Inhibitory Effects of Prior Low-dose X-ray Irradiation on Carbon Tetrachloride-induced Hepatopathy in Acatalasemic Mice

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  • YAMAOKA Kiyonori
    Chair of Medical Radioscience, and Department of Public Health and Pharmacology, Okayama University Medical School
  • KATAOKA Takahiro
    Chair of Medical Radioscience, and Department of Public Health and Pharmacology, Okayama University Medical School
  • NOMURA Takaharu
    Low Dose Radiation Research Center, Central Research Institute of Electric Power Industry
  • TAGUCHI Takehito
    Chair of Medical Radioscience, and Department of Public Health and Pharmacology, Okayama University Medical School
  • WANG Da-Hong
    Public Health, Okayama University Medical School
  • MORI Shuji
    Pharmacology, Okayama University Medical School
  • HANAMOTO Katsumi
    Chair of Medical Radioscience, and Department of Public Health and Pharmacology, Okayama University Medical School
  • KIRA Shohei
    Public Health, Okayama University Medical School

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The catalase activities in blood and organs of the acatalasemic (C3H/AnLCsbCsb) mouse of C3H strain are lower than those of the normal (C3H/AnLCs aCsa) mouse. We examined the effects of prior low-dose (0.5 Gy) X-ray irradiation, which reduced the oxidative damage under carbon tetrachloride-induced hepatopathy in the acatalasemic or normal mice. The acatalasemic mice showed a significantly lower catalase activity and a significantly higher glutathione peroxidase activity compared with those in the normal mice. Moreover, low-dose irradiation increased the catalase activity in the acatalasemic mouse liver to a level similar to that of the normal mouse liver. Pathological examinations and analyses of blood glutamic oxaloacetic and glutamic pyruvic transaminase activity and lipid peroxide levels showed that carbon tetrachloride induced hepatopathy was inhibited by low-dose irradiation. These findings may indicate that the free radical reaction induced by the lack of catalase and the administration of carbon tetrachloride is more properly neutralized by high glutathione peroxidase activity and low-dose irradiation in the acatalasemic mouse liver.<br>

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