Abstract
The brain has the highest metabolic rate of all organs and depends predominantly on oxidative metabolism as a source of energy. Thus, it utilizes about 20% of respired oxygen for normal function, even though it represents only 5% of the body weight. Much of oxygen taken up by neurons is utilized for producing ATP, which is needed not only for maintaining the appropriate ionic gradients across the neural membranes but also creating the proper cellular redox potentials. Full and transient deficits in glucose and oxygen can rapidly compromise ATP production and threaten cellular integrity by either not maintaining or abnormally modulating ion homeostasis and cellular redox. The initial response to a transient insufficiency of energy is depolarization resulting in Na+ influx into axons.
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References
Abe K, Aoki M, Kawagoe J, Yoshida T, Hattori A, Kogure K, Itoyama Y (1995) Ischemic delayed neuronal death: a mitochondrial hypothesis. Stroke 26:1478–1489
Acarin L, Paris J, González B, Castellano B (2002) Glial expression of small heat shock proteins following an excitotoxic lesion in the immature rat brain. Glia 38:1–14
Akin Sp, Liu PK, Hsu CY (1996) Immediate early gene expression in response to cerebral ischemia: friend or foe? Stroke 27:1682–1687
Al-Bahrani A, Taha S, Shaath H, Bakhiet M (2007) TNF-alpha and IL-8 in acute stroke and the modulation of these cytokines by antiplatelet agents. Curr Neurovasc Res 4:31–37
Almeida A, Heales SJ, Bolanos JP, Medina JM (1998) Glutamate neurotoxicity is associated with nitric oxide-mediated mitochondrial dysfunction and glutathione depletion. Brain Res 790:209–216
An G, Lin TN, Liu JS, Xue JJ, He YY, Hsu CY (1993) Expression of c-fos and c-jun family genes after focal cerebral ischemia. Ann Neurol 33:457–464
An JJ, Lee YP, Kim SY, Lee SH, Lee MJ, Jeong MS, Kim DW, Jang SH, Yoo KY, Won MH, Kang TC, Kwon OS, Cho SW, Lee KS, Park J, Eum WS, Choi SY (2008) Transduced human PEP-1-heat shock protein 27 efficiently protects against brain ischemic insult. FEBS J 275:1296–1308
Annunziato L, Pignataro G, Di Renzo GF (2004) Pharmacology of brain Na+/Ca2+ exchanger: from molecular biology to therapeutic perspectives. Pharmacol Rev 56:633–654
Anrather J, Racchumi G, Iadecola C (2006) NF-kappaB regulates phagocytic NADPH oxidase by inducing the expression of gp91phox. J Biol Chem 281:5657–5667
Atlante A, Calissano P, Bobba A, Azzariti A, Marra E, Passarella S (2000) Cytochrome c is released from mitochondria in a reactive oxygen species (ROS)-dependent fashion and can operate as a ROS scavenger and as a respiratory substrate in cerebellar neurons undergoing excitotoxic death. J Biol Chem 275:37159–37166
Auger C, Attwell D (2000) Fast removal of synaptic glutamate by postsynaptic transporters. Neuron 28:547–558
Baltan S (2006) Surviving anoxia: a tale of two white matter tracts. Crit Rev Neurobiol 18:95–103
Baltan S (2009) Ischemic injury to white matter: an age-dependent process. Neuroscientist 15:126–133
Beckman KB, Ames BN (1997) Oxidative decay of DNA. J Biol Chem 272:19633–19636
Benavides A, Pastor D, Santos P, Traque P, Calvo S (2005) CHOP plays a pivotal role in the astrocyte death induced by oxygen and glucose deprivation. Glia 52:261–275
Bergeron M, Gidday JM, Yu AY, Semenza GL, Ferriero DM, Sharp FR (2000) Role of hypoxia-inducible factor-1 in hypoxia-induced ischemic tolerance in neonatal rat brain. Ann Neurol 48:285–296
Blaustein MP, Lederer WJ (1999) Sodium/calcium exchange: its physiological implications. Physiol Rev 79:763–854
