Oxidative stress markers in surgically treated patients with refractory epilepsy

Clinical Biochemistry

Volumn 40, Issue 5-6, 2007, Pages 292-298

  López, Jeffrey ^a   González, María E ^a   Lorigados, Lourdes ^a   Morales, Lilia ^a   Riverón, Gretel ^b   Bauzá, José Y ^a  

^a CENTRO INTERNACIONAL DE RESTAURACIÓN NEUROLÓGICA CIREN   (Cuba)

^b National Center of Medical Genetics   (Cuba)

Author keywords

Advanced oxidation protein products; Antioxidant enzymes; Epilepsy surgery; Malondialdehyde; Oxidative stress; Temporal lobe epilepsy

Indexed keywords

CATALASE; GLUTATHIONE PEROXIDASE; SUPEROXIDE DISMUTASE;

ADULT; ARTICLE; CLINICAL ARTICLE; ENZYME ACTIVITY; EPILEPSY; FEMALE; HUMAN; MALE; OXIDATIVE STRESS; PREOPERATIVE EVALUATION; PRIORITY JOURNAL;

ADULT; ANTIOXIDANTS; BIOLOGICAL MARKERS; CATALASE; EPILEPSY; FEMALE; GLUTATHIONE PEROXIDASE; HUMANS; MALE; MALONDIALDEHYDE; OXIDATIVE STRESS; SUPEROXIDE DISMUTASE;

EID: 33847250334     PISSN: 00099120     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clinbiochem.2006.11.019     Document Type: Article

References (51)

