Radiolytic yield of cardiolipin peroxidation by gamma rays in large unilamellar vesicles of phosphatidylcholine

Radiation Research

Volumn 171, Issue 5, 2009, Pages 622-630

  Ahmed Adrar, Nazha Sid ^a   Collin, Fabrice ^a   Couturier, Martine ^b   Vitrac, Heidi ^a   Bonnefont Rousselot, Dominique ^c   Jore, Daniel ^a   Gards Albert, Monique ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b Dyslipoproteinemia and Atherosclerosis Research Unit   (France)

^c UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CARDIOLIPIN; HYDROXYL RADICAL; PHOSPHATIDYLCHOLINE; LIPOSOME;

ARTICLE; GAMMA RADIATION; LIPID PEROXIDATION; PHOSPHOLIPID MEMBRANE; PHOSPHOLIPID VESICLE; PRIORITY JOURNAL; RADIATION DOSE; RADIOLYSIS; METABOLISM; RADIATION EXPOSURE;

RHODOCOCCUS RHODOCHROUS;

CARDIOLIPINS; GAMMA RAYS; LIPID PEROXIDATION; PHOSPHATIDYLCHOLINES; UNILAMELLAR LIPOSOMES;

EID: 67650686822     PISSN: 00337587     EISSN: None     Source Type: Journal    
DOI: 10.1667/RR1473.1     Document Type: Article

References (30)

