Non-thermal plasma elicits ferrous chloride-catalyzed DMPO-OH

References

• Toyokuni S, Ikehara Y, Kikkawa F, et al. Plasma medical science. London: Academic Press; 2018. p. 438.
   Google Scholar
• Privat-Maldonado A, Schmidt A, Lin A, et al. ROS from physical plasmas: redox chemistry for biomedical therapy. Oxid Med Cell Longev. 2019;2019:9062098.
   PubMed Web of Science ®Google Scholar
• Tanaka H, Mizuno M, Ishikawa K, et al. Molecular mechanisms of non-thermal plasma-induced effects in cancer cells. Biol Chem. 2018;400(1):87–91.
   PubMed Web of Science ®Google Scholar
• Yan D, Sherman JH, Keidar M. Cold atmospheric plasma, a novel promising anti-cancer treatment modality. Oncotarget. 2017;8(9):15977–15995.
   PubMedGoogle Scholar
• Yan D, Nourmohammadi N, Bian K, et al. Stabilizing the cold plasma-stimulated medium by regulating medium’s composition. Sci Rep. 2016;6:26016.
   PubMed Web of Science ®Google Scholar
• Jiang L, Zheng H, Lyu Q, et al. Lysosomal nitric oxide determines transition from autophagy to ferroptosis after exposure to plasma-activated ringer’s lactate. Redox Biol. 2021;43:101989.
   PubMed Web of Science ®Google Scholar
• Tanaka H, Bekeschus S, Yan D, et al. Plasma-treated solutions (PTS) in cancer therapy. Cancers. 2021;13(7):1737.
   PubMed Web of Science ®Google Scholar
• Tanaka H, Hosoi Y, Ishikawa K, et al. Low temperature plasma irradiation products of sodium lactate solution that induce cell death on U251SP glioblastoma cells were identified. Sci Rep. 2021;11(1):18488.
   PubMed Web of Science ®Google Scholar
• Bernhardt T, Semmler ML, Schafer M, et al. Plasma medicine: applications of cold atmospheric pressure plasma in dermatology. Oxid Med Cell Longev. 2019;2019:3873928.
   PubMed Web of Science ®Google Scholar
• Harley JC, Suchowerska N, McKenzie DR. Cancer treatment with gas plasma and with gas plasma-activated liquid: positives, potentials and problems of clinical translation. Biophys Rev. 2020;12(4):989–1006.
   PubMedGoogle Scholar
• Sies H, Belousov VV, Chandel NS, et al. Defining roles of specific reactive oxygen species (ROS) in cell biology and physiology. Nat Rev Mol Cell Biol. 2022;23(7):499–515.
   PubMed Web of Science ®Google Scholar
• Toyokuni S. The origin and future of oxidative stress pathology: from the recognition of carcinogenesis as an iron addiction with ferroptosis-resistance to non-thermal plasma therapy. Pathol Int. 2016;66(5):245–259.
   PubMed Web of Science ®Google Scholar
• Utsumi F, Kajiyama H, Nakamura K, et al. Effect of indirect nonequilibrium atmospheric pressure plasma on anti-proliferative activity against chronic chemo-resistant ovarian cancer cells in vitro and in vivo. PLOS One. 2013;8(12):e81576.
   PubMed Web of Science ®Google Scholar
• Okazaki Y, Wang Y, Tanaka H, et al. Direct exposure of non-equilibrium atmospheric pressure plasma confers simultaneous oxidative and ultraviolet modifications in biomolecules. J Clin Biochem Nutr. 2014;55(3):207–215.
   PubMed Web of Science ®Google Scholar
• Okazaki Y, Sasaki K, Ito N, et al. Tetrachloroaurate (III)-induced oxidation increases non-thermal plasma-induced oxidative stress. Free Radic Res. 2022;56(1):17–27.
   PubMed Web of Science ®Google Scholar
• Shi L, Ito F, Wang Y, et al. Non-thermal plasma induces a stress response in mesothelioma cells resulting in increased endocytosis, lysosome biogenesis and autophagy. Free Radic Biol Med. 2017;108:904–917.
   PubMed Web of Science ®Google Scholar
• Shi L, Wang Y, Ito F, et al. Biphasic effects of l-ascorbate on the tumoricidal activity of non-thermal plasma against malignant mesothelioma cells. Arch Biochem Biophys. 2016;605:109–116.
   PubMed Web of Science ®Google Scholar
• Sato K, Shi L, Ito F, et al. Non-thermal plasma specifically kills oral squamous cell carcinoma cells in a catalytic Fe(II)-dependent manner. J Clin Biochem Nutr. 2019;65(1):8–15.
   PubMed Web of Science ®Google Scholar
• Adachi T, Nonomura S, Horiba M, et al. Iron stimulates plasma-activated medium-induced A549 cell injury. Sci Rep. 2016;6:20928.