Block ML, Hong JS (2005) Microglia and inflammation-mediated neurodegeneration: multiple triggers with a common mechanism. Prog Neurobiol 76:77–98
Bojarski C, Meloni BP, Moore SR, Majda BT, Knuckey NW (2008) Na+/Ca2+ exchanger subtype (NCX1, NCX2, NCX3) protein expression in the rat hippocampus following 3 min and 8 min durations of global cerebral ischemia. Brain Res 1189:198–202
Bolanos JP, Almeida A, Stewart V, Peuchen S, Land JM, Clark JB, Heales SJ (1997) Nitric oxide-mediated mitochondrial damage in the brain: mechanisms and implications for neurodegenerative diseases. J Neurochem 68:2227–2240
Brea D, Sobrino T, Ramos-Cabrer P, Castillo J (2009) Inflammatory and neuroimmunomodulatory changes in acute cerebral ischemia. Cerebrovasc Dis 27(Suppl 1):48–64
Büttner F, Cordes C, Gerlach F, Heimann A, Alessandri B, Luxemburger U, Türeci O, Hankeln T, Kempski O, Burmester T (2009) Genomic response of the rat brain to global ischemia and reperfusion. Brain Res 1252:1–14
Camandola S, Poli G, Mattson MP (2000) The lipid peroxidation product 4-hydroxy-2,3-nonenal increases AP-1-binding activity through caspase activation in neurons. J Neurochem 74:159–168
Cande C, Cohen I, Daugas E, Ravagnan L, Larochette N, Zamzami N, Kroemer G (2002) Apoptosis-inducing factor (AIF): a novel caspase-independent death effector released from mitochondria. Biochimie 84:215–222
Cao G, Pei W, Lan J, Stetler RA, Luo Y, Nagayama T, Graham SH, Yin XM, Simon RP, Chen J (2001) Caspase-activated DNase/DNA fragmentation factor 40 mediates apoptotic DNA fragmentation in transient cerebral ischemia and in neuronal cultures. J Neurosci 21:4678–4690
Carlezon WA Jr., Duman RS, Nestler EJ (2005) The many faces of CREB. Trends Neurosci 28:436–445
Chabot C, Gagné J, Giguère C, Bernard J, Baudry M, Massicotte G (1998) Bidirectional modulation of AMPA receptor properties by exogenous phospholipase A2 in the hippocampus. Hippocampus 8:299–309
Chaitanya GV, Babu PP (2008) Multiple apoptogenic proteins are involved in the nuclear translocation of Apoptosis Inducing Factor during transient focal cerebral ischemia in rat. Brain Res 1246:178–190
Chen J, Jin K, Chen M, Pei W, Kawaguchi K, Greenberg DA, Simon RP (1997) Early detection of DNA strand breaks in the brain after transient focal ischemia: implications for the role of DNA damage in apoptosis and neuronal cell death. J Neurochem 69:232–245
Choi DW (1988) Glutamate neurotoxicity and diseases of the nervous system. Neuron 1:628–634
Clark JD, Schievella AR, Nalefski EA, Lin L-L (1995) Cytosolic phospholipase A2. J Lipid Mediat Cell Signal 12:83–117
Clemens JA, Stephenson DT, Smalstig EB, Roberts EF, Johnstone EM, Sharp JD, Little SP, Kramer RM (1996) Reactive glia express cytosolic phospholipase A2 after transient global forebrain ischemia in the rat. Stroke 27:527–535
Cui J, Holmes EH, Liu PK (1999) Oxidative damage to the c-fos gene and reduction of its transcription after focal cerebral ischemia. J Neurochem 73:1164–1174
Cui J, Holmes EH, Greene TG, Liu PK (2000) Oxidative DNA damage precedes DNA fragmentation after experimental stroke in rat brain. FASEB J 14:955–967
Dawson VL, Dawson TM (2004) Deadly conversations: nuclear-mitochondrial cross-talk. J Bioenerg Biomembr 36:287–294
DeCoster MA, Mukherjee PK, Davis RJ, Bazan NG (1998) Platelet-activating factor is a downstream messenger of kainate-induced activation of mitogen-activated protein kinases in primary hippocampal neurons. J Neurosci Res 53:297–303
DeGracia DJ, Kumar R, Owen CR, Krause GS, White BC (2002) Molecular pathways of protein synthesis inhibition during brain reperfusion: implications for neuronal survival or death. J Cereb Blood Flow Metab 22:127–141
