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Development of the new therapeutic drug for sepsis, focusing on protein farnesylation in the skeletal muscle

Research Project

Project/Area Number 17K18084
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Emergency medicine
Anesthesiology
Research InstitutionKyorin University

Principal Investigator

Nakazawa Harumasa  杏林大学, 医学部, 准教授 (10458888)

Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2018: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2017: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Keywords敗血症 / ミトコンドリア機能障害 / ファルネシル化変換酵素阻害薬 / ミトコンドリアDNA / ミトコンドリア障害 / ファルネシル化 / DAMPs / ファルネシル変換酵素阻害薬 / インスリン抵抗性 / 筋萎縮
Outline of Final Research Achievements

This study is aimed to investigate the effect of farnesyltransferase inhibiter on sepsis-induced mitochondrial dysfunction/integrity in mouse skeletal muscle. Our data indicate that FTI treatment reverses sepsis-induced mitochondrial dysfunction/disintegrity in skeletal muscle, and tends to decrease circulating-mitochondrial DNA in plasma. As the result, FTI improved a mortality of sepsis model mouse.
These data highlight FTI as a potential new strategy to prevent mitochondrial damage and metabolic dysfunction in sepsis patients.

Academic Significance and Societal Importance of the Research Achievements

敗血症は、発症率と死亡率が高く、その要因がさまざまであるため治療が困難な病態である。とくに敗血症に伴う骨格筋のミトコンドリア機能障害の合併は、患者のよごを増悪させる因子として重要である。本研究で、我々はファルネシル化変換酵素阻害薬(FTI)が、ミトコンドリア機能を完全させる可能性に注目し、敗血市モデルマウスに対するFTIの効果について検討した。その結果、FTIの投与は敗血症マウスのミトコンドリア形態異常を改善し、生命予後を向上させることが示された。本研究の結果は、今後の敗血症治療においてミトコンドリア機能をターゲットとした新しい治療法につながる可能性があり意義深いと考える。

Report

(4 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • Research Products

    (4 results)

All 2019 2018 2017

All Journal Article (3 results) (of which Int'l Joint Research: 2 results,  Peer Reviewed: 3 results,  Open Access: 2 results) Presentation (1 results)

  • [Journal Article] Coenzyme Q10 protects against burn-induced mitochondrial dysfunction and impaired insulin signaling in mouse skeletal muscle2019

    • Author(s)
      Nakazawa Harumasa、Ikeda Kazuhiro、Shinozaki Shohei、Yasuhara Shingo、Yu Yong-Ming、Martyn J.A. Jeevendra、Tompkins Ronald G.、Yorozu Tomoko、Inoue Satoshi、Kaneki Masao
    • Journal Title

      FEBS Open Bio

      Volume: 9 Issue: 2 Pages: 348-363

    • DOI

      10.1002/2211-5463.12580

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] 重症敗血症治療の新たな可能性:偽性低酸素血症とミトコンドリア機能障害の改善を目指して2018

    • Author(s)
      中澤春政
    • Journal Title

      臨床麻酔

      Volume: 3 Pages: 471-477

    • Related Report
      2017 Research-status Report
    • Peer Reviewed
  • [Journal Article] Burn-induced muscle metabolic derangements and mitochondrial dysfunction are associated with activation of HIF-1α and mTORC1: Role of protein farnesylation2017

    • Author(s)
      Nakazawa Harumasa、Ikeda Kazuhiro、Shinozaki Shohei、Kobayashi Masayuki、Ikegami Yuichi、Fu Ming、Nakamura Tomoyuki、Yasuhara Shingo、Yu Yong-Ming、Martyn J. A. Jeevendra、Tompkins Ronald G.、Shimokado Kentaro、Yorozu Tomoko、Ito Hideki、Inoue Satoshi、Kaneki Masao
    • Journal Title

      Scientific Reports

      Volume: 7 Issue: 1 Pages: 6618-6618

    • DOI

      10.1038/s41598-017-07011-3

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] 敗血症に伴う骨格筋ミトコンドリア機能障害に対するファルネシル化変換酵素阻害薬の効果とメカニズムの解明2019

    • Author(s)
      中澤春政
    • Organizer
      第47回日本集中治療医学会学術集会
    • Related Report
      2019 Annual Research Report

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Published: 2017-04-28   Modified: 2021-02-19  

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