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Glutathione Peroxidase-Catalase Cooperativity Is Required for Resistance to Hydrogen Peroxide by Mature Rat Oligodendrocytes
Open accessAbstract
Oxidative mechanisms of injury are important in many neurological disorders, including hypoxic-ischemic brain damage. Cerebral palsy after preterm birth is hypothesized to be caused by hypoxic-ischemic injury of developing oligodendrocytes (OLs). Here we examined the developmental sensitivity of OLs to exogenous hydrogen peroxide (H2O2) with stage-specific rat oligodendrocyte cultures. We found that H2O2 itself or that generated by glucose oxidase was more toxic to developing than to mature OLs. Mature OLs were able to degrade H2O2 faster than developing OLs, suggesting that higher antioxidant enzyme activity might be the basis for their resistance. Catalase expression and activity were relatively constant during oligodendrocyte maturation, whereas glutathione peroxidase (GPx) was upregulated with a twofold to threefold increase in its expression and activity. Thus, it appeared that the developmental change in resistance to H2O2 was caused by modulation of GPx but not by catalase expression. To test the relative roles of catalase and GPx in the setting of oxidative stress, we measured enzyme activity in cells exposed to H2O2 and found that H2O2 induced a decrease in catalase activity in developing but not in mature OLs. Inhibition of GPx by mercaptosuccinate led to an increase in the vulnerability of mature OLs to H2O2 as well as a reduction in catalase activity. Finally, H2O2-dependent inactivation of catalase in developing OLs was prevented by the GPx mimic ebselen. These data provide evidence for a key role for GPx-catalase cooperativity in the resistance of mature OLs to H2O2-induced cell death.
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“In vitro studies show that oligodendrocytes are susceptible to oxidative stress due to their high metabolic activity and iron content combined with low antioxidant levels (Back et al., 1998; Baud et al., 2004; Fragoso et al., 2004).”
From Redox dysregulation, neuroinflammation, and NMDA receptor hypofunction: A “central hub” in schizophrenia pathophysiology? (2016) · cites this paper as Baud et al., 2004
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Cites
Free radicals in biology and medicine
Gutteridge, J. M. C. (1991) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(91)90478-o · Cited by 17,178
Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue.
McCarthy, K. D., & de Vellis, J. (1980) · The Journal of Cell Biology · doi:10.1083/jcb.85.3.890 · Cited by 3,845
Reactive Oxygen Species and the Central Nervous System
Halliwell, B. (1992) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1992.tb10990.x · Cited by 2,947
Wang, H., & Joseph, J. A. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00107-0 · Cited by 2,355
Self-citationYakes, F. M., & Van Houten, B. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.2.514 · Cited by 1,854
(1964) · The Medical Journal of Australia · doi:10.5694/j.1326-5377.1964.tb115841.x · Cited by 1,411
Neurobiology of Periventricular Leukomalacia in the Premature Infant
Volpe, J. J. (2001) · Pediatric Research · doi:10.1203/00006450-200111000-00003 · Cited by 945
Self-citationBack, S. A., Luo, N. L., Borenstein, N. S., Levine, J. M., Volpe, J. J., & Kinney, H. C. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-04-01302.2001 · Cited by 936
Self-citationSelective Vulnerability of Late Oligodendrocyte Progenitors to Hypoxia–Ischemia