1. E. Fahy, S. Subramaniam, H. A. Brown, C. K. Glass, A. H. Merrill, Jr., R. C. Murphy, C. R. H. Raetz, D. W. Russell, Y. Seyama and E. A. Dennis, A comprehensive classification system for lipids. J. Lipid Res. 46, 839-861 (2005).
2. G. Daum, Lipids of mitochondria. Biochim. Biophys. Acta 822, 1-42 (1985).
3. F. E. McAuley, P. K. Fyfe, J. P. Ridge, N. W. Isaacs, R. J. Cogdell and M. R. Jones, Structural details of interaction between cardiolipin and an integral membrane protein. Proc. Natl. Acad. Sci. USA 96, 14706-14711 (1999).
4. A. I. de Kroon, D. Dolis, A. Mayer, R. Lill and B. de Kruijff, Phospholipid composition of highly purified mitochondrial outer membranes of rat liver and Neurospora crassa. Is cardiolipin present in the mitochondrial outer membrane? Biochim. Biophys. Acta 1325, 108-116 (1997).
5. M. Schlame, S. Shanske, S. Doty, T. Konig, T. Sculco, S. DiMauro and T. J. J. Blanck, Microanalysis of cardiolipin in small biopsies including skeletal muscle from patients with mitochondrial disease. J. Lipid Res. 40, 1585-1592 (1999).
6. F. L. Hoch, Cardiolipin and biomembrane function. Biochim. Biophys. Acta 1113, 71-133 (1992).
7. F. Gonzalvez and E. Gottlieb, Cardiolipin: setting the beat of apoptosis. Apoptosis 12, 877-885 (2007).
8. J. B. McMillin and W. Dowhan, Cardiolipin and apoptosis. Biochim. Biophys. Acta 1585, 97-107 (2002).
9. G. C. Sparagna, C. A. Johnson, S. A. McCune, R. L. Moore and R. C. Murphy, Quantitation of cardiolipin molecular species in spontaneously hypertensive heart failure rats using electrospray ionisation mass spectrometry. J. Lipid Res. 46, 1196-1204 (2005).
10. G. Paradies, G. Petrosillo, M. Pistolese and F. M. Ruggiero, Reactive species generated by the mitochondrial respiratory chain affect the complex III activity via cardiolipin peroxidation in beef-heart sub-mitochondrial particles. Mitochondrion 1, 151-159 (2001).
11. G. Petrosillo, F. M. Roggiero, M. Pistolese and G. Paradies, Reactive oxygen species generated from the mitochondrial electron transport chain induce cytochrome c dissociation from beef-heart submitochondrial particles via cardiolipin peroxidation. Possible role in the apoptosis. FEBS Lett. 509, 435-438 (2001).
12. V. E. Kagan, G. G. Borisenko, Y. Y. Tyurina, V. A. Tyurin, J. Jiang, A. I. Potapovich, V. Kini, A. A. Amoscato and Y. Fujii, Oxidative lipidomics of apoptosis: redox catalytic interactions of cytochrome c with cardiolipin and phosphatidylserine. Free Radic. Biol. Med. 37, 1963-1985 (2004).
13. F. Valianpour, R. J. A. Wanders, P. G. Barth, H. Overmars and A. H. Van Gennip, Quantitative and compositional study of cardiolipin in platelets by electrospray ionization. Mass spectrometry: Application for the identification of Barth syndrome patients. Clin. Chem. 48, 1390-1397 (2002).
14. K. D. Hauff and G. M. Hatch, Cardiolipin metabolism and Barth syndrome. Prog. Lipid Res. 45, 91-101 (2006).
15. H. Vitrac, M. Courrègelongue, M. Couturier, F. Collin, P. Thérond, S. Rémita, P. Peretti, D. Jore and M. Gardès-Albert, Radiation-induced peroxidation of small unilamellar vesicles of phosphatidylcho-line generated by sonication. Can. J. Physiol. Pharmacol. 82, 153-160 (2004).
16. -free radicals produced by gamma radiolysis. Radiat. Res. 134, 271-282 (1993).
17. J. W. T. Spinks and R. J. Woods, Water and inorganic aqueous systems. In Introduction to Radiation Chemistry, 3rd ed., pp. 243-313. Wiley-Interscience, New York, 1990.
18. H. Fricke and S. Morse, The chemical action of Roentgen rays on dilute ferrosulfonate solutions as a measure of dose. Am. J. Roentgenol. Radium Ther. 18, 430-432 (1927).
19. -radicals in aqueous solutions. J. Phys. Chem. Ref. Data 14, 1041-1051 (1985).
20. D. G. Hendry, T. Mil, L. Piskziewicz, J. A. Howard and H. K. Eigenmann, A critical review of H-atom transfer in the liquid phase: chlorine atom, alkyl, trichloromethyl, alkoxy, and alkylperoxy radicals. J. Phys. Chem. Ref. Data 3, 937-978 (1974).
21. K. Hasegawa and L. K. Patterson, Pulse radiolysis studies in model lipid system: formation and behavior of peroxy radicals in fatty acids. Photochem. Photobiol. 28, 817-823 (1978).
22. M. Al Sheikly and M. G. Simic, Chain-propagation length of linoleic acid peroxidation in aqueous monomeric and micellar systems. J. Phys. Chem. 93, 3103-3106 (1989).
23. M. Hicks and J. M. Gebicki, Continuous measurement of oxygen consumption by linoleic acid membranes exposed to free radicals generated by gamma-radiation. Int. J. Radiat. Biol. 60, 143-148 (1993).
24. W A. Pryor and L. Castle, Chemical methods for the detection of lipid hydroperoxides. Methods Enzymol. 105, 293-299 (1984).
25. P. Thérond, M. Couturier, J. F. Demelier and F. Lemonnier, Simultaneous determination of the main molecular species of soybean phosphatidylcholine or phosphatidylethanolamine and their corresponding hydroperoxides obtained by lipoxygenase treatment. Lipids 28, 245-249 (1993).
26. J. Hindo, C. Hauville, S. Remita, P. Thérond, M. Couturier, D. Jore and M. Gardès-Albert, Evidence of the formation of different hydroperoxides in irradiated gamma-linolenate solutions: Effect of micelle formation. Radiat. Res. 153, 201-207 (2000).
27. C. Hauville, S. Rémita, P. Thérond, D. Jore and M. Gardès-Albert, Radiation induced peroxidation of polyunsaturated fatty acids: Recent results on formation of hydroperoxides. Can. J. Physiol. Pharmacol. 79, 176-179 (2001).
28. Y. Y. Tyurina, V. A. Tyurin, M. W Epperly, J. S. Greenberger and V. E. Kagan, Oxidative lipidomics of γ-irradiation-induced intestinal injury. Free Radic. Biol. Med. 44, 299-314 (2008).
29. O. Shadiro, I. Yurkova, M. Kisel, O. Brede and J. Arnhold, Formation of phosphatidic acid, ceramide and diglyceride on radiolysis of lipids: identification by MALDI-TOF mass spectrometry. Free Radic. Biol. Med. 36, 1612-1624 (2004).
30. G. Paradies, G. Petrosillo, M. Pistolese, N. Di Venosa, D. Serena and F. M. Ruggiero, Lipid oxidation and alterations to oxidative metabolism in mitochondria isolated from rat heart subjected to ischemia and reperfusion. Free Radic. Biol. Med. 27, 42-50 (1999).