論文

2016年12月

Orally administered conjugated linoleic acid ameliorates allergic dermatitis induced by repeated applications of oxazolone in mice

ANIMAL SCIENCE JOURNAL
  • Tomonori Nakanishi
  • ,
  • Yuzo Tokunaga
  • ,
  • Masao Yamasaki
  • ,
  • Laurie Erickson
  • ,
  • Satoshi Kawahara

87
12
開始ページ
1554
終了ページ
1561
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1111/asj.12603
出版者・発行元
WILEY-BLACKWELL

Conjugated linoleic acid (CLA) is one of the constituents of animal products with possible health benefits such as anti-carcinogenic and anti-obesity effects. In this study, we investigated the immunomodulatory effects of CLA using a mouse model of allergic dermatitis. Mice were orally administered either a CLA mixture containing equal amounts of 9c, 11t-CLA and 10t, 12c-CLA, or high linoleic acid safflower oil, and allergic dermatitis was induced on the ear by repeated topical applications of oxazolone. Oral administration of the CLA mixture but not the high linoleic safflower oil attenuated the symptoms of allergic dermatitis in both ear weights and clinical scores. This effect was associated with decreased levels of ear interleukin-4 (IL-4) and plasma immunoglobulin E. The immunomodulatory effects of the CLA isomers were compared by an in vitro cytokine production assay. The results showed that 9c, 11t-CLA, the most predominant isomer in animal products, significantly inhibited IL-4 and interferon- production from mouse splenocytes with similar potency to 10t, 12c-CLA. These findings suggest that CLA, a constituent of animal products, has a potentially beneficial effect for amelioration of allergic dermatitis.

リンク情報
DOI
https://doi.org/10.1111/asj.12603
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/26990926
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000389323700013&DestApp=WOS_CPL
URL
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84961275868&origin=inward
ID情報
  • DOI : 10.1111/asj.12603
  • ISSN : 1344-3941
  • eISSN : 1740-0929
  • PubMed ID : 26990926
  • SCOPUS ID : 84961275868
  • Web of Science ID : WOS:000389323700013

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