Calcium loading capacity and morphological changes in mitochondria in an ischemic preconditioned model

Neuroscience Letters

Volumn 448, Issue 3, 2008, Pages 268-272

  Iijima, Takehiko ^a   Tanaka, Kensuke ^a   Matsubara, Sachie ^a   Kawakami, Hayato ^a   Mishima, Tatsuya ^a   Suga, Kei ^a   Akagawa, Kimio ^a   Iwao, Yasuhide ^a  

^a KYORIN UNIVERSITY   (Japan)

Author keywords

Calcium; Membrane potential; Mitochondria; Permeability transition; Preconditioning

Indexed keywords

CALCIUM; GLUCOSE; GLUTAMIC ACID; OXYGEN;

ANIMAL CELL; ARTICLE; CALCIUM BLOOD LEVEL; CALCIUM TRANSPORT; CELL CULTURE; CELL ULTRASTRUCTURE; CONTROLLED STUDY; CYTOSOL; HIPPOCAMPUS; ISCHEMIA; ISCHEMIC PRECONDITIONING; MEMBRANE DAMAGE; MITOCHONDRIAL PERMEABILITY; NERVE CELL; NONHUMAN; PRIORITY JOURNAL; RAT;

ANIMALS; CALCIUM; CELLS, CULTURED; CYTOSOL; FLUORESCENT DYES; GLUTAMATES; HYPOXIA, BRAIN; ISCHEMIC PRECONDITIONING; MITOCHONDRIA; MITOCHONDRIAL MEMBRANES; MODELS, NEUROLOGICAL; PERMEABILITY; RATS; RATS, WISTAR;

EID: 56249140763     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2008.10.056     Document Type: Article

References (33)

