pubmed-article:20149620 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0010453 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0035143 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0031715 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0521447 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0042878 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0079189 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0021467 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0333348 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C1150571 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C1521761 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0021469 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C1879547 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
pubmed-article:20149620 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
pubmed-article:20149620 | pubmed:issue | 11 | lld:pubmed |
pubmed-article:20149620 | pubmed:dateCreated | 2010-10-25 | lld:pubmed |
pubmed-article:20149620 | pubmed:abstractText | Vitamin K is essential for blood coagulation and bone metabolism in mammals. This vitamin functions as a cofactor in the posttranslational synthesis of ?-carboxyglutamic acid (Gla) from glutamic acid residues. However, other functions of vitamin K have been reported recently. We previously found that vitamin K suppresses the inflammatory reaction induced by lipopolysaccharide (LPS) in rats and human macrophage-like THP-1 cells. In this study, we further investigated the mechanism underlying the anti-inflammatory effect of vitamin K by using cultures of LPS-treated human- and mouse-derived cells. All the vitamin K analogues analyzed in our study exhibited varied levels of anti-inflammatory activity. The isoprenyl side chain structures, except geranylgeraniol, of these analogues did not show such activity; warfarin did not interfere with this activity. The results of our study suggest that the 2-methyl-1,4-naphtoquinone ring structure contributes to express the anti-inflammatory activity, which is independent of the Gla formation activity of vitamin K. Furthermore, menaquinone-4, a form of vitamin K?, reduced the activation of nuclear factor ?B (NF?B) and inhibited the phosphorylation of IKK?/? after treatment of cells with LPS. These results clearly show that the anti-inflammatory activity of vitamin K is mediated via the inactivation of the NF?B signaling pathway. | lld:pubmed |
pubmed-article:20149620 | pubmed:language | eng | lld:pubmed |
pubmed-article:20149620 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20149620 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:20149620 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20149620 | pubmed:month | Nov | lld:pubmed |
pubmed-article:20149620 | pubmed:issn | 1873-4847 | lld:pubmed |
pubmed-article:20149620 | pubmed:author | pubmed-author:KomaiMichioM | lld:pubmed |
pubmed-article:20149620 | pubmed:author | pubmed-author:ShirakawaHito... | lld:pubmed |
pubmed-article:20149620 | pubmed:author | pubmed-author:GotoTomokoT | lld:pubmed |
pubmed-article:20149620 | pubmed:author | pubmed-author:SatoShokoS | lld:pubmed |
pubmed-article:20149620 | pubmed:author | pubmed-author:OhsakiYusukeY | lld:pubmed |
pubmed-article:20149620 | pubmed:author | pubmed-author:MiuraAkihitoA | lld:pubmed |
pubmed-article:20149620 | pubmed:author | pubmed-author:GiriwonoPuspo... | lld:pubmed |
pubmed-article:20149620 | pubmed:author | pubmed-author:OhashiAiA | lld:pubmed |
pubmed-article:20149620 | pubmed:author | pubmed-author:IribeMaikoM | lld:pubmed |
pubmed-article:20149620 | pubmed:copyrightInfo | Copyright © 2010 Elsevier Inc. All rights reserved. | lld:pubmed |
pubmed-article:20149620 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20149620 | pubmed:volume | 21 | lld:pubmed |
pubmed-article:20149620 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20149620 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20149620 | pubmed:pagination | 1120-6 | lld:pubmed |
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pubmed-article:20149620 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20149620 | pubmed:articleTitle | Vitamin K suppresses the lipopolysaccharide-induced expression of inflammatory cytokines in cultured macrophage-like cells via the inhibition of the activation of nuclear factor ?B through the repression of IKK?/? phosphorylation. | lld:pubmed |
pubmed-article:20149620 | pubmed:affiliation | Laboratory of Nutrition, Graduate School of Agricultural Science, Tohoku University, Sendai 981-8555, Japan. | lld:pubmed |
pubmed-article:20149620 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20149620 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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