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Immunohistochemical studies on early changes of components of the nervous system after head injury and application to forensic diagnosis

Research Project

Project/Area Number 10670395
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Legal medicine
Research InstitutionKagoshima University

Principal Investigator

OGATA Mamoru  Kagoshima University, Faculty of Medicine, Professor, 医学部, 教授 (10152373)

Project Period (FY) 1998 – 1999
Project Status Completed (Fiscal Year 1999)
Budget Amount *help
¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 1999: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 1998: ¥1,300,000 (Direct Cost: ¥1,300,000)
KeywordsHead injury / Diffuse axonal injury / Immunohistochemistry / Neuron-specific enolase / Astrocyte / 0ligodendroglia / Microglia / Glial fibrillary acidic protein / RCA、レクチン / カーボニック・アンヒドラーゼ / CNPアーゼ / RCA,レクチン
Research Abstract

1. Immunohistochemical studies on axonal injury after head trauma: Further studies were performed to determine whether immunostaining for neuron-specific enolase (NSE) can detect early post-traumatic axonal changes. NSE as well as amyloid precursor protein (APP) could label so-called axonal bulbs and swollen axons in cases with only 1.5 hours' survival after head trauma, so that NSE should be one of useful markers for detection of early axonal changes.
2. Changes of astrocytes after brain injury: Antibodies against glial fibrillary acidic protein (GFAP), S100 protein, vimentin, laminin and glutamine synthetase (GS) were used. Immunostaining for GFAP and S100 labelled both reactive astrocytes in cases of head injury with more than 7 days' survival and swollen astrocytes in cases with 9 hours' to 7 days' survival. Further, in cases with less than 1.5 hours' survival, clasmatodendrosis and pyknosis of the nucleus were detected by GFAP and S100 staining. Immunostaining for vimentin, laminin and GS also labelled these astrocytes, suggesting that immunostaining for astrocytes should be useful for evaluating early brain damage after head injury.
3. Changes of oligodendrocytes after brain injury: Immnostaining for CNPase label oligodendrocytes of head trauma, though did not label cells of control brain. Therefore it is suggested that CNPase staining is very useful for detection of early oligodendrocytic changes after head injury.
4. Changes of microglia after brain injury: Lectin staining for Ricinus Communis agglutinin-1 (RCA1) labelled so-called foamy cells in cases of head injury with more than 2 weeks' survival and hypertrophic microglia in cases with more than 9 hours' survival, so that lectin staining for RCA1 may be useful for estimating the duration of posttraumatic survival.

Report

(3 results)
  • 1999 Annual Research Report   Final Research Report Summary
  • 1998 Annual Research Report
  • Research Products

    (4 results)

All Other

All Publications (4 results)

  • [Publications] M. Ogata: "Neuron-specific enolase as an effctive immunohistochemical marker for injured axons after fatal brain injury"International Journal of Legal Medicine. 113. 19-25 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Mamoru Ogata: "Neuron-specific enolase as an effective immunohistochemical marker for injured axons after fatal brain injury"International Journal of Legal Medicine. 113. 19-25 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] M.Ogata: "Neuron-specific enolose as an effective immunohistochemical Marker for injured axons after fatal brain injury"Intaernatinal Jourmal of Legal Medicine. 113巻1号. 19-25 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] M.ogata: "Internationnal journal of legal medicine"Neuron-specific enolase as an effective immunohistochemical makker for injured axons affer fatal brain injury. 19-25 (1999)

    • Related Report
      1999 Annual Research Report

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Published: 1998-04-01   Modified: 2016-04-21  

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