フッ化カドミウム静脈内単回投与後の急性有害影響(第2報) : カドミウムおよびフッ素の胆汁および尿中排出量の経時的変化 Acute Harmful Effects after Single Intravenous Dose of Cadmium Fluoride in Rats (Second report) : Changes of cadmium and fluoride excretion in bile and urine

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著者

    • 足立 和也 ADACHI Kazuya
    • 大阪医科大学 衛生学・公衆衛生学教室 Department of Hygiene and Public Health, Osaka Medical College
    • 三井 剛 MITSUI Go
    • 大阪医科大学 衛生学・公衆衛生学教室 Department of Hygiene and Public Health, Osaka Medical College
    • 河野 公一 KONO Koichi
    • 大阪医科大学 衛生学・公衆衛生学教室 Department of Hygiene and Public Health, Osaka Medical College

抄録

Cadmium fluoride(CdF<sub>2</sub>)have been recently used for electronics device in industrial fields. In previous study, we investigated the dose-effect relationships of acute toxicities from the standpoint of occupational health. It would be strongly influenced by metabolism of CdF<sub>2</sub>. Therefore, this study was designed to investigate the early dynamic state of Cd and F in bile and urine after the acute exposure of CdF<sub>2</sub>. Rats were received a single intravenous injection of saline or CdF<sub>2</sub>(1.34, 2.67, or 4.01 mg/kg)which were the same doses of the previous study. Bile was collected at intervals of 30 min until 300 min. Urine was collected for 300 min. Volume of bile and urine were decreased in CdF<sub>2</sub> treated groups. Total biliary Cd was excreted in the 2.67 and 4.01 group much more than 1.34 group. The peaks of maximum excretion were 30-60 min in the 2.67 group and 60-90 min in the 4.01 group respectively. Our previous study indicated that CdF<sub>2</sub> caused severe liver dysfunction at a dose of 2.67 and 4.01 mg/kg and proximal tubular damage at a dose of 4.01 mg/kg. Abnormalities in Cd kinetics could be resulted from extensive hepatic damage at a toxic dose. The differences of kinetics would be caused by the saturation of the accumulation capacity of the liver. Although biliary ionized F(F)was dose-relatedly excreted, urinary F did not show dose-related excretion. Therefore, the metabolism of F was mainly disordered by renal dysfunction rather than hepatic damage. The toxicity of CdF<sub>2</sub> may be enhanced by kinetics abnormalities caused by liver and kidneys dysfunctions.

収録刊行物

  • Biomedical research on trace elements  

    Biomedical research on trace elements 18(4), 405-409, 2007-12-31 

    Japan Society for Biomedical Research on Trace Elements

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各種コード

  • NII論文ID(NAID)
    10021097807
  • NII書誌ID(NCID)
    AN10423256
  • 本文言語コード
    JPN
  • 資料種別
    SHO
  • ISSN
    0916717X
  • NDL 記事登録ID
    9412637
  • NDL 雑誌分類
    ZS8(科学技術--医学--解剖学・生理学・生化学)
  • NDL 請求記号
    Z19-3255
  • データ提供元
    CJP書誌  CJP引用  NDL  J-STAGE 
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