Back, S. A., Han, B. H., Luo, N. L., Chricton, C. A., Xanthoudakis, S., Tam, J., Arvin, K. L., & Holtzman, D. M. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-02-00455.2002 · Cited by 795
Pigeolet, E., Corbisier, P., Houbion, A., Lambert, D., Michiels, C., Raes, M. J., Zachary, M.-D., & Remacle, J. (1990) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(90)90078-t · Cited by 747
Research works printed but not linked: 2
- 1984, Methods of enzymatic analysis, 3, 273
- 1996, Pediatr Res, 39, 204
Cited by
Sorted by citations
Ferriero, D. M. (2004) · New England Journal of Medicine · doi:10.1056/nejmra041996 · Cited by 1,148
Singh, N., Savanur, M. A., Srivastava, S., D’Silva, P., & Mugesh, G. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201708573 · Cited by 665
Tomlinson, D. R., & Gardiner, N. J. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2294 · Cited by 578
White matter injury in the preterm infant: pathology and mechanisms
Back, S. A. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1718-6 · Cited by 473
Shields, H. J., Traa, A., & Van Raamsdonk, J. M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.628157 · Cited by 478
Peroxide detoxification by brain cells
Dringen, R., Pawlowski, P. G., & Hirrlinger, J. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20280 · Cited by 455
The developing oligodendrocyte: key cellular target in brain injury in the premature infant
Volpe, J. J., Kinney, H. C., Jensen, F. E., & Rosenberg, P. A. (2011) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2011.02.012 · Cited by 394
Self-citationOxidative Stress in the Newborn – A 30-Year Perspective
Saugstad, O. D. (2005) · Neonatology · doi:10.1159/000087586 · Cited by 356
Maturation-Dependent Vulnerability of Perinatal White Matter in Premature Birth
Back, S. A., Riddle, A., & McClure, M. M. (2007) · Stroke · doi:10.1161/01.str.0000254729.27386.05 · Cited by 346
Arrested oligodendrocyte lineage maturation in chronic perinatal white matter injury
Segovia, K. N., McClure, M., Moravec, M., Luo, N. L., Wan, Y., Gong, X., Riddle, A., Craig, A., Struve, J., Sherman, L. S., et al. (2008) · Annals of Neurology · doi:10.1002/ana.21359 · Cited by 340
Back, S. A. (2006) · Mental Retardation and Developmental Disabilities Research Reviews · doi:10.1002/mrdd.20107 · Cited by 327
Radical changes in multiple sclerosis pathogenesis
van Horssen, J., Witte, M. E., Schreibelt, G., & de Vries, H. E. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2010.06.011 · Cited by 325
Inhibition of Cystine Uptake Disrupts the Growth of Primary Brain Tumors
Chung, W. J., Lyons, S. A., Nelson, G. M., Hamza, H., Gladson, C. L., Gillespie, G. Y., & Sontheimer, H. W. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.5258-04.2005 · Cited by 316
Free radicals, mitochondria, and hypoxia–ischemia in the developing brain
Blomgren, K., & Hagberg, H. (2005) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2005.08.040 · Cited by 310
Steullet, P., Cabungcal, J. H., Monin, A., Dwir, D., O'Donnell, P., Cuenod, M., & Do, K. Q. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2014.06.021 · Cited by 262
Oxidative stress disrupts oligodendrocyte maturation
French, H. M., Reid, M., Mamontov, P., Simmons, R. A., & Grinspan, J. B. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22139 · Cited by 246
Oxidative stress and its impact on neurons and glia in multiple sclerosis lesions
Lassmann, H., & van Horssen, J. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2015.09.018 · Cited by 245
Spaas, J., van Veggel, L., Schepers, M., Tiane, A., van Horssen, J., Wilson, D. M., Moya, P. R., Piccart, E., Hellings, N., Eijnde, B. O., et al. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03802-0 · Cited by 224