   PubMed Web of Science ®Google Scholar
• Okazaki Y, Ishidzu Y, Ito F, et al. L-dehydroascorbate efficiently degrades non-thermal plasma-induced hydrogen peroxide. Arch Biochem Biophys. 2021;700:108762.
   PubMed Web of Science ®Google Scholar
• Okazaki Y, Tanaka H, Hori M, et al. L-dehydroascorbic acid recycled by thiols efficiently scavenges non-thermal plasma-induced hydroxyl radicals. Arch Biochem Biophys. 2019;669:87–95.
   PubMed Web of Science ®Google Scholar
• Okazaki Y, Tanaka H, Matsumoto KI, et al. Non-thermal plasma-induced DMPO-OH yields hydrogen peroxide. Arch Biochem Biophys. 2021;705:108901.
   PubMed Web of Science ®Google Scholar
• Matsumoto K, Ueno M, Nakanishi I, et al. Density of hydroxyl radicals generated in an aqueous solution by irradiating carbon-ion beam. Chem Pharm Bull. 2015;63(3):195–199.
   PubMed Web of Science ®Google Scholar
• Kakhlon O, Cabantchik ZI. The labile iron Pool: characterization, measurement, and participation in cellular processes. Free Radic Biol Med. 2002;33(8):1037–1046.
   PubMed Web of Science ®Google Scholar
• Halliwell B, Gutteridge JMC. Free radicals in biology and medicine. Croydon: Oxford University Press; 2015.
   Google Scholar
• Makino K, Mossoba MM, Riesz P. Chemical effects of ultrasound on aqueous-solutions – formation of hydroxyl radicals and hydrogen-atoms. J Phys Chem. 1983;87(8):1369–1377.
   Web of Science ®Google Scholar
• Moritake T, Tsuboi K, Anzai K, et al. ESR spin trapping of hydroxyl radicals in aqueous solution irradiated with high-LET carbon-ion beams. Radiat Res. 2003;159(5):670–675.
   PubMed Web of Science ®Google Scholar
• Nishi M, Hagi A, Ide H, et al. Comparison of 2,5,5-trimethyl-1-pyrroline-N-oxide (M3PO) and 3,3,5,5-tetramethyl-1-pyrroline-N-oxide (M4PO) with 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) as spin traps. Biochem Int. 1992;27(4):651–659.
   PubMedGoogle Scholar
• Reinke LA, Rau JM, McCay PB. Characteristics of an oxidant formed during iron (II) autoxidation. Free Radic Biol Med. 1994;16(4):485–492.
   PubMed Web of Science ®Google Scholar
• Yamazaki I, Piette LH. ESR spin-trapping studies on the reaction of Fe2+ ions with H2O2-reactive species in oxygen toxicity in biology. J Biol Chem. 1990;265(23):13589–13594.
   PubMed Web of Science ®Google Scholar
• Lloyd RV, Hanna PM, Mason RP. The origin of the hydroxyl radical oxygen in the Fenton reaction. Free Radic Biol Med. 1997;22(5):885–888.
   PubMed Web of Science ®Google Scholar
• Halliwell B, Gutteridge JM. Biologically relevant metal ion-dependent hydroxyl radical generation. An update. FEBS Lett. 1992;307(1):108–112.
   PubMed Web of Science ®Google Scholar
• Rachmilovich-Calis S, Masarwa A, Meyerstein N, et al. The Fenton reaction in aerated aqueous solutions revisited. Eur J Inorg Chem. 2005;2005(14):2875–2880.
   Google Scholar
• Koppenol WH, Hider RH. Iron and redox cycling. Do’s and don’ts. Free Radic Biol Med. 2019;133:3–10.
   PubMed Web of Science ®Google Scholar
• Enami S, Sakamoto Y, Colussi AJ. Fenton chemistry at aqueous interfaces. Proc Natl Acad Sci USA. 2014;111(2):623–628.
   PubMed Web of Science ®Google Scholar
• Deguillaume L, Leriche M, Chaumerliac N. Impact of radical versus non-radical pathway in the Fenton chemistry on the iron redox cycle in clouds. Chemosphere. 2005;60(5):718–724.
   PubMed Web of Science ®Google Scholar
• Rush JD, Koppenol WH. Oxidizing intermediates in the reaction of ferrous EDTA with hydrogen peroxide. Reactions with organic molecules and ferrocytochrome c. J Biol Chem. 1986;261(15):6730–6733.
   PubMed Web of Science ®Google Scholar
• Burkitt MJ. ESR spin trapping studies into the nature of the oxidizing species formed in the Fenton reaction: pitfalls associated with the use of 5,5-dimethyl-1-pyrroline-N-oxide in the detection of the hydroxyl radical. Free Radic Res Commun. 1993;18(1):43–57.