1. Commission on Classification and Terminology of the International League Against Epilepsy. Proposal for revised clinical and electroencephalographic classification of epileptic seizures. Epilepsia 22 (1981) 489-501
2. Commission on Classification and Terminology of the International League Against Epilepsy. Proposal for classification of epilepsies and epileptic syndromes. Epilepsia 26 (1985) 268-278
3. Fisher R.S., Emde B.W., Blume W., Elger C., Genton P., and Lee P. Epileptic seizures and epilepsy: definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE). Epilepsia 46 (2005) 470-472
4. Yañez-Lermanda A. Cirugía de la epilepsia. Actualización y conceptos básicos. ¿Es factible en países en desarrollo?. Rev. Neur. Arg. 19 (1994) 21-28
5. Cascino G.D. Surgical treatment for epilepsy. Epilepsy Res. 60 (2004) 179-186
6. Sies H. Chapter 1: oxidative stress: introductory remarks. In: Sies H. (Ed). Oxidative stress (1985), Academic Press, London
7. Valentine J.S., Wertz D., Lyons T., Liou L., Goto J., and Butler E. The dark side of dioxygen biochemistry. Curr. Opin. Chem. Biol. 2 (1998) 253-262
8. Clarke D. Circulation and energy metabolism of the brain. In: Siegel G.J. (Ed). Basic neurochemistry: molecular, cellular and clinical aspects (1999), Lippincott-Raven Publishers, Philadelphia 639-669
9. Chaudiére J., and Ferrari-Iliou R. Intracellular Antioxidants: from Chemical to Biochemical Mechanisms. Food Chem. Toxicol. 37 (1999) 949-962
10. Matés J.M., Pérez C., and Núñez de Castro I. Antioxidant enzymes and human diseases. Clin. Biochem. 32 (1999) 595-603
11. Meldrum B.S. Glutamate as a neurotransmitter in the brain: review of physiology and pathology. J. Nutr. 130 (2000) S1007-S1015
12. Borlongan C, Kanning K, Poulos SG, Freeman B, Cahill W, Sanberg PR. Free radical damage and oxidative stress in Huntington's disease. J. Florida, M.A. 83 (1996) 335-341.
13. Singh R., and Pathak D.N. Lipid peroxidation and glutathione peroxidase, glutathione reductase, superoxide dismutase, catalase, and glucose-6-phosphate dehydrogenase activities in FeCl3-induced epileptogenic foci in the rat brain. Epilepsia 31 (1990) 15-26
14. Hurd R.W., Wilder B.J., and Perchalski B.J. Increased extracellular superoxide dismutase in Baltic myoclonus. Epilepsia 34 (1993) 14-15
15. Ben-Menachem E., Kyllerman M., and Marklund S. Superoxide dismutase and glutathione peroxidase function in progressive myoclonus epilepsies. Epilepsy Res. 40 (2000) 33-39
16. Kim H., Choi D., Jhoo W., Lee D., Koo C., and Kim C. Aspalactone, a new antiplatelet agent, attenuates the neurotoxicity induced by kainic acid in the rat. Life Sci. 61 (1997) 373-381
17. Ueda Y., Yokohama H., Niwa R., Konaka R., Ohya-Nishiguchi H., and Kamada H. Generation of lipid radicals in the hippocampus extracellular space during kainic acid-induced seizures in rats. Epilepsy Res. 26 (1997) 329-333
18. Tang L., Reiter R., Li Z., Ortiz G.G., Yu B.P., and Garcia J.J. Melatonin reduces the increase in 8-hydroxy-deoxyguanosine levels in the brain and liver of kainic acid-treated rats. Mol. Cell. Biochem. 178 (1998) 299-303
19. Gluck M.R., Jayatilleke E., Shaw S., Rowan A.J., and Haroutunian V. CNS oxidative stress associated with the kainic acid rodent model of experimental epilepsy. Epilepsy Res. 39 (2000) 63-71
20. Sudha K., Rao A.V., and Rao A. Oxidative stress and antioxidants in epilepsy. Clin. Chim. Acta 303 (2001) 19-24
21. Marklund S., and Marklund G. Involvement of the superoxide anion radical in the autoxidation of pryrogallol and a convenient assay for superoxide dismutase. J. Biochem. 47 (1974) 469-474
22. Aebi H.E. Catalase in vitro. Methods Enzymol. 105 (1984) 121-125
23. Flohé L., and Günzler W.A. Assays of glutathione peroxidase. Methods Enzymol. 105 (1984) 114-121
24. Beige J.A., and Aust S.D. Microsomal lipid peroxidation. Methods Enzymol. 52 (1978) 302-310
25. Witko-Sarsat V., Friedlander M., Capeillère-Blandin C., Nguyen-Khoa T., Nguyen A.T., and Zingraff J. Advanced oxidation protein products as a novel marker of oxidative stress in uremia. Kidney Int. 49 (1996) 1304-1313
26. Bai J., Rodríguez A.M., Melendez J.A., and Cederbaum A.I. Overexpression of catalase in cytosolic or mitochondrial compartment protects HepG2 cells against oxidative injury. J. Biol. Chem. 274 (1999) 26217-26224
27. Röhrdanz E., Schmuck G., Ohler S., and Kahl R. The influence of oxidative stress on catalase and MnSOD gene transcription in astrocytes. Brain Res. 900 (2001) 128-136