Pathophysiology of glia in perinatal white matter injury
Back, S. A., & Rosenberg, P. A. (2014) · Glia · doi:10.1002/glia.22658 · Cited by 202
Self-citationCirculating Oxidative Stress Biomarkers in Clinical Studies on Type 2 Diabetes and Its Complications
Bigagli, E., & Lodovici, M. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/5953685 · Cited by 208
Emerging concepts in periventricular white matter injury
Back, S. A., & Rivkees, S. A. (2004) · Seminars in Perinatology · doi:10.1053/j.semperi.2004.10.010 · Cited by 192
Hyperoxia Causes Maturation-Dependent Cell Death in the Developing White Matter
Gerstner, B., DeSilva, T. M., Genz, K., Armstrong, A., Brehmer, F., Neve, R. L., Felderhoff‐Mueser, U., Volpe, J. J., & Rosenberg, P. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3213-07.2008 · Cited by 179
Self-citationOxidative and Nitrative Injury in Periventricular Leukomalacia: A Review
Haynes, R. L., Baud, O., Li, J., Kinney, H. C., Volpe, J. J., & Folkerth, R. D. (2005) · Brain Pathology · doi:10.1111/j.1750-3639.2005.tb00525.x · Cited by 177
Self-citationDo, K. Q., Cuenod, M., & Hensch, T. K. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv065 · Cited by 158
Singh, N., Savanur, M. A., Srivastava, S., D’Silva, P., & Mugesh, G. (2017) · Angewandte Chemie · doi:10.1002/ange.201708573 · Cited by 153
Folkerth, R. D., Haynes, R. L., Borenstein, N. S., Belliveau, R. A., Trachtenberg, F. L., Rosenberg, P. A., Volpe, J. J., & Kinney, H. C. (2004) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/63.9.990 · Cited by 143
Self-citationButts, B. D., Houde, C., & Mehmet, H. (2008) · Cell Death and Differentiation · doi:10.1038/cdd.2008.70 · Cited by 132
Li, J., Ramenaden, E. R., Peng, J., Koito, H., Volpe, J. J., & Rosenberg, P. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3995-07.2008 · Cited by 130
Self-citationNeuropathologic Substrate of Cerebral Palsy
Folkerth, R. D. (2005) · Journal of Child Neurology · doi:10.1177/08830738050200120301 · Cited by 130
Cellular antioxidant enzyme activity and biomarkers for oxidative stress are affected by heat stress
Habashy, W. S., Milfort, M. C., Rekaya, R., & Aggrey, S. E. (2019) · International Journal of Biometeorology · doi:10.1007/s00484-019-01769-z · Cited by 126
Oxidative stress in surgery in an ageing population: Pathophysiology and therapy
Rosenfeldt, F., Wilson, M. D., Lee, G., Kure, C., Ou, R., Braun, L. A., & de Haan, J. B. (2012) · Experimental Gerontology · doi:10.1016/j.exger.2012.03.010 · Cited by 126
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Olivier, P., Fontaine, R. H., Loron, G., Van Steenwinckel, J., Biran, V., Massonneau, V., Kaindl, A., Dalous, J., Charriaut-Marlangue, C., Aigrot, M.-S., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007128 · Cited by 119
Self-citationOligodendrocyte Pathophysiology and Treatment Strategies in Cerebral Ischemia
Mifsud, G., Zammit, C., Muscat, R., Giovanni, G. D., & Valentino, M. (2014) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12263 · Cited by 123
Ketones prevent synaptic dysfunction induced by mitochondrial respiratory complex inhibitors
Kim, D. Y., Vallejo, J., & Rho, J. M. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06728.x · Cited by 113
Oxidative stress in head trauma in aging
Shao, C., Roberts, K. N., Markesbery, W. R., Scheff, S. W., & Lovell, M. A. (2006) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2006.03.007 · Cited by 111
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Folkerth, R. D. (2006) · Pediatric and Developmental Pathology · doi:10.2350/06-01-0024.1 · Cited by 109
