Mitochondrial dysfunction in the hippocampus of rats caused by chronic oxidative stress

Neuroscience

Volumn 252, Issue , 2013, Pages 384-395

  Rodriguez Martinez E ^a   Martinez F ^a   Espinosa Garcia M T ^a   Maldonado, P ^b   Rivas Arancibia, S ^a  

^a UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^b NATIONAL INSTITUTE OF NEUROLOGY AND NEUROSURGERY   (Mexico)

Author keywords

Hippocampus; Mitochondria; Oxidative stress; Ozone

Indexed keywords

CYTOCHROME C; EOSIN; GLUTATHIONE PEROXIDASE; HEMATOXYLIN; INDUCIBLE NITRIC OXIDE SYNTHASE; MANGANESE SUPEROXIDE DISMUTASE; OZONE; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA COACTIVATOR 1ALPHA; PROTEIN BAX; PROTEIN BCL 2; SUCCINATE DEHYDROGENASE;

ANIMAL EXPERIMENT; ARTICLE; CELL DAMAGE; CELL ORGANELLE; CELL STRUCTURE; CONTROLLED STUDY; DISEASE ASSOCIATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ELECTRON MICROSCOPY; ENZYME ACTIVITY; HIPPOCAMPUS; HISTOPATHOLOGY; LONG TERM EXPOSURE; MITOCHONDRIAL CRISTAE; MITOCHONDRION SWELLING; NERVE DEGENERATION; NONHUMAN; OXIDATION; OXIDATIVE STRESS; OXYGEN CONSUMPTION; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; SPECTROPHOTOMETRY; WESTERN BLOTTING;

2,4-DINITROPHENYLHYDRAZINE; 4-(2-HYDROXYETHYL-1-PIPERAZINEETHANE SULFONIC ACID; APAF-1; APOPTOSIS PROTEASE-ACTIVATING FACTOR; B-CELL LYMPHOMA; BCL-2; BOVINE SERUM ALBUMIN; BSA; DDC; DIETHYLDITHIOCARBAMATE; DNPH; EDTA; EGTA; ELECTRON TRANSPORT CHAIN; ENDOTHELIAL NITRIC OXIDE SYNTHASE; ENOS; ETC; ETHYLENE GLYCOL TETRAACETIC ACID; ETHYLENEDIAMINETETRAACETIC ACID; GLUTATHIONE PEROXIDASE; GPX; H&E; HEMATOXYLIN AND EOSIN; HEPES; HIPPOCAMPUS; INDUCIBLE NITRIC OXIDE SYNTHASE; INOS; MANGANESE SUPEROXIDE DISMUTASE; MITOCHONDRIA; MN-SOD; NADPH; NBT; NEURONAL NITRIC OXIDE SYNTHASE; NITRIC OXIDE; NITRO-BLUE TETRAZOLIUM; NNOS; NO; OXIDATIVE STRESS; OZONE; PBS; PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR Γ CO-ACTIVATOR 1Α; PGC-1Α; PHOSPHATE SALINE BUFFER; RC; REDUCED FORM OF NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; RESPIRATORY CONTROL; SDH; SOD; SUCCINATE DEHYDROGENASE; SUPEROXIDE DISMUTASE;

ANIMALS; BLOTTING, WESTERN; HIPPOCAMPUS; IMMUNOHISTOCHEMISTRY; MITOCHONDRIA; OXIDANTS, PHOTOCHEMICAL; OXIDATIVE STRESS; OZONE; RATS; RATS, WISTAR;

EID: 84884545904     PISSN: 03064522     EISSN: 18737544     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2013.08.018     Document Type: Article

References (45)

