Radical scavenging and chemical repair of rutin observed by pulse radiolysis: as a basis for radiation protection

References

• Painter RB. The role of DNA damage and repair in cell killing induced by ionizing radiation. In: Meyn RE, Withers HR, editors. Radiation biology in cancer research. New York (NY): Raven Press; 1980. p. 59–68.
   Google Scholar
• Hall EJ, Giaccia AJ. Radiobiology for the radiologist. Philadelphia: Lippincott Williams & Wilkins; 2006.
   Google Scholar
• O’Neill P, Fielden EM. Primary free radical processes in DNA. Adv Radiat Biol. 1993;17:53–120.
   Google Scholar
• Douki T, Cadet J. Radiation-induced damage to DNA: from model compounds to cell. In: Spotheim-Maurizot M, Mostafavi M, Douki T, et al., editors. Radiation chemistry: from basics to applications in material and life sciences. Les Ulis: EDP Sciences; 2008. p. 177–191.
   Google Scholar
• Buxton GV. An overview of the radiation chemistry of liquids. In: Spotheim-Maurizot M, Mostafavi M, Douki T, et al., editors. Radiation chemistry: from basics to applications in material and life sciences. Les Ulis: EDP Sciences; 2008. p. 3–12.
   Google Scholar
• Ward JF. Mechanisms of radiation action on DNA in model systems-their relevance to cellular DNA. In: Fielden EM, O'Neill P,editors. The early effects of radiation on DNA. Berlin: Springer; 1991. p. 1–16.
   Google Scholar
• deLara CM, Jenner TJ, Townsend KM, et al. The effect of dimethyl sulfoxide on the induction of DNA double-strand breaks in V79-4 mammalian cells by alpha particles. Radiat Res. 1995;144(1):43–49.
   PubMed Web of Science ®Google Scholar
• Roots R, Okada S. Estimation of life times and diffusion distances of radicals involved in X-ray-induced DNA strand breaks of killing of mammalian cells. Radiat Res. 1975;64(2):306–320.
   PubMed Web of Science ®Google Scholar
• Kouvaris JR, Kouloulias VE, Vlahos LJ. Amifostine: the first selective-target and broad-spectrum radioprotector. Oncologist. 2007;12(6):738–747.
   PubMed Web of Science ®Google Scholar
• Rades D, Fehlauer F, Bajrovic A, et al. Serious adverse effects of amifostine during radiotherapy in head and neck cancer patients. Radiother Oncol. 2004;70(3):261–264.
   PubMed Web of Science ®Google Scholar
• Kligerman MM, Glover DJ, Turrisi AT, et al. Toxicity of WR-2721 administered in single and multiple doses. Int J Radiat Oncol Biol Phys. 1984;10(9):1773–1776.
   PubMed Web of Science ®Google Scholar
• O’Neill P. Pulse radiolytic study of the interaction of thiols and ascorbate with OH adducts of dGMP and dG: implications for DNA repair processes. Radiat Res. 1983;96(1):198–210.
   PubMed Web of Science ®Google Scholar
• Fu H, Lin M, Muroya Y, et al. Free radical scavenging reactions and antioxidant activities of silybin: mechanistic aspects and pulse radiolytic studies. Free Radic Res. 2009;43(9):887–897.
   PubMed Web of Science ®Google Scholar
• Anderson RF, Amarasinghe C, Fisher LJ, et al. Reduction in free-radical-induced DNA strand breaks and base damage through fast chemical repair by flavonoids. Free Radic Res. 2000;33(1):91–103.
   PubMed Web of Science ®Google Scholar
• Agarwal OP, Nagaratnam A. Radioprotective property of flavonoids in mice. Toxicon. 1981;19(2):201–204.
   PubMed Web of Science ®Google Scholar
• Shimoi K, Masuda S, Furugori M, et al. Radioprotective effect of antioxidative flavonoids in γ-ray irradiated mice. Carcinogenesis. 1994;15(11):2669–2672.
