Trolox protection of myelin membrane in hydrogen peroxide-treated mature oligodendrocytes

References

• Larkin EC, Rao GA. Importance of fetal and neonatal iron: Adequacy for normal development of central nervous system. Brain behavior and iron in the infant diet, J Dobbing, 1990; 43–63
   Google Scholar
• Richter-Landsberg C, Vollgraf U. Mode of cell injury and death after hydrogen peroxide exposure in cultured oligodendroglia cells. Exp Cell Res 1998; 244: 218–229
   PubMedGoogle Scholar
• Connor RJ, Menzies SL. Relationship of iron to oligodendrocytes and myelination. Glia 1996; 17: 83–93
   PubMed Web of Science ®Google Scholar
• Bhat NR. Signal transduction mechanisms in glial cells. Dev Neurosci 1995; 17: 267–284
   PubMedGoogle Scholar
• Fergusson B, Matyszak MK, Esivi MM. Axonal damage in acute multiple sclerosis lesions. Brain 1997; 120: 292–399
   Google Scholar
• Trapp BD, Peterson J, Ransohoff RM, et al. Axonal transection in the lesions of multiple sclerosis. N Engl J Med 1998; 338: 278–285
   PubMed Web of Science ®Google Scholar
• De Stefano N, Naroyoanan S, Matthews PM, et al. In vivo evidence for axonal dysfunction remote from focal cerebral demyelination of the type seen in multiple sclerosis. Brain 1999; 122: 1933–1939
   PubMed Web of Science ®Google Scholar
• Silber E, Sharief MK. Axonal degeneration in the pathogenesis of multiple sclerosis. J Neurol Sci 1999; 170: 11–18
   PubMed Web of Science ®Google Scholar
• Trapp BD, Ransohoff R, Rudick R. Axonal pathology in multiple sclerosis: Relationship to neurologic disability. Curr Opin Neurol 1999; 12: 295–302
   PubMed Web of Science ®Google Scholar
• Gilgun-Sherki Y, Melamed E, Offen D. The role of oxidative stress in the pathogenesis of multiple sclerosis: The need for effective antioxidant therapy. J Neurol 2004; 251: 261–268
   PubMed Web of Science ®Google Scholar
• LeVine SM. The role of reactive oxygen species in the pathogenesis of multiple sclerosis. Med Hypotheses 1992; 39: 271–274
   PubMed Web of Science ®Google Scholar
• Langemann H, Kabiersch A, Newcombe J. Measurement of low molecular-weight antioxidants, uric acid, tyrosine and tryptofan in plagues and white matter from patients with multiple sclerosis. Eur Neurol 1992; 32: 248–252
   PubMed Web of Science ®Google Scholar
• Butterfield DA, Castegna A, Drake J, Scapagnini G, Callabrese V. Vitamin E and neurodegenerative disorders associated with oxidative stress. Nutr Neurosci 2002; 5: 229–239
   PubMed Web of Science ®Google Scholar
• Craft S, Watson GS. Insulin and neurodegenerative disease: Shared and specific mechanisms. Lancet Neurol 2004; 3: 169–178
   PubMed Web of Science ®Google Scholar
• Duarte AI, Santos MS, Oliveira CR, Rego AC. Insulin neuroprotection against oxidative stress in cortical neurons—involvement of uric acid and gluthathione antioxidant defenses. Free Radic Biol Med 2005; 39: 876–889
   PubMed Web of Science ®Google Scholar
• Duarte AI, Proença T, Oliveira CR, Santos MS, Rego AC. Insulin restores metabolic function in cultured cortical neurons subjected to oxidative stress. Diabetes 2006; 55: 2863–2870
   PubMed Web of Science ®Google Scholar
• Masters BA, Werner H, Roberts CT, Jr, LeRoith D, Raizada MK. Insulin-like growth factor 1 (IGF-1) receptors and IGF-1 action in oligodendrocytes from rat brains. Regul Pept 1991; 33: 117–131
   PubMedGoogle Scholar
• Baumann N, Pham-Dinh D. Biology of oligodendrocyte and myelin in the mammalian central nervous system. Physiol Rev 2001; 81(2)871–927
   PubMed Web of Science ®Google Scholar
