Acknowledgement
Supported by : Dongguk Research Fund
References
- Anderson CM, Swanson RA. (2000). Astrocyte glutamate transport: review of properties, regulation, and physiological functions. Glia 32: 1-14 https://doi.org/10.1002/1098-1136(200010)32:1<1::AID-GLIA10>3.0.CO;2-W
- Audinat E, Lambolez B, Rossier J, Crepel F. (1994). Activity-dependent regulation of N-methyl-D-aspartate receptor subunit expression in rat cerebellar granule cells. Eur J Neurosci 6: 1792-1800 https://doi.org/10.1111/j.1460-9568.1994.tb00572.x
- Beck T, Weber M, Horvath E, Wree A. (1996). Functional cerebral activity during regeneration from entorhinal lesions in the rat. J Cereb Blood Flow Metab 16: 342-352 https://doi.org/10.1097/00004647-199603000-00021
-
Ben-Ari Y. (1990). Modulation of ATP sensitive
$K^+$ channels: a novel strategy to reduce the deleterious effects of anoxia. Adv Exp Med Biol 268: 481-489 - Benveniste H, Drejer J, Schousboe A, Diemer NH. (1984). Elevation of the extracellular concentrations of glutamate and aspartate in rat hippocampus during transient cerebral ischemia monitored by intracerebral microdialysis. J Neurochem 43: 1369-1374 https://doi.org/10.1111/j.1471-4159.1984.tb05396.x
- Besancon E, Guo S, Lok J, Tymianski M, Lo EH. (2008). Beyond NMDA and AMPA glutamate receptors: emerging mechanisms for ionic imbalance and cell death in stroke. Trends Pharmacol Sci 29: 268-275 https://doi.org/10.1016/j.tips.2008.02.003
- Blaustein MP, Lederer WJ. (1999). Sodium/calcium exchange: its physiological implications. Physiol Rev 79: 763-854 https://doi.org/10.1152/physrev.1999.79.3.763
-
Boscia F, Gala R, Pignataro G, et al. (2006). Permanent focal brain ischemia induces isoform-dependent changes in the pattern of
$Na^+/Ca^{2+}$ exchanger gene expression in the ischemic core, periinfarct area, and intact brain regions. J Cereb Blood Flow Metab 26: 502-517 https://doi.org/10.1038/sj.jcbfm.9600207 -
Czyz A, Baranauskas G, Kiedrowski L. (2002). Instrumental role of
$Na^+ in NMDA excitotoxicity in glucose-deprived and depolarized cerebellar granule cells. J Neurochem 81: 379-389 https://doi.org/10.1046/j.1471-4159.2002.00851.x - D'Ambrosio R, Gordon DS, Winn HR. (2002). Differential role of KIR channel and Na(+)/K(+)-pump in the regulation of extracellular K(+) in rat hippocampus. J Neurophysiol 87: 87-102 https://doi.org/10.1152/jn.00240.2001
-
Fuller W, Parmar V, Eaton P, Bell JR, Shattock MJ. (2003). Cardiac ischemia causes inhibition of the
$Na^+/K^+$ ATPase by a labile cytosolic compound whose production is linked to oxidant stress. Cardiovasc Res 57: 1044-1051 https://doi.org/10.1016/S0008-6363(02)00810-6 - Gegelashvili G, Schousboe A. (1997). High affinity glutamate transporters: regulation of expression and activity. Mol Pharmacol 52: 6-15 https://doi.org/10.1124/mol.52.1.6
- Hansen AJ, Zeuthen T. (1981). Extracellular ion concentrations during spreading depression and ischemia in the rat brain cortex. Acta Physiol Scand 113: 437-445 https://doi.org/10.1111/j.1748-1716.1981.tb06920.x
- Hardingham GE, Fukunaga Y, Bading H. (2002). Extrasynaptic NMDARs oppose synaptic NMDARs by triggering CREB shut-off and cell death pathways. Nat Neurosci 5: 405-414 https://doi.org/10.1038/nn835
- Hasegawa Y, Fisher M, Latour LL, Dardzinski BJ, Sotak CH. (1994). MRI diffusion mapping of reversible and irreversible ischemic injury in focal brain ischemia. Neurology 44: 1484-1490 https://doi.org/10.1212/WNL.44.8.1484
- Ishii T, Moriyoshi K, Sugihara H, et al. (1993). Molecular characterization of the family of the N-methyl-D-aspartate receptor subunits. J Biol Chem 268: 2836-2843