Hyperoxia and the Immature Brain
Reich, B., Hoeber, D., Bendix, I., & Felderhoff‐Mueser, U. (2016) · Developmental Neuroscience · doi:10.1159/000454917 · Cited by 112
LaFemina, M. J., Sheldon, R. A., & Ferriero, D. M. (2006) · Pediatric Research · doi:10.1203/01.pdr.0000214891.35363.6a · Cited by 107
Comprehensive analysis of oxidative stress markers and antioxidants status in preeclampsia
Taravati, A., & Tohidi, F. (2018) · Taiwanese Journal of Obstetrics and Gynecology · doi:10.1016/j.tjog.2018.10.002 · Cited by 106
Back, S. A., Craig, A., Kayton, R. J., Luo, N. L., Meshul, C. K., Allcock, N., & Fern, R. F. (2006) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600344 · Cited by 105
Antioxidant therapy in multiple sclerosis
Mirshafiey, A., & Mohsenzadegan, M. (2008) · Immunopharmacology and Immunotoxicology · doi:10.1080/08923970802331943 · Cited by 105
Mechanism and Treatment Related to Oxidative Stress in Neonatal Hypoxic-Ischemic Encephalopathy
Qin, X., Cheng, J., Zhong, Y., Mahgoub, O. K., Akter, F., Fan, Y., Aldughaim, M. S., Xie, Q., Qin, L., Gu, L., et al. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00088 · Cited by 105
Prenatal Ischemia and White Matter Damage in Rats
Olivier, P., Baud, O., Evrard, P., Gressèns, P., & Verney, C. (2005) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/01.jnen.0000187052.81889.57 · Cited by 104
Self-citationZiabreva, I., Campbell, G. R., Rist, J. M., Zambonin, J. L., Rorbach, J., Wydro, M. M., Lassmann, H., Franklin, R. J. M., & Mahad, D. (2010) · Glia · doi:10.1002/glia.21052 · Cited by 102
Wang, H., Li, J., Follett, P. L., Zhang, Y., Cotanche, D. A., Jensen, F. E., Volpe, J. J., & Rosenberg, P. A. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03650.x · Cited by 97
Self-citationPolyphenols of virgin coconut oil prevent pro-oxidant mediated cell death
Illam, S. P., Narayanankutty, A., & Raghavamenon, A. C. (2017) · Toxicology Mechanisms and Methods · doi:10.1080/15376516.2017.1320458 · Cited by 107
Hypoxic-Ischemic Encephalopathy: Biochemical and Physiological Aspects
Volpe, J. J. (2008) · Elsevier eBooks · doi:10.1016/b978-1-4160-3995-2.10006-8 · Cited by 95
Self-citationBuser, J. R., Segovia, K. N., Dean, J. M., Nelson, K., Beardsley, D. J., Gong, X., Luo, N. L., Ren, J., Wan, Y., Riddle, A., et al. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2009.286 · Cited by 88
Naturally Occurring Antioxidant Therapy in Alzheimer’s Disease
Collins, A. E., Saleh, T. M., & Kalisch, B. E. (2022) · Antioxidants · doi:10.3390/antiox11020213 · Cited by 93
Fragoso, G., Martínez‐Bermúdez, A. K., Liu, H., Khorchid, A., Chemtob, S., Mushynski, W. E., & Almazan, G. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02488.x · Cited by 82
Liddell, J. R., Hoepken, H. H., Crack, P. J., Robinson, S. R., & Dringen, R. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.20957 · Cited by 82
Madhavan, L., Ourednik, V., & Ourednik, J. (2006) · Stem Cells · doi:10.1634/stemcells.2006-0018 · Cited by 80
Zhao, M., Wen, J., Wang, L., Wang, X., & Chen, T. (2019) · Cell Stress and Chaperones · doi:10.1007/s12192-019-00993-1 · Cited by 80
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Đokić, I., Hartmann, C. J., Herold‐Mende, C. C., & Régnier‐Vigouroux, A. (2012) · Glia · doi:10.1002/glia.22397 · Cited by 75
Kishido, T., Unno, K., Yoshida, H., Choba, D., Fukutomi, R., Asahina, S., Iguchi, K., Oku, N., & Hoshino, M. (2007) · Biogerontology · doi:10.1007/s10522-007-9085-7 · Cited by 75
Brain susceptibility to oxidative stress in the perinatal period
