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papers

Neonatal Borna disease virus infection in rats is associated with increased extracellular levels of glutamate and neurodegeneration in the striatum

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Pages 185-194 | Received 05 Nov 2006, Accepted 23 Jan 2007, Published online: 10 Jul 2009

References

  • Alexander G M, Deitch J S, Seeburger J L, Del Valle L, Heiman-Patterson T D. Elevated cortical extracellular fluid glutamate in transgenic mice expressing human mutant (G93A) Cu/Zn superoxide dismutase. J Neurochem 2000; 74: 1666–1673
  • Anderson C M, Swanson R A. Astrocyte glutamate transport: review of properties, regulation, and physiological functions. Glia 2000; 32: 1–14
  • Baker D A, Xi Z X, Shen H, Swanson C J, Kalivas P W. The origin and neuronal function of in vivo nonsynaptic glutamate. J Neurosci 2002; 22: 9134–9141
  • Bautista J R, Rubin S A, Moran T H, Schwartz G J, Carbone K M. Developmental injury to the cerebellum following perinatal borna disease virus infection. Brain Res Dev Brain Res 1995; 90: 45–53
  • Billaud J N, Ly C, Phillips T R, de la Torre J C. Borna disease virus persistence causes inhibition of glutamate uptake by feline primary cortical astrocytes. J Virol 2000; 74: 10438–10446
  • Briese T, Hornig M, Lipkin W I. Bornavirus immunopathogenesis in rodents: models for human neurological diseases. J NeuroVirol 1999; 5: 604–612
  • Carbone K M, Park S W, Rubin S A, Waltrip R W, 2nd, Vogelsang G B. Borna disease: association with a maturation defect in the cellular immune response. J Virol 1991; 65: 6154–6164
  • Chen Y, Swanson R A. Astrocytes and brain injury. J Cereb Blood Flow Metab 2003; 23: 137–149
  • Danbolt N C. Glutamate uptake. Prog Neurobiol 2001; 65: 1–105
  • de l a, Torre J C. Bornavirus and the brain. J Infect Dis 2002; 186: S241–S247, (Suppl 2)
  • Deitch J S, Alexander G M, Del Valle L, Heiman-Patterson T D. GLT-1 glutamate transporter levels are unchanged in mice expressing G93A human mutant SOD1. J Neurol Sci 2002; 193: 117–126
  • Dietz D, Vogel M, Rubin S, Moran T, Carbone K, Pletnikov M. Developmental alterations in serotoninergic neurotransmission in Borna disease virus (BDV)-infected rats: a multidisciplinary analysis. J Neurovirol 2004; 10: 267–277
  • Eisenman L M, Brothers R, Tran M H, Kean R B, Dickson G M, Dietzschold B, Hooper D C. Neonatal borna disease virus infection in the rat causes a loss of purkinje cells in the cerebellum. J NeuroVirol 1999; 5: 181–189
  • Espey M G, Kustova Y, Sei Y, Basile A S. Extracellular glutamate levels are chronically elevated in the brains of LP-BM5-infected mice: a mechanism of retrovirus-induced encephalopathy. J Neurochem 1998; 71: 2079–2087
  • Gochenauer G E, Robinson M B. Dibutyryl-cAMP (dbcAMP) up-regulates astrocytic chloride-dependent l-[3H]glutamate transport and expression of both system xc(−) subunits. J Neurochem 2001; 78: 276–286
  • Gonzalez-Dunia D, Watanabe M, Syan S, Mallory M, Masliah E, De La Torre J C. Synaptic pathology in borna disease virus persistent infection. J Virol 2000; 74: 3441–3448
  • Gonzalez-Dunia D, Volmer R, Mayer D, Schwemmle M. Borna disease virus interference with neuronal plasticity. Virus Res 2005; 111: 224–234
  • Gosztonyi G, Ludwig H. Neurotrasnmitter receptors and vial neurotropism. Neuropsychiatr Clin 1984; 3: 107–114
  • Gosztonyi G, Ludwig H. Borna disease—neuropathology and pathogenesis. Curr Top Microbiol Immunol 1995; 190: 39–73
  • Gosztonyi G, Ludwig H. Interaction of viral proteins with neurotransmitter receptors may protect or destroy neurons. Curr Top Microbiol Immunol 2001; 253: 121–144
