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Erythropoietin attenuates the sequels of ischaemic spinal cord injury with enhanced recruitment of CD34+ cells in mice

Research Project

Project/Area Number 24592058
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Thoracic surgery
Research InstitutionMie University

Principal Investigator

HIRANO KOJI  三重大学, 医学(系)研究科(研究院), リサーチアソシエート (40378394)

Co-Investigator(Kenkyū-buntansha) SHIMPO HIDETO  三重大学, 医学系研究科, 教授 (70179076)
Co-Investigator(Renkei-kenkyūsha) SHIMAMOTO AKIRA  三重大学, 医学部附属病院, 講師 (90324524)
MAESHIRO RYO  三重大学, 医学系研究科, 助教 (90647124)
MATSUO ERI  三重大学, 医学系研究科, 特定事業技術補佐員 (40751665)
Project Period (FY) 2012-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2014: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2013: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords脊髄虚血 / エリスロポエチン / 血管再生 / 神経再生 / 脊髄虚血障害
Outline of Final Research Achievements

In this study, we investigated whether erythropoietin (EPO) could ameliorate ischaemic spinal cord injury in mice. EPO (5000 IU/kg) was administrated before aortic cross-clamping for 7 minutes to develop spinal cord ischaemia in mice. Neurological function was assessed using the paralysis score for 7 and 28 days after the operation (POD). Spinal cords were histologically evaluated with immunohistochemistry to detect CD31, CD34, brain-derived neurotrophic factor (BDNF), vascular endothelial growth factor (VEGF), and NeuN. Treated mice demonstrated significant improvement of neurological function at POD 28. Motor neurons in treated mice were more preserved at POD 7 and 28. Although expressions of BDNF and VEGF, also CD31+CD34 cells in treated mice were significantly increased at POD 7, NeuN+CD34 cells was significantly increased at POD 28. We conclude that EPO could induce micro-angiogenesis and promote motor nerve regeneration to preserve ischaemic spinal cord injury.

Report

(5 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • 2013 Research-status Report
  • 2012 Research-status Report
  • Research Products

    (1 results)

All 2012

All Journal Article (1 results) (of which Peer Reviewed: 1 results)

  • [Journal Article] Erythropoietin attenuates the sequels of ischaemic spinal cord injury with enhanced recruitment of CD34+ cells in mice2012

    • Author(s)
      Koji Hirano, Klaus Wagner, Peter Mark, Erik Pittermann, Ralf Gäbel, Dario Furlani, Wenzhong Li, Brigitte Vollmar, Tomomi Yamada, Gustav Steinhoff, Nan Ma
    • Journal Title

      Journal of Cellular and Molecular Medicine

      Volume: 16 Issue: 8 Pages: 1792-1802

    • DOI

      10.1111/j.1582-4934.2011.01489.x

    • Related Report
      2012 Research-status Report
    • Peer Reviewed

URL: 

Published: 2013-05-31   Modified: 2019-07-29  

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