Low dose gamma-irradiation differentially modulates antioxidant defense in liver and lungs of Balb/c mice

References

• Amundson S A, Lee R A, Koch-Paiz C A, Bittner M L, Meltzer P, Trent J M, Fornace A J, Jr. Differential responses of stress genes to low-dose-rate γ-irradiation. Molecular Cancer Research 2003; 1: 445–452
   PubMed Web of Science ®Google Scholar
• Brenner D J, Doll R, Goodhead D T, Hall E J, Land C E, Little J B, Lubin J H, Preston D L, Preston R J, Puskin J S, Ron E, Sachs R K, Samet J M, Setlow R B, Zaider M. Cancer risks attributable to low-doses of ionizing radiation: assessing what we really know. Proceedings of the National Academy of Sciences of the USA 2003; 100: 13761–13766
   PubMed Web of Science ®Google Scholar
• Calabrese E J, Baldwin L A. Radiation hormesis and cancer. Human and Ecological Risk Assessment 2002; 8: 327–353
   Web of Science ®Google Scholar
• Carlberg I, Mannervik B. Purifications and characterization of the flavoenzyme glutathione reductase from rat liver. Journal of Biological Chemistry 1975; 250: 5475–5480
   PubMed Web of Science ®Google Scholar
• Cuttler J M, Pollycove M. Can cancer be treated with low-doses of radiation?. Journal of American Physicians and Surgeons 2003; 8: 108–111
   Google Scholar
• Dasu A, Denekamp J. Inducible repair and intrinsic radiosensitivity: A complex but predictable relationship?. Radiation Research 2000; 153: 279–288
   PubMed Web of Science ®Google Scholar
• Djordjevic V B. Free radicals in cell biology. International Review of Cytology 2004; 237: 57–89
   PubMed Web of Science ®Google Scholar
• Grant C M, Dawes I W. Synthesis and role of glutathione in protein against oxidative stress in yeast. Redox Report 1996; 2: 223–229
   PubMed Web of Science ®Google Scholar
• Ibuki Y, Goto R. Adaptive response to low-doses of gamma-ray in Chinese hamster cells: determined by cell survival and DNA synthesis. Biological & Pharmaceutical Bulletin 1994; 17: 1111–1113
   PubMed Web of Science ®Google Scholar
• Ibuki Y, Goto R. Ionizing radiation-induced macrophage activation: augmentation of nitric oxide production and its significance. Cellular & Molecular Biology 2004; 50: 617–626
   Google Scholar
• Ikushima T, Aritomi H, Morisita J. Radioadaptive response: Efficient repair of radiation-induced DNA damage in adapted cells. Mutation Research 1996; 358: 193–198
   PubMed Web of Science ®Google Scholar
• Ina Y, Sakai K. Prolongation of life span associated with immunological modification by chronic low-dose-rate irra-diation in MRL-lpr/lpr mice. Radiation Research 2004; 161: 168–173
   PubMed Web of Science ®Google Scholar
• Ina Y, Tanooka H, Yamada T, Sakai K. Suppression of thymic lymphoma induction by life-long low-dose-rate irradiation accompanied by immune activation in C57BL/6 mice. Radiation Research 2005; 163: 153–158
   PubMed Web of Science ®Google Scholar
• ICRP. 1990 Recommendations of the International Commission on Radiological Protection. Pergamon Press, Oxford 1991, ICRP Publication 60, Annals of the ICRP 21(1 – 3)
   Google Scholar
• Jain A, Martensson J, Stole E, Auld P A, Meister A. Glutathione deficiency leads to mitochondrial damage in the brain. Proceedings of the National Academy of Sciences of the USA 1991; 88: 1913–1917
   PubMed Web of Science ®Google Scholar
• James S J, Makinodan T. T cell potentiation in normal and autoimmune-prone mice after extended exposure to low-doses of ionizing radiation and/or caloric restriction. International Journal of Radiation Biology and Related Studies in Physics, Chemistry and Medicine 1988; 53: 137–152
   PubMedGoogle Scholar
• Kawakita Y, Ikekita M, Kurozumi R, Kojima S. Increase of intracellular glutathione by low-dose gamma-ray irradiation is mediated by transcription factor AP-1 in RAW 264.7 cells. Biological and Pharmaceutical Bulletin 2003; 26: 19–23
