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Development of new treatment strategy in peripheral artery disease using apoA-I mimetic peptide

Research Project

Project/Area Number 26860591
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Cardiovascular medicine
Research InstitutionFukuoka University

Principal Investigator

Imaizumi Satoshi  福岡大学, 医学部, 准教授 (60609478)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2016: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2015: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2014: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
KeywordsApoA-I模倣ペプチド / 下肢虚血 / 血管新生 / NO / HDL / FAMP / アポA-I模倣ペプチド / NO
Outline of Final Research Achievements

It is unclear whether an apoA-I mimetic peptide can promote neovascularization in vivo. Here, we investigated the effect of FAMP on endothelial nitric oxide synthase (eNOS) activation and angiogenesis in a murine hindlimb ischemia model. As a result, FAMP promoted recovery from hindlimb ischemia through a nitric oxide (NO)-related pathway by activation of a PI3K / Akt pathway. FAMP may become a new therapeutic agent for the future clinical treatment of peripheral artery disease (PAD).

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (4 results)

All 2016 2015 2014

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

  • [Journal Article] Newly developed apolipoprotein A-I mimetic peptide promotes macrophage reverse cholesterol transport in vivo.2015

    • Author(s)
      Shimizu T, Tanigawa H, Miura S, Kuwano T, Takata K, Suematsu Y, Imaizumi S, Yahiro E, Zhang B, Uehara Y, Saku K.
    • Journal Title

      Int J Cardiol.

      Volume: 192 Pages: 82-88

    • DOI

      10.1016/j.ijcard.2016.01.012

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] Inhibition of lipopolysaccharide induced gene expression by HDL from healthy subjects and patients with acute myocardial infarction.2016

    • Author(s)
      Imaizumi S, Takata K, Yahiro E, Kawachi E, Iwata A, Uehara Y, Zhang B, Miura S, Saku K.
    • Organizer
      ESC congress 2016
    • Place of Presentation
      Rome
    • Year and Date
      2016-08-27
    • Related Report
      2016 Annual Research Report
    • Int'l Joint Research
  • [Presentation] FAMP (Fukuoka University Apo A-1 Mimetic peptide) ameliorates impaired HDL function with activation of NO related pathway2015

    • Author(s)
      高田 耕平
    • Organizer
      第79回日本循環器学会学術集会
    • Place of Presentation
      大阪
    • Year and Date
      2015-04-26
    • Related Report
      2014 Research-status Report
  • [Presentation] ApoA-I mimetic peptide FAMP induces neovascularization through activation of endothelial cell nitric oxide related pathway2014

    • Author(s)
      高田 耕平
    • Organizer
      ESC(欧州心臓病学会)
    • Place of Presentation
      バルセロナ(スペイン)
    • Year and Date
      2014-09-02
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2018-03-22  

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