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タイトル
  • en Morphological assessment of bone mineralization in tibial metaphyses of ascorbic acid-deficient ODS rats
作成者
アクセス権 open access
主題
  • NDC 497
内容注記
  • Abstract en Osteogenic disorder shionogi (ODS) rats carry a hereditary defect in ascorbic acid synthesis, mimicking human scurvy when fed with an ascorbic acid-deficient (aa-def) diet. As aa-def ODS rats were shown to feature disordered bone formation, we have examined the bone mineralization in this rat model. A fibrous tissue layer surrounding the trabeculae of tibial metaphyses was found in aa-def ODS rats, and this layer showed intense alkaline phosphatase activity and proliferating cell nuclear antigen-immunopositivity. Many osteoblasts detached from the bone surfaces and were characterized by round-shaped rough endoplasmic reticulum (rER), suggesting accumulation of malformed collagen inside the rER. Accordingly, fine, fragile fibrillar collagenous structures without evident striation were found in aa-def bones, which may result from misassembling of the triple helices of collagenous α-chains. Despite a marked reduction in bone formation, ascorbic acid deprivation seemed to have no effect on mineralization: while reduced in number, normal matrix vesicles and mineralized nodules could be seen in aa-def bones. Fine needle-like mineral crystals extended from these mineralized nodules, and were apparently bound to collagenous fibrillar structures. In summary, collagen mineralization seems unaffected by ascorbic acid deficiency in spite of the fine, fragile collagenous fibrils identified in the bones of our animal model.
出版者 en Biomedical Research Press
日付
    Issued2011-08-30
言語
  • eng
資源タイプ journal article
出版タイプ VoR
資源識別子 HDL http://hdl.handle.net/2115/72292
関連
  • isIdenticalTo DOI https://doi.org/10.2220/biomedres.32.259
収録誌情報
    • PISSN 0388-6107
    • EISSN 1880-313X
    • NCID AA00110128
      • en Biomedical Research
      • 32 4 開始ページ259 終了ページ269
ファイル
    • fulltext A4_32_259.pdf
    • 1.6 MB (application/pdf)
      • Issued2011-08-30
コンテンツ更新日時 2023-07-26