DeGracia DJ, Montee HL (2004) Cerebral ischemia and the unfolded protein response. J Neurochem 91:1–8
DeGracia DJ (2004) Acute and persistent protein synthesis inhibition following cerebral reperfusion. J Neurosci Res 77:771–776
Demple B, Sung JS (2005) Molecular and biological roles of Ape1 protein in mammalian base excision repair. DNA Repair (Amst) 4:1442–1449
Dienel GA (1984) Regional accumulation of calcium in postischemic rat brain. J Neurochem 43:913–925
Edgar AD, Strosznajder J, Horrocks LA (1982) Activation of ethanolamine phospholipase A2 in brain during ischemia. J Neurochem 39:1111–1116
Enari M, Sakahira H, Yokoyama H, Okawa K, Iwamatsu A, Nagata S (1998) A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD. Nature (London) 391:43–50
Epe B, Ballmaier D, Roussyn I, Briviba K, Sies H (1996) DNA damage by peroxynitrite characterized with DNA repair enzymes. Nucleic Acids Res 24:4105–4110
Farooqui AA, Horrocks LA (1994) Excitotoxicity and neurological disorders: involvement of membrane phospholipids. Int Rev Neurobiol 36:267–323
Farooqui AA, Horrocks LA (2007) Glycerophospholipids in brain. Springer, New York, NY
Farooqui AA, Horrocks LA (2006) Phospholipase A2-generated lipid mediators in the brain: the good, the bad, and the ugly. Neuroscientist 12:245–260
Farooqui AA, Horrocks LA (2009) Glutamate and cytokine-mediated alterations of phospholipids in head injury and spinal cord trauma. In: Banik N, Ray SK (eds) Brain and spinal cord trauma, Handbook of neurochemistry Lajtha, A. Springer, New York, NY, pp 71–89
Farooqui AA (2009) Hot topics in neural membrane lipidology. Springer, New York, NY
Farooqui AA, Horrocks LA, Farooqui T (2007) Modulation of inflammation in brain: a matter of fat. J Neurochem 101:577–599
Farooqui AA, Ong WY, Horrocks LA (2008) Neurochemical aspects of excitotoxicity. Springer, New York, NY
Feigin VL, Lawes CM, Bennett DA, Anderson CS (2003) Stroke epidemiology: a review of population-based studies of incidence, prevalence, and case-fatality in the late 20th century. Lancet Neurol 2:43–53
Formisano L, Saggese M, Secondo A, Sirabella R, Vito P, Valsecchi V, Molinaro P, Di Renzo G, Annunziato L (2008) The two isoforms of the Na+/Ca2+ exchanger, NCX1 and NCX3, constitute novel additional targets for the prosurvival action of Akt/protein kinase B pathway. Mol Pharmacol 73(3):727–737 13 Dec 2007 [Epub ahead of print]
Fradejas N, Pastor MD, Mora-Lee S, Tranque P, Calvo S (2008) SEPS1 gene is activated during astrocyte ischemia and shows prominent antiapoptotic effects. J Mol Neurosci 35:259–265
Frangogiannis NG (2007) Chemokines in ischemia and reperfusion. Thromb Haemost 97:738–747
Gavrieli Y, Sherman Y, Ben-Sasson SA (1992) Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J Cell Biol 119:493–501
Giffard RG, Yenari MA (2004) Many mechanisms for Hsp70 protection from cerebral ischemia. J Neurosurg Anesthesiol 16:53–61
Greenberg DA, Jin K, Khan AA (2008) Neuroglobin: an endogenous neuroprotectant. Curr Opin Pharmacol 8:20–24
Hamrick SE, McQuillen PS, Jiang X, Mu D, Madan A, Ferriero DM (2005) A role for hypoxia-inducible factor-1alpha in desferoxamine neuroprotection. Neurosci Lett 379:96–100
Hanawalt PC (1994) Transcription-coupled repair and human disease. Science 266:1957–1958
Hayashi T, Abe K (2004) Ischemic neuronal cell death and organelle damage. Neurol Res 26:827–834
Haze K, Yoshida H, Yanagi H, Yura T, Mori K (1999) Mammalian transcription factor ATF6 Is synthesized as a transmembrane protein and activated by proteolysis in response to endoplasmic reticulum stress. Mol Biol Cell 10:3787