- Kasischke KA, Vishwasrao HD, Fisher PJ, Zipfel WR, Webb WW. (2004). Neural activity triggers neuronal oxidative metabolism followed by astrocytic glycolysis. Science 305: 99-103 https://doi.org/10.1126/science.1096485
- Kiedrowski L. (1999). N-methyl-D-aspartate excitotoxicity: relationships among plasma membrane potential, Na(+)/Ca(2+) exchange, mitochondrial Ca(2+) overload, and cytoplasmic concentrations of Ca(2+), H(+), and K(+). Mol Pharmacol 56: 619-632 https://doi.org/10.1124/mol.56.3.619
- Kiedrowski L. (2001). Repolarization of the plasma membrane shapes NMDA-induced cytosolic [Ca2+] transients. Neuroreport 12: 3579-3582 https://doi.org/10.1097/00001756-200111160-00041
- Kolker S, Okun JG, Ahlemeyer B, et al. (2002). Chronic treatment with glutaric acid induces partial tolerance to excitotoxicity in neuronal cultures from chick embryo telencephalons. J Neurosci Res 68: 424-431 https://doi.org/10.1002/jnr.10189
-
Lees GJ, Leong W. (1996). Interactions between excitotoxins and the
$Na^+/K^+$ -ATPase inhibitor ouabain in causing neuronal lesions in the rat hippocampus. Brain Res 714: 145-155 https://doi.org/10.1016/0006-8993(95)01518-3 - Lipton SA, Rosenberg PA. (1994). Excitatory amino acids as a final common pathway for neurologic disorders. N Engl J Med 330: 613-622 https://doi.org/10.1056/NEJM199403033300907
-
MacDonald JF, Xiong ZG, Jackson MF. (2006). Paradox of
$Ca^{2+}$ signaling, cell death and stroke. Trends Neurosci 29: 75-81 https://doi.org/10.1016/j.tins.2005.12.001 - Madl JE, Burgesser K. (1993). Adenosine triphosphate depletion reverses sodium-dependent, neuronal uptake of glutamate in rat hippocampal slices. J Neurosci 13: 4429-4444
- Martin RL, Lloyd HG, Cowan AI. (1994). The early events of oxygen and glucose deprivation: setting the scene for neuronal death? Trends Neurosci 17: 251-257 https://doi.org/10.1016/0166-2236(94)90008-6
-
Matsuda T, Arakawa N, Takuma K, et al. (2001). SEA0400, a novel and selective inhibitor of the
$Na^+-Ca^{2+}$ exchanger, attenuates reperfusion injury in the in vitro and in vivo cerebral ischemic models. J Pharmacol Exp Ther 298: 249-256 - Meguro H, Mori H, Araki K, et al. (1992). Functional characterization of a heteromeric NMDA receptor channel expressed from cloned cDNAs. Nature 357: 70-74 https://doi.org/10.1038/357070a0
- Monyer H, Sprengel R, Schoepfer R, et al. (1992). Heteromeric NMDA receptors: molecular and functional distinction of subtypes. Science 256: 1217-1221. https://doi.org/10.1126/science.256.5060.1217
- Mori H, Mishina M. (1995). Structure and function of the NMDA receptor channel. Neuropharmacology 34: 1219-1237 https://doi.org/10.1016/0028-3908(95)00109-J
-
Perkel DJ, Petrozzino JJ, Nicoll RA, Connor JA. (1993). The role of
$Ca^{2+} entry via synaptically activated NMDA receptors in the induction of long-term potentiation. Neuron 11: 817-823 https://doi.org/10.1016/0896-6273(93)90111-4 -
Pignataro G, Tortiglione A, Scorziello A, et al. (2004). Evidence for a protective role played by the
$Na^+/Ca^{2+}$ exchanger in cerebral ischemia induced by middle cerebral artery occlusion in male rats. Neuropharmacology 46: 439-448 https://doi.org/10.1016/j.neuropharm.2003.09.015 -
Quednau BD, Nicoll DA, Philipson KD. (1997). Tissue specificity and alternative splicing of the
$Na^+/Ca^{2+}$ exchanger isoforms NCX1, NCX2, and NCX3 in rat. Am J Physiol 272: C1250-1261 https://doi.org/10.1152/ajpcell.1997.272.4.C1250 - Resink A, Villa M, Benke D, Hidaka H, Mohler H, Balazs R. (1996). Characterization of agonist-induced down-regulation of NMDA receptors in cerebellar granule cell cultures. J Neurochem 66: 369-377
- Rumbaugh G, Vicini S. (1999). Distinct synaptic and extrasynaptic NMDA receptors in developing cerebellar granule neurons. J Neurosci 19: 10603-10610.