   PubMed Web of Science ®Google Scholar
• Patil SL, Rao NB, Somashekarappa HM, et al. Antigenotoxic potential of rutin and quercetin in Swiss mice exposed to gamma radiation. Biomed J. 2014;37(5):305–313.
   PubMedGoogle Scholar
• Suzuki Y, Suzuki K. Enzymatic formation of 4G-α-d-glucopyranosyl-rutin. Agric Biol Chem. 1991;55(1):181–187.
   PubMed Web of Science ®Google Scholar
• Shimoi K, Yoshizumi K, Kido T, et al. Absorption and urinary excretion of quercetin, rutin, and αG-rutin, a water soluble flavonoid, in rats. J Agric Food Chem. 2003;51(9):2785–2789.
   PubMed Web of Science ®Google Scholar
• Matsumoto M, Chiji H, Hara H. Intestinal absorption and metabolism of a soluble flavonoid, αG-rutin, in portal cannulated rats. Free Radic Res. 2005;39(10):1139–1146.
   PubMed Web of Science ®Google Scholar
• Hata K, Urushibara A, Yamashita S, et al. Chemical repair activity of free radical scavenger edaravone: reduction reactions with dGMP hydroxyl radical adducts and suppression of base lesions and AP sites on irradiated plasmid DNA. J Radiat Res. 2015;56(1):59–66.
   PubMed Web of Science ®Google Scholar
• Hata K, Lin M, Katsumura Y, et al. Pulse radiolysis study on free radical scavenger edaravone (3-methyl-1-phenyl-2-pyrazolin-5-one). 2: a comparative study on edaravone derivatives. J Radiat Res. 2011;52(1):15–23.
   PubMed Web of Science ®Google Scholar
• Buxton GV, Greenstock CL, Helman WP, et al. Critical review of rate constants for reactions of hydrated electrons, hydrogen atoms and hydroxyl radicals (•OH/•O− in aqueous solution. J Phys Chem Ref Data. 1988;17(2):513–886.
   Web of Science ®Google Scholar
• Steenken S, Jovanovic SV. How easily oxidizable is DNA? One-electron reduction potentials of adenosine and guanosine radicals in aqueous solution. J Am Chem Soc. 1997;119(3):617–618.
   Web of Science ®Google Scholar
• Milligan JR, Aguilera JA, Ward JF. Redox equilibrium between guanyl radicals and thiocyanate influences base damage yields in gamma irradiated plasmid DNA. Estimation of the reduction potential of guanyl radicals in plasmid DNA in aqueous solution at physiological ionic strength. Int J Radiat Biol. 2001;77(12):1195–1205.
   PubMed Web of Science ®Google Scholar
• Buxton GV, Stuart CR. Re-evaluation of the thiocyanate dosimeter for pulse radiolysis. Faraday Trans. 1995;91(2):279–281.
   Google Scholar
• Scholes G, Shaw P, Willson RL, et al. Pulse radiolysis studies of aqueous solutions of nucleic acid and related compounds. In: Ebert M, Keene JP, Swallow AJ, editors. Pulse radiolysis. New York (NY): Academic Press; 1965. p. 151–164.
   Google Scholar
• Fu H, Katsumura Y, Lin M, et al. Fast repair activities towards dGMP hydroxyl radical adducts by silybin and its analogues. J Radiat Res. 2008;49(6):609–614.
   PubMed Web of Science ®Google Scholar
• Elliot AJ. A pulse radiolysis study of the reaction of •OH with I2 and the decay of I2•−. Can J Chem. 1992;70(6):1658–1661.
   Web of Science ®Google Scholar
• Muroya Y, Yamashita S, Lertnaisat P, et al. Rate constant for the H•+H2O → •OH + H2 reaction at elevated temperatures measured by pulse radiolysis. Phys Chem Chem Phys. 2017;19(45):30834–30841.
   PubMed Web of Science ®Google Scholar
• Savel’eva O, Shevchuk L, Vysotskaya N. Reactions of substituted phenols with hydroxyl radicals and their dissociated form O−. J Org Chem USSR. 1972;8(2):283–286.
   Google Scholar