Involvement of Hydrogen Peroxide in the Manganese-Induced Myocytes Mitochondrial Membrane Potential Loss

REFERENCES

• F. S. Archibald, and I. Fridovich. (1982). The scavenging of superoxide radical by manganeous complexes: in vitro. Arch. Biochem. Biophys. 214:452–463.
   PubMed Web of Science ®Google Scholar
• W. W. Barrington, C. R. Angle, N. K. Willcockson, M. A. Padula, and T. Korn. (1998). Autonomic function in manganese alloy workers. Environ. Res. 78:50–58.
   PubMed Web of Science ®Google Scholar
• G. Bellomo, and S. Orrenius. (1985). Altered thiol and calcium homeostasis in oxidative hepatocellular injury. Hepatology 5:876–882.
   PubMed Web of Science ®Google Scholar
• V. Bencko, and M. Cikrt. (1984). Manganese: a review of occupational and environmental toxicology. J. Hyg. Epidemiol. Microbiol. Immunol. 28:139–148.
   PubMedGoogle Scholar
• A. H. Boulares, F. J. Contreras, L. A. Espinoza, and M. E. Smulson. (2002). Role of oxidative stress and glutathione depletion in JP-8 jet fuel-induced apoptosis in rat lung epithelial cells. Toxicol. Appl. Pharm. 180:92–99.
   PubMed Web of Science ®Google Scholar
• H. Brurok, K. Berg, L. Sneen, D. Grant, J. O. G. Karlsson, and P. Jynge. (1999). Cardiac metal contents after infusions of manganese: an experimental evaluation in the isolated rat heart. Invest. Radiol. 34:470–476.
   PubMed Web of Science ®Google Scholar
• H. Brurok, J. Schjott, K. Berg, J. O. G. Karlsson, and P. Jynge. (1997a). Effects of MnDPDP, DPDP −−, and MnCl2 on cardiac energy metabolism and manganese accumulation: an experimental study in the isolated perfused rat heart. Invest. Radiol. 32:205–211.
   PubMed Web of Science ®Google Scholar
• H. Brurok, J. Schjott, K. Berg, J. O. G. Karlsson, and P. Jynge. (1997b). Manganese and the heart: acute cardiodepression and myocardial accumulation of manganese. Acta Physiol. Scand. 159:33–40.
   PubMedGoogle Scholar
• B. Collin, D. Busseuil, M. Zeller, C. Perrin, O. Barthez, L. Duvillard, C. Vergely, M. Bardou, M. Dumas, Y. Cottin, and L. Rochette. (2007). Increased superoxide anion production is associated with early atherosclerosis and cardiovascular dysfunctions in a rabbit model. Mol. Cell Biol. 294:225–235.
   Google Scholar
• J. P. Crow. (1997). Dichlorodihydrofluorescein and dihydrorhodamine 123 are sensitive indicators of peroxynitrite in vitro: implications for intracellular measurement of reactive nitrogen and oxygen species. Nitric Oxide 1:145–157.
   PubMed Web of Science ®Google Scholar
• J. M. Davis, A. M. Jarabek, D. T. Mage, and J. A. Graham. (1999). Inhalation health risk assessment of MMT. Environ. Res. 80:103–104.
   PubMed Web of Science ®Google Scholar
• M. S. Desole, L. Sciola, M. R. Delogu, S. Sircana, R. Migheli, and E. Miele. (1997). Role of oxidative stress in the manganese and 1-methyl-4-(2′-ethylphenyl)-1,2,3,6-tetrahydropyridine-induced apoptosis in PC12 cells. Neurochem. Int. 31:169–176.
   PubMed Web of Science ®Google Scholar
• P. C. Elwood, M. Abernethy, and M. Morton. (1974). Mortality in adults and trace elements in water. Lancet 2:1470–1472.
   PubMed Web of Science ®Google Scholar
• E. Gumpricht, M. W. Devereaux, R. H. Dahl, and R. J. Sokol. (2000). Glutathione status of isolated rat hepatocytes affects bile acid-induced cellular necrosis but not apoptosis. Toxicol. Appl. Pharm. 164:102–111.
   PubMed Web of Science ®Google Scholar
• T. E. Gunter, L. M. Miller, C. E. Gavin, R. Eliseev, J. Salter, L. Buntinas, A. Alexandrov, S. Hammond, and K. K. Gunter. (2004). Determination of the oxidation states of manganese in brain, liver, and heart mitochondria. J. Neurochem. 88:266–280.
   PubMed Web of Science ®Google Scholar
• H. C. Ha, P. M. Woster, J. D. Yager, and R. A. CaseroJr.. (1997). The role of polyamine catabolism in polyamine analogue-induced programmed cell death. Proc. Natl. Acad. Sci. USA 94:11557–11562.
   PubMed Web of Science ®Google Scholar
• G. Isenberg, and U. Klöckner. (1982). Isolated bovine ventricular myocytes. Characterization of action potential. Pflugers Arch. 395:19–29.
   PubMed Web of Science ®Google Scholar
• Y. M. Jiang, and W. Zheng. (2005). Cardiovascular toxicities upon manganese exposure. Cardiovasc. Toxicol. 5:345–354.
