<?xml version="1.0" encoding="UTF-8"?>
<records>
<record>
<language>eng</language>
<publisher>Science and Education Publishing</publisher>
<journalTitle>Journal of Food and Nutrition Research</journalTitle>
<eissn>2333-1240</eissn>
<publicationDate>2016-08-19</publicationDate>
<volume>4</volume>
<issue>8</issue>
<startPage>515</startPage>
<endPage>521</endPage>
<doi>10.12691/jfnr-4-8-5</doi>
<publisherRecordId>JFNR2016485</publisherRecordId>
<documentType>article</documentType>
<title language="eng">Silibinin Suppresses Mediators of Inflammation through the Inhibition of TLR4-TAK1 Pathway in LPS-induced RAW264.7 Cells</title>
<authors>
<author>
<name>Ji-Hyeon Song</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Kui-Jin Kim</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Boo-Yong Lee</name>
<email>bylee@cha.ac.kr</email>
<affiliationId>1</affiliationId>
</author>

</authors>
<affiliationsList>
<affiliationName affiliationId="1">Department of Food Science and Biotechnology, CHA University, Kyonggi 463-400, South Korea</affiliationName>


</affiliationsList>
<abstract language="eng">Silibinin is the major bioactive compound of silymarin which is the mixture of flavonolignans extracted from milk thistle. Silibinin has been shown to possess anti-inflammatory activity. However, the underlying mechanisms still remain unclear. The aims of this study were to determine the effect of silibinin on molecular mechanism in lipopolysaccharide (LPS)-induced RAW264.7 macrophage cells. Here, we observed that silibinin attenuated the production of nitric oxide (NO) and its regulatory protein inducible nitric oxide synthase (iNOS) expression. The pro-inflammatory cytokine interleukin (IL)-1β was inhibited by silibinin in a time dependent manner. Moreover, silibinin decreased the expression of toll-like receptor (TLR)-4, TAK1, and IRF3. TLR- associated MAPK signaling pathway was also dramatically down-regulated in LPS-induced RAW 264.7 cells with presence of silibinin. Silibinin repressed oxidative stress-associated proteins including NOX4, G6PDH, and CuZnSOD, while silibinin increased the expression of GR and catalase in LPS-induced RAW264.7 cells. In the current study, silibinin suppresses the LPS-induced inflammation via modulation of TLR4-TAK1 signaling and subsequently attenuated the production of inflammation mediators in RAW264.7 cells. Therefore, we suggest that silibinin has a potential bioactivity for prevention and intervention of endotoxin-mediated inflammation and TLR4-TAK1-associated chronic diseases.</abstract>
<fullTextUrl format="pdf">http://pubs.sciepub.com/jfnr/4/8/5/jfnr-4-8-5.pdf</fullTextUrl>
<keywords language="eng"><keyword>silibinin</keyword>
<keyword>TLR4</keyword>
<keyword>TAK1</keyword>
<keyword>MAPK</keyword>
<keyword>Inflammation</keyword>
<keyword>LPS</keyword>
<keyword>RAW2647</keyword>
</keywords>
</record>
</records>
