课题基金 / 基金详情

Study on biological effectiveness of organic bound tritium by using DNA deficient cells.

Study on biological effectiveness of organic bound tritium by using DNA deficient cells.
利用DNA缺陷细胞研究有机结合氚的生物有效性。
批准号:
06680482
负责人:
KOMATSU Kenshi
金额:
$1.41万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1994
资助国家:
日本
项目状态:
已结题
起止时间:
1994 至 1995

项目摘要

项目成果

KOMATSU Kenshi的其他基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
Tritium is one of radioactive isotopic element, which constitute of the cell DNA.There is two majour factors for the risk of tritium in environment, which should enhance the biological effects, namely ; (1) DNA (organic)-bound tritium microdosimetricaly cause the large lession of DNA,(2) amount of tritium incorperated into organisms are increased through a food chain. In previous paper, we reported that a food chain results in 2.1-fold increase in liver cell nucleus and DNA,leading to several times higher biological effects in comparison with that of tritiated water. Our review study confirmed these high biological effectiveness of organic-bound tritium, except that tritiated amino acid have tremendous effectiveness in embryo.It is known that a low concentration or low dose rate of organic-bound tritium from environment will result in reduction of biological effectiveness, so called, dose rate effect. DNA repair from radiation-induced damage is majour factor of this low dose rate. In this experiment we estimated the effect of DNA repair on tritium biological effectiveness by using DNA repair deficient mutants, mouse scid cells and human Nijmegen Breakage Syndrome cells. The mean lethal dose Do of scid cells and NBS cells were 0.7 and 0.6 Gy, respectively and they were about half of that of normal cells. Hence, we concluded that an adequate ALI for organic bound tritium in environment is a quarter of 2.8 x 10^9 Bq presently recommended by ICRP.
期刊论文(64)
专著(0)
科研奖励(0)
会议论文
Komatsu, K.: Ataxia telangiectasia."Clinical DNA Diagnosis" (Ed.by T.Kosho, et.al.).Kanehara Inc.Tokyo, 855-857 (1994)
Komatsu,K.:共济失调毛细血管扩张症。“临床 DNA 诊断”(T.Kosho 等编)。Kanehara Inc.Tokyo,855-857 (1994)
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Komatsu,K.et.al.: "Inhibitory effects of Rooibos tea. Aspalathus linealis,on X-ray-induced C3H1Qt1/2 cell transformation." Cancer Left.77. 33-38 (1994)
Komatsu,K.et.al.:“Rooibos 茶的抑制作用。Aspalathus linealis,对 X 射线诱导的 C3H1Qt1/2 细胞转化的抑制作用。”
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
小松賢志: "In“核融合研究"名古屋大学出版会" 晩発効果・発ガン(In press), (1995)
Kenji Komatsu:“名古屋大学出版社《核聚变研究》中的晚期效应/致癌作用(正在出版),(1995 年)
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Matsuo,T.,Komatsu,K.,et.al.: "Inhibition of epidermal growth factor binding system by ionizing radiation in A431 human squamous carcinoma cells." Cancer Lett.89. 153-159 (1995)
Matsuo,T.,Komatsu,K.,et.al.:“通过电离辐射抑制 A431 人鳞状癌细胞中的表皮生长因子结合系统。”
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
30
    Contribution of translesional DNA synthesis to UV-induced damage during embryogenesis and at low dose-rate.
    • 批准号:
      25550025
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.58万
    • 财政年份:
      2013
    • 负责人:
      KOMATSU Kenshi
    • 依托单位:
    Roles of newly discovered NBS1 domains in ubiquitin signals and rejoining of double-strand breaks after irradiation
    • 批准号:
      23241021
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $24.13万
    • 财政年份:
      2011
    • 负责人:
      KOMATSU Kenshi
    • 依托单位:
    Molecular mechanism of radiation/NBS1-associated microcephaly
    • 批准号:
      23651045
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.58万
    • 财政年份:
      2011
    • 负责人:
      KOMATSU Kenshi
    • 依托单位:
    Induction of DNA double strand break by environmental genotoxic and carcinogenic agents
    • 批准号:
      18101002
    • 项目类别:
      Grant-in-Aid for Scientific Research (S)
    • 资助金额:
      $69.56万
    • 财政年份:
      2006
    • 负责人:
      KOMATSU Kenshi
    • 依托单位: