Long-Term Astroglial Reaction and Neuronal Plasticity in the Subcortical Visual Pathways After a Complete Ablation of Telencephalon in Pigeons (Columba livia)

REFERENCES

• Ajtai B. M., Kalman M. Reactive glia support and guide axon growth in the rat thalamus during the first postnatal week: A sharply timed transition from permissive to non-permissive stage. International Journal of Developmental Neuroscience 2001; 19(6)589–597
   PubMedGoogle Scholar
• Aldskogius H., Kozlova E. N. Central neuron–glial and glial–glial interactions following axon injury. Progress in Neurobiology 1998; 55(1)1–26
   PubMedGoogle Scholar
• Allen N. J., Barres B. A. Signaling between glia and neurons: Focus on synaptic plasticity. Current Opinion in Neurobiology 2005; 15(5)542–548
   PubMedGoogle Scholar
• Alvarez-Maubecin V., Garcia-Hernandez F., Williams J. T., Van Bockstaele E. J. Functional coupling between neurons and glia. Journal of Neuroscience 2000; 20(11)4091–4098
   PubMedGoogle Scholar
• Atwal G. S. Dynamic plasticity in coupled avian midbrain maps. Physical Review: E; Statistical, Nonlinear, and Soft Matter Physics 2004; 70(6 Pt. 1)061904
   Google Scholar
• Bahr M., Bonhoeffer F. Perspectives on axonal regeneration in the mammalian CNS. Trends in Neurosciences 1994; 17(11)473–479
   PubMedGoogle Scholar
• Bjorklund H., Olson L., Dahl D., Schwarcz R. Short-and long-term consequences of intracranial injections of the excitotoxin, quinolinic acid, as evidenced by GFA immunohistochemistry of astrocytes. Brain Research 1986; 371(2)267–277
   PubMedGoogle Scholar
• Britto L. R. Inhibition of tectal neurons from telencephalic visual areas in pigeons. Revista Brasileira Pesquisas Medicine and Biology 1978; 11(Britto)223–227
   PubMedGoogle Scholar
• Cao L., Jiao X., Zuzga D. S., Liu Y., Fong D. M., et al. VEGF links hippocampal activity with neurogenesis, learning and memory. Nature Genetics 2004; 36(8)827–835
   PubMedGoogle Scholar
• Carmignoto G. Reciprocal communication systems between astrocytes and neurones. Progress in Neurobiology 2000; 62(6)561–581
   PubMed Web of Science ®Google Scholar
• Cavaglia M., Dombrowski S. M., Drazba J., Vasanji A., Bokesch P. M., Janigro D. Regional variation in brain capillary density and vascular response to ischemia. Brain Research 2001; 910(1–2)81–93
   PubMedGoogle Scholar
• Cerutti S. M., Chadi G. S100 immunoreactivity is increased in reactive astrocytes of the visual pathways following a mechanical lesion of the rat occipital cortex. Cell Biology International 2000; 24(1)35–49
   PubMed Web of Science ®Google Scholar
• Cerutti S. M., Diaz-Cintra S., Cintra L., Ferrari E. A. Operant discriminative learning and evidence of subtelencephalic plastic changes after long-term detelencephalation in pigeons. Neural Plasticity 2003; 10(4)247–266
   PubMedGoogle Scholar
• Cerutti S. M., Ferrari E. A. Operant discrimination learning in detelencephalated pigeons (Columba livia). Brazilian Journal of Medical and Biological Research 1995; 28(10)1089–1095
   PubMedGoogle Scholar
• Chadi G., Cao Y., Pettersson R. F., Fuxe K. Temporal and spatial increase of astroglial basic fibroblast growth factor synthesis after 6-hydroxydopamine–induced degeneration of the nigrostriatal dopamine neurons. Neuroscience 1994; 61(4)891–910
   PubMedGoogle Scholar
• Chadi G., Moller A., Rosen L., Janson A. M., Agnati L. A., Goldstein M., et al. Protective actions of human recombinant basic fibroblast growth factor on MPTP-lesioned nigrostriatal dopamine neurons after intraventricular infusion. Experimental Brain Research 1993; 97(1)145–158
   PubMed Web of Science ®Google Scholar
• Collombet J. M., Four E., Bernabe D., Masqueliez C., Burckhart M. F., Baille V., et al. Soman poisoning increases neural progenitor proliferation and induces long-term glial activation in mouse brain. Toxicology 2005; 208(3)319–334
   PubMedGoogle Scholar
• Di Giovanni S., Movsesyan V., Ahmed F., Cernak I., Schinelli S., Stoica B., et al. Cell cycle inhibition provides neuroprotection and reduces glial proliferation and scar formation after traumatic brain injury. Proceedings of the National Academy of Sciences of the United States of America 2005; 102(23)8333–8338
   PubMed Web of Science ®Google Scholar
