Structural patterns of injured mitochondria in human oedematous cerebral cortex

References

• Koizumi, J. and SHIRAISHI, H.: Fine structural changes of mitochondria in cerebral edema and dehydration. Archives Histologicum Japonicum, 32: 241–249, 1970.
   PubMedGoogle Scholar
• BROWN, A. W. and BRIERLEY, J. B.: The earliest alteration in rat neurons and astrocytes after anoxia-ischemia. Acta Neuropathologica (Berlin), 23: 9–22, 1973.
   PubMedGoogle Scholar
• CLENDENON, N. R. and ALLEN, N.: Organelle, and membrane defects: lysosomes, mitochondria, and cell membrane. In: A. J. Popp, R. S. Bourke, L. R. Nelson et al. (editors), Seminars in Neurological Surgery (Raven Press), pp. 115–129, 1979.
   Google Scholar
• HOSSMANN, K. A., GROSSE OPHOFF, B., SCIMIDT-KASTNER, R. et al.: Mitochondrial calcium sequestration in cortical and hippocampal neurons after prolonged ischemia of the cat brain. Acta Neurophatologica (Berlin), 68: 230–238, 1985.
   Google Scholar
• NoviKov, V. E. and NAPERSTNIKO V. V.: The effect of fenibut on the ultrastructure of the brain mitochondria in traumatic edema and swelling. Eksperimental'naia Klinischekaia Farmkologiia, 57: 13–16, 1994.
   PubMedGoogle Scholar
• ROMANSKY, K. and STAMENOV, B.: Ultrastructural study of cerebral cortex and subcortical white matter following ligation of bridging veins in cats. Zentralblatl far Neurochirurgie, 56: 111–116, 1995.
   PubMedGoogle Scholar
• IKKENY, K., Doi, E., HAjos, F. et al.: Metabolic and electron microscopic studies post mortem in brain mitochondria. Advances in Experimental Medicine and Biology, 75: 159–164, 1976.
   PubMedGoogle Scholar
• GuriERKEz-DIAz, J. A., CUEVAS, P., REIMERS, D. et al.: Quantitative electron microscopic study of calcium accumulation in cerebral ischemia mitochondria. Surgical Neurology, 24: 67–72, 1985.
   Google Scholar
• DZHAFAROV, A. I., MAGOMEDOV, N. M., BABAEV, Kw F. et al.: Lipid peroxidation in the synap-tosomal and mitochondrial fraction of separate brain structures in hypoxia. Biulleten' Eksperimental'noi Biologii Meditsiny, 107: 305–307, 1989.
   PubMedGoogle Scholar
• WAGNER, K. R., KLEINHOLZ, M. and MYERS, R. E.: Delayed decreases in specific brain mito-chondrial electron transfer complex activities and cytochrome concentration following anoxia/ ischemia. Journal of Neurological Sciences, 100: 142–151, 1990.
   PubMed Web of Science ®Google Scholar
• MAYEVSKY, A. and Zw, I.: Oscillations of cortical oxidative metabolism and microcirculation in the ischaennic brain. Neurological Research, 13: 39–47, 1991.
   PubMedGoogle Scholar
• ROSENTHAL, M., MUMFORD, P. L., SICK, T. J. et al.: Mitochondrial hyperoxidaton after cerebral anoxia/ischemia. Epiphenomenon or precursor to residual damage? Advances in Experimental Medicine and Biology, 428: 189–195, 1997.
   PubMedGoogle Scholar
• NEWCOMB, R., PIERCE, A. R., KANO, T. et al.: Characterization of mitochondrial glutaminase and amino acids at prolonged times after experimental focal cerebral ischemia. Brain Research, 813: 103–111, 1998.
   PubMed Web of Science ®Google Scholar
• Du, G., MOUITHYS-MICHALAD, A. and SLUSE, F. E.: Generation of superoxide anion by mitochondria and impairment of their functions during anoxia and reoxygeneration in vitro. Free Radical Biology and Medicine, 25: 1066–1074, 1998.
