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Regulation of cardiac metabolism by Akt signaling

Research Project

Project/Area Number 20390217
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Circulatory organs internal medicine
Research InstitutionChiba University

Principal Investigator

SHIOJIMA Ichiro  Chiba University, 医学系研究科, 寄附講座准教授 (90376377)

Project Period (FY) 2008 – 2010
Project Status Completed (Fiscal Year 2010)
Budget Amount *help
¥18,590,000 (Direct Cost: ¥14,300,000、Indirect Cost: ¥4,290,000)
Fiscal Year 2010: ¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2009: ¥6,240,000 (Direct Cost: ¥4,800,000、Indirect Cost: ¥1,440,000)
Fiscal Year 2008: ¥7,020,000 (Direct Cost: ¥5,400,000、Indirect Cost: ¥1,620,000)
KeywordsAkt / 糖代謝 / 脂肪酸代謝 / 心不全
Research Abstract

Akt is a serine/threonine protein kinase that is situated downstream of PI3-kinase and regulates multiple cellular processes including cell growth and glucose metabolism. The purpose of the present study was to investigate the mechanism of metabolic regulation by Akt signaling in the heart. We found that Akt activation leads to downregulation of fatty acid oxidation and that downregulation of Akt pathway in the heart leads to contractile dysfunction. These data suggest that Akt maintains cardiac function in part through regulation of ATP synthesis in the heart.

Report

(4 results)
  • 2010 Annual Research Report   Final Research Report ( PDF )
  • 2009 Annual Research Report
  • 2008 Annual Research Report
  • Research Products

    (9 results)

All 2010 2009 2008

All Journal Article (9 results) (of which Peer Reviewed: 9 results)

  • [Journal Article] Wnt signaling and aging-related heart disorders.2010

    • Author(s)
      Naito AT, Shiojima I, Komuro I.
    • Journal Title

      Circ Res 107

      Pages: 1295-1303

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Journal Article] Promotion of CHIP-mediated p53 degradation protects the heart from ischemic injury.2010

    • Author(s)
      Naito AT, Okada S, Minamino T, Iwanaga K, Liu ML, Sumida T, Nomura S, Sahara N, Mizoroki T, Takashima A, Akazawa H, Nagai T, Shiojima I, Komuro I.
    • Journal Title

      Circ Res 106

      Pages: 1692-1702

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Journal Article] Excessive cardiac insulin signaling exacerbates systolic dysfunction induced by pressure overload in rodents.2010

    • Author(s)
      Shimizu I, Minamino T, Toko H, Okada S, Ikeda H, Yasuda N, Tateno K, Moriya J, Yokoyama M, Nojima A, Koh GY, Akazawa H, Shiojima I, Kahn CR, Abel ED, Komuro I.
    • Journal Title

      J Clin Invest 120

      Pages: 1506-1514

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Journal Article] Chronic doxorubicin cardiotoxicity is mediated by oxidative DNA damage-ATM-p53-apoptosis pathway and attenuated by pitavastatin through the inhibition of Rac1 activity.2009

    • Author(s)
      Yoshida M, Shiojima I, Ikeda H, Komuro I.
    • Journal Title

      J Mol Cell Cardiol 47

      Pages: 698-705

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Journal Article] Interaction of myocardial insulin receptor and IGF receptor signaling in exercise-induced cardiac hypertrophy.2009

    • Author(s)
      Ikeda H, Shiojima I, Ozasa, Y, Yoshida M, Holzenberger M, C Ronald Kahn, Kenneth Walsh, Takashi Igarashi, E Dale Abel, Issei Komuro.
    • Journal Title

      J Mol Cell Cardiol 47

      Pages: 664-675

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Journal Article] mTORC1 activation regulates beta-cell mass and proliferation by modulation of cyclin D2 synthesis and stability.2009

    • Author(s)
      Balcazar N, Sathyamurthy A, Elghazi L, Gould A, Weiss A, Shiojima I, Walsh K, Bernal-Mizrachi E.
    • Journal Title

      J Biol Chem 284

      Pages: 7832-7842

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Journal Article] IGFBP-4 is an inhibitor of canonical Wnt signalling required for cardiogenesis.2008

    • Author(s)
      Zhu W, Shiojima I, Ito Y, Li Z, Ikeda H, Yoshida M, Naito AT, Nishi J, Ueno H, Umezawa A, Minamino T, Nagai T, Kikuchi A, Asashima M, Komuro I.
    • Journal Title

      Nature 454

      Pages: 345-349

    • NAID

      120007069172

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Journal Article] Gremlin enhances the determined path to cardiomyogenesis.2008

    • Author(s)
      Kami D, Shiojima I, Makino H, Matsumoto K, Takahashi Y, Ishii R, Naito AT, Toyoda M, Saito H, Watanabe M, Komuro I, Umezawa A.
    • Journal Title

      PLoS ONE 3

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Journal Article] A crucial role of a high mobility group protein HMGA2 in cardiogenesis.2008

    • Author(s)
      Monzen K, Ito Y, Naito AT, Kasai H, Hiroi Y, Hayashi D, Shiojima I, Yamazaki T, Miyazono K, Asashima M, Naigai R, Komuro I.
    • Journal Title

      Nat Cell Biol 10

      Pages: 567-574

    • Related Report
      2010 Final Research Report
    • Peer Reviewed

URL: 

Published: 2008-04-01   Modified: 2016-04-21  

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