• Diekamp B., Hellmann B., Troje N. F., Wang S. R., Gunturkun O. Electrophysiological and anatomical evidence for a direct projection from the nucleus of the basal optic root to the nucleus rotundus in pigeons. Neuroscience Letters 2001; 305(2)103–106
   PubMedGoogle Scholar
• Fawcett J. W., Asher R. A. The glial scar and central nervous system repair. Brain Research Bulletin 1999; 49(6)377–391
   PubMed Web of Science ®Google Scholar
• Finger S., Almli C. R. Brain damage and neuroplasticity: Mechanisms of recovery or development?. Brain Research 1985; 357(3)177–186
   PubMed Web of Science ®Google Scholar
• Froes M. M., de Carvalho A. C. Gap junction-mediated loops of neuronal-glial interactions. Glia 1998; 24(1)97–107
   PubMedGoogle Scholar
• Giulian D. Reactive glia as rivals in regulating neuronal survival. Glia 1993; 7(1)102–110
   PubMed Web of Science ®Google Scholar
• Gomes F. C., Spohr T. C., Martinez R., Moura Neto V. Cross-talk between neurons and glia: Highlights on soluble factors. Brazilian Journal of Medical and Biological Research 2001; 34(5)611–620
   PubMedGoogle Scholar
• Gomide V. C., Silveira G. A., Chadi G. Transient and widespread astroglial activation in the brain after a striatal 6-OHDA–induced partial lesion of the nigrostriatal system. The International Journal of Neuroscience 2005; 115(1)99–117
   PubMed Web of Science ®Google Scholar
• Gunturkun O., Hahmann U. Functional subdivisions of the ascending visual pathways in the pigeon. Behavioural Brain Research 1999; 98(2)193–201
   PubMedGoogle Scholar
• Heidmann S., Luksch H. Development of retino-recipient projection neurons in the optic tectum of the chicken. Brain Research. Developmental Brain Research 2001; 128(2)149–156
   PubMedGoogle Scholar
• Hellmann B., Gunturkun O. Visual-field-specific heterogeneity within the tecto-rotundal projection of the pigeon. The European Journal of Neuroscience 1999; 11(8)2635–2650
   PubMedGoogle Scholar
• Hodos W., Bonbright J. C. Intensity difference thresholds in pigeons after lesions of the tectofugal and thalamofugal visual pathways. Journal of Comparative Physiology Psychology 1974; 87(6)1013–1031
   PubMedGoogle Scholar
• Hodos W., Karten H. J. Brightness and pattern discrimination deficits in the pigeon after lesions of nucleus rotundus. Experimental Brain Research 1966; 2(2)151–167
   PubMedGoogle Scholar
• Horner P. J., Gage F. H. Regenerating the damaged central nervous system. Nature 2000; 407(6807)963–970
   PubMed Web of Science ®Google Scholar
• Hsu S. M., Raine L., Fanger H. Use of avidin–biotin–peroxidase complex (ABC) in immunoperoxidase techniques: A comparison between ABC and unlabeled antibody (PAP) procedures. The Journal of Histochemistry and Cytochemistry 1981; 29(4)577–580
   PubMed Web of Science ®Google Scholar
• Hunt S. P., Kunzle H. Observations on the projections and intrinsic organization of the pigeon optic tectum: An autoradiographic study based on anterograde and retrograde, axonal and dendritic flow. The Journal of Comparative Neurology 1976; 170(2)153–172
   PubMedGoogle Scholar
• Jeglinski W., Koczyk D., Zaremba M., Oderfeld-Nowak B. Bilateral gliosis in unilaterally lesioned septohippocampal system: Changes in GFAP immunoreactivity and content. Journal of Neuroscience Research 1995; 41(3)394–402
   PubMedGoogle Scholar
• Kalman M., Csillag A., Schleicher A., Rind C., Hajos F., Zilles K. Long-term effects of anterograde degeneration on astroglial reaction in the rat geniculo-cortical system as revealed by computerized image analysis. Anatomy and Embryology (Berlin) 1993; 187(1)1–7
   PubMedGoogle Scholar
• Karten H. J., Hodos W. A stereotaxic atlas of the pigeon brain (Columba livia), et al. The Johns Hopkins Press, Baltimore, MD 1967
   Google Scholar
• Kolb B., Gibb R., Gorny G. Experience-dependent changes in dendritic arbor and spine density in neocortex vary qualitatively with age and sex. Neurobiology of Learning and Memory 2003; 79(1)1–10
   PubMed Web of Science ®Google Scholar
• Kolb B., Whishaw I. Q. Plasticity in the neocortex: mechanisms underlying recovery from early brain damage. Progress in Neurobiology 1989; 32(4)235–276
   PubMedGoogle Scholar
• Leme R. J., Chadi G. Distant microglial and astroglial activation secondary to experimental spinal cord lesion. Arquivos De Neuro-Psiquiatria 2001; 59(3-A)483–492
   PubMedGoogle Scholar