Hinman JD, Peters A, Cabral H, Rosene DL, Hollander W, Rasband MN, Abraham CR (2006) Age-related molecular reorganization at the node of Ranvier. J Comp Neurol 495:351–362
Ho MC, Lo AC, Kurihara H, Yu AC, Chung SS, Chung SK (2001) Endothelin-1 protects astrocytes from hypoxic/ischemic injury. FASEB J 15:618–626
Honda Z, Ishii S, Shimizu T (2002) Platelet-activating factor receptor. J Biochem 131:773–779
Hou ST, MacManus JP (2002) Molecular mechanisms of cerebral ischemia-induced neuronal death. Int Rev Cytol 221:93–148
Huang D, Shenoy A, Cui JK, Huang W, Liu PK (2000) In situ detection of AP sites and DNA strand breaks with 3′-phosphate ends in ischemic mouse brain. FASEB J 14:407–417
Ishii S, Nagase T, Shimizu T (2002) Platelet-activating factor receptor. Prostaglandins Other Lipid Mediat 68–69:599–609
Janaky R, Ogita K, Pasqualotto BA, Bains JS, Oja SS, Yoneda Y, Shaw CA (1999) Glutathione and signal transduction in the mammalian CNS. J Neurochem 73:889–902
Ji L, Nazarali AJ, Paterson PG (2008) Protein-energy malnutrition increases activation of the transcription factor, nuclear factor-κB, in the gerbil hippocampus following global ischemia. J Nutr Biochem 19:770–777
Jian Liu K, Rosenberg GA (2005) Matrix metalloproteinases and free radicals in cerebral ischemia. Free Rad Biol Med 39:71–80
Jin K, Mao XO, Eshoo MW, Nagayama T, Minami M, Simon RP, Greenberg DA (2001) Microarray analysis of hippocampal gene expression in global cerebral ischemia. Ann Neurol 50:93–103
Kamath-Loeb AS, Hizi A, Tabone J, Solomon MS, Loeb LA (1997) Inefficient repair of RNA × DNA hybrids. Eur J Biochem 250:492–501
Kamii H, Mikawa S, Murakami K, Kinouchi H, Yoshimoto T, Reola L, Carlson E, Epstein CJ, Chan PH (1996) Effects of nitric oxide synthase inhibition on brain infraction in SOD-1-transgenic mice following transient focal cerebral ischemia. J Cereb Blood Flow Metab 16:1153–1157
Kato H, Araki T, Itoyama Y, Kogure K, Kato K (1995a) An immunohistochemical study of heat shock protein-27 in the hippocampus in a gerbil model of cerebral ischemia and ischemic tolerance. Neurosci 68:65–71
Kato H, Kogure K, Liu XH, Araki T, Kato K, Itoyama Y (1995b) Immunohistochemical localization of the low molecular weight stress protein Hsp27 following focal cerebral ischemia in the rat. Brain Res 679:1–7
Khan AA, Mao XO, Banwait S, DerMardirossian CM, Bokoch GM, Jin K, Greenberg DA (2006) Regulation of hypoxic neuronal death signaling by neuroglobin. FASEB J 22:1737–1747
Kiessling M, Stumm G, Xie Y, Herdegen T, Aguzzi A, Bravo R, Gass P (1993) Differential transcription and translation of immediate early genes in the gerbil hippocampus after transient global ischemia. J Cereb Blood Flow Metab 13:914–924
Kim JS (1996) Cytokines and adhesion molecules in stroke and related diseases. J Neurol Sci 137:69–78
Koistinaho J, Hökfelt T (1997) Altered gene expression in brain ischemia. Neuroreport 8:i–viii
Kuwabara K, Matsumoto M, Ikeda J, Hori O, Ogawa S, Maeda Y, Kitagawa K, Imuta N, Kinoshita T, Stern DM, Yanagi H, Kamada T (1996) Purification and characterization of a novel stress protein, the 150-kDa oxygen-regulated protein (ORP150), from cultured rat astrocytes and its expression in ischemic mouse brain. J Biol Chem 271:5025–5032
Lee HT, Chang YC, Wang LY, Wang ST, Huang CC, Ho CJ (2004) cAMP response element-binding protein activation in ligation preconditioning in neonatal brain. Ann Neurol 56:611–623