Perrone, S., Tataranno, M. L., Stazzoni, G., Ramenghi, L. A., & Buonocore, G. (2013) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.3109/14767058.2013.796170 · Cited by 74
Hohnholt, M. C., Geppert, M., & Dringen, R. (2011) · Acta Biomaterialia · doi:10.1016/j.actbio.2011.06.052 · Cited by 73
Effect of tumor necrosis factor-? on developing optic nerve oligodendrocytes in culture
Pang, Y., Cai, Z., & Rhodes, P. G. (2005) · Journal of Neuroscience Research · doi:10.1002/jnr.20450 · Cited by 73
Marrazzo, P., Paduano, F., Palmieri, F., Marrelli, M., & Tatullo, M. (2016) · Stem Cells International · doi:10.1155/2016/7230987 · Cited by 72
Zhang, Y., Chen, L., Sun, R., Lv, R., Du, T., Li, Y., Zhang, X., Sheng, R., & Qi, Y. (2022) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.1c01286 · Cited by 73
Maturation-dependent oligodendrocyte apoptosis caused by hyperoxia
Gerstner, B., Bührer, C., Rheinländer, C., Polley, O., Schüller, A., Berns, M., Obladen, M., & Felderhoff‐Mueser, U. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.20880 · Cited by 72
White matter injury and neurodevelopmental disabilities: A cross-disease (dis)connection
Cainelli, E., Arrigoni, F., & Vedovelli, L. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101845 · Cited by 74
Disorders of Endogenous and Exogenous Antioxidants in Neurological Diseases
Korczowska-Łącka, I., Słowikowski, B. K., Piekut, T., Hurła, M., Banaszek, N., Szymanowicz, O., Jagodziński, P. P., Kozubski, W. P., Permoda-Pachuta, A., & Dorszewska, J. (2023) · Antioxidants · doi:10.3390/antiox12101811 · Cited by 84
Helgesen, K. O., Romstad, H., Aaen, S. M., & Horsberg, T. E. (2015) · Aquaculture Reports · doi:10.1016/j.aqrep.2015.01.001 · Cited by 69
Regulation of Glutamate Transport in Developing Rat Oligodendrocytes
DeSilva, T. M., Kabakov, A. Y., Goldhoff, P., Volpe, J. J., & Rosenberg, P. A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6129-08.2009 · Cited by 71
Self-citationGlutamate Transport and Preterm Brain Injury
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Furumoto, H., Nanthirudjanar, T., Kume, T., Izumi, Y., Park, S., Kitamura, N., Kishino, S., Ogawa, J., Hirata, T., & Sugawara, T. (2016) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2016.02.012 · Cited by 68
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Carlson, N. G., & ROSE, J. W. (2006) · CNS Drugs · doi:10.2165/00023210-200620060-00001 · Cited by 66
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Schmidt, M., & Dringen, R. (2011) · Advances in neurobiology · doi:10.1007/978-1-4614-1788-0_36 · Cited by 66
Ribeiro, M., Maria, V. L., Scott-Fordsmand, J. J., & Amorim, M. J. B. (2015) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph120809589 · Cited by 65
PTU‐induced hypothyroidism modulates antioxidant defence status in the developing cerebellum
Bhanja, S., & Chainy, G. B. N. (2010) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2010.01.005 · Cited by 64
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Lee, B., Jung, J., & Kim, H. (2012) · Food and Chemical Toxicology · doi:10.1016/j.fct.2012.08.004 · Cited by 64
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Ruffini, F., Arbour, N., Blain, M., Olivier, A., & Antel, J. P. (2004) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63266-x · Cited by 61
Volpe, J. J., Kinney, H. C., Jensen, F. E., & Rosenberg, P. A. (2011) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2011.07.008 · Cited by 59
Self-citationOxidative Stress and Neurobiology of Demyelination
Ljubisavljević, S. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-9041-x · Cited by 60
