4.7 Article

Saponarin from barley sprouts inhibits NF-κB and MAPK on LPS-induced RAW 264.7 cells

Journal

FOOD & FUNCTION
Volume 5, Issue 11, Pages 3005-3013

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4fo00612g

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Funding

  1. Cooperative Research Program for Agriculture Science & Technology Development (Project title: Investigation and evaluation of biological activity for functional compounds on alcoholic fatty liver and detoxification using barley sprouts) [PJ01052801]
  2. Rural Development Administration (RDA), Republic of Korea

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Saponarin (SA), a natural flavonoid, is known for its antioxidant and hepatoprotective activities. SA is the predominant compound (1142.7 +/- 0.9 mg per 100 g) in barley sprouts, constituting 72% of the total polyphenol content. We investigated, for the first time, the effects of SA from barley sprouts on cellular anti-inflammatory responses. In lipopolysaccharide (LPS)-induced RAW 264.7 macrophages, SA suppressed the activation of NF-kappa B, as evidenced by the inhibition of NF-kappa B DNA binding, nuclear translocation, I kappa B alpha phosphorylation, and reporter gene expression, and it downregulated the expression of the pro-inflammatory mediator IL-6. Furthermore, SA reduced the transcription of NF-kappa B target molecules COX2 and FLIP inhibited the phosphorylation of mitogen-activated protein kinases ERK and p38. These results suggest that SA isolated from barley sprouts exerts anti-inflammatory effects in LPS-induced RAW 264.7 macrophages via inhibition of NF-kappa B, ERK and p38 signaling. Thus, SA may be a promising natural anti-inflammatory agent.

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