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The Research for the cause of hydrocephaulus associated with spina bifida using delayd Splotch mouse with myeloschisis

Research Project

Project/Area Number 04670875
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Cerebral neurosurgery
Research InstitutionJikei University of Medicine

Principal Investigator

NAKAHARA Shigehiro  Jikei University, Neurosurgery, Lecturer, 医学部, 講師 (80147339)

Co-Investigator(Kenkyū-buntansha) SHUKUYA Ikuo  Jikei University, Neurosurgery, assistant, 医学部, 助手 (90226291)
TANAKA Hideaki  Jikei University, Neursurgery, assistant, 医学部, 助手 (70227164)
Project Period (FY) 1992 – 1994
Project Status Completed (Fiscal Year 1994)
Budget Amount *help
¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1994: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1993: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1992: ¥800,000 (Direct Cost: ¥800,000)
KeywordsChiari II malformation / Delayd Splotch mouse / Hydrocephalus / Myeloschisis / Spina bifida / hydrocephalus / myeloschisis / spina bifida / Chari II malformation / Luschka / Magendie / subarachnoid space / delayed Splotch
Research Abstract

We have already reported our unified theory of the cause of Chiari II malformation : failure of correct timing of apposition and transient occulusion of spinal neurocele, which leads to failure to maintain distention of the rhombencephalic vesicles, which alters the inductive effect of pressure on the surrounding mesenchyme. Therefore, we hypothesize the cause of hydrocephalus associated with myeloschisis is related to lack of driving force on the surrounding mesenchyme, especially arachnoid membrane. To test the possibility, we tried to investigate sagittal and coronal sections of the embryonic brain in normal and neural tube defect (NTD) in delayd Splotch mouse using Richardson's staining and the fetal arachnoid membrane of normal and NTD (myeloschisis) in delayd Splotch mouse using scanning electron microscope (SEM) and to make a baby model with myeloschisis using surgical glue for repairing myeloschisis to investigate arrachnoid membrane.
Finally, we failed to make a baby model with myeloschisis which caused by respiratory disorder associated with Chiari II malformation. However, SEM finding of fetal arachnoid membrane and subarachnoid space of the posterior fossa and vertex of the parenchyma in myeloschisis was quite different with that of normal fetus.
Our data suggest that the cause of hydrocephalus with Chiari II malformation associated with myeloschisis is related to this maldevelopment of the embryonic subarachnoid system, which leads to lack of distention of the embryonic ventricular system.

Report

(4 results)
  • 1994 Annual Research Report   Final Research Report Summary
  • 1993 Annual Research Report
  • 1992 Annual Research Report
  • Research Products

    (5 results)

All Other

All Publications (5 results)

  • [Publications] McLone D.G.: "The cause of Chiari II malformation:An unified theory." Pediatric Neuroscience. 15. 1-12 (1989)

    • Related Report
      1992 Annual Research Report
  • [Publications] McLone D.G.: "The Chiari II malformation:Pathogenesis and dynamics." Concepts in Pediatric Neurosurgery. 11. 1-17 (1990)

    • Related Report
      1992 Annual Research Report
  • [Publications] 中原 成浩: "先天性myeloschisisにChiari II奇形、水頭症を合併するマウス胎仔脳の形態学的研究" 小児の脳神経. 16. 421-428 (1991)

    • Related Report
      1992 Annual Research Report
  • [Publications] 中原 成浩: "正常マウス胎仔脳室内髄液吸引後の後頭蓋窩Chiari II奇形様変化について" 小児の脳神経. 17. 81-87 (1992)

    • Related Report
      1992 Annual Research Report
  • [Publications] 中原 成浩: "ビタミンA誘発マウス二分脊椎に合併するChiari II奇形について" 小児の脳神経. 17. 135-142 (1992)

    • Related Report
      1992 Annual Research Report

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Published: 1992-04-01   Modified: 2016-04-21  

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