Manganese-induced single strand breaks of mitochondrial DNA in vitro and in vivo

Environmental Toxicology and Pharmacology

Volumn 26, Issue 2, 2008, Pages 123-127

  Jiao, Jian ^a   Qi, Yanmin ^a   Fu, Juanling ^a   Zhou, Zongcan ^a  

^a PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

Author keywords

Manganese; Mitochondrial DNA; Oxidative stress; Reactive oxygen species; Single strand breakage

Indexed keywords

GLUTATHIONE; MALONALDEHYDE; MANGANESE; MANGANESE CHLORIDE; MITOCHONDRIAL DNA; REACTIVE OXYGEN METABOLITE;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; BRAIN MITOCHONDRION; CONTROLLED STUDY; DNA STRAND BREAKAGE; DOSE RESPONSE; FEMALE; IN VITRO SELECTION; IN VIVO STUDY; LIVER MITOCHONDRION; MALE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; RAT;

RATTUS;

EID: 47849088897     PISSN: 13826689     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.etap.2007.12.009     Document Type: Article

References (36)

1. Archibald F.S., and Fridovich I. The scavenging of superoxide radical by manganous complexes: in vitro. Arch. Biochem. Biophys. 214 2 (1982) 452-463
2. Balasubramanian B., Pogozelski W.K., and Tullius T.D. DNA strand breaking by the hydroxyl radical is governed by the accessible surface areas of the hydrogen atoms of the DNA backbone. Proc. Natl. Acad. Sci. U.S.A. 95 17 (1998) 9738-9743
3. Beuege J.A., and Aust S.D. Microsomal lipid peroxidation. Methods Enzymol. 30 (1978) 302-310
4. Bhattacharjee C., and Sharan R.N. UV-C radiation induced conformational relaxation of pMTa4 DNA in Escherichia coli may be the cause of single strand breaks. Int. J. Radiat. Biol. 81 12 (2005) 919-927
5. Bradford M.M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of dye-binding. Anal. Biochem. 72 (1976) 248-254
6. Brenneman K.A., Cattley R.C., Ali S.F., and Dorman D.C. Manganese-induced developmental neurotoxicity in the CD rat: is oxidative damage a mechanism of action. Neurotoxicology 20 2-3 (1999) 477-487
7. Brown S., and Taylor N.I. Could mitochondrial dysfunction play a role in manganese toxicity?. Environ. Toxicol. Pharmacol. 7 (1999) 49-57
8. Chen M.T., Yiin S.J., Sheu J.Y., and Huang Y.L. Brain lipid peroxidation and changes of trace metals in rats following chronic manganese chloride exposure. J. Toxicol. Environ. Health. A 65 3-4 (2002) 305-316
9. Darley-Usmar V., and Schapira A.H.V. Mitochondrial: DNA, Proteins and Disease (1994), Portland Press, London
10. Davis J.M. Manganese and Rhenium. In: Bingham E., Cohrssen B., and Powell C.H. (Eds). Patty's Industrial Hygiene and Toxicology. 5th ed. vol. 3 (2001), John Wiley & Sons Inc. pp. 129-168
11. Dobson A.W., Erikson K.M., and Aschner M. Manganese neurotoxicity. Ann. NY Acad. Sci. 1012 (2004) 115-128
12. Epe B., and Hegler J. Oxidative DNA damage: endonuclease fingerprinting. Methods Enzymol. 234 (1994) 122-131
13. Erikson K.M., Dobson A.W., Dorman D.C., and Aschner M. Manganese exposure and induced oxidative stress in the rat brain. Sci. Total Environ. 334/335 (2004) 409-416
14. Galvani P., Fumagalli P., and Santagostino A. Vulnerability of mitochondrial complex I in PC12 cells exposed to manganese. Eur. J. Pharmacol. 293 4 (1995) 377-383
15. 2+sequestration by mitochondria and inhibition of oxidative phosphorylation. Toxicol. Appl. Pharmacol. 115 1 (1992) 1-5
16. Gerber G.B., Léonard A., and Hantson Ph. Carcinogenicity, mutagenicity and teratogenicity of manganese compounds. Crit. Rev. Oncol. Hematol. 42 (2002) 25-34
