Linarin down-regulates phagocytosis, pro-inflammatory cytokine production, and activation marker expression in RAW264.7 macrophages

Plant-extracted flavonoid glycosides have been reported to be bioactive compounds with pleiotropic functions, including antioxidant, anti-inflammatory, and anti-cancer effects. This study investigated the anti-inflammatory role of linarin (acacetin-7-rutinoside, which is found in Chrysanthemum indic...

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Published inFood science and biotechnology Vol. 25; no. 5; pp. 1437 - 1442
Main Authors Kim, Bomi, Lee, Jong Hun, Seo, Myung-Ji, Eom, Seok Hyun, Kim, Wooki
Format Journal Article
LanguageEnglish
Published Seoul The Korean Society of Food Science and Technology 01.10.2016
Springer Nature B.V
한국식품과학회
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ISSN1226-7708
2092-6456
2092-6456
DOI10.1007/s10068-016-0223-3

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Summary:Plant-extracted flavonoid glycosides have been reported to be bioactive compounds with pleiotropic functions, including antioxidant, anti-inflammatory, and anti-cancer effects. This study investigated the anti-inflammatory role of linarin (acacetin-7-rutinoside, which is found in Chrysanthemum indicum (Gam-Guk) and Dendranthema zawadskii (Gu-Jul-Cho)), on lipopolysaccharide-stimulated RAW264.7 macrophages. Linarin treatments exhibited no cytotoxicity up to a concentration of 30 μM, as assessed by MTT assay. The production of nitric oxide, an inflammatory mediator, was decreased by addition of linarin. The secretion of pro-inflammatory cytokines, interleukin-1β and interleukin-6, was significantly decreased in a dose-dependent manner. Linarin also decreased the phagocytic ability of macrophages following co-culture with fluorescent beads. In addition, expression levels of antigenpresenting surface markers, MHC II and CD80, were suppressed by linarin. Taken together, these results indicate that the flavonoid glycoside linarin has an anti-inflammatory effect, in part through the suppression of phagocytosis, cytokine production, and antigen presentation in macrophages.
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G704-000139.2016.25.5.008
ISSN:1226-7708
2092-6456
2092-6456
DOI:10.1007/s10068-016-0223-3