28. Bruce A.J., and Baudry M. Oxygen free radicals in rat limbic structures after kainate-induced seizures. Free Radic. Biol. Med. 18 (1995) 993-1002
29. Freitas R.M., Nascimento V.S., Vasconcelos S.M.M., Sousa F.C.F., Viana G.S.B., and Fonteles M.M.F. Catalase activity in cerebellum, hippocampus, frontal cortex and striatum after status epilepticus induced by pilocarpine in Wistar rats. Neurosci. Lett. 365 (2004) 102-105
30. Buschfort C., Müller M.R., Seeber S., Rajewsky M.F., and Thomale J. DNA excision repair profiles of normal and leukemic human lymphocytes: functional analysis at the single-cell level. Cancer Res. 57 (1997) 651-658
31. Ookawara T., Matsuura N., Oh-ishi T., Okazaki M., Kizaki T., Suzuki K., et al. Serum extracellular superoxide dismutase in pediatric patients with various diseases as judged by an ELISA. Res. Commun. Mol. Pathol. Pharmacol. 107 (2000) 291-296
32. Mori N., and Yokoyama H. Role of superoxide dismutase in a kindled model of epilepsy. Comp. Biochem. Physiol. 104 (1993) 373-376
33. Bellissimo M.I., Amado D., Abadía D.C.P., Ferreira E.C., Cavalheiro E.A., and Naffah-Mazzacoratti M.G. Superoxide dismutase, glutathione peroxidase activities the hydroperoxide concentration are modified hippocampus of epileptic rats. Epilepsy Res. 46 (2001) 121-128
34. Ilhan A., Aladag M.A., Kocer A., Boluk A., Gurel A., and Armutcu F. Erdosteine ameliorates PTZ-induced oxidative stress in mice seizure model. Brain Res. Bull. 65 (2005) 495-499
35. Erakovic V., Zupan G., Varljen J., Laginja J., and Smonic A. Lithium plus pilocarpine induced status epilepticus biochemical changes. Neurosci. Res. 36 (2000) 157-166
36. Beutler E., Curnutte J.T., and Forman L. Glutathione peroxidase deficiency and childhood seizures. Lancet 337 (1991) 1443-1444
37. Nikushkin E.V., Kryzhanovskii G.N., Tupeev I.R., Bordiukov M.M., and Iuzefova S.M. Blood antioxidative enzymes during epileptic activity Biull Eksp. Biol. Med. Mar. 103 (1987) 297-299
38. Lores Arnaiz S., Travacio M., Llesuy S., and Lores Arnaiz G. Regional vulnerability to oxidative stress in a model of experimental epilepsy. Neurochem. Res. 23 (1998) 1477-1483
39. Erakovic V., Upana G., Varljenb J., and Simonia A. Pentylenetetrazol-induced seizures and kindling: changes in free fatty acids, superoxide dismutase, and glutathione peroxidase activity. Neurochem. Int. 42 (2003) 173-178
40. Capeillére-Blandin C.H., Gausson V., Descamps-Latscha B., and Witko-Sarsat V. Biochemical and spectrophotometric significance of advanced oxidized protein products. Biochim. Biophys. Acta 1689 (2004) 91-102
41. Shacter E. Quantification and significance of protein oxidation in biological samples. Drug Metab. Rev. 32 (2000) 307-326
42. Morrell F., Smith M.C., and de ToledoMorrell L. Secondary epileptogenesis and kindling. In: Wyllie E. (Ed). The treatment of epilepsy. Principles and practice (1993), Lea and Febiger, Philadelphia 126-144
43. DeFelipe-Oroquieta J., Arellano J.I., Alonso L., and Muñoz A. Neuropatología de la epilepsia del lóbulo temporal. Alteraciones primarias y secundarias de los circuitos corticales y epileptogenicidad. Rev. Neurol. 34 (2002) 401-408
44. Kandel E., and Conrad G. Cap 46: Crisis epilépticas y epilepsia. In: Kandel E., Schwartz J., and Jessell T. (Eds). Neurociencia y Conducta (2000), McGraw Hill, New York 910-935
45. Uchida K., and Stadtman E.R. Quantitation of 4-hydroxynonenal protein adducts. Methods Enzymol. 233 (1994) 371-380
46. Volterra A., Trotti D., Tromba C., Floridi S., and Racagni G. Glutamate uptake inhibition by oxygen free radicals in rat cortical astrocytes. J. Neurosci. 14 (1994) 2924-2932
47. Trotti D., Volterra A., Lehre K.P., Rossi D., Gjesdal O., Racagni G., et al. Arachidonic acid inhibits a purified and reconstituid glutamate transporter directly from the water phase and not via the phospholipid membrane. J. Biol. Chem. 270 (1995) 9890-9895
48. Trotti D., Rossi D., Gjesdal O., Levy L.M., Racagni G., Danbolt N.C., et al. Peroxynitrite inhibits glutamate transporters subtypes. J. Biol. Chem. 27 (1996) 5976-5979
49. Patel M. Mitochondrial dysfunction and oxidative stress: Cause and consequence of epileptic seizures. Free Radic. Biol. Med. 37 (2004) 1951-1962
50. Cahng B.S., and Lowenstein D.H. Epilepsy. N. Engl. J. Med. 349 (2003) 1257-1266
51. Morimoto K., Fahnestock M., and Racine R.J. Kindling and status epilepticus models of epilepsy: rewiring the brain. Progr. Neurobiol. 73 (2004) 1-60