Skip to main content
Log in

Spin trapping endogenous radicals in MC-1010 cells: Evidence for hydroxyl radical and carbon-centered ascorbyl radical adducts

  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Abstract

Incubation of MC-1010 cells with the spin-trapping agent 5,5-dimethyl-1-pyrroline 1-oxide (DMPO) followed by brief treatment with the solid oxidant lead dioxide (PbO2) yielded, after filtration, a cell-free solution that contained two nitroxyl adducts. The first was the hydroxyl radical adduct, 5,5-dimethyl-2-hydroxypyrrolidine-1-oxyl (DMPO-OH), which formed immediately upon PbO2 oxidation. The second had a 6-line EPR spectrum typical of a carbon-centered radical (AN=15.9 G; AH=22.4 G) and formed more slowly. No radical signals were detected in the absence of either cells or PbO2 treatment. The 6-line spectrum could be duplicated in model systems that contained ascorbate, DMPO and DMPO-OH, where the latter was formed from hydroxyl radicals generated by sonolysis or the cleavage of hydrogen peroxide with Fe2+ (Fenton reaction). In addition, enrichment of MC-1010 cells with ascorbate prior to spin trapping yielded the 6-line EPR spectrum as the principal adduct following PbO2 oxidation and filtration. These results suggest that ascorbate reacted with DMPO-OH to form a carbon-centered ascorbyl radical that was subsequently trapped by DMPO. The requirement for mild oxidation to detect the hydroxyl radical adduct suggests that DMPO-OH formed in the cells was reduced to an EPR-silent form (i.e., the hydroxylamine derivative). Alternatively, the hydroxylamine derivative was the species initially formed. The evidence for endogenous hydroxyl radical formation in unstimulated leukocytes may be relevant to the leukemic nature of the MC-1010 cell line. The spin trapping of the ascorbyl radical is the first report of formation of the carbon-centered ascorbyl radical by means other than pulse radiolysis. Unless it is spin trapped, the carbon-centered ascorbyl radical immediately rearranges to the more stable oxygen-centered species that is passive to spin trapping and characterized by the well-known EPR doublet of AH4=1.8 G.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

EPR:

Electron Paramagnetic Resonance

References

  1. Halliwell B, Aruoma OI: DNA damage by oxygen-derived species. Its mechanism and measurement in mammalian systems. FEBS Lett 281: 9–19, 1991

    Google Scholar 

  2. Floyd RA, West MS, Eneff KL, Hogsett WE, Tingey DT: Hydroxyl free radical mediated formation of 8-hydroxyguanine in isolated DNA. Arch Biochem Biophys 262:266–272, 1988

    Google Scholar 

  3. Kasai K, Nishimura S: Formation of 8-hydroxydeoxyguanosine in DNA by oxygen radicals and its biological significance. In H. Sies (ed.). Oxidative Stress: Oxidants and Antioxidants. Academic Press, London, 1991, pp 99–116

    Google Scholar 

  4. Shibutani S, Takeshita M, Grollman AP: Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG. Nature 349:431–434, 1991

    Google Scholar 

  5. Simic MG, Grossman L, Upton AC (eds). Mechanisms of DNA Damage and Repair. Implications for carcinogenesis and Risk Assessment. Plenum Press, New York, 1986

    Google Scholar 

  6. Cerutti PA, Nygaard OF, Simic MG (eds). Anticarcinogenesis and Radiation Protection. Plenum Press, New York, 1987

    Google Scholar 

  7. Kuroda Y, Shankel DM, Waters MD (eds). Antimutagenesis and Anticarcinogenesis Mechanisms II. Plenum Press, New York, 1990

    Google Scholar 

  8. Halliwell B, Aruoma OI (eds). DNA and Free Radicals. Ellis Horwood, New York, 1993

    Google Scholar 

  9. Frenkel K: Carcinogen-mediated oxidant formation and oxidative DNA damage. Pharmacol Therapeut 53:127–166, 1992

    Google Scholar 

  10. Janzen EG, Haire DL: Two decades of spin trapping. In: D.D. Tanner (ed). Advances in Free Radical Chemistry, vol 1. JAI Press, Greenwich, Conn, 1990, pp 253–295

    Google Scholar 

  11. Aust SD, Chignell CF, Bray TM, Kalyanaraman B, Mason RP. Contemporary issues in toxicology. Free radicals in toxicology. Toxicol Appl Pharmacol 120:168–178, 1993

    Google Scholar 

  12. Bielski BHJ: Chemistry of Ascorbic Acid Radicals. In: P.A Seib, B.M. Tolbert (eds). Ascorbic Acid: Chemistry, Metabolism, and Uses. Amer Chem Soc, Washington, D.C., 1982, pp 81–100