   PubMed Web of Science ®Google Scholar
• ANDERSON, M. F. and Sims, N. R.: Mitochondrial respiratory function and cell death in focal cerebral ischemia. Journal of Neurochemistry, 73: 1189–1199, 1999.
   PubMed Web of Science ®Google Scholar
• PEREz/PINzoN, M. A., Zu, G. P. and BORN, J.: Cytochrome C is released from mitochondria into the cytosol after cerebral anoxia or ischemia. Journal of Cerebral Blood Flow and Metabolism, 19: 39–43, 1999.
   Google Scholar
• GNAIGER, E., KUZNETSOV, A. V., REIGER, G. et al.: Mitochondrial defects by intracellular calcium overload versus endothelial cold ischemia/reperfusion injury. Transplant International, Supplement 1: S555—S557, 2000.
   Google Scholar
• MARTIN, L. J., BRANMBRINK, A. M., PRICE, A. C. et al.: Neuronal death in newborn striatum after hypoxia-ischemia is necrosis and evolves with oxidative stress. Neurobiology of Diseases, 7: 169–191, 2000.
   PubMed Web of Science ®Google Scholar
• CHEN, H., Hu, C. J., HE, Y. Y. et al.: Reduction and restoration of mitochondrial dna content after focal cerebral ischemia/reperfusion. Stroke, 32: 2382–2387, 2001.
   PubMed Web of Science ®Google Scholar
• CHEN, D., MINAMI, M., HENSHALL, D. C. et al.: Upregulation of mitochondrial base-excision repair capability within rat brain after brief ischemia. Journal of Cerebral Blood Flow and Metabolism, 23: 88–98, 2003.
   PubMed Web of Science ®Google Scholar
• CASTEJON, O. J.: Electron microscopic study of capillary wall in human cerebral edema. Journal of Neuropathology and Experimental Neurology, 49: 296–328, 1980.
   Google Scholar
• CASTEJON, O. J.: Electron microscopic study of central axons degeneration in traumatic human brain edema. Journal of Submicroscopic Cytology, 17: 703–718, 1985.
   PubMedGoogle Scholar
• CASTEJON, O. J.: Ultraestructurg alterations of human cortical capillary basement membrane in perifocal brain edema. Journal of Submicroscopic Cytology and Pathology, 20: 519–536, 1988.
   PubMedGoogle Scholar
• CASTEJON, O. J.: Transmission electron microscope study of human hydrocephalic cerebral cortex. Journal of Submicroscopic Cytology and Pathology, 26: 29–39, 1994.
   PubMedGoogle Scholar
• CASTEJON, O. J., VALERO, C. and Duz, M.: Synaptic degenerative changes in human traumatic brain edema. An electron microscopic study of cerebral cortical biopsies. Journal of Neurosurgical Sciences, 39: 47–65, 1995.
   Google Scholar
• CASTEJON, O. J., VALERO, C. and DIAZ, M.: Light and electron microscope study of nerve cells in traumatic oedematous human cerebral cortex. Brain Injury, 5: 363–388, 1997.
   Google Scholar
• CASTEJON, O. J.: Ultrastructural pathology of Golgi apparatus of nerve cells in human brain edema associated to brain congenital malformations, tumours and trauma. Journal of Submicroscpic Cytology and Pathology, 31: 203–213, 1999.
   PubMedGoogle Scholar
• CASTEJON, O. J.: Astrocyte subtypes in the gray matter of injured human cerebral cortex: a transmission electon microscope study. Brain Injury, 4: 291–304.
   Google Scholar
• CASTEJON, O. J. and CASTEJON, H. V.: Oligodendroglial cell behaviour in traumatic oedematous cerebral cortex: a light and electron microscopic study. Brain Injury, 14: 303–317.
   Google Scholar
• SOLENSKI, J. J., DIPIERRo, C. G., TRIMMER, P. A. et al.: Ultrastructurg changes of neuronal mitochondria after transient and permanent cerebral ischemia. Stroke, 33: 816–824, 2002.
   PubMed Web of Science ®Google Scholar
• LEHNINGER, A. L.: Respiration and ATP formation in the mitochondria. In: Bioenergetics (WA. Benjaminc, Inc), pp. 73–98, 1971.
