論文

査読有り
2016年4月

10-Oxo-trans-11-octadecenoic acid generated from linoleic acid by a gut lactic acid bacterium Lactobacillus plantarum is cytoprotective against oxidative stress

TOXICOLOGY AND APPLIED PHARMACOLOGY
  • Hidehiro Furumoto
  • ,
  • Tharnath Nanthirudjanar
  • ,
  • Toshiaki Kume
  • ,
  • Yasuhiko Izumi
  • ,
  • Si-Bum Park
  • ,
  • Nahoko Kitamura
  • ,
  • Shigenobu Kishino
  • ,
  • Jun Ogawa
  • ,
  • Takashi Hirata
  • ,
  • Tatsuya Sugawara

296
開始ページ
1
終了ページ
9
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.taap.2016.02.012
出版者・発行元
ACADEMIC PRESS INC ELSEVIER SCIENCE

Oxidative stress is a well-known cause of multiple diseases. The nuclear factor erythroid 2-related factor 2 (Nrf2)-antioxidant response element (ARE) pathway plays a central role in cellular antioxidative responses. In this study, we investigated the effects of novel fatty acid metabolite derivatives of linoleic acid generated by the gut lactic acid bacteria Lactobacillus plantarum on the Nrf2-ARE pathway. 10-Oxo-trans-11-octadecenoic acid (KetoC) protected HepG2 cells from cytotoxicity induced by hydrogen peroxide. KetoC also significantly increased cellular Nrf2 protein levels, ARE-dependent transcription, and the gene expression of antioxidative enzymes such as heme oxygenase-1 (HO-1), glutamate-cysteine ligase modifier subunit (GCLM), and NAD(P)H:quinone oxidoreductase 1 (NQO1) in HepG2 cells. Additionally, a single oral dose administration of KetoC also increased antioxidative gene expression and protein levels of Nrf2 and HO-1 in mouse organs. Since other fatty acid metabolites and linoleic acid did not affect cellular antioxidative responses, the cytoprotective effect of KetoC may be because of its a,(3-unsaturated carbonyl moiety. Collectively, our data suggested that KetoC activated the Nrf2-ARE pathway to enhance cellular antioxidative responses in vitro and in vivo, which further suggests that KetoC may prevent multiple diseases induced by oxidative stress. (C) 2016 Published by Elsevier Inc.

リンク情報
DOI
https://doi.org/10.1016/j.taap.2016.02.012
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000372681600001&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.taap.2016.02.012
  • ISSN : 0041-008X
  • eISSN : 1096-0333
  • Web of Science ID : WOS:000372681600001

エクスポート
BibTeX RIS