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Identification of molecular mechanisms and therapy target in the closure of ductus arteriosus

Research Project

Project/Area Number 22791042
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeSingle-year Grants
Research Field Embryonic/Neonatal medicine
Research InstitutionKurume University

Principal Investigator

KAJIMOTO Hidemi  久留米大学, 循環器病研究所, 助教 (50349700)

Project Period (FY) 2010 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2012: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2011: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2010: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Keywords新生児医学 / 動脈管 / 閉鎖 / 血管内皮 / 新生児 / 遺伝子
Research Abstract

Patent DA accounts for significant morbidity in preterm newborns.Phosphatase and tensin homolog that is a protein phosphatase in PI3 kinase/Akt pathway increases after ductus arteriosus closure. Analysis of the comprehensive gene expression profile changes provided new insight into understanding the mechanism of DA closure

Report

(4 results)
  • 2012 Annual Research Report   Final Research Report ( PDF )
  • 2011 Annual Research Report
  • 2010 Annual Research Report
  • Research Products

    (14 results)

All 2012 2011 2010

All Journal Article (6 results) (of which Peer Reviewed: 6 results) Presentation (8 results)

  • [Journal Article] Inhibition of eNOS Phosphorylation Mediates Endothelial Dysfunction in Renal Failure : New Effect of Asymmetric Dimethylarginine2012

    • Author(s)
      Kajimoto H, Kai H, Imaizumi T(他6人9番目)
    • Journal Title

      Kidney International

      Volume: 81 Issue: 8 Pages: 762-768

    • DOI

      10.1038/ki.2011.476

    • Related Report
      2012 Annual Research Report 2012 Final Research Report 2011 Annual Research Report
    • Peer Reviewed
  • [Journal Article] High-sensitive troponin T is associated with atrial fibrillation in a general population.2012

    • Author(s)
      Anegawa T, Kai H, Kajimoto H, YasuokaS
    • Journal Title

      Int J Cardiol

      Volume: 156 Issue: 1 Pages: 98-100

    • DOI

      10.1016/j.ijcard.2011.12.117

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Selective gene expression analysis of muscular and vascular components in hearts using laser microdissection method.2012

    • Author(s)
      Ikeda A, Kai H, Kajimoto H, Yasuoka S
    • Journal Title

      Int J Vasc Med

      Volume: Article ID 863410 Pages: 2012-2012

    • DOI

      10.1155/2012/863410

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Ultrasound stimulation restores impaired neovascularization-related capacities of human circulating angiogenic cells2012

    • Author(s)
      Toyama Y, Sasaki K, Tachibana K, Ueno T, Kajimoto H, Yokoyama S, Ohtsuka M, Koiwaya H, Nakayoshi T, Mitsutake Y, Chibana H, Itaya N, Imaizumi T.
    • Journal Title

      Cardiovasc Res

      Volume: 1:95(4) Issue: 4 Pages: 448-59

    • DOI

      10.1093/cvr/cvs173

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Simvastatin prevents large blood pressure variability induced aggravation of cardiac hypertrophy in hypertensive rats by inhibiting RhoA/Ras-ERK pathways2011

    • Author(s)
      Takayama N, Kai H, Imaizumi T(他7人10番目)
    • Journal Title

      Hypertens Res

      Volume: 34 Issue: 3 Pages: 341-347

    • DOI

      10.1038/hr.2010.229

    • NAID

      10031163179

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] A Central role for CD68 (+) macrophages in hepatopulmonary syndrome: Reversal by macrophage depletion.2011

    • Author(s)
      Thenappan T, Kajimoto H
    • Journal Title

      Am J Resp Crit Care Med

      Volume: 183 Issue: 8 Pages: 1080-1091

    • DOI

      10.1164/rccm.201008-1303oc

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Presentation] Inhibition of CaMKII/ERK-mediated eNOS phosphorylation by asymmetric dimethylarginine is novel molecular mechanism of endothelial dysfunction in chronic kidney disease mice2012

    • Author(s)
      Hidemi Kajimoto
    • Organizer
      第76回日本循環器学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2012-03-16
    • Related Report
      2011 Annual Research Report
  • [Presentation] Increased Phosphatase and Tensin Homolog Plays a Crucial Role in Endothelial Dysfunction in Mice with Renal Failure.2012

    • Author(s)
      Kajimoto H, et al
    • Organizer
      (American Heart Association's Scientific Sessions
    • Place of Presentation
      Los Angeles, USA
    • Related Report
      2012 Final Research Report
  • [Presentation] Inhibition of CaMKII/ERK-mediated eNOS phosphorylation by asymmetric dimethylarginine is novel molecular mechanism of endothelial dysfunction in chronic kidney disease mice. (2012

    • Author(s)
      Kajimoto H, et al
    • Organizer
      76th Annual Scientific Meeting of the Japanese Circulation Society
    • Place of Presentation
      Fukuoka, Japan
    • Related Report
      2012 Final Research Report
  • [Presentation] Increased Phosphatase and Tensin Homolog Plays a Crucial Role in Endothelial Dysfunction in Mice with Renal Failure.2012

    • Author(s)
      Hidemi Kajimoto
    • Organizer
      American Heart Association’s Scientific Sessions
    • Place of Presentation
      Los Angeles, USA
    • Related Report
      2012 Annual Research Report
  • [Presentation] Inhibition of CaMKII-and ERK-mediated eNOS phosphorylation impairs endothelial function in renal failure mice : New effect of asymmetric dimethylarginine2011

    • Author(s)
      Hidemi Kajimoto
    • Organizer
      American Heart Association's Scientific Sessions
    • Place of Presentation
      オーランド
    • Year and Date
      2011-11-15
    • Related Report
      2011 Annual Research Report
  • [Presentation] Inhibition of CaMKII- and ERK-mediated eNOS phosphorylation impairs endothelial function in renal failure mice: New effect of asymmetric dimethylarginine. (2011

    • Author(s)
      Kajimoto H, et al
    • Organizer
      American Heart Association's Scientific Sessions
    • Place of Presentation
      Orlando, USA
    • Related Report
      2012 Final Research Report
  • [Presentation] Increased circulating asymmetric dimethylarginine in chronic kidney disease mice induces endothelial dysfunction by inhibitingCa/Calmodulin-dependent protein kinase II-eNOS signaling.2010

    • Author(s)
      Kajimoto H, et al
    • Organizer
      American Heart Association's Scientific Sessions
    • Place of Presentation
      Chicago, USA
    • Related Report
      2012 Final Research Report
  • [Presentation] Asymmetric dimethylarginine impairs endothelial function in CKD mice.2010

    • Author(s)
      Kajimoto H, et al
    • Organizer
      ISN-Nexus Symposium 2010
    • Place of Presentation
      Kyoto, Japan
    • Related Report
      2012 Final Research Report

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Published: 2010-08-23   Modified: 2019-07-29  

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