   PubMed Web of Science ®Google Scholar
• Kojima S, Ishida H, Takahashi M, Yamaoka K. Elevation of glutathione induced by low-dose gamma rays and its involvement in increased natural killer activity. Radiation Research 2002; 157: 275–280
   PubMedGoogle Scholar
• Kojima S, Matsuki O, Kinoshita I, Gonzalez T V, Shimura N, Kubodera A. Does small dose gamma-ray radiation induce endogenous antioxidant potential in vivo?. Biological and Pharmaceutical Bulletin 1997; 20: 601–604
   PubMed Web of Science ®Google Scholar
• Kojima S, Matsuki O, Nomura T, Kubodera A, Honda Y, Honda S, Tanooka H, Wakasugi H, Yamaoka K. Induction of mRNAs for glutathione synthesis-related proteins in mouse liver by low-doses of gamma-rays. Biochimica et Biophysica Acta 1998b; 1381: 312–318
   PubMed Web of Science ®Google Scholar
• Kojima S, Matsuki O, Nomura T, Kubodera A, Yamaoka K. Elevation of mouse liver glutathione level by low-dose γ-ray irradiation and its effect on CCl4-induced liver damage. Anticancer Research 1998c; 18: 2471–2476
   PubMed Web of Science ®Google Scholar
• Kojima S, Matsuki O, Nomura T, Shimura N, Kubodera A, Yamaoka K, Tanooka H, Wakasugi H, Honda Y, Honda S, Sasaki T. Localization of glutathione and induction of glutathione synthesis-related proteins in mouse brain by low-doses of gamma-rays. Brain Research 1998a; 808: 262–269
   PubMed Web of Science ®Google Scholar
• Kojima S, Matsuki O, Nomura T, Yamaoka K, Takahashi M, Niki E. Elevation of antioxidant potency in the brain of mice by low-dose γ-ray irradiation and its effect on 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced brain damage. Free Radical Biology & Medicine 1999; 26: 388–395
   PubMed Web of Science ®Google Scholar
• Kojima S, Matsumori S, Ishida H, Yamaoka K. Possible role of elevation of glutathione in the acquisition of enhanced proliferation of mouse splenocytes exposed to small-dose gamma-rays. International Journal of Radiation Biology 2000; 76(12)1641–1647
   PubMed Web of Science ®Google Scholar
• Kojima S, Nakayama K, Ishida H. Low-dose gamma-rays activate immune functions via induction of glutathione and delay tumor growth. Journal of Radiation Research (Tokyo) 2004; 45: 33–39
   PubMed Web of Science ®Google Scholar
• Kojima S, Yamaoka K. Induction of glutathione in mouse brain by low doses of γ-rays. Biological effects of low dose radiation, Yamada, et al. Elsevier Science BV, Arizona, USA 2000; 117–127
   Google Scholar
• Kono Y. Generation of superoxide radical during autooxidation of hydroxylamine and an assay for superoxide dismutase. Archives of Biochemistry & Biophysics 1978; 186: 189–195
   PubMed Web of Science ®Google Scholar
• Lawrence R A, Burk R F. Glutathione peroxidase activity in selenium-deficient rat liver. Biochemistry & Biophysical Research Communication 1976; 71: 952–958
   PubMed Web of Science ®Google Scholar
• Liu S Z, Liu W H, Sun J B. Radiation hormesis: Its expression in the immune system. Health Physics 1987; 52: 579–583
   PubMed Web of Science ®Google Scholar
• Lowry O H, Rosebrough N J, Farr A L, Randall R J. Protein measurement with folin-phenol reagent. Journal of Biological Chemistry 1951; 193: 265–275
   PubMed Web of Science ®Google Scholar
• Luck H. Catalase. Methods of enzymatic analysis, H W Bergmeyer. Academic Press, New York 1963; 885–894, Section 3
   Google Scholar
• Luckey T D. Physiological benefits from low levels of ionizing radiation. Health Physics 1982; 43: 771–789
   PubMed Web of Science ®Google Scholar
• Martensson J, Jain A, Stole E, Frayer W, Auld P A, Meister A. Inhibition of glutathione synthesis in the newborn rat: A model of endogenously produced oxidative stress. Proceedings of the National Academy of Sciences of the USA 1991; 88: 9360–9364
