-stimulated macrophages. The extract showed potent anti-inflammatory activity against COX-2/PGE2 and NLRP3/mir-223, possibly due to synergistic effects with FX and simple phenolic compounds. T. lutea F&M-M36 may be a potential source of anti-inflammatory compounds for further evaluation in inflammation models.
In this study, we compared the effects of a Tisochrysis lutea (T. lutea) F&M-M36 methanolic extract with those of fucoxanthin (FX) at equivalent concentration, on lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages. The T. lutea F&M-M36 methanolic extract contained 4.7 mg of FX and 6.22 mg of gallic acid equivalents of phenols per gram. HPLC analysis revealed the presence of simple phenolic acid derivatives. The T. lutea F&M-M36 extract exhibited a potent and concentration-dependent inhibitory activity against COX-2 dependent PGE2 production compared to FX alone. Compared to LPS, T. lutea F&M-M36 extract and FX reduced the expression of IL-6 and of Arg1 and enhanced that of IL-10 and of HO-1; T. lutea F&M-M36 extract also significantly abated the expression of NLRP3, enhanced mir-223 expression and reduced that of mir-146b, compared to LPS (p < 0.05). These findings indicate that T. lutea F&M-M36 methanolic extract has a peculiar anti-inflammatory activity against COX-2/PGE2 and NLRP3/mir-223 that might be attributable to the known anti-inflammatory effects of simple phenolic compounds found in the extract that may synergize with FX. Our data suggest that T. lutea F&M-M36 may serve as a source of anti-inflammatory compounds to be further evaluated in in vivo models of inflammation.

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