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Alterations in cellular iron metabolism caused by oxidative stress

Research Project

Project/Area Number 15K16534
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Applied health science
Research InstitutionHyogo Medical University

Principal Investigator

Yoshihara Daisaku  兵庫医科大学, 医学部, 助教 (00567266)

Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2016: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords酸化ストレス / 鉄代謝 / SOD1
Outline of Final Research Achievements

The aim of this study was to investigate the relationship between oxidative stress and age-related disturbance of iron metabolism. It was shown that the 2,3-Dimethoxy-1,4-naphtoquinone (DMNQ), a superoxide generator, and 4-hydroxy-2-nonenal (4-HNE), a lipid peroxidation product, increased ferrous ion and inhibited IRP1 (Iron regulatory protein 1) activity in mProx24 cell (mouse proximal tubular cell) and HEK293 cell (human embryonic kidney cells). In addition, SOD1 KO (animal model of oxidative stress) mice showed abnormalities of brain iron metabolism and exhibited impaired motivational behavior in three-chamber social interaction tests. These results suggest that age-related oxidative stress may induce disturbance of iron metabolism.

Report

(3 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • Research Products

    (6 results)

All 2016 2015

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Acknowledgement Compliant: 1 results) Presentation (5 results)

  • [Journal Article] The absence of the SOD1 gene causes abnormal monoaminergic neurotransmission and motivational impairment-like behavior in mice.2016

    • Author(s)
      Daisaku Yoshihara, Noriko Fujiwara, Nobue Kitanaka, Junichi Kitanaka, Haruhiko Sakiyama, Hironobu Eguchi, Motohiko Takemura and Keiichiro Suzuki
    • Journal Title

      Free Radical Research

      Volume: 50(11) Issue: 11 Pages: 1245-1256

    • DOI

      10.1080/10715762.2016.1234048

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Presentation] フェロトーシス誘導時における鉄イオン動態の解析2016

    • Author(s)
      吉原大作、藤原範子、平山祐、丹羽正人、江口裕伸、崎山晴彦、永澤秀子、鈴木敬一郎
    • Organizer
      第40回 日本鉄バイオサイエンス学会学術集会
    • Place of Presentation
      名古屋大学豊田講堂(愛知県名古屋市)
    • Year and Date
      2016-09-10
    • Related Report
      2016 Annual Research Report
  • [Presentation] SOD1欠損はモチベーションの低下を引き起こす2016

    • Author(s)
      吉原大作、藤原範子、北中順惠、北中純一、崎山晴彦、江口裕伸、竹村基彦、鈴木敬一郎
    • Organizer
      第69回 日本酸化ストレス学会学術集会
    • Place of Presentation
      仙台国際センター(宮城県仙台市)
    • Year and Date
      2016-08-30
    • Related Report
      2016 Annual Research Report
  • [Presentation] 吉原大作、藤原範子、江口裕伸、崎山晴彦、鈴木敬一郎2015

    • Author(s)
      SOD1欠損マウスにおける行動学的異常
    • Organizer
      BMB2015
    • Place of Presentation
      神戸国際展示場(兵庫県神戸市)
    • Year and Date
      2015-12-03
    • Related Report
      2015 Research-status Report
  • [Presentation] NOおよびROSが鉄代謝調節機構に及ぼす影響2015

    • Author(s)
      吉原大作、藤原範子、崎山晴彦、江口裕伸、鈴木敬一郎
    • Organizer
      第15回 日本NO学会学術集会
    • Place of Presentation
      千里ライフサイエンスセンター(大阪府豊中市)
    • Year and Date
      2015-06-26
    • Related Report
      2015 Research-status Report
  • [Presentation] 吉原大作、藤原範子、崎山晴彦、江口裕伸、鈴木敬一郎2015

    • Author(s)
      SOD1欠損は脳内モノアミン代謝異常と行動異常を引き起こす
    • Organizer
      第68回 日本酸化ストレス学会学術集会
    • Place of Presentation
      かごしま県民交流センター(鹿児島県鹿児島市)
    • Year and Date
      2015-06-11
    • Related Report
      2015 Research-status Report

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Published: 2015-04-16   Modified: 2018-03-22  

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