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Pathomechanism of oteonecrosis in a serum sickness rabbit osteonecrosis model

Research Project

Project/Area Number 08671657
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Orthopaedic surgery
Research InstitutionOsaka University

Principal Investigator

SUGANO Nobuhiko (1997-1998)  Osaka University Medical School Department of Orthopaedic Surgery Assistant Professor, 医学部, 助手 (70273620)

松井 稔 (1996)  大阪大学, 医学部, 助手 (20238950)

Co-Investigator(Kenkyū-buntansha) MASUHARA Kensaku  Osaka University Medical School Department of Orthopaedic Surgery Lecturer, 医学部, 講師 (90238915)
MATSUI Minoru  Osaka University Medical School Department of Orthopaedic Surgery Assistant Prof, 医学部, 助手 (20238950)
菅野 伸彦  大阪大学, 医学部, 助手 (70273620)
Project Period (FY) 1996 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1998: ¥400,000 (Direct Cost: ¥400,000)
Fiscal Year 1997: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1996: ¥1,000,000 (Direct Cost: ¥1,000,000)
KeywordsOsteonecrosis / Animal model / Rabbit / Pathomechanism / Magnetic Resonance Imaging / Avascular Necrosis of the Femoral Head / 微小循環障害 / 血清病 / 免疫複合体
Research Abstract

We investigated early osteonecrosis (ON) using in vivo magnetic resonance imaging (MRI) in a non-traumatic rabbit serum sickness ON model, in which ON was induced after two intravenous injections of horse serum with a three-week interval. One week (group A, 17 rabbits) and three weeks (group B, 13 rabbits) after the second serum injection, coronal MRI of the rabbit femora was obtained and the femur itself was removed for histological study. While some part of the necrotic lesions in the diaphysis was detected on T1-weighted, T2-weighted, and fat suppression T1-weighted images (6/24 necrotic lesions in group A and 16/18 necrotic lesions iii group B), all of the necrotic lesions in the epiphysis, the metaphysis and the diaphysis were detected on Gd-DTPA enhanced T1-weighted (Gd-T1W) or Gd-DTPA enhanced fat suppression T1 -weighted (Gd-FST1W) images. All focal homogeneous enhanced areas on Gd-T1W or Gd-FST1W images corresponded to necrotic lesions (22124 necrotic lesions in group A, 18/18 necrotic lesions in group B), which may result from extravasation of erythrocytes in the bone marrow. The contours of the enhanced areas were displayed more clearly on Gd-FST1W images than on Gd-T1W images. The Gd-FST1W image was thus the most sensitive and the most specific of five kinds of MR images for the detection of early necrotic lesions, The results suggest that the Gd-FST1W image may reflect be useful for early diagnosis of clinical ON and for obtaining information about the pathomechanism of ON.

Report

(4 results)
  • 1998 Annual Research Report   Final Research Report Summary
  • 1997 Annual Research Report
  • 1996 Annual Research Report
  • Research Products

    (16 results)

All Other

All Publications (16 results)

  • [Publications] 坂井孝司,他: "ウサギ骨壊死モデルにおける早期MRI画像と病理組織像との比較" 厚生省特定疾患 骨・関節系疾患調査研究班 平成9年度研究報告書. 162-163 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 大園健二,他: "特発生大腿骨頭壊死症の病態と治療" Pharma Medica. 16. 67-78 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 坂井孝司,他: "ウサギ骨壊死モデルにおける早期MR画像" 日本整形外科学会雑誌. 72(8). S1599 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 坂井孝司,他: "ウサギ骨壊死モデルにおける処置後1週のMRI画像と病理組織像との比較" 厚生省特定疾患 骨・関節系疾患調査研究班 平成10年度研究報告書. (印刷中). (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 坂井孝司,他: "ウサギ骨壊死モデルに対するFK506投与処置後3週群での比較" 厚生省特定疾患 骨・関節系疾患調査研究班 平成10年度研究報告書. (印刷中). (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Sakai T,Sugano S,et al.: "Contrast-enhanced magnetic resonance imaging in a non-traumatic rabbit osteonecrosis model." Journal of Orthopaedic Research. (印刷中).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Sakai T.Sugano S,et al.: "Contrast-enhanced magnetic resonance imaging in a non-traumatic eabbit osteonecrosis model." Journal of Orthopaedic Research. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] 坂井孝司、他: "ウサギ骨壊死モデルにおける早期MRI画像と病理組織像との比較" 厚生省特定疾患 骨・関節系疾患検査研究班平成9年度研究報告書. 162-163 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 大園健二、他: "特発性大腿骨頭壊死症の病態と治療" Pharma Medica. 16. 67-78 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 坂井孝司、他: "ウサギ骨壊死モデルにおける早期MRI画像" 日本整形外科学会雑誌. 72(8). S1559- (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 坂井孝司、他: "ウサギの骨壊死モデルにおける処置後1週のMRI画像と病理組織像との比較" 厚生省特定疾患 骨・関節系疾患検査研究班平成10年度研究報告書. 印刷中. (1999)

    • Related Report
      1998 Annual Research Report
  • [Publications] 坂井孝司、他: "ウサギ骨壊死モデルに対するFK506投与処置後3週群での比較" 厚生省特定疾患 骨・関節系疾患検査研究班平成10年度研究報告書. 印刷中. (1999)

    • Related Report
      1998 Annual Research Report
  • [Publications] Sakai t. Sugano s, et al.: "Contrast-enhanced magnetic resonance imaging in a non-traumatic rabbit osteonecrosis model" Joumal of Orthopaeduc Research. 印刷中.

    • Related Report
      1998 Annual Research Report
  • [Publications] 大園健二、中田活也、松井 稔、菅野伸彦、増原建作: "特発性大腿骨頭壊死症の自然経過からみた発症機序" 整形外科. 48巻9号. 1265-1272 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Katsuya Nakata: "INDUCIBLE OSTEONECROSIS IN A RABBIT SERUM SICKNESS MODEL : DEPOSITION OF IMMUNE COMPLEXES IN BONE MARROW" Bone. 18・6. 609-615 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] 中田活也,増原建作,松井稔: "血小板活性化因子阻害剤による骨壊死発生の抑制" 日本整形外科学会誌. 70(8). 1513 (1996)

    • Related Report
      1996 Annual Research Report

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Published: 1996-04-01   Modified: 2016-04-21  

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