    Google Scholar 

  13. Chang SCS, Bernofsky C: Correlation between DNA synthesis and intracellular NAD in cultured human leukemic lymphocytes. Biochem Biophys Res Commun 64:539–545, 1975

    Google Scholar 

  14. Phillips HJ: Dye exclusion tests for cell viability. In: P.F. Kruse Jr, M.K. Patterson Jr (eds). Tissue Culture Methods and Applications. Academic Press, New York, 1973, pp 406–408

    Google Scholar 

  15. Jacob RA: Vitamin C. In: M.E. Shils, J.A. Shike (eds). Modern Nutrition in Health and Disease, 8th ed, vol 1. Lea & Febiger, Philadelphia, 1994, pp 432–448

    Google Scholar 

  16. Bergsten P, Amitai G, Kehrl J, Dhariwal KR, Klein HG, Levine M: Millimolar concentrations of ascorbic acid in purified human mononuclear leukocytes. J Biol Chem 265:2584–2587, 1990

    Google Scholar 

  17. Bernofsky C, Bandara BMR, Hinojosa O: Fate of the free radical 5,5-dimethyl-2-pyrrolidone 1-oxyl (DMPOX) in activated neutrophils. FASEB J 7:A598, 1993

    Google Scholar 

  18. Mottley C, Mason RP: Nitroxide radical adducts in biology: chemistry, applications, and pitfalls. Biol Mag Res 8:489–546, 1989

    Google Scholar 

  19. Riesz P, Kondo T, Krishna CM: Free radical formation by ultrasound in aqueous solutions. A spin trapping study. Free Radic Res Commun 10:27–35, 1990

    Google Scholar 

  20. Weis W: Ascorbic acid and electron transport. Ann N Y Acad Sci 258:190–200, 1975

    Google Scholar 

  21. Halliwell B, Gutteridge JMC: The role of iron in free radical reactions. In: O. Hayaishi, E. Niki, M. Kondo, T. Yoshikawa (eds). Medical, Biochemical and Chemical Aspects of Free Radicals, vol 1. Elsevier Science Publ, Amsterdam, 1989, pp 21–32

    Google Scholar 

  22. Goldstein S, Meyerstein D, Czapski G: The Fenton reagents. Free Radic Biol Med 15:435–445, 1993

    Google Scholar 

  23. Golubev VA, Kozlov YN, Petrov AN, Purmal AP: Catalysis of redox processes by nitroxyl radicals. In: R.I. Zhdanov (ed.), Bioactive Spin Labels. Springer-Verlag, Berlin, 1992, pp 119–140

    Google Scholar 

  24. Clark VM, Sklarz B, Todd A: Experiments towards the synthesis of corrins. Part VII. The reductive dimerisation of a Δ1-pyrroline 1-oxide. Oxidative degradation of 2∶2′- and 2∶3′-bipyrrolidinyl derivatives. J Chem Soc 2123–2127, 1959

  25. Fessenden RW, Verma NC: A time-resolved electron spin resonance study of the oxidation of ascorbic acid by hydroxyl radical. Biophys J 24:93–100, 1978

    Google Scholar 

  26. Keana JFW, Pou S, Rosen GM: Nitroxides as potential contrast enhancing agents for MRI application: influence of structure on the rate of reduction by rat hepatocytes, whole liver homogenate, subcellular fractions, and ascorbate. Magn Reson Med 5:525–536, 1987

    Google Scholar 

  27. Eriksson UG, Brasch RC, Tozer TN: Nonenzymatic bioreduction in rat liver and kidney of nitroxyl spin labels, potential contrast agents in magnetic resonance imaging. Drug Med Disp 15:155–160, 1987

    Google Scholar 

  28. Swartz HM: Principles of the metabolism of nitroxides and their implications for spin trapping. Free Radic Res Commun 9:399–405, 1990

    Google Scholar 

  29. Buettner GR: The pecking order of free radicals and antioxidants: lipid peroxidation, α-tocopherol, and ascorbate. Arch Biochem Biophys 300:535–543, 1993

    Google Scholar 

  30. Frei B, England L, Ames BN: Ascorbate is an outstanding antioxidant in human blood plasma. Proc Nat Acad Sci USA 86:6377–6381, 1989

    Google Scholar 

  31. Halliwell B, Gutteridge JMC: Free Radicals in Biology and Medicine, 2 ed Clarendon Press, Oxford, 1989

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bernofsky, C., Bandara, B.M.R. Spin trapping endogenous radicals in MC-1010 cells: Evidence for hydroxyl radical and carbon-centered ascorbyl radical adducts. Mol Cell Biochem 148, 155–164 (1995). https://doi.org/10.1007/BF00928153

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00928153

Key Words

Navigation