Li X, Nemoto M, Xu Z, Yu SW, Shimoji M, Andrabi SA, Haince JF, Poirier GG, Dawson TM, Dawson VL, Koehler RC (2007) Influence of duration of focal cerebral ischemia and neuronal nitric oxide synthase on translocation of apoptosis-inducing factor to the nucleus. Neurosci 144:56–65
Lilienbaum A, Israel A (2003) From calcium to NF-kappa B signaling pathways in neurons. Mol Cell Biol 23:2680–2698
Lin L, Cao S, Yu L, Cui J, Hamilton WJ, Liu PK (2000) Up-regulation of base excision repair activity for 8–2′ deoxyhydroxyl guanosine in the mouse brain after forebrain ischemia-reperfusion. J Neurochem 74:101–108
Lin JH, Li H, Yasumura D, Cohen HR, Zhang C, Panning B, Shokat KM, Lavail MM, Walter P (2007) IRE1 signaling affects cell fate during the unfolded protein response. Science 318:944–949
Lipton P (1999) Ischemic cell death in brain neurons. Physiol Rev 79:1431–1568
Lipton SA, Gu Z, Nakamura T (2007) Inflammatory mediators leading to protein misfolding and uncompetitive/fast off-rate drug therapy for neurodegenerative disorders. Int Rev Neurobiol 82:1–27
Lipton SA (2007) Pathologically-activated therapeutics for neuroprotection: mechanism of NMDA receptor block by memantine and S-nitrosylation. Curr Drug Targets 8:621–632
Liu PK, Hsu CY, Dizdaroglu M, Floyd RA, Kow YW, Karakaya A, Rabow LE, Cui JK (1996) Damage, repair and mutagenesis in nuclear genes after mouse forebrain ischemia-reperfusion. J Neurosci 16:6795–6806
Liu XS, Zou H, Slaughter C, Wang XD (1997) DFF: a heterodimeric protein that functions downstream of caspase-3 to trigger DNA fragmentation during apoptosis. Cell 89:175–184
Love S (1999) Oxidative stress in brain ischemia. Brain Pathol 9:119–131
Lu A, Tang Y, Ran R, Clark JF, Aronow BJ, Sharp FR (2003) Genomics of the periinfarction cortex after focal cerebral ischemia. J Cereb Blood Flow Metab 23:786–810
Luo Y, Ji X, Ling F, Li W, Zhang F, Cao G, Chen J (2007) Impaired DNA repair via the base-excision repair pathway after focal ischemic brain injury: a protein phosphorylation-dependent mechanism reversed by hypothermic neuroprotection. Front Biosci 12:1852–1862
Ma Y, Hendershot LM (2004) ER chaperone functions during normal and stress conditions. J Chem Neuroanat 28:51–65
Maclennan KM, Smith PF, Darlington CL (1996) Platelet-activating factor in the CNS. Prog Neurobiol 50:585–596
Marchetti L, Klein M, Schlett K, Pfizenmaier K, Eisel UL (2004) Tumor necrosis factor (TNF)-mediated neuroprotection against glutamate-induced excitotoxicity is enhanced by N-methyl-D-aspartate receptor activation. Essential role of a TNF receptor 2-mediated phosphatidylinositol 3-kinase-dependent NF-kappa B pathway. J Biol Chem 279:32869–32881
Mark RJ, Lovell MA, Markesbery WR, Uchida K, Mattson MP (1997) A role for 4-hydroxynonenal, an aldehydic product of lipid peroxidation, in disruption of ion homeostasis and neuronal death induced by amyloid β-peptide. J Neurochem 68:255–264
Mattson MP, Meffert MK (2006) Roles for NF-kappaB in nerve cell survival, plasticity, and disease. Cell Death Differ 13:852–860
Matute C, Domercq M, Sánchez-Gómez MV (2006) Glutamate-mediated glial injury: mechanisms and clinical importance. Glia 53:212–224
Miao B, Yin XH, Pei DS, Zhang QG, Zhang GY (2005) Neuroprotective effects of preconditioning ischemia on ischemic brain injury through down-regulating activation of JNK1/2 via N-methyl-D-aspartate receptor-mediated Akt1 activation. J Biol Chem 280:21693–21699
Millán M, Arenillas J (2006) Gene expression in cerebral ischemia: a new approach for neuroprotection. Cerebrovasc Dis 21(Suppl 2):30–37
Minami M, Satoh M (2000) Chemokines as mediators for intercellular communication in the brain. Nippon Yakurigaku Zasshi 115:193–200