-
Schroder UH, Breder J, Sabelhaus CF, Reymann KG. (1999). The novel
$Na^+/Ca^{2+}$ exchange inhibitor KB-R7943 protects CA1 neurons in rat hippocampal slices against hypoxic/hypoglycemic injury. Neuropharmacology 38: 319-321 https://doi.org/10.1016/S0028-3908(98)00198-1 - Silver IA, Deas J, Erecinska M. (1997). Ion homeostasis in brain cells: differences in intracellular ion responses to energy limitation between cultured neurons and glial cells. Neuroscience 78: 589-601 https://doi.org/10.1016/S0306-4522(96)00600-8
- Storck T, Schulte S, Hofmann K, Stoffel W. (1992). Structure, expression, and functional analysis of a Na(+)-dependent glutamate/aspartate transporter from rat brain. Proc Natl Acad Sci U S A 89: 10955-10959 https://doi.org/10.1073/pnas.89.22.10955
-
Stys PK, Waxman SG, Ransom BR. (1992). Ionic mechanisms of anoxic injury in mammalian CNS white matter: role of
$Na^+$ channels and$Na^+-Ca^{2+}$ exchanger. J Neurosci 12: 430-439 - Tasker RC, Coyle JT, Vornov JJ. (1992). The regional vulnerability to hypoglycemia-induced neurotoxicity in organotypic hippocampal culture: protection by early tetrodotoxin or delayed MK-801. J Neurosci 12: 4298-4308
-
Veldhuis WB, van der Stelt M, Delmas F, et al. (2003). In vivo excitotoxicity induced by ouabain, a
$Na^+/K^+$ -ATPase inhibitor. J Cereb Blood Flow Metab 23: 62-74 https://doi.org/10.1097/01.WCB.0000039287.37737.50 - Witte OW, Bidmon HJ, Schiene K, Redecker C, Hagemann G. (2000). Functional differentiation of multiple perilesional zones after focal cerebral ischemia. J Cereb Blood Flow Metab 20: 1149-1165 https://doi.org/10.1097/00004647-200008000-00001
- Yu AC, Gregory GA, Chan PH. (1989). Hypoxia-induced dysfunctions and injury of astrocytes in primary cell cultures. J Cereb Blood Flow Metab 9: 20-28. https://doi.org/10.1038/jcbfm.1989.3
Cited by
- Oligodendrocyte N-Methyl-d-aspartate Receptor Signaling: Insights into Its Functions vol.47, pp.2, 2010, https://doi.org/10.1007/s12035-013-8408-8
- Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study vol.2, pp.1, 2010, https://doi.org/10.1186/2193-1801-2-46
- Naringin ameliorates sodium arsenite-induced renal and hepatic toxicity in rats: decisive role of KIM-1, Caspase-3, TGF-β, and TNF-α vol.37, pp.8, 2015, https://doi.org/10.3109/0886022x.2015.1074462
- Cofilin as a Promising Therapeutic Target for Ischemic and Hemorrhagic Stroke vol.7, pp.1, 2010, https://doi.org/10.1007/s12975-015-0438-2
- Affinity of Tau antibodies for solubilized pathological Tau species but not their immunogen or insoluble Tau aggregates predicts in vivo and ex vivo efficacy vol.11, pp.None, 2010, https://doi.org/10.1186/s13024-016-0126-z
- The Functional and Molecular Properties, Physiological Functions, and Pathophysiological Roles of GluN2A in the Central Nervous System vol.54, pp.2, 2010, https://doi.org/10.1007/s12035-016-9715-7
- Cofilin: Molecular and Cellular Functions and Its Role in the Functioning of the Nervous System vol.13, pp.1, 2019, https://doi.org/10.1134/s1819712419010124
- Dynamics of Internalization and Intracellular Interaction of Tau Antibodies and Human Pathological Tau Protein in a Human Neuron-Like Model vol.11, pp.None, 2010, https://doi.org/10.3389/fneur.2020.602292