Effects of irradiation conditions on the radiation sensitivity of microorganisms in the presence of OH-radical scavengers

References

• Adhikari M, Dhaker A, Adhikari J, Ivanov V, Singh V, Chawla R, Kumar R, Sharma R, Karamalakova Y, Gadjeva V, et al. 2013. In vitro studies on radioprotective efficacy of silymarin against γ-irradiation. Int J Radiat Biol. 89:200–211.
   PubMed Web of Science ®Google Scholar
• Alizadeh E, Sanz AG, Madugundu GS, Garcia G, Wagner JR, Sanche L. 2014. Thymidine decomposition induced by low energy electrons and soft X rays under N2 and O2 atmospheres. Radiat Res. 181:629–640.
   PubMed Web of Science ®Google Scholar
• Alya G, Ekhtiar A, Saour G. 2015. Effects of lethal dose of γ-radiation and partial body hyperthermia on Wistar rats. Int J Hyperthermia. 31:460–463.
   PubMed Web of Science ®Google Scholar
• Barilla J, Lokajíček MV, Pisaková H, Simr P. 2016. Influence of oxygen on the chemical stage of radiobiological mechanism. Radiat Phys Chem. 124:116–123.
   Web of Science ®Google Scholar
• Buxton GV, Greenstock CL, Helman WP, Ross AB. 1988. 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. 17:513–886.
   Web of Science ®Google Scholar
• Chapman JD, Reuvers AP, Borsa J, Greenstock CL. 1973. Chemical radioprotection and radiosensitization of mammalian cells growing in vitro. Radiat Res. 56:291–306.
   PubMed Web of Science ®Google Scholar
• Cui L, Tse K, Zahedi P, Harding SM, Zafarana G, Jaffray DA, Bristow RG, Allen C. 2014. Hypoxia and cellular localization influence the radiosensitizing effect of gold nanoparticles (AuNPs) in breast cancer cells. Radiat Res. 182:475–488.
   PubMed Web of Science ®Google Scholar
• Czapski G, Goldstein S, Andorn N, Aronovitch J. 1992. Radiation-induced generation of chlorine derivatives in N2O-saturated phosphate buffered saline: toxic effects on Escherichia coli cells. Free Radic Biol Med. 12:353–364.
   PubMed Web of Science ®Google Scholar
• Ewing D. 1987. Application of radiation chemistry to studies in the radiation biology of microorganisms. In: Farhathaziz, Rodgers MAJ, editors. Radiation chemistry. Principles and applications, Inc; p. 501–526.
   Google Scholar
• Hirayama R, Matsumoto Y, Kase Y, Noguchi M, Ando K, Ito A, Okayasu R, Furusawa Y. 2009. Radioprotection by DMSO in nitrogen-saturated mammalian cells exposed to helium ion beams. Radiat Phys Chem. 78:1175–1178.
   Web of Science ®Google Scholar
• Hirayama R, Ito A, Noguchi M, Matsumoto Y, Uzawa A, Kobashi G, Okayasu R, Furusawa Y. 2013. OH radicals from the indirect actions of X-rays induce cell lethality and mediate the majority of the oxygen enhancement effect. Radiat Res. 180:514–523.
   PubMed Web of Science ®Google Scholar
• Hou Y, Li X, Zhao Q, Quan X, Chen G. 2010. Electrochemically assisted photocatalytic degradation of 4-chlorophenol by ZnFe2O4-modified TiO2 nanotube array electrode under visible light irradiation. Environ Sci Technol. 44:5098–5103.
   PubMed Web of Science ®Google Scholar
• Johansen I, Howard-Flanders P. 1965. Macromolecular repair and free radical scavenging in the protection of bacteria against X-Rays. Radiat Res. 24:184–200.
   PubMed Web of Science ®Google Scholar
• Liu C, Lin Q, Yun Z. 2015. Cellular and molecular mechanisms underlying oxygen-dependent radiosensitivity. Radiat Res. 183:487–496.
   PubMed Web of Science ®Google Scholar
• Mairani A, Böhlen TT, Dokic I, Cabal G, Brons S, Haberer T. 2013. Modelling of cell killing due to sparsely ionizing radiation in normoxic and hypoxic conditions and an extension to high LET radiation. Int J Radiat Biol. 89:782–793.