• Martinez G., Carnazza M. L., Di Giacomo C., Sorrenti V., Avitabile M., Vanella A. GFAP, S-100 and vimentin proteins in rat after cerebral post-ischemic reperfusion. International Journal of Developmental Neuroscience 1998; 16(6)519–526
   PubMedGoogle Scholar
• McMillian M. K., Thai L., Hong J. S., O’Callaghan J. P., Pennypacker K. R. Brain injury in a dish: A model for reactive gliosis. Trends in Neurosciences 1994; 17(4)138–142
   PubMedGoogle Scholar
• Menon V. K., Landerholm T. E. Intralesion injection of basic fibroblast growth factor alters glial reactivity to neural trauma. Experimental Neurology 1994; 129(1)142–154
   PubMedGoogle Scholar
• Moonen G., Rogister B., Leprince P., Rigo J. M., Delree P., Lefebvre P. P., et al. Neurono-glial interactions and neural plasticity. Progress in Brain Research 1990; 86: 63–73
   PubMedGoogle Scholar
• Nagy J. I., Dudek F. E., Rash J. E. Update on connexins and gap junctions in neurons and glia in the mammalian nervous system. Brain Research. Brain Research Reviews 2004; 47(1–3)191–215
   PubMedGoogle Scholar
• Nakajima K., Kohsaka S. Functional roles of microglia in the brain. Neuroscience Research 1993; 17(3)187–203
   PubMed Web of Science ®Google Scholar
• O’Dowd B. S., Gibbs M. E., Sedman G. L., Ng K. T. Astrocytes implicated in the energizing of intermediate memory processes in neonate chicks. Brain Research. Cognitive Brain Research 1994; 2(2)93–102
   PubMedGoogle Scholar
• Paulson O. B. Blood-brain barrier, brain metabolism and cerebral blood flow. European Neuropsychopharmacology 2002; 12(6)495–501
   PubMed Web of Science ®Google Scholar
• Petrova T. V., Hu J., Van Eldik L. J. Modulation of glial activation by astrocyte-derived protein S100B: differential responses of astrocyte and microglial cultures. Brain Research 2000; 853(1)74–80
   PubMedGoogle Scholar
• Petzold A. Neurofilament phosphoforms: Surrogate markers for axonal injury, degeneration and loss. The Journal of Neurological 2005; 233(1–2)183–198
   PubMed Web of Science ®Google Scholar
• Phelps C. H. Neural plasticity in aging and Alzheimer's disease: Some selected comments. Progress in Brain Research 1990; 86: 3–9
   PubMedGoogle Scholar
• Pisani A., Centonze D., Bernardi G., Calabresi P. Striatal synaptic plasticity: Implications for motor learning and Parkinson's disease. Movement Disorders 2005; 20(4)395–402
   PubMed Web of Science ®Google Scholar
• Prickaerts J., Koopmans G., Blokland A., Scheepens A. Learning and adult neurogenesis: survival with or without proliferation?. Neurobiology of Learning and Memory 2004; 81(1)1–11
   PubMedGoogle Scholar
• Rekart J. L., Meiri K., Routtenberg A. Hippocampal-dependent memory is impaired in heterozygous GAP-43 knockout mice. Hippocampus 2005; 15(1)1–7
   PubMed Web of Science ®Google Scholar
• Shimizu T., Bowers A. N. Visual circuits of the avian telencephalon: Evolutionary implications. Behavioural Brain Research 1999; 98(2)183–191
   PubMedGoogle Scholar
• Suk K., Lee J., Hur J., Kim Y. S., Lee M., Cha S., et al. Activation-induced cell death of rat astrocytes. Brain Research 2001; 900(2)342–347
   PubMedGoogle Scholar
• Swanson R. A., Ying W., Kauppinen T. M. Astrocyte influences on ischemic neuronal death. Current Molecular Medicine 2004; 4(2)193–205
   PubMed Web of Science ®Google Scholar
• Theis M., Sohl G., Eiberger J., Willecke K. Emerging complexities in identity and function of glial connexins. Trends in Neurosciences 2005; 28(4)188–195
   PubMedGoogle Scholar
• Torre E. R., Lothman E., Steward O. Glial response to neuronal activity: GFAP-mRNA and protein levels are transiently increased in the hippocampus after seizures. Brain Research 1993; 631(2)256–264
   PubMedGoogle Scholar
• Winocur G., Roder J., Lobaugh N. Learning and memory in S100-beta transgenic mice: an analysis of impaired and preserved function. Neurobiology of Learning and Memory 2001; 75(2)230–243
   PubMed Web of Science ®Google Scholar
• Xu Z., Tung V. W. Temporal and spatial variations in slow axonal transport velocity along peripheral motoneuron axons. Neuroscience 2001; 102(1)193–200
   PubMedGoogle Scholar
• Yamaguchi Y., Pasquale E. B. Eph receptors in the adult brain. Current Opinion in Neurobiology 2004; 14(3)288–296
   PubMedGoogle Scholar
• Zonta M., Angulo M. C., Gobbo S., Rosengarten B., Hossmann K. A., Pozzan T., et al. Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation. Nature Neuroscience 2003; 6(1)43–50
   PubMed Web of Science ®Google Scholar