Minami M, Satoh M (2003) Chemokines and their receptors in the brain: pathophysiological roles in ischemic brain injury. Life Sci 74:321–327
Mukherjee PK, DeCoster MA, Campbell FZ, Davis RJ, Bazan NG (1999) Glutamate receptor signaling interplay modulates stress-sensitive mitogen-activated protein kinases and neuronal cell death. J Biol Chem 274:6493–6498
Niimura M, Takagi N, Takagi K, Mizutani R, Ishihara N, Matsumoto K, Funakoshi H, Nakamura T, Takeo S (2006) Prevention of apoptosis-inducing factor translocation is a possible mechanism for protective effects of hepatocyte growth factor against neuronal cell death in the hippocampus after transient forebrain ischemia. J Cereb Blood Flow Metab 26:1354–1365
Nishino K, Nowak TS Jr (2004) Time course and cellular distribution of hsp27 and hsp72 stress protein expression in a quantitative gerbil model of ischemic injury and tolerance: thresholds for hsp72 induction and hilar lesioning in the context of ischemic preconditioning. J Cereb Blood Flow Metab 24:167–178
Nito C, Kamada H, Endo H, Niizuma K, Myer DJ, Chan PH (2008) Role of the p38 mitogen-activated protein kinase/cytosolic phospholipase A2 signaling pathway in blood-brain barrier disruption after focal cerebral ischemia and reperfusion. J Cereb Blood Flow Metab 28:1686–1696
Oka A, Belliveau MJ, Rosenberg PA, Volpe JJ (1993) Vulnerability of oligodendroglia to glutamate: pharmacology, mechanisms, and prevention. J Neurosci 13:1441–1453
Olney JW, Fuller T, de Gubareff T (1979) Acute dendrotoxic changes in the hippocampus of kainate treated rats. Brain Res 176:91–100
Park EM, Cho S, Frys K, Racchumi G, Zhou P, Anrather J, Iadecola C (2004) Interaction between inducible nitric oxide synthase and poly(ADP-ribose) polymerase in focal ischemic brain injury. Stroke 35:2896–2901
Parker MA, Bazan HEP, Marcheselli V, Rodriguez de Turco EB, Bazan NG (2002) Platelet-activating factor induces permeability transition and cytochrome c release in isolated brain mitochondria. J Neurosci Res 69:39–50
Perez-Pinzon MA, Dave KR, Raval AP (2005) Role of reactive oxygen species and protein kinase C in ischemic tolerance in the brain. Antioxid Redox Signal 7:1150–1157
Phillis JW, Horrocks LA, Farooqui AA (2006) Cyclooxygenases, lipoxygenases, and epoxygenases in CNS: their role and involvement in neurological disorders. Brain Res Rev 52:201–243
Pignataro G, Gala R, Cuomo O, Tortiglione A, Giaccio L, Castaldo P, Sirabella R, Matrone C, Canitano A, Amoroso S, Di Renzo G, Annunziato L (2004) Two sodium/calcium exchanger gene products, NCX1 and NCX3, play a major role in the development of permanent focal cerebral ischemia. Stroke 35:2566–2570
Pilitsis JG, Diaz FG, O‘Regan MH, Phillis JW (2001) Inhibition of Na+/Ca2+ exchange by KB-R7943, a novel selective antagonist, attenuates phosphoethanolamine and free fatty acid efflux in rat cerebral cortex during ischemia-reperfusion injury. Brain Res 916:192–198
Pizzi M, Sarnico I, Lanzillotta A, Battistin L, Spano P (2009) Post-ischemic brain damage: NF-kappaB dimer heterogeneity as a molecular determinant of neuron vulnerability. FASEB J 276:27–35
Popa-Wagner A, Carmichael ST, Kokaja Z, Kessler C, Walker LC (2007) The response of the aged brain to stroke: too much, too soon? Curr Neurovas Res 4:216–227
Pryor WA, Squadrito GL (1995) The chemistry of peroxynitrite: a product from the reaction of nitric oxide with superoxide. Am J Physiol 268:L699–L722
Qi W, Reiter RJ, Tan DX, Manchester LC, Siu AW, Garcia JJ (2000) Increased levels of oxidatively damaged DNA induced by chromium(III) and H2O2: protection by melatonin and related molecules. J Pineal Res 29:54–61