   PubMed Web of Science ®Google Scholar
• Millar BC, Sapora O, Fielden EM, Loverock PS. 1981. The application of rapid-lysis techniques in radiobiology IV. The effect of glycerol and DMSO on Chinese Hamster Cell Survival and DNA Single-Strand Break Production. Radiat Res. 86:506–514.
   PubMed Web of Science ®Google Scholar
• Múčka V, Bláha P, Čuba V, Červenák J. 2013. Influence of various scavengers of •OH radicals on the radiation sensitivity of yeast and bacteria. Int J Radiat Biol. 89:1045–1052.
   PubMed Web of Science ®Google Scholar
• Múčka V, Červenák J, Čuba V, Bláha P. 2015. Determination of the survival of yeast and bacteria under the influence of gamma or UV radiation in the presence of some scavengers of OH radicals. J Radioanal Nucl Chem. 304:237–244.
   Web of Science ®Google Scholar
• Noguchi M, Hirayama R, Druzhinin S, Okayasu R. 2009. Enhanced radiation-induced cell killing by Herbimycin A pre-treatment. Radiat Phys Chem. 78:1184–1187.
   Web of Science ®Google Scholar
• Olsson MG, Nilsson EJC, Rutardóttir S, Paczesny J, Pallon J, Åkerström B. 2010. Bystander cell death and stress response is inhibited by the radical scavenger α1-microglobulin in irradiated cell cultures. Radiat Res. 174:590–600.
   PubMed Web of Science ®Google Scholar
• Petin VG, Kim JK. 2004. Survival and recovery of yeast cells after combined treatment with ionizing radiation and heat. Radiat Res. 161:56–63.
   PubMed Web of Science ®Google Scholar
• Roos A, Boron WF. 1981. Intracellular pH. Physiol Rev. 61:296–434.
   PubMed Web of Science ®Google Scholar
• Roots R, Okada S. 1972. Protection of DNA molecules of cultured mammalian cells from radiation induced single-strand scissions by various alcohols and SH compounds. Int J Radiat Biol. 21:329–342.
   Web of Science ®Google Scholar
• Saran M, Bertram H, Bors W, Czapski G. 1993. On the cytotoxicity of irradiated media. To what extent are stable products of radical chain reactions in physiological saline responsible for cell death? Int J Radiat Biol. 64:311–318.
   PubMed Web of Science ®Google Scholar
• Stevens DL, Bradley S, Goodhead DT, Hill MA. 2014. Influence of dose rate on the induction of chromosome aberrations and gene mutation after exposure of plateau phase V 79-4 cells with high-LET alpha particles. Radiat Res. 182:331–337.
   PubMed Web of Science ®Google Scholar
• Sun J, Li X, Zhao Q, Ke J, Zhang D. 2014. Novel V2O5/BiVO4/TiO2 nanocomposites with high visible-light-induced photocatalytic activity for the degradation of toluene. J Phys Chem C. 118:10113–10121.
   Web of Science ®Google Scholar
• Von Sontag C. 1987. The chemical bases of radiation biology. London: Taylor and Francis LtD (Inc.).
   Google Scholar
• Wardman P, Rothkamm K, Folkes LK, Woodcock M, Johnston PJ. 2007. Radiosensitization by nitric oxide at low radiation doses. Radiat Res. 167:475–484.
   PubMed Web of Science ®Google Scholar
• Wardman P. 2016. Time as a variable in radiation biology: the oxygen effect. Radiat Res. 185:1–3.
   PubMed Web of Science ®Google Scholar
• Yang H, Magpayo N, Rusek A, Chiang I-H, Sivertz M, Held KD. 2011. Effects of very low fluences of high-energy protons or iron ions on irradiated and bystander cells. Radiat Res. 176:695–705.
   PubMed Web of Science ®Google Scholar
• Yokota Y, Funayama T, Mutou-Yoshihara Y, Ikeda H, Kobayashi Y. 2015. The bystander cell-killing effect mediated by nitric oxide in normal human fibroblasts varies with irradiation dose but not with radiation quality. Int J Radiat Biol. 91:383–388.
   PubMed Web of Science ®Google Scholar
• Yu H, Li X, Quan X, Chen S, Zhang Y. 2009. Effective utilization of visible light (including λ > 600 nm) in phenol degradation with p-silicon nanowire/TiO2 core/shell heterojunction array cathode. Environ Sci Technol. 43:7849–7855.
   PubMed Web of Science ®Google Scholar