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Analysis of the process of inflammatory response induced by trans fatty acids and development of the suppression method

Research Project

Project/Area Number 25350138
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Eating habits
Research InstitutionSeitoku University

Principal Investigator

KANOU Kazutaka  聖徳大学, 人間栄養学部, 教授 (70111507)

Co-Investigator(Kenkyū-buntansha) YOKOYAMA Yoshiko  聖徳大学, 人間栄養学部, 准教授 (40202395)
IWASAKI Yuki  人間総合科学大学, 人間科学部, 助手 (60762078)
Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2013: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywordsトランス脂肪酸 / アテローム性動脈硬化症 / TNF-α / Toll様受容体4 / アディポネクチン / 食作用 / エライジン酸 / TLR-4 / マクロファージ / Toll様受容体(TLR)-4 / NF-κB / TNF-α受容体 / 細胞内情報伝達系
Outline of Final Research Achievements

【Aim】High intake of trans fatty acid (TFA) increases the risk of cardiovascular disease and atherosclerosis. This study analyzed the mechanism of atherosclerosis induction by elaidic acid (EA), which is a component of industrially produced TFA. 【Methods】Human breast carcinoma-derived YMB-1-E cells and human monocytic leukemia-derived U937 cells were used for the exsperiments. 【Results】EA strongly suppressed the anti-arteriosclerosis protein adiponectin expression. EA promoted in PMA-stimulated U937 cells, expression of differentiation marker antigens CD68 and CD147, expression of TNF-α, lipid accumulation and activation of phagocytosis. Experiments with TLR4 inhibitors indicated that elaidic acid exacerbates atherosclerotic changes via TLR4 signal transduction pathway. These facts suggest the possibility to suppress the development of pathogenesis of atherosclerosis by control the function of TLR4.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (5 results)

All 2015

All Journal Article (2 results) (of which Peer Reviewed: 2 results,  Acknowledgement Compliant: 2 results) Presentation (3 results)

  • [Journal Article] エライジン酸によるアディポネクチン発現抑制作用2015

    • Author(s)
      岩﨑有希、白石弘美、久保宏隆、横山嘉子、加納和孝
    • Journal Title

      日本臨床栄養学会雑誌

      Volume: 37 Pages: 44-53

    • Related Report
      2015 Annual Research Report 2014 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Journal Article] エライジン酸によるマクロファージの食作用の亢進2015

    • Author(s)
      岩﨑有希、白石弘美、久保宏隆、横山嘉子、加納和孝
    • Journal Title

      日本臨床栄養学会雑誌

      Volume: 37 Pages: 54-59

    • Related Report
      2015 Annual Research Report 2014 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Presentation] エライジン酸は TLR-4 を介して TNF- αを増加させアディポネクチン発現を抑制する2015

    • Author(s)
      岩崎 有希、白石 弘美、久保 宏隆、横山 嘉子、加納 和孝
    • Organizer
      日本臨床栄養学会 第13回大連合大会
    • Place of Presentation
      都市センターホテル(東京都・千代田区)
    • Year and Date
      2015-10-04
    • Related Report
      2015 Annual Research Report
  • [Presentation] エライジン酸はTLR-4 情報伝達系を介してアディポネクチン発現を抑制する2015

    • Author(s)
      岩崎 有希、白石 弘美、横山 嘉子、加納 和孝
    • Organizer
      第24回 日本油脂栄養学会
    • Place of Presentation
      ホテルグランデはがくれ(佐賀県・佐賀市)
    • Year and Date
      2015-08-28
    • Related Report
      2015 Annual Research Report
  • [Presentation] エライジン酸によるマクロファージの食作用の亢進2015

    • Author(s)
      田口 祐未、岩崎 有希、白石 弘美、加納 和孝、横山 嘉子
    • Organizer
      第62回日本栄養改善学会学術総会
    • Place of Presentation
      福岡国際会議場(福岡県・福岡市)
    • Year and Date
      2015-08-25
    • Related Report
      2015 Annual Research Report

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Published: 2014-07-25   Modified: 2019-07-29  

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