   PubMed Web of Science ®Google Scholar
• H. Karppanen, R. Pennanen, and L. Passinen. (1978). Mineral, coronary heart disease and sudden coronary death. Adv. Cardiol. 25:9–24.
   PubMedGoogle Scholar
• K. S. Kasprzak. (1995). Possible role of oxidative damage in metal-induced carcinogenesis. Cancer Invest. 13:411–430.
   PubMed Web of Science ®Google Scholar
• C. L. Keen, B. Lonnerdal, and L. S. Hurley. (1984). Manganese. In: E. Frieden, (Ed.), Biochemistry of the Essential Ultratrace Elements, Plenum Press, New York, pp. 89–132.
   Google Scholar
• M. Korc. (1988). Manganese homeostasis in humans and its role in disease states. In: A. S. Prasad, (Ed.), Essential and Toxic Trace Elements in Human Health and Disease, John Wiley & Sons, Chichester, pp. 253–273.
   Google Scholar
• R. Kovacs, J. Kardos, U. Heinemann, and O. Kann. (2005). Mitochondrial calcium ion and membrane potential transients follow the pattern of epileptiform discharges in hippocampal slice cultures. J. Neurosci. 25:4260–4269.
   PubMed Web of Science ®Google Scholar
• Y. X. Ma, T. Ogino, T. Kawabata, J. Li, K. Eguchi, and S. Okada. (1999). Cupric nitrilotriacetate-induced apoptosis in HL-60 cells association with lipid peroxidation, release of cytochrome c from mitochondria, and activation of caspases-3. Free Radic. Biol. Med. 27:227–233.
   PubMed Web of Science ®Google Scholar
• E. A. Malecki. (2001). Manganese toxicity is associated with mitochondrial dysfunction and DNA fragmentation in rat primary striatal neurons. Brain Res. Bull. 55:225–228.
   PubMed Web of Science ®Google Scholar
• M. Merad-Boudia, A. Nicole, D. Santiard-Baron, C. Saillé, and I. Ceballos-Picot. (1998). Mitochondrial impairment as an early event in the process of apoptosis induced by glutathione depletion in neuronal cells: relevance to Parkinson's disease. Biol. Pharmacol. 56:645–655.
   PubMed Web of Science ®Google Scholar
• C. Parmentier, M. Wellman, A. Nicolas, G. Siest, and P. Leroy. (1999). Simultaneous measurement of reactive oxygen species and reduced glutathione using capillary electrophoresis and laser-induced fluorescence detection in cultured cell lines. Electrophoresis 20:2938–2944.
   PubMed Web of Science ®Google Scholar
• M. A. Retamal, C. J. Cortes, L. Reuss, M. V. L. Bennett, and J. C. Saez. (2006). S-nitrosylation and permeation through connexin 43 hemichannels in astrocytes: induction by oxidant stress and reversal by reducing agents. Proc. Natt. Acad. Sci. USA 103:4475–4480.
   PubMed Web of Science ®Google Scholar
• M. Sargazi, A. Shenkin, and N. B. Roberts. (2006). Aluminium-induced injury to kidney proximal tubular cells: effects on markers of oxidative damage. J. Trace Elem. Med. Biol. 19:267–273.
   PubMed Web of Science ®Google Scholar
• X. Q. Shan, T. Y. Aw, and D. P. Jones. (1990). Glutathione-dependent protection against oxidative injury. Pharmacol. Ther. 47:61–71.
   PubMed Web of Science ®Google Scholar
• H. L. Shi, L. G. Hudson, and K. J. Liu. (2004). Oxidative stress and apoptosis in metal ion-induced carcinogenesis. Free Radic. Biol. Med. 37:582–593.
   PubMed Web of Science ®Google Scholar
• A. Takeda. (2003). Manganese action in brain function. Brain Res. Rev. 41:79–87.
   PubMed Web of Science ®Google Scholar
• H. Wiseman, and B. Halliwell. (1996). Damage to DNA by reactive oxygen and nitrogen species: role in inflammatory disease and progression to cancer. Biochem. J. 313:17–29.
   PubMed Web of Science ®Google Scholar
• H. J. Yang, Y. G. Sun, and X. X. Zheng. (2007). Manganese-induced apoptosis in rat myocytes. J. Biochem. Mol. Toxicol. 21:94–100.
   PubMed Web of Science ®Google Scholar
• H. J. Yang, T. N. Wang, J. Y. Li, L. Gu, and X. X. Zheng. (2006). Decreasing expression of α1C calcium L-type channel subunit mRNA in rat ventricular myocytes upon manganese exposure. J. Biol. Mol. Toxicol. 20:159–166.
   PubMed Web of Science ®Google Scholar
• X. A. Zhan, M. Wang, Z. R. Xu, W. F. Li, and J. X Li. (2006). Effects of fluoride on hepatic antioxidant system and transcription of Cu/Zn SOD gene in young pigs. J. Trace Elem. Med. Biol. 20:83–87.
   PubMed Web of Science ®Google Scholar
• S. R. Zhang, J. L. Fu, and Z. C. Zhou. (2004). In vitro effect of manganese chloride exposure on reactive oxygen species generation and respiratory chain complexes activities of mitochondrial isolated from rat brain. Toxicol. in Vitro 18:71–77.
   PubMed Web of Science ®Google Scholar