1. Andreyev A.Y., Kushnareva Y.E., Starkov A.A. Mitochondrial metabolism of reactive oxygen species. Biochemistry (Mosc) 2005, 70(2):200-214.
2. Antonsson B., Conti F., Ciavatta A., Montessuit S., Lewis S., Martinou I., Bernasconi L., Bernard A., Mermod J.J., Mazzei G., Maundrell K., Gambale F., Sadoul R., Martinou J.C. Inhibition of Bax channel-forming activity by Bcl-2. Science 1997, 277(5324):370-372.
3. Basañez G., Nechushtan A., Drozhinin O., Chanturiya A., Choe E., Tutt S., Wood K.A., Hsu Y., Zimmerberg J., Youle R.J. Bax, but not Bcl-xL, decreases the lifetime of planar phospholipid bilayer membranes at subnanomolar concentrations. Proc Natl Acad Sci USA 1999, 96(10):5492-5497.
4. Beal M.F. Mitochondrial dysfunction in neurodegenerative diseases. Biochim Biophys Acta 1998, 1366(1-2):211-223.
5. Beal M.F. Mitochondria take center stage in aging and neurodegeneration. Ann Neurol 2005, 58:495-505.
6. Bensadoun A., Weinstein D. Assay of proteins in the presence of interfering material. Anal Biochem 1976, 70:241-250.
7. Brouillet E., Conde F., Beal M.F., Hantraye P. Replicating Huntington's disease phenotype in experimental animals. Prog Neurobiol 1999, 59:427-468.
8. Browne S.E., Bowling A.C., MacGarvey U., Baik M.J., Berger S.C., Muqit M.M., Bird E.D., Beal M.F. Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia. Ann Neurol 1997, 41(5):646-653.
9. Campbell G.R., Mahad D.J. Mitochondria as crucial players in demyelinated axons: lessons from neuropathology and experimental demyelination. Autoimmune Dis 2011, 8:262847.
10. Chang W.L. Introduction to basic principles of neurocytology and general concepts on neuropathology. Principles of neurotoxicology 1993, 88. Marcel Dekker, Inc., New York. L.W. Chang (Ed.).
11. Desagher S., Martinou J.C. Mitochondria as the central control point of apoptosis. Trends Cell Biol 2000, 10(9):369-377.
12. Dispersyn G., Nuydens R., Connors R., Borgers M., Geerts H. Bcl-2 protects against FCCP-induced apoptosis and mitochondrial membrane potential depolarization in PC12 cells. Biochim Biophys Acta 1999, 1428(2-3):357-371.
13. Facecchia K., Fochesato L.A., Ray S.D., Stohs S.J., Pandey S. Oxidative toxicity in neurodegenerative diseases: role of mitochondrial dysfunction and therapeutic strategies. J Toxicol 2011, 683728:14.
14. Fernandez-Marcos P.J., Auwerx J. Regulation of PGC-1α, a nodal regulator of mitochondrial biogenesis. Am J Clin Nutr 2011, 93(4):884S-890S.
15. Ghafourifar P., Schenk U., Klein S.D., Richter C. Mitochondrial nitric-oxide synthase stimulation causes cytochrome c release from isolated mitochondria. Evidence for intramitochondrial peroxynitrite formation. J Biol Chem 1999, 274:31185-31188.
16. Green D.R., Reed J.C. Mitochondria and apoptosis. Science 1998, 281(5381):1309-1312.
17. Guy W.J.M., Bernard M.C., Gareth J.G., Angela T., John A.H., Caroline D. Damage-induced Bax N-terminal change, translocation to mitochondria and formation of Bax dimers/complexes occur regardless of cell fate. EMBO J 2001, 20:6306-6315.
18. Hüttemann M., Pecina P., Rainbolt M., Sanderson T.H., Kagan V.E., Samavati L., Doan J.W., Lee I. The multiple functions of cytochrome c and their regulation in life and death decisions of the mammalian cell: from respiration to apoptosis. Mitochondrion 2011, 11(3):369-381.
19. Knott A.B., Bossy-Wetzel E. Nitric oxide in health and disease of the nervous system. Antioxid Redox Signal 2009, 11:541-554.
20. Knott A.B., Bossy-Wetzel E. Impact of nitric oxide on metabolism in health and age-related disease. Diabetes Obes Metab 2010, 12:126-133.
21. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970, 227:680-685.
22. Li P., Nijhawan D., Budihardjo I., Srinivasula S.M., Ahmad M., Alnemri E.S., Wang X. Cytochrome c and dATP-dependent formation of Apaf-1/caspase-9 complex initiates an apoptotic protease cascade. Cell 1997, 91(4):479-489.