   Google Scholar
• MORLEY, P., TAUSICELA, J. S. and HAICIM, A. M.: Calcium overload. In: W. Walz (editor), Cerebral Ischemia. Molecular and Cellular Pathophysiology (Humana Press), pp. 69–104, 1999.
   Google Scholar
• DUBINSKY, J. M., BRUSTOVETSHKY, N., PINELIS, V. et al.: The mitochondrial permeability transi-tion: the brain's point of view. Biochemical Society Symposium, 66: 75–84, 1999.
   PubMedGoogle Scholar
• ANICARCRONA, M., DYPICBUKT, J. M., BONFOCO, E. et al.: Glutamate-induced neuronal death: a succession of necrosis or apoptosis depending on mitochondrial function. Neuron, 115: 961–973, 1995.
   Google Scholar
• LEMASTERS, J. J., NMMINEN, A. L., QIAN, T. et al.: The mitochondrial permeability transition in toxic, hypoxic and reperfusion injury. Molecular Cell Biochemistry, 174: 159–1165, 1997.
   PubMed Web of Science ®Google Scholar
• NicHous, D. G., Bunn, S. L., WARD, M. W. et al.: Excitotoxicity and mitochondria. Biochemical Society Symposium, 66: 55–67, 1999.
   PubMedGoogle Scholar
• KRISTIAN, T., WATHERBY, T. M., BATES, T. E. et al.: Heterogeneity of the calcium-induced permeability transition in isolated non-synaptic brain mitochondria. Journal of Neurochemistry, 83: 1297-1308.
   Google Scholar
• BROWN, G. C. and BORUTAITE, V.: Nitric oxide, cytochrome c and mitochondria. Biochemical Society Symposium, 66: 17–25, 1999.
   PubMedGoogle Scholar
• WULLNER, U., SEYFRIED, J., GROSCURTH, P. et al.: Glutathione depletion and neuronal cell death: the role of reactive oxigen intermediates and mitochondrial function. Brain Research, 826: 530–562, 1999.
   Google Scholar
• HILLEKED, L. and CHANG, P. H.: Brain mitochondrial swelling induced by arachidonic acid and other long chain free fatty acids. Journal of Neuroscience Research, 24: 247–250, 1989.
   PubMedGoogle Scholar
• KYICENS, J. A.: Isolated cerebral and cerebellar mitochondria produce free radicals when exposed to elevated Ca2± and Nat: implications for neurodegeneration. Journal of Neurochemistry, 63: 584–591, 1994.
   Google Scholar
• GINSBERG, M. D., WATSON, B. D. and BUSTOS, R.: Peroxidative damage to cell membrane following cerebral ischemia. A cause of ischemic brain injury. Neurochemistry and Pathology, 9: 171–193, 1988.
   Google Scholar
• NOVIKOF, V. E. and SHARov, A.: The effect of GABA-ergic agents on oxidative phosphorylation in the brain mitochondria in traumatic edema. Farmakologiia i Toksikologiia, 54: 44–46.
   Google Scholar
• MUIZELAAR, J. P. and DORE-DUFFY, P.: Advances in experimental research, and clinical interven-tion for catastrophic brain injury: the early twenty-first century. In: H. S. Levini, A. L. Benton and J. P. Muizelaar (editors), Catastrophic Brain Injury (Oxford University Press), pp. 233–251, 1996.
   Google Scholar
• HAYES, R. L.: Neurochemical changes in traumatic brain injuries. In: H. S. Levini, A. L. Benton and J. P. Muizelaar (editors), Catastrophic Brain Injury (Oxford University Press), pp. 183–207, 1996.
   Google Scholar
• BONDY, S. C.: Evaluation of free radical- initiated oxidants events within nervous system. In: R. Perez-Polo (editor), Paradigms of Nerve Injury (Academic Press), pp. 243–259, 1996.
   Google Scholar
• Mc CLuRE, M. J., PANCHALINGAM, K., KLUNK, W. E. et al.: Magnetic resonance spectroscopy of neural tissue. In: R. Perez-Polo (editor), Paradigms of Nerve Injury (Academic Press), pp. 178–202, 1996.
   Google Scholar