• McCarthy KD, de Vellis J. Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue. J Cell Biol 1980; 85: 890–902
   PubMed Web of Science ®Google Scholar
• Mosmann T. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J Immunol Methods 1983; 65(1–2)55–63
   PubMed Web of Science ®Google Scholar
• Rego AC, Santos MS, Oliveira CR. Influence of the antioxidants vitamin E and idebenone on retinal cell injury mediated by chemical ischemia, hypoglycemia, or oxidative stress. Free Radic Biol Med 1999; 26: 1405–1417
   PubMed Web of Science ®Google Scholar
• Nishiyama A, Chang A, Trapp BD. NG2+ glial cells: A novel glial cell population in the adult brain. J Neuropathol Exp Neurol 1999; 58: 1113–1124
   PubMed Web of Science ®Google Scholar
• Mronga T, Stahnke T, Goldbaum O, Richter-Landsberg C. Mitochondrial pathway is involved in hydrogen-peroxide-induced apoptotic cell death of oligodendrocytes. Glia 2004; 46: 446–455
   PubMedGoogle Scholar
• Liu Y, Pu Y, Zhang X. Role of mitochondrial signaling pathway in murine coronavirus-induced oligodendrocyte apoptosis. J Virol 2006; 80: 395–403
   PubMedGoogle Scholar
• Antonsson B, Montesuuit S, Lauper S, Eskes R, Martinou JC. Bax oligomerization is required for channel-forming activity in liposomes and to trigger cytochrome c release from mitochondria. Biochem J 2000; 345: 271–278
   PubMed Web of Science ®Google Scholar
• Nechusthan A, Smith CL, Lamensdorf I, Yoon SH, Youle RJ. Bax and Bak coalesce into novel mitochondria-associated clusters during apoptosis. J Cell Biol 2001; 153: 1265–1276
   PubMedGoogle Scholar
• Green DR. Apoptotic pathways: Ten minutes to dead. Cell 2005; 121: 671–674
   PubMed Web of Science ®Google Scholar
• Gutteridge JM, Halliwell B. Free radicals and antioxidants in the year 2000. A historical look to the future. Ann NY Acad Sci 2000; 899: 136–147
   PubMed Web of Science ®Google Scholar
• McCord JM. The evolution of free radicals and oxidative stress. Am J Med 2000; 108: 652–659
   PubMed Web of Science ®Google Scholar
• Thomas MJ. The role of free radicals and antioxidants. Nutrition 2000; 16: 716–718
   PubMed Web of Science ®Google Scholar
• Fragoso G, Martínez-Bermúdez AK, Liu H-N, Khorchid A, Chemtob S, Mushynski WE, Almazan G. Development differences in H2O2-induced oligodendrocyte cell death: A role of glutathione, mitogen-activated protein kinases and caspase 3. J Neurochem 2004; 90: 392–404
   PubMed Web of Science ®Google Scholar
• Juurlink BH, Thorburne SK, Hertz L. Peroxide-scavenging deficit underlies oligodendrocyte susceptibility to oxidative stress. Glia 1998; 22: 371–378
   PubMed Web of Science ®Google Scholar
• Shibata M, Hisahara S, Hara H, Yamawaki T, Fukuuchi Y, Yuan J, Okano H, Miura M. Caspases determine the vulnerability of oligodendrocytes in the ischemic brain. J Clin Invest 2000; 106: 643–653
   PubMedGoogle Scholar
• Baud O, Greene AE, Li J, Wang H, Volpe JJ, Rosenberg PA. Glutathione peroxidase-catalase cooperativity is required for resistance to hydrogen peroxide by mature rat oligodendrocytes. J Neurosci 2004; 24(7)1531–1540
   PubMed Web of Science ®Google Scholar
• Quintanilla RA, Munoz FJ, Metcalfe MJ, Hitschfeld M, Olivares G, Godoy JA, Inestrosa NC. Trolox and 17β-estradiol protect against amyloid β-peptide neurotoxicity by a mechanism that involves modulation of the wnt signalling pathway. J Biol Chem 2005; 280: 11615–11625
   PubMed Web of Science ®Google Scholar
• Alberdi E, Sanchez-Gomez MV, Torre I, Domercq M, Perez-Samartin A, Perez-Cerda F, Matute C. Activation of kainate receptors sensitizes oligodendrocytes to complement attack. J Neurosci 2006; 26: 3220–3228
   PubMedGoogle Scholar