『徳島大学 教育・研究者情報データベース (EDB)』---[学外] /
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EID=236644EID:236644, Map:0, LastModified:2012年11月8日(木) 13:46:07, Operator:[三木 ちひろ], Avail:TRUE, Censor:承認済, Owner:[美原(和田) 智恵], Read:継承, Write:継承, Delete:継承.
種別 (必須): 学術論文 (審査論文) [継承]
言語 (必須): 英語 [継承]
招待 (推奨):
審査 (推奨): Peer Review [継承]
カテゴリ (推奨):
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学究種別 (推奨):
組織 (推奨):
著者 (必須): 1.美原(和田) 智恵 ([徳島大学.病院.中央診療施設等.総合歯科診療部])
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学籍番号 (推奨):
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2.片岡 正俊
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3.瀬戸 浩行
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学籍番号 (推奨):
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4. (英) Hayashi Noriko (日) (読)
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学籍番号 (推奨):
[継承]
5. (英) Kido Jun-ichi (日) (読)
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[継承]
6.篠原 康雄 ([徳島大学.先端酵素学研究所.基幹研究部門])
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学籍番号 (推奨):
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7.永田 俊彦
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題名 (必須): (英) High-turnover osteoporosis is induced by cyclosporin A in rats.  (日)    [継承]
副題 (任意):
要約 (任意): (英) Cyclosporin A (CsA) is used widely as an immunosuppressive agent, but it induces osteoporosis as a prominent side effect. To elucidate the mechanisms involved in CsA-induced osteoporosis, the effects of CsA on bone metabolism were investigated in a rat experimental model. Fifteen-day-old rats were fed a powdered diet containing or lacking CsA for 8-30 days. Analysis was performed by micro-computed tomography (muCT) and light microscopy to examine histomorphometric changes in rat tibiae on days 8, 16, and 30. Plasma parathyroid hormone (PTH) and osteocalcin (OCN) levels were determined by enzyme-linked immunosorbent assay (ELISA) on days 8, 16, and 30. The expression of OCN, osteopontin (OPN), and cathepsin K mRNAs in tibial bone marrow was examined by Northern blot analysis on days 8 and 16. Although no significant differences were observed in tibial length during the experimental periods, or in histomorphometric parameters on day 8, an apparent decrease in bone volume was observed in the CsA-treated group after day 16. Histologic analysis showed that the number of osteoblasts and osteoclasts on the surface of trabecular bone in the CsA-treated group had increased significantly on day 16. Plasma PTH and OCN levels in CsA-treated rats were significantly higher than those in control animals on day 8. Northern blot analysis revealed that the CsA-treated group showed an increase in the expression of OCN, OPN, and cathepsin K mRNAs on day 8 compared with the controls. These findings suggest that bone resorption in CsA-treated rats is induced by high-turnover osteoporosis and that bone remodeling activity may be activated by PTH.  (日)    [継承]
キーワード (推奨): 1. (英) Animals (日) (読) [継承]
2. (英) Bone Remodeling (日) (読) [継承]
3. (英) Bone Resorption (日) (読) [継承]
4. (英) Cyclosporine (日) (読) [継承]
5. (英) Gingival Overgrowth (日) (読) [継承]
6. (英) Immunosuppressive Agents (日) (読) [継承]
7. (英) Male (日) (読) [継承]
8. (英) Osteocalcin (日) (読) [継承]
9. (英) Osteogenesis (日) (読) [継承]
10. (英) Osteoporosis (日) (読) [継承]
11. (英) Parathyroid Hormone (日) (読) [継承]
12. (英) Rats (日) (読) [継承]
13. (英) Rats, Inbred F344 (日) (読) [継承]
14. (英) Tibia (日) (読) [継承]
15. (英) Tomography, X-Ray Computed (日) (読) [継承]
発行所 (推奨):
誌名 (必須): Journal of Bone and Mineral Metabolism ([Springer-Verlag])
(pISSN: 0914-8779, eISSN: 1435-5604)

ISSN (任意): 0914-8779
ISSN: 0914-8779 (pISSN: 0914-8779, eISSN: 1435-5604)
Title: Journal of bone and mineral metabolism
Title(ISO): J Bone Miner Metab
Supplier: Springer Online Journal Archive
Publisher: Springer
 (NLM Catalog  (医中誌Web  (Scopus  (CrossRef (Scopus information is found. [need login])
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年月日 (必須): 西暦 2006年 5月 初日 (平成 18年 5月 初日) [継承]
URL (任意):
DOI (任意): 10.1007/s00774-005-0672-x    (→Scopusで検索) [継承]
PMID (任意): 16622732    (→Scopusで検索) [継承]
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備考 (任意): 1.(英) Affiliation: Division of Gene Expression, Institute for Genome Research, The University of Tokushima, Kuramoto 3-18-15, Tokushima 770-8503, Japan.  (日)    [継承]
2.(英) PublicationType: Journal Article  (日)    [継承]

標準的な表示

和文冊子 ● Chie Wada -Mihara, Masatoshi Kataoka, Hiroyuki Seto, Noriko Hayashi, Jun-ichi Kido, Yasuo Shinohara and Toshihiko Nagata : High-turnover osteoporosis is induced by cyclosporin A in rats., Journal of Bone and Mineral Metabolism, 24, 3, 199-205, 2006.
欧文冊子 ● Chie Wada -Mihara, Masatoshi Kataoka, Hiroyuki Seto, Noriko Hayashi, Jun-ichi Kido, Yasuo Shinohara and Toshihiko Nagata : High-turnover osteoporosis is induced by cyclosporin A in rats., Journal of Bone and Mineral Metabolism, 24, 3, 199-205, 2006.

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