   PubMed Web of Science ®Google Scholar
• Yamazaki I, Piette LH. EPR spin-trapping study on the oxidizing species formed in the reaction of the ferrous ion with hydrogen-peroxide. J Am Chem Soc. 1991;113(20):7588–7593.
   Web of Science ®Google Scholar
• Makino K, Hagiwara T, Hagi A, et al. Cautionary note for DMPO spin trapping in the presence of iron ion. Biochem Biophys Res Commun. 1990;172(3):1073–1080.
   PubMed Web of Science ®Google Scholar
• Hanna PM, Chamulitrat W, Mason RP. When are metal ion-dependent hydroxyl and alkoxyl radical adducts of 5,5-dimethyl-1-pyrroline N-oxide artifacts? Arch Biochem Biophys. 1992;296(2):640–644.
   PubMed Web of Science ®Google Scholar
• Leinisch F, Jiang J, DeRose EF, et al. Investigation of spin-trapping artifacts formed by the Forrester-Hepburn mechanism. Free Radic Biol Med. 2013;65:1497–1505.
   PubMed Web of Science ®Google Scholar
• Beltran FJ, Rivas FJ, Montero-de-Espinosa R. Iron type catalysts for the ozonation of oxalic acid in water. Water Res. 2005;39(15):3553–3564.
   PubMed Web of Science ®Google Scholar
• Tada M, Kohno M, Kasai S, et al. Generation mechanism of radical species by tyrosine-tyrosinase reaction. J Clin Biochem Nutr. 2010;47(2):162–166.
   PubMed Web of Science ®Google Scholar
• Ito S, Ikuta K, Kato D, et al. Non-transferrin-bound iron assay system utilizing a conventional automated analyzer. Clin Chim Acta. 2014;437:129–135.
   PubMed Web of Science ®Google Scholar
• Okazaki Y. Asbestos-induced mesothelial injury and carcinogenesis: involvement of iron and reactive oxygen species. Pathol Int. 2022;72(2):83–95.
   PubMed Web of Science ®Google Scholar
• Okazaki Y. The role of ferric nitrilotriacetate in renal carcinogenesis and cell death: from animal models to clinical implications. Cancers. 2022;14(6):1495.
   PubMed Web of Science ®Google Scholar
• Badu-Boateng C, Naftalin RJ. Ascorbate and ferritin interactions: consequences for iron release in vitro and in vivo and implications for inflammation. Free Radic Biol Med. 2019;133:75–87.
   PubMed Web of Science ®Google Scholar
• Furuta T, Shi L, Toyokuni S. Non-thermal plasma as a simple ferroptosis inducer in cancer cells: a possible role of ferritin. Pathol Int. 2018;68(7):442–443.
   PubMed Web of Science ®Google Scholar
• Klinkhammer C, Verlackt C, Śmiłowicz D, et al. Elucidation of plasma-induced chemical modifications on glutathione and glutathione disulphide. Sci Rep. 2017;7(1):13828.
   PubMedGoogle Scholar
• Śmiłowicz D, Kogelheide F, Stapelmann K, et al. Study on chemical modifications of glutathione by cold atmospheric pressure plasma (CAP) operated in air in the presence of Fe(II) and Fe(III) complexes. Sci Rep. 2019;9(1):18024.
   PubMedGoogle Scholar
• Giamalva D, Church DF, Pryor WA. A comparison of the rates of ozonation of biological antioxidants and oleate and linoleate esters. Biochem Biophys Res Commun. 1985;133(2):773–779.
   PubMed Web of Science ®Google Scholar
• Kanofsky JR, Sima PD. Reactive absorption of ozone by aqueous biomolecule solutions: implications for the role of sulfhydryl compounds as targets for ozone. Arch Biochem Biophys. 1995;316(1):52–62.
   PubMed Web of Science ®Google Scholar
• Spear N, Aust SD. Thiol-mediated NTA-Fe(III) reduction and lipid peroxidation. Arch Biochem Biophys. 1994;312(1):198–202.
   PubMed Web of Science ®Google Scholar
• Ke Z, Huang Q. Haem-assisted dityrosine-cross-linking of fibrinogen under non-thermal plasma exposure: one important mechanism of facilitated blood coagulation. Sci Rep. 2016;6:26982.
   PubMed Web of Science ®Google Scholar
• Śmiłowicz D, Kogelheide F, Schöne AL, et al. Catalytic oxidation of small organic molecules by cold plasma in solution in the presence of molecular iron complexes. Sci Rep. 2020;10(1):21652.
   PubMed Web of Science ®Google Scholar
• Pelalak R, Heidari Z, Forouzesh M, et al. High performance ozone based advanced oxidation processes catalyzed with novel argon plasma treated iron oxyhydroxide hydrate for phenazopyridine degradation. Sci Rep. 2021;11(1):964.
   PubMed Web of Science ®Google Scholar