23. Liu Y., Fiskum G., Schubert D. Generation of reactive oxygen species by the mitochondrial electron transport chain. J Neurochem 2002, 80(5):780-787.
24. Lowry O.H., Rosebrough N.J., Rarr A.L., Randall R.J. Protein measurement with the Folin-Phenol reagent. J Biol Chem 1951, 193:265-275.
25. Luna G., Heffes M.D., Mullick M.D. Métodos histotecnológicos, Instituto de Patología de las Fuerzas Armadas de los Estados Unidos de América (AFIP) 1995, McGraw-Hill, New York.
26. Mills G.C. Hemoglobin catabolism. I. Glutathione peroxidase, an erythrocyte enzyme which protects hemoglobin from oxidative breakdown. J Biol Chem 1957, 229(1):189-197.
27. Navarrete J., Flores-Herrera O., Uribe A., Martinez F. Differences in cholesterol incorporation into mitochondria from hepatoma AS-30D and human term placenta. Placenta 1999, 20:285-291.
28. Nisoli E., Carruba M.O. Nitric oxide and mitochondrial biogenesis. J Cell Sci 2006, 119:2855-2862.
29. Oberley L.W., Spitz D.R. Assay of superoxide dismutase activity in tumor tissue of reactive oxygen species. Biochemistry (Mosc) 1984, 70:200-214.
30. Okado-Matsumoto A., Fridovich I. Subcellular distribution of superoxide dismutases (SOD) in rat liver: Cu, Zn-SOD in mitochondria. J Biol Chem 2001, 276:38388-38393.
31. Panfili E., Sandri G., Ernest L. Distribution of glutathione peroxidase and glutathione reductase in rat brain mitochondrial. FEBS Lett 1991, 290:35-37.
32. Pereverzev M.O., Vygodina T.V., Konstantinov A.A., Skulachev V.P. Cytochrome c, an ideal antioxidant. Biochem Soc Trans 2003, 3:1312-1315.
33. Pereyra-Muñoz N., Rugerio-Vargas C., Angoa-Pérez M., Borgonio-Pérez G., Rivas-Arancibia S. Oxidative damage in substantia nigra and striatum of rats chronically exposed to ozone. J Chem Neuroanat 2006, 31(2):114-123.
34. Reddy P.H. Mitochondrial dysfunction in aging and Alzheimer's disease: strategies to protect neurons. Antioxidant Redox Signal 2007, 9(10):1647-1658.
35. Reed J.C., Doctor K.S., Godzik A. The domains of apoptosis: a genomics perspective. Sci STKE 2004, 9.
36. Reznick A.Z., Packer L. Oxidative damage to proteins: spectrophotometric method for carbonyl assay. Methods Enzymol 1994, 233:357-363.
37. Rivas-Arancibia S., Guevara-Guzmán R., López-Vidal Y., Rodríguez-Martínez E., Zanardo-Gomes M., Angoa-Pérez M., Raisman-Vozari R. Oxidative stress caused by ozone exposure induces loss of brain repair in the hippocampus of adult rats. Toxicol Sci 2010, 113(1):187-197.
38. Sasaki T., Shimizu T., Koyama T., Sakai M., Uchiyama S., Kawakami S., Noda Y., Shirasawa T., Kojima S. Superoxide dismutase deficiency enhances superoxide levels in brain tissues during oxygenation and hypoxia-reoxygenation. J Neurosci Res 2011, 89(4):601-610.
39. Scott D.M., Storey B.T., Lee C.P. L-3-glycerol phosphate oxidation with energy coupling in submitochondria particles from skeletal muscle mitochondria. Biochem Biophys Res Commun 1978, 83:641-648.
40. Susnow N., Zeng L., Margineantu D., Hockenbery D.M. Bcl-2 family proteins as regulators of oxidative stress. Semin Cancer Biol 2009, 19(1):42-49.
41. Szibor M., Holtz J. Mitochondrial ageing. Basic Res Cardiol 2003, 98(4):210-218.
42. Valko M., Leibfritz D., Moncol J., Cronin M.T., Mazur M., Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol 2007, 39(1):44-84.
43. Wang Z.B., Li M., Zhao Y., Xu J.X. Cytochrome c is a hydrogen peroxide scavenger in mitochondria. Protein Pept Lett 2003, 10:247-253.
44. Wei M.C., Zong W.X., Cheng E.H., Lindsten T., Panoutsakopoulou V., Ross A.J., Roth K.A., MacGregor G.R., Thompson C.B., Korsmeyer S.J. Proapoptotic BAX and BAK: a requisite gateway to mitochondrial dysfunction and death. Science 2001, 292(5517):727-730.
45. Yang L., Matthews R., Schulz B., Klockgether T., Liao A., Martinou J., Penney J., Hyman B., Beal F. 1-Methyl-4-86phenyl-1,2,3,6-tetrahydropyride neurotoxicity is attenuated in mice overexpressing Bcl-2. J Neurosci 1998, 18(29):8145-8152.