   PubMed Web of Science ®Google Scholar
• Meister A, Anderson M E. Glutahione. Annual Review of Biochemistry 1983; 52: 711–760
   PubMed Web of Science ®Google Scholar
• Moron M S, Dipierre J W, Mannervik B. Levels of glutathione, glutathione reductase and glutathione-s-transferase activities in rat lungs and liver. Biochemica et Biophysica Acta 1979; 582: 67–78
   PubMed Web of Science ®Google Scholar
• Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry 1979; 95: 351–358
   PubMed Web of Science ®Google Scholar
• Pollycove M. Radiobiological basis of low-dose irradiation in prevention and therapy of cancer. 14th Pacific Basin Nuclear Conference. Honolulu, HI March 21 – 25 2004, 2004; 647–653
   Google Scholar
• Safwat A. The immunobiology of low-dose total-body irradiation: More questions than answers. Radiation Research 2000; 153: 599–604
   PubMed Web of Science ®Google Scholar
• Sankaranarayanan K, von Duyn A, Loos M J, Natarajan A T. Adaptive response of human lymphocytes to low-level radiation from radioisotopes or X-rays. Mutation Research 1989; 211: 7–12
   PubMed Web of Science ®Google Scholar
• Shadley J D, Afzal V, Wolff S. Characterization of the adaptive response to ionizing radiation induced by low-doses of X rays to human lymphocytes. Radiation Research 1987; 111: 511–517
   PubMed Web of Science ®Google Scholar
• Skov K A. Radioresponsiveness at low-doses: Hyper-radiosensitivity and increased radioresistance in mammalian cells. Mutation Research 1999; 430: 241–253
   PubMed Web of Science ®Google Scholar
• Tiku A B, Kale R K. Adaptive response and split-dose effect of radiation on the survival of mice. Journal of Biosciences 2004; 29: 111–117
   PubMed Web of Science ®Google Scholar
• United Nations Scientific Committee on the Effects of Atomic Radiation, Genetic and Somatic Effects of Ionizing Radiation, 1986 report to the General Assembly, with annexes. New YorkUnited Nations 1986
   Google Scholar
• Wang B, Ohyama H, Shang Y, Tanaka K, Aizawa S, Yukawa O, Hayata I. Adaptive response in embryogenesis: V. Existence of two efficient dose-rate ranges for 0.3 Gy of priming irradiation to adapt mouse fetuses. Radiation Research 2004; 161: 264–272
   PubMed Web of Science ®Google Scholar
• Wang Z Q, Saigusa S, Sasaki M S. Adaptive response to chromosome damage in cultured human lymphocytes primed with low-doses of X-rays. Mutation Research 1991; 246: 179–186
   PubMed Web of Science ®Google Scholar
• Wolff S. Aspects of the adaptive response to very low-doses of radiation and other agents. Mutation Research 1996; 358: 135–142
   PubMed Web of Science ®Google Scholar
• Wolff S. The adaptive response in radiobiology: Evolving insights and implications. Environmental Health Perspectives 1998; 106: 277–283
   PubMed Web of Science ®Google Scholar
• Yamaoka K, Edamatsu R, Mori A. Increased SOD activities and decreased lipid peroxide levels induced by low-dose X-irradiation in rat organs. Free Radical Biology and Medicine 1991; 11: 299–306
   PubMed Web of Science ®Google Scholar
• Yamaoka K, Komoto Y, Suzuka I, Edamatsu R, Mori A. Effects of radon inhalation on biological function – lipid peroxide level, superoxide dismutase activity, and membrane fluidity. Archives of Biochemistry and Biophysics 1993; 302: 37–41
   PubMed Web of Science ®Google Scholar
• Yonezawa M, Misonoh J, Hosokawa Y. Two types of X-ray-induced radioresistance in mice: Presence of 4 dose ranges with distinct biological effects. Mutation Research 1996; 358: 237–243
   PubMed Web of Science ®Google Scholar
• Yonezawa M, Takeda A, Misonoh J. Acquired radioresistance after low-dose X-irradiation in mice. Journal of Radiation Research 1990; 31: 256–262
   PubMedGoogle Scholar