Biological bases of neuroplasticity – in vivo and in vitro studies: Interest for the auditory system

References

• Díaz Arribas MJ, Pardo-Hervás P, Tabares-Lavado M, Rios-Lago M, Maestú F. Plasticidad del sistema nervioso central y estrategias de tratamiento para la reprogramación sensorimotora: comparación de dos casos de accidente cerebrovascular isquémico en el territorio de la arteria cerebral media. Rev Neurol. 2006; 42: 153–8
   PubMed Web of Science ®Google Scholar
• Shimojo S, Sams L. Sensory modalities are not separate modalities: plasticity and interactions. Curr Opin Neurobiol. 2001; 11: 505–9
   PubMed Web of Science ®Google Scholar
• Bergado-Rosado JA, Almaguer-Melian W. Cellular mechanisms of neuroplasticity. Rev Neurol. 2000; 31: 1074–95
   PubMed Web of Science ®Google Scholar
• Gil-Loyzaga P. Neuroplasticidad y Sistema Auditivo. Tratado Otorrinolaringología & Cirugía Cabeza & Cuello2nd edn, C Suarez, LM Gil-Carcedo, J Marco, J Medina, P Ortega, J Trinidad. Panamericana, Madrid 2007; II: 1057–67
   Google Scholar
• Nitsche MA, Liebetanz D, Paulus W, Tergau F. Pharmacological characterization and modulation of neuroplasticity in humans. Curr Neuropharmacol. 2005; 3: 217–29
   Google Scholar
• Syka J. Plastic changes in the central auditory system after hearing loss, restoration of function, and during learning. Physiol Rev. 2002; 82: 601–36
   PubMed Web of Science ®Google Scholar
• Gil-Loyzaga P. Neuroplasticity in the auditory system. Eur Rev ENT. 2005; 126: 203–8
   Google Scholar
• Irvine DR. Auditory cortical neuroplasticity: does it provide evidence for cognitive processing in the auditory cortex?. Hear Res. 2007; 229: 158–70
   PubMed Web of Science ®Google Scholar
• Gil-Loyzaga P. Regeneración del epitelio del oído interno. Libro del Año Otorrinolaringología 1999, C Suarez. SANED Publ., Madrid 1999; 181–97
   Google Scholar
• Haberny KA, Paule MG, Scallet AC, Sistare FD, Lester DS, Hanig JP, et al. Ontogeny of the N-methyl-D-aspartate (NMDA) receptor system and susceptibility to neurotoxicity. Toxicol Sci. 2002; 68: 9–17
   PubMed Web of Science ®Google Scholar
• Deacon TW. Prefrontal cortex and symbol learning: why a brain capable of language evolved only once. Communicating meaning: the evolution and development of language, BM Velichkovsky, DM Rumbaugh. LEA Publishers, New York 1996; 103–38
   Google Scholar
• Gil-Loyzaga P. Fisiología del receptor auditivo. Fisiología y fisiopatología de la cóclea. Suppl. Act. ORL, P Gil-Loyzaga. SANED Publ, Madrid 2005; 1–7
   Google Scholar
• Gil-Loyzaga P. Estructura y función de la corteza auditiva. Bases de la vía auditiva ascendente. Tratado de Audiologia, E Salesa, E Perelló, A Bonavida. Masson-Elsevier, Barcelona 2005; 23–38
   Google Scholar
• Moller AR. Symptoms and signs caused by neural plasticity. Neurol Res. 2001; 23: 565–72
   PubMed Web of Science ®Google Scholar
• Bartels H, Staal MJ, Albers FWJ. Tinnitus and neural plasticity of the brain. Otol Neurotol. 2007; 28: 178–84
   PubMed Web of Science ®Google Scholar
• Cacace AT. Expanding the biological bases of tinnitus: cross-modal origins and the role of neuroplasticity. Hear Res. 2003; 175: 112–32
   PubMed Web of Science ®Google Scholar
• Jin YM, Godfrey DA. Effects of cochlear ablation on muscarinic acetylcholine receptor binding in the rat cochlear nucleus. J Neurosci Res. 2006; 83: 157–66
   PubMed Web of Science ®Google Scholar
• Barbacid M. Neurotrophic factors and their receptors. Current Opin Cell Biol. 1995; 7: 148–55
   PubMed Web of Science ®Google Scholar
• Ramón y Cajal S. Acción neurotrópica de los epitelios (Algunos detalles sobre el mecanismo genético de las ramificaciones nerviosas intra-epiteliales, sensitivas y sensoriales). Trab Lab Inv Biol. 1919; 17: 181–228
   Google Scholar
• Levi-Montalcini R. Developmental neurobiology and the natural history of nerve growth factor. Ann Rev Neurosci. 1982; 5: 341–62
   PubMed Web of Science ®Google Scholar
• Oudega M, Xu XM. Schwann cell transplantation for repair of the adult spinal cord. J Neurotrauma. 2006; 23: 453–67
   PubMed Web of Science ®Google Scholar
• Castro Soubriet F. Moléculas quimiotrópicas como mecanismo de orientación del crecimiento axonal y de la migración neuronal durante el desarrollo del sistema nervioso de los mamíferos. Rev Neurol. 2001; 33: 54–68
   PubMed Web of Science ®Google Scholar
• Brors D, Aletsee C, Dazert S, Huverstuhl J, Ryan AF, Bodmer D. Clostridium difficile toxin B, an inhibitor of the small GTPases Rho, Rac and Cdc42, influences spiral ganglion neurite outgrowth. Acta Otolaryngol (Stockh) 2003; 123: 20–5
   PubMed Web of Science ®Google Scholar
• Korsching S. The neurotrophic factor concept: a re-examination. J Neurosci. 1993; 13: 2739–48
   PubMed Web of Science ®Google Scholar
• Chao MV, Hempstead BL. p75 and Trk: a two-receptor system. TINS. 1995; 18: 321–6
   PubMed Web of Science ®Google Scholar
• Pirvola U, Hallböök F, Xing-Qun L, Virkkala J, Saarma M, Ylikoski J, et al. Expression of neurotrophins and Trk receptors in the developing, adult, and regenerating avian cochlea. J Neurobiol. 1997; 33: 1019–33
   PubMed Web of Science ®Google Scholar
• Represa J, Bernd P. Nerve growth factor and serum differentially regulate development of the embryonic otic vesicle and cochleovestibular ganglion in vitro. Dev Biol. 1989; 134: 21–9
   PubMed Web of Science ®Google Scholar
• Lefebvre PP, Leprince P, Weber T, Rigo JM, Delree P, Moonen G. Neuronotrophic effect of developing otic vesicle on cochleo-vestibular neurons: evidence for nerve growth factor involvement. Brain Res. 1990; 507: 254–60
   PubMed Web of Science ®Google Scholar
• Lefebvre PP, van de Water TR, Represa J, Liu W, Bernd P, Modlin S, et al. Temporal pattern of nerve growth factor (NGF) binding in vivo and the in vitro effects of NGF on cultures of developing auditory and vestibular neurons. Acta Otolaryngol (Stockh) 1991; 111: 304–11
   PubMed Web of Science ®Google Scholar
• Lefebvre PP, van de Water TR, Staecker H, Weber T, Galinovic-Schwartz V, Moonen G, et al. Nerve growth factor stimulates neurite regeneration but not survival of adult auditory neurons in vitro. Acta Otolaryngol (Stockh) 1992; 112: 288–93
   PubMed Web of Science ®Google Scholar
• Represa J, van de Water TR, Bernd P. Temporal pattern of nerve growth factor receptor expression in developing cochlear and vestibular ganglia in quail and mouse. Anat Embryol. 1991; 184: 421–32
   PubMedGoogle Scholar
• Cotanche DA, Lee KH. Regeneration of hair cells in the vestibulocochlear system of birds and mammals. Curr Opin Neurobiol. 1994; 4: 508–14
   Google Scholar
• Staecker H, van de Water TR. Factors controlling hair cell regeneration/repair in the inner ear. Curr Opin Neurobiol. 1998; 8: 480–7
   PubMed Web of Science ®Google Scholar
• Cotanche DA. Hair cell regeneration in the avian cochlea. Ann Otol Rhinol Laryngol. 1997; 106: 9–15
   Web of Science ®Google Scholar
• Schimmang T, Represa J. Neurotrophins gain a hearing. TINS. 1997; 20: 100–2
   PubMed Web of Science ®Google Scholar
• Lefebvre PP, Malgrange B, Staecker H, Moonen G, van de Water TR. Retinoic acid stimulates regeneration of mammalian auditory hair cells. Science. 1993; 260: 692–5
   PubMed Web of Science ®Google Scholar
• Pirvola U, Ylikoski J, Palgi J, Lehtonen E, Arumae U, Saarma M. Brain-derived neurotrophic factor and neurotrophin 3 mRNAs in the peripheral target fields of developing inner ear ganglia. Proc Natl Acad Sci USA. 1992; 89: 9915–9
   PubMed Web of Science ®Google Scholar
• Zhou X, Hossain WA, Rutledge A, Baier C, Morest DK. Basic fibroblast growth factor (FGF-2) affects development of acoustico-vestibular neurons in the chick embryo brain in vitro. Hear Res. 1996; 93: 147–66
   PubMed Web of Science ®Google Scholar
• Ylikoski J, Pirvola U, Virkkala J, Suvanto P, Liang XQ, Magal E, et al. Guinea pig auditory neurons are protected by glial cell-line derived growth factor from degeneration after noise trauma. Hear Res. 1998; 124: 17–26
   PubMed Web of Science ®Google Scholar