Radi R, Beckman JS, Bush KM, Freeman BA (1991) Peroxynitrite oxidation of sulfhydryls. The cytotoxic potential of superoxide and nitric oxide. J Biol Chem 266:4244–4250
Ran A, Lu A, Xu H, Tang Y, Sharp FR (2007) Heat-shock protein regulation of protein folding, protein degradation, protein function, and apoptosis. In Handbook of neurochemistry and molecular biology. Springer, New York, NY, pp 89–107
Ravagnan L, Gurbuxani S, Susin SA, Maisse C, Daugas E, Zamzami N, Mak T, Jaattela M, Penninger JM, Garrido C, Kroemer G (2001) Heat-shock protein 70 antagonizes apoptosis-inducing factor. Nat Cell Biol 3:839–843
Rosamond W, Flegal K, Friday G, Furie K, Go A, Greenlund K, Haase N, Ho M, Howard V, Kissela B et al (2007) Heart disease and stroke statistics – 2007 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation 115:e69–e171
Rothwell NJ, Relton JK (1993) Involvement of cytokines in acute neurodegeneration in the CNS. Neurosci Biobehav Rev 17:217–227
Salaycik KJ, Kelly-Hayes M, Beiser A, Nguyen AH, Brady SM, Kase CS, Wolf PA (2007) Depressive symptoms and risk of stroke: the Framingham Study. Stroke 38:16–21
Sarnico I, Lanzillotta A, Boroni F, Benarese M, Alghisi M, Schwaninger M, Inta I, Battistin L, Spano P, Pizzi M (2009) NF-kappaB p50/RelA and c-Rel-containing dimers: opposite regulators of neuron vulnerability to ischaemia. J Neurochem 108:475–485
Savitz SI, Malhotra S, Gupta G, Rosenbaum DM (2003) Cell transplants offer promise for stroke recovery. J Cardiovasc Nurs 18:57–61
Savitz SI, Dinsmore JH, Wechsler LR, Rosenbaum DM, Caplan LR (2004) Cell therapy for stroke. NeuroRx 1:406–414
Sawe N, Steinberg G, Zhao H (2008) Dual roles of the MAPK/ERK1/2 cell signaling pathway after stroke. J Neurosci Res 86:1659–1669
Sirabella R, Secondo A, Pannaccione A, Scorziello A, Valsecchi V, Adornetto A, Bilo L, Di Renzo G, Annunziato L (2009) Anoxia-induced NF-kappaB-dependent upregulation of NCX1 contributes to Ca2+ refilling into endoplasmic reticulum in cortical neurons. Stroke 40(3):922–929 22 Jan 2009 [Epub ahead of print]
Skaper SD (2003a) Poly(ADP-Ribose) polymerase-1 in acute neuronal death and inflammation: a strategy for neuroprotection. Ann NY Acad Sci 993:217–228
Skaper SD (2003b) Poly(ADP-ribosyl)ation enzyme-1 as a target for neuroprotection in acute central nervous system injury. Curr Drug Targets CNS Neurol Disord 2:279–291
Sobol RW, Horton JK, Kuhn R, Gu H, Singhal RK, Prasad R, Rajewsky K, Wilson SH (1996) Requirement of mammalian DNA polymerase-β in base-excision repair. Nature (London) 379:183–186
Stephenson D, Yin T, Smalstig EB, Hsu MA, Panetta J, Little S, Clemens J (2000) Transcription factor nuclear factor-kappa B is activated in neurons after focal cerebral ischemia. J Cereb Blood Flow Metab 20:592–603
Stetler RA, Cao G, Gao Y, Zhang F, Wang S, Weng Z, Vosler P, Zhang L, Signore A, Graham SH, Chen J (2008) Hsp27 protects against ischemic brain injury via attenuation of a novel stress-response cascade upstream of mitochondrial cell death signaling. J Neurosci 28:13038–13055
Sun GY, Horrocks LA, Farooqui AA (2007) The role of NADPH oxidase and phospholipases A2 in mediating oxidative and inflammatory responses in neurodegenerative diseases. J Neurochem 103:1–16
Terao Y, Ohta H, Oda A, Nakagaito Y, Kiyota Y, Shintani Y (2009) Macrophage inflammatory protein-3alpha plays a key role in the inflammatory cascade in rat focal cerebral ischemia. Neurosci Res 64:75–82