Mitozo, P. A., de Souza, L. F., Loch-Neckel, G., Flesch, S., Maris, A. F., Figueiredo, C. P., Santos, A. R. S., Farina, M., & Dafré, A. L. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.03.017 · Cited by 58
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Xi, J., Zhu, C., Wang, Y., Zhang, Q., & Fan, L. (2019) · RSC Advances · doi:10.1039/c9ra01227c · Cited by 58
Shi, L., Xu, Y., Mao, C., Wang, Z., Guo, S., Jin, X., Yan, S., & Shi, B. (2020) · International Journal of Biometeorology · doi:10.1007/s00484-020-02000-0 · Cited by 56
Farhat, Z., Browne, R. W., Bonner, M. R., Tian, L., Deng, F., Swanson, M. K., & Mu, L. (2018) · Environment International · doi:10.1016/j.envint.2017.12.033 · Cited by 53
Nakamichi, N., Kambe, Y., Oikawa, H., Ogura, M., Takano, K., Tamaki, K., Inoue, M., Hinoi, E., & Yoneda, Y. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.02999.x · Cited by 52
Masuda, T., Hida, H., Kanda, Y., Aihara, N., Ohta, K., Yamada, K., & Nishino, H. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21089 · Cited by 51
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Huarte‐Bonnet, C., Juárez, M. P., & Pedríni, N. (2014) · Current Genetics · doi:10.1007/s00294-014-0452-z · Cited by 51
Abdallah, D. M., & Eid, N. I. (2004) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.20037 · Cited by 51
Carlström, K. E., Zhu, K., Ewing, E., Krabbendam, I. E., Harris, R. A., Falcão, A. M., Jagodic, M., Castelo‐Branco, G., & Piehl, F. (2020) · Nature Communications · doi:10.1038/s41467-020-17871-5 · Cited by 50
Kure, C., Rosenfeldt, F., Scholey, A. B., Pipingas, A., Kaye, D. M., Bergin, P. J., Croft, K. D., Wesnes, K. A., Myers, S. P., & Stough, C. K. K. (2016) · Journal of Cardiac Failure · doi:10.1016/j.cardfail.2016.03.006 · Cited by 48
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Vosloo, D., Rensburg, L. D. V., & Vosloo, A. (2013) · Aquaculture · doi:10.1016/j.aquaculture.2013.09.031 · Cited by 48
Zhao, H., Yi, X., Hu, Z., Hu, M., Chen, S., Rizwan‐ul‐Haq, M., Dong, X., & Gong, L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0059527 · Cited by 46
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Metadata
- Authors
- Baud, O., Greene, A. E., Li, J., Wang, H., Volpe, J. J., & Rosenberg, P. A.
- Affiliations
- Boston Children's Hospital (US)
- Corresponding author
- Rosenberg, Paul A.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2004-02-18
- Volume
- 24
- Issue
- 7
- Pages
- 1531-1540
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6730475
- OpenAlex
- W2024367623
- Cited by
- 292
- References
- 46
- Citations by year
- 2026: 4 · 2025: 17 · 2024: 7 · 2023: 12 · 2022: 10 · 2021: 14 · 2020: 14 · 2019: 13 · 2018: 16 · 2017: 17 · 2016: 13 · 2015: 12 · 2014: 15 · 2013: 14 · 2012: 12
- FWCI
- 5.70
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (NS38475, P01NS038475)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD18655, P30HD018655)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Neonatal and fetal brain pathology
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Keywords
- glutathione peroxidase, catalase, hydrogen peroxide, oligodendrocyte maturation, oxidative stress, antioxidant enzymes, catalase inactivation, ebselen, mercaptosuccinic acid, hypoxic-ischemic brain injury, cerebral palsy, oxidative cell death, developmental vulnerability
- MeSH terms
- Animals, Catalase, Cell Differentiation, Cells, Cultured, Drug Resistance, Glutathione Peroxidase, Hydrogen Peroxide, Oligodendroglia, Peroxides, Time Factors, Up-Regulation, Oxidants, Rats, Sprague-Dawley, Apoptosis, Oxidative Stress, In Situ Nick-End Labeling, Rats
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