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Effects of Brain derived neurotrophic factor (BDNF) and assessment using MRI on experimentally spinal cord Injury

Research Project

Project/Area Number 12671396
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Orthopaedic surgery
Research InstitutionCHIBA UNIVERSITY

Principal Investigator

MURAKAMI Masazumi  Chiba University, University Hospital, Lecturer, 医学部・附属病院, 講師 (50219903)

Co-Investigator(Kenkyū-buntansha) YAMAZAKI Masashi  Chiba University, University Hospital, Assistant, 医学部・附属病院, 助手 (50281712)
Project Period (FY) 2000 – 2001
Project Status Completed (Fiscal Year 2001)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,900,000)
Fiscal Year 2001: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 2000: ¥2,900,000 (Direct Cost: ¥2,900,000)
Keywordsspinal cord injury / brain derived neurotrophic factor / rat / oligodendrocyte / apoptosis / MRI / apoptosis
Research Abstract

We evaluated the effect of brain-derived neurotrophic factor (BDNF) on apoptosis after spinal cord injury. A rat spinal cord injury model was produced by static load, and continuous intrathecal BDNF or vehicle infusion was carried out either immediately or 3 days after the injury. Apoptotic cells were examined by nuclear staining and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL). After injury, typical apoptotic cells were observed. Double staining with TUNEL and specific cell markers revealed that soon after the injury the apoptotic cells at the injury site were neurons and microglia. One week after the injury, apoptotic oligodendrocytes but not apoptotic astrocytes were observed in the white matter rostral and caudal to the injury site, whereas few apoptotic cells were found in the gray matter. The immediate BDNF treatment significantly reduced the number of TUNEL-positive cells in the adjacent rostral site 1 and 2 weeks after the injury, and in the adjacent caudal site 3 days and 1 week after the injury, even though there was no significant difference between BDNF-treated and control rats at the injury site itself. In addition, similar anti-apoptotic effects were observed in these regions 1 week after injury in rats that received BDNF treatment from the third day after injury. These findings suggest that BDNF suppresses delayed apoptosis of oligodendrocytes after spinal cord injury, for which even injections started late are effective. BDNF administration may therefore be useful for the clinical treatment of spinal cord injury through the suppression of secondary events.

Report

(3 results)
  • 2001 Annual Research Report   Final Research Report Summary
  • 2000 Annual Research Report
  • Research Products

    (1 results)

All Other

All Publications (1 results)

  • [Publications] Osamu Ikeda, et al.: "Acute up-regulation of brain-derived neurotrophic factor expression resulting from experimentally induced injury in the rat spinal cord"Acta Neuropathol. 102. 239-245 (2001)

    • Related Report
      2001 Annual Research Report

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Published: 2000-04-01   Modified: 2016-04-21  

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