17. Haddad J.J. Redox and oxidant-mediated regulation of apoptosis signaling pathways: immuno-pharmaco-redox conception of oxidative siege versus cell death commitment. Int. Immunopharmacol. 4 (2004) 475-493
18. Husain R., Seth P.K., and Chandra S.V. Early inhibition of succinic dehydrogenase by manganese in rat gonads. Bull. Environ. Contam. Toxicol. 16 (1976) 118-121
19. Johnson D., and Lardy H. Isolation of liver and kidney mitochondria. Methods Enzymol. IV (1967) 94-95
20. Koehker C.M., Beverly K.N., and Leverich E.P. Redox pathways of the mitochondrion. Antioxid. Redox Signal. 8 5&6 (2006) 813-822
21. LeBel C.P., Ishiropoulos H., and Bondy S.C. Evaluation of the probe 29, 79-dichlorofluorescin as an indicator of reactive oxygen species formation and oxidative stress. Chem. Res. Toxicol. 5 (1992) 227-231
22. Lφvtrup S., and Zelander T. Isolation of brain mitochondria. Exp. Cell Res. 22 (1962) 468-473
23. Marklund S., and Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur. J. Biochem. 47 (1974) 469-474
24. Moron M.S., Depierre J.W., and Mannervik B. Concentrations of glutathione, glutathione reductase and glutathione-s-transferase activities in rat lung and liver. Biochim. Biophys. Acta 582 (1979) 67-78
25. Odyuo M.M., and Sharan R.N. Differential DNA strand breaking abilities of {radical dot}OH and ROS generating radiomimetic chemicals and g-rays: study of plasmid DNA, pMTa4, in vitro. Free Radic. Res. 39 May (5) (2005) 499-505
26. Richter C., Gogvadze V., Laffranchi R., Schlapbach R., Schweizer M., Suter M., Walter P., and Yaffee M. Oxidants in mitochondria: from physiology to diseases. Biochim. Biophys. Acta 1271 1 (1995) 67-74
27. Sazuka Y., Tanizawa H., and Takino Y. Effect of adriamycin on the activities of superoxide dismutase, glutathione peroxidase and catalase in tissues of mice. Jpn. J. Cancer Res. 80 (1989) 89-94
28. Shukla G.S., and Chandra S.V. Manganese toxicity: lipid peroxidation in rat brain. Acta Pharmacol. Toxicol. 48 2 (1981) 95-100
29. Taylor M.D., Erikson K.M., Dobson A.W., Fitsanakis V.A., Dorman D.C., and Aschner M. Effects of inhaled manganese on biomarkers of oxidative stress in the rat brain. NeuroToxicology 27 (2006) 788-797
30. US ASTDR. Toxicicology Profile: Manganese http://www.atsdr.cdc.gov/toxprofiles/tp151.pdf, 2000.
31. Vamvakas S., Bittner D., Dekant W., and Anders M.W. Covalent binding of reactive intermediates of xenobiotics to mitochondrial DNA. In: Lash L.H., and Jones D.P. (Eds). Mitochondrial Dysfunction (1993), Academic Press Inc. pp. 453-9
32. Van Houten B., Woshner V., Janine H., and Santos J.H. Role of mitochondrial DNA in toxic responses to oxidative stress. DNA Repair 5 (2006) 145-152
33. Zhang S., Fu J., and Zhou Z. In vitro effect of manganese chloride exposure on reactive oxygen species generation and respiratory chain complexes activities of mitochondria isolated from rat brain. Toxicol. In Vitro 18 (2004) 71-77
34. Zhang S., Fu J., and Zhou Z. Changes in the brain mitochondrial proteome of male Sprague-Dawley rats treated with manganese chloride. Toxicol. Appl. Pharmcol. 202 (2005) 13-17
35. Zhang S., Zhou Z., and Fu J. Effect of manganese chloride exposure on liver and brain mitochondria function in rats. Environ. Res. 93 (2003) 149-157
36. Zhu F., Jiang Y., Fu J., and Zhou Z. Effect of sub-acute Mn exposure on mitochondrial function of rat brain and hemakaryocyte. China Ind. Health Occup. Dis. 28 2 (2002) 107-109