  • Haas B, Becht H, Rott R. Purification and properties of an intranuclear virus-specific antigen from tissue infected with Borna disease virus. J Gen Virol 1986; 67: 235–241, (Pt 2)
  • Hara M R, Snyder S H. Cell signaling and neuronal death. Annu Rev Pharmacol Toxicol 2006
  • Hornig M, Chian D, Sindelar M, Hoffman K, Lipkin W I (2001) AMPA receptor disturbances and apoptosis in a rodent model of neurodevelopemtnal damage. Program, 1st Annual International Meeting for Autism Research, San Diego, CA, 2001, B-49, Abstract no. 21.02
  • Hornig M, Weissenböck H, Horscroft N, Lipkin W I. An infection-based model of neurodevelopmental damage. Proc Natl Acad Sci U S A 1999; 96: 12102–12107
  • Kaul M, Lipton S A. Mechanisms of neuronal injury and death in HIV-1 associated dementia. Curr HIV Res 2006; 4: 307–318
  • Maragakis N J, Rothstein J D. Glutamate transporters: animal models to neurologic disease. Neurobiol Dis 2004; 15: 461–473
  • McBean G J. Cerebral cystine uptake: a tale of two transporters. Trends Pharmacol Sci 2002; 23: 299–302
  • Melendez R I, Vuthiganon J, Kalivas P W. Regulation of extracellular glutamate in the prefrontal cortex: Focus on the cystine glutamate exchanger and group I metabotropic glutamate receptors. J Pharmacol Exp Ther 2005; 314: 139–147
  • Mitchell I J, Cooper A J, Griffiths M R. The selective vulnerability of striatopallidal neurons. Prog Neurobiol 1999; 59: 691–719
  • Nyitrai G, Kekesi K A, Juhasz G. Extracellular level of GABA and Glu: in vivo microdialysis-HPLC measurements. Curr Top Med Chem 2006; 6: 935–940
  • Pasantes-Morales H. Volume regulation in brain cells: cellular and molecular mechanisms. Metab Brain Dis 1996; 11: 187–204
  • Paxinos Watson. The rat brain in stereotaxic coordinates, 2nd ed. Academic Press, New York 1986
  • Pletnikov M V, Moran T H, Carbone K M. Borna disease virus infection of the neonatal rat: Developmental brain injury model of autism spectrum disorders. Front Biosci 2002a; 7: d593–d607
  • Pletnikov M V, Rubin S A, Vogel M W, Moran T H, Carbone K M. Effects of genetic background on neonatal borna disease virus infection-induced neurodevelopmental damage. I. brain pathology and behavioral deficits. Brain Res 2002b; 944: 97–107
  • Richt J A, Rott R. Borna disease virus: a mystery as an emerging zoonotic pathogen. Vet J 2001; 161: 24–40
  • Sauder C, de la Torre J C. Cytokine expression in the rat central nervous system following perinatal borna disease virus infection. J Neuroimmunol 1999; 96: 29–45
  • Sonsalla P K, Albers D S, Zeevalk G D. Role of glutamate in neurodegeneration of dopamine neurons in several animal models of parkinsonism. Amino Acids 1998; 14: 69–74
  • Tang X C, Kalivas P W. Bidirectional modulation of cystine/glutamate exchanger activity in cultured cortical astrocytes. Ann N Y Acad Sci 2003; 1003: 472–475
  • Timmerman W, Westerink B H. Brain microdialysis of GABA and glutamate: what does it signify?. Synapse 1997; 27: 242–261
  • Tomonaga K, Kobayashi T, Ikuta K. Molecular and cellular biology of borna disease virus infection. Microbes Infect 2002; 4: 491–500
  • Weissenböck H, Hornig M, Hickey W F, Lipkin W I. Microglial activation and neuronal apoptosis in bornavirus infected neonatal lewis rats. Brain Pathol 2000; 10: 260–272
  • West M J. New stereological methods for counting neurons. J Neuropathol Exp Neurol 1993; 14: 275–285
  • Williams B L, Lipkin W I. Endoplasmic reticulum stress and neurodegeneration in rats neonatally infected with borna disease virus. J Virol 2006; 80: 8613–8626

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