Truettner JS, Hu K, Liu CL, Dietrich WD, Hu B (2009) Subcellular stress response and induction of molecular chaperones and folding proteins after transient global ischemia in rats. Brain Res 1249:9–18
Tuttolomondo A, Di Raimondo D, di Sciacca R, Pinto A, Licata G (2008) Inflammatory cytokines in acute ischemic stroke. CurrPharm Des 14:3574–3589
van Wijk SJ, Haegeman GJ (2005) Poly(ADP-ribose) polymerase-1 mediated caspase-independent cell death after ischemia/reperfusion. Free Rad Biol Med 39:81–90
Walton M, Sirimanne E, Williams C, Gluckman P, Dragunow M (1996) The role of the cyclic AMP-responsive element binding protein (CREB) in hypoxic-ischemic brain damage and repair. Brain Res Mol Brain Res 43:21–29
Wen YD, Zhang HL, Oin ZH (2006) Inflammatory mechanism in ischemic neuronal injury. Neurosci Bull 22:171–182
Widlak P (2000) The DFF40/CAD endonuclease and its role in apoptosis. Acta Biochem Pol 47:1037–1044
Wissing D, Mouritzen H, Egeblad M, Poirier GG, Jäättelä M (1997) Involvement of caspase-dependent activation of cytosolic phospholipase A2 in tumor necrosis factor-induced apoptosis. Proc Natl Acad Sci USA 94:5073–5077
Won MH, Kang TC, Jeon GS, Lee JC, Kim DY, Choi EM, Lee KH, Choi CD, Chung MH, Cho SS (1999) Immunohistochemical detection of oxidative DNA damage induced by ischemia-reperfusion insults in gerbil hippocampus in vivo. Brain Res 836:70–78
Wong CH, Crack PJ (2008) Modulation of neuro-inflammation and vascular response by oxidative stress following cerebral ischemia-reperfusion injury. Curr Med Chem 15:1–14
Woo EJ, Kim YG, Kim MS, Han WD, Shin S, Robinson H, Park SY, Oh BH (2004) Structural mechanism for inactivation and activation of CAD/DFF40 in the apoptotic pathway. Mol Cell 14:531–539
Yagita Y, Sakoda S, Kitagawa K (2008) Gene expression in brain ischemia. Brain Nerve 60:1347–1355
Yakubov E, Gottlieb M, Gil S, Dinerman P, Fuchs P, Yavin E (2004) Overexpression of genes in the CA1 hippocampus region of adult rat following episodes of global ischemia. Mol Brain Res 127:10–25
Yamamoto Y, Gaynor RB (2004) I-κB kinases: key regulators of the NF-κB pathway. Trends Biochem Sci 29:72–79
Yenari MA, Han HS (2006) Influence of hypothermia on post-ischemic inflammation: role of nuclear factor kappa B (NFkappaB). Neurochem Int 49:164–169
Yilmaz G, Granger DN (2008) Cell adhesion molecules and ischemic stroke. Neurol Res 30:783–793
Yoshida T, Limmroth V, Irikura K, Moskowitz MA (1994) The NOS inhibitor, 7-nitroindazole, decreases focal infract volume but not the response to topical acetylcholine in pial vessels. J Cereb Blood Flow Metab 14:924–929
Zaleska MM, Wilson DF (1989) Lipid hydroperoxides inhibit reacylation of phospholipids in neuronal membranes. J Neurochem 52:255–260
Zaman K, Ryu H, Hall D, O‘Donovan K, Lin KI, Miller MP, Marquis JC, Baraban JM, Semenza GL, Ratan RR (1999) Protection from oxidative stress-induced apoptosis in cortical neuronal cultures by iron chelators is associated with enhanced DNA binding of hypoxia-inducible factor-1 and ATF-1/CREB and increased expression of glycolytic enzymes, p21(waf1/cip1), and erythropoietin. J Neurosci 19:9821–9830
Zhang W, Potrovita I, Tarabin V, Herrmann O, Beer V, Weih F, Schneider A, Schwaninger M (2005) Neuronal activation of NF-kappaB contributes to cell death in cerebral ischemia. J Cereb Blood Flow Metab 25:30–40
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Farooqui, A.A. (2010). Neurochemical Aspects of Ischemic Injury. In: Neurochemical Aspects of Neurotraumatic and Neurodegenerative Diseases. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-6652-0_2
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