1. Brustovetsky N., Brustovetsky T., Jemmerson R., and Dubinsky J.M. Calcium-induced cytochrome c release from CNS mitochondria is associated with the permeability transition and rupture of the outer membrane. J. Neurochem. 80 (2002) 207-218
2. Cortese J.D., Voglino A.L., and Hackenbrock C.R. Ionic strength of the intermembrane space of intact mitochondria as estimated with fluorescein-BSA delivered by low pH fusion. J. Cell. Biol. 113 (1991) 1331-1340
3. Crompton M., Virji S., Doyle V., Johnson N., and Ward J.M. The mitochondrial permeability transition pore. Biochem. Soc. Symp. 66 (1999) 167-179
4. Dave K.R., DeFazio R.A., Raval A.P., Torraco A., Saul I., Barrientos A., and Perez-Pinzon M.A. Ischemic preconditioning targets the respiration of synaptic mitochondria via protein kinase C epsilon. J. Neurosci. 28 (2008) 4172-4182
5. Dirnagl U., Simon R.P., and Hallenbeck J.M. Ischemic tolerance and endogenous neuroprotection. Trends Neurosci. 26 (2003) 248-254
6. Hackenbrock C.R. Ultrastructural bases for metabolically linked mechanical activity in mitochondria. I. Reversible untrastructural changes with change in metabolic steady state in isolated liver mitochondria. J. Cell. Biol. 30 (1966) 269-297
7. Hackenbrock C.R. Ultrastructural bases for metabolically linked mechanical activity in mitochondria. II. Electron transport-linked ultrastructural transformations in mitochondria. J. Cell. Biol. 37 (1968) 345-369
8. Hossmann K.A., Grosse Ophoff B., Schmidt-Kastner R., and Oschlies U. Mitochondrial calcium sequestration in cortical and hippocampal neurons after prolonged ischemia of the cat brain. Acta Neuropathol. 68 (1985) 230-238
9. Iijima T. Mitochondrial membrane potential and ischemic neuronal death. Neurosci. Res. 55 (2006) 234-243
10. Iijima T., Mishima T., Akagawa K., and Iwao Y. Mitochondrial hyperpolarization after transient oxygen-glucose deprivation and subsequent apoptosis in cultured rat hippocampal neurons. Brain Res. 993 (2003) 140-145
11. Iijima T., Mishima T., Tohyama M., Akagawa K., and Iwao Y. Mitochondrial membrane potential and intracellular ATP content after transient experimental ischemia in the cultured hippocampal neuron. Neurochem. Int. 43 (2003) 263-269
12. Kadenbach B. Intrinsic and extrinsic uncoupling of oxidative phosphorylation. Biochim. Biophys. Acta 1604 (2003) 77-94
13. Kadenbach B., Arnold S., Lee I., and Huttemann M. The possible role of cytochrome c oxidase in stress-induced apoptosis and degenerative diseases. Biochim. Biophys. Acta 1655 (2004) 400-408
14. 2+ is coupled with reactive oxygen species generation in cultured hippocampal neurons but not in astrocytes. J. Neurosci. Res. 79 (2005) 262-271
15. Kristian T., Pivovarova N.B., Fiskum G., and Andrews S.B. Calcium-induced precipitate formation in brain mitochondria: composition, calcium capacity, and retention. J. Neurochem. 102 (2007) 1346-1356
16. Kroemer G., Petit P., Zamzami N., Vayssiere J.L., and Mignotte B. The biochemistry of programmed cell death. Faseb J. 9 (1995) 1277-1287
17. Kushnareva Y.E., Wiley S.E., Ward M.W., Andreyev A.Y., and Murphy A.N. Excitotoxic injury to mitochondria isolated from cultured neurons. J. Biol. Chem. 280 (2005) 28894-28902
18. Lee I., Bender E., Arnold S., and Kadenbach B. New control of mitochondrial membrane potential and ROS formation-a hypothesis. Biol. Chem. 382 (2001) 1629-1636
19. Nicholls D.G., Johnson-Cadwell L., Vesce S., Jekabsons M., and Yadava N. Bioenergetics of mitochondria in cultured neurons and their role in glutamate excitotoxicity. J. Neurosci. Res. 85 (2007) 3206-3212
20. Nicholls D.G., and Ward M.W. Mitochondrial membrane potential and neuronal glutamate excitotoxicity: mortality and millivolts. Trends Neurosci. 23 (2000) 166-174
21. Nogueira V., Devin A., Walter L., Rigoulet M., Leverve X., and Fontaine E. Effects of decreasing mitochondrial volume on the regulation of the permeability transition pore. J. Bioenerg. Biomembr. 37 (2005) 25-33
22. 2+ dynamics in soma and neurites of individual adult mouse sympathetic neurons. J. Physiol. 580 (2007) 385-395
23. Pasdois P., Beauvoit B., Tariosse L., Vinassa B., Bonoron-Adele S., and Santos P.D. MitoK(ATP)-dependent changes in mitochondrial volume and in complex II activity during ischemic and pharmacological preconditioning of Langendorff-perfused rat heart. J. Bioenerg. Biomembr. 38 (2006) 101-112
24. Perry S.W., Norman J.P., Litzburg A., Zhang D., Dewhurst S., and Gelbard H.A. HIV-1 transactivator of transcription protein induces mitochondrial hyperpolarization and synaptic stress leading to apoptosis. J. Immunol. 174 (2005) 4333-4344
25. Pivovarova N.B., Hongpaisan J., Andrews S.B., and Friel D.D. Depolarization-induced mitochondrial Ca accumulation in sympathetic neurons: spatial and temporal characteristics. J. Neurosci. 19 (1999) 6372-6384
26. Pivovarova N.B., Nguyen H.V., Winters C.A., Brantner C.A., Smith C.L., and Andrews S.B. Excitotoxic calcium overload in a subpopulation of mitochondria triggers delayed death in hippocampal neurons. J. Neurosci. 24 (2004) 5611-5622
27. Reynolds I.J. Mitochondrial membrane potential and the permeability transition in excitotoxicity. Ann. N.Y. Acad. Sci. 893 (1999) 33-41
28. Riess M.L., Costa A.D., Carlson Jr. R., Garlid K.D., Heinen A., and Stowe D.F. Differential increase of mitochondrial matrix volume by sevoflurane in isolated cardiac mitochondria. Anesth. Analg. 106 (2008) 1049-1055 table of contents
29. Scalettar B.A., Abney J.R., and Hackenbrock C.R. Dynamics, structure, and function are coupled in the mitochondrial matrix. Proc. Natl. Acad. Sci. U.S.A. 88 (1991) 8057-8061
30. 2+ rise upon hypoxia/reoxygenation for functional breakdown and morphological disintegration. J. Biol. Chem. 278 (2003) 25454-25460
31. Tanaka K., Iijima T., Mishima T., Suga K., Akagawa K., and Iwao Y. Ca(2+) buffering capacity of mitochondria after oxygen-glucose deprivation in hippocampal neurons. Neurochem. Res. (2008)
32. Ward M.W., Huber H.J., Weisova P., Dussmann H., Nicholls D.G., and Prehn J.H. Mitochondrial and plasma membrane potential of cultured cerebellar neurons during glutamate-induced necrosis, apoptosis, and tolerance. J. Neurosci. 27 (2007) 8238-8249
33. Wigdal S.S., Kirkland R.A., Franklin J.L., and Haak-Frendscho M. Cytochrome c release precedes mitochondrial membrane potential loss in cerebellar granule neuron apoptosis: lack of mitochondrial swelling. J. Neurochem. 82 (2002) 1029-1038