• Ditlevsen DK, Povlsen GK, Berezin V, Boek E. NCAM-induced intracellular signalling revisited. J Neurosci Res. 2008; 86: 727–43
   PubMed Web of Science ®Google Scholar
• Kolkova K, Novitskaya V, Pedersen N, Berezin V, Bock E. Neural cell adhesion molecule-stimulated neurite outgrowth depends on activation of protein kinase C and the Ras-mitogen-activated protein kinase pathway. J Neurosci. 2000; 20: 2238–46
   PubMed Web of Science ®Google Scholar
• Emerit MB, Riad M, Hamon M. Trophic effects of neurotransmitters during brain maturation. Biol Neonate. 1992; 62: 193–201
   PubMedGoogle Scholar
• Puel JL, Ruel J, Guitton M, Wang J, Pujol R. The inner hair cell synaptic complex: physiology, pharmacology and new therapeutic strategies. Audiol Neurootol. 2002; 7: 49–54
   PubMed Web of Science ®Google Scholar
• Zamanillo D, Sprengel R, Hvalby O, Jensen V, Burnashev N, Rozov A, et al. Importance of AMPA receptors for hippocampal synaptic plasticity but not for spatial learning. Science. 1999; 284: 1805–11
   PubMed Web of Science ®Google Scholar
• Jones TA, Kleim JA, Greenough WT. Synaptogenesis and dendritic growth in the cortex opposite unilateral sensorymotor cortex damage in adult rats: a quantitative electron microscopic examination. Brain Res. 1996; 773: 142–8
   Google Scholar
• Pavon N, Vidal L, Blanco L, Alvarez-Fonseca P, Torres-Montoya A, Lorigados L, et al. Factores que desencadenan la muerte neuronal en enfermedades neurodegenerativas. Rev Neurol. 1998; 26: 544–60
   PubMed Web of Science ®Google Scholar
• Puel JL. Chemical synaptic transmission in the cochlea. Progress Neurobiol. 1995; 47: 449–76
   PubMed Web of Science ®Google Scholar
• Ruel J, Chen C, Pujol R, Bobbin RP, Puel JL. AMPA-preferring glutamate receptors in cochlear physiology of adult guinea pig. J Physiol. 1999; 518: 667–80
   PubMed Web of Science ®Google Scholar
• Canlon B, Agerman K, Dauman R, Puel JL. Pharmacological strategies for preventing cochlear damage induced by noise trauma. Noise Health. 1998; 1: 13–23
   PubMedGoogle Scholar
• Bohne BA, Harding GW. Neural regeneration in the noise-damaged chinchilla cochlea. Laryngoscope. 1992; 102: 693–703
   PubMed Web of Science ®Google Scholar
• Lawner BE, Harding GW, Bohne BA. Time course of nerve fibre regeneration in the noise damaged mammalian cochlea. Int J Devel Neurosci. 1997; 15: 601–17
   PubMed Web of Science ®Google Scholar
• D'Aldin CG, Ruel J, Assie R, Pujol R, Puel JL. Implication of NMDA type glutamate receptors in neural regeneration and neoformation of synapses after excitotoxic injury in the guinea pig cochlea. Int J Devel Neurosci. 1997; 15: 619–29
   PubMed Web of Science ®Google Scholar
• Lipsky RH, Jiang X, Xu K, Marko AJ, Neyer KM, Anderson TR, Marini AM. Genomics and variation of ionotropic glutamate receptors: implications for neuroplasticity. Amino Acids. 2005; 28: 169–75
   PubMed Web of Science ®Google Scholar
• Portera-Cailliau C, Yuste R. On the function of dendritic filopodia. Rev Neurol. 2001; 33: 1158–66
   PubMed Web of Science ®Google Scholar
• Toyama K, Komatsu Y, Yamamoto N, Kurotami T, Yamada K. In vitro approach to visual cortical development and plasticity. Neurosci Res. 1991; 12: 57–71
   PubMed Web of Science ®Google Scholar
• Bufill E, Carbonell E. Are symbolic behaviour and neuroplasticity an example of gene-culture coevolution?. Rev Neurol. 2004; 39: 48–55
   PubMed Web of Science ®Google Scholar
• Letourneau PC. Regulation of nerve fibre elongation during embryogenesis. Developmental Neuropsychobiology, WT Greennough, JM Juraska. Acad. Press Ibc. Harc. Brace Jovanovich Publishers, OrlandoUSA 1986; 33–71
   Google Scholar
• Ladrech S, Lenoir M, Ruel J, Puel JL. Microtubule-associated protein 2 (MAP2) expression during synaptic plasticity in the guinea pig cochlea. Hear Res. 2003; 186: 85–90
   PubMed Web of Science ®Google Scholar
• Futerman AH, Banker GA. The economics of neurite outgrowth. The addition of new membrane to growing axons. Trends Neurosci. 1996; 19: 144–9
   PubMed Web of Science ®Google Scholar