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Neurological Research
A Journal of Progress in Neurosurgery, Neurology and Neurosciences
Volume 30, 2008 - Issue 10: Nerve Regeneration and Nerve Repair
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Articles

Real-time multi-site multi-parametric monitoring of rat brain subjected to traumatic brain injury

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Pages 1075-1083 | Published online: 19 Jul 2013

  • Sandvig A, Berry M, Barrett LB, et al. Myelin-, reactive glia-, and scar-derived CNS axon growth inhibitors: Expression, receptor signaling, and correlation with axon regeneration. Glia 2004; 46: 225-251
  • Silver J, Miller JH. Regeneration beyond the glial scar. Nat Rev Neurosci 2004; 5: 146–156
  • Yiu G, He Z. Glial inhibition of CNS axon regeneration. Nat Rev Neurosci 2006; 7: 617–627
  • Narakas AO. Lesions found when operating traction injuries of the brachial plexus. Clin Neurol Neurosurg 1993; 95 (Suppl.): S56—S64
  • Bonney G. The value of axon responses in determining the site of lesion in traction injuries of the brachial plexus. Brain 1954; 77: 588–609
  • Terzis JK, Vekris MD, Soucacos PN. Outcomes of brachial plexus reconstruction in 204 patients with devastating paralysis. Plast Reconstr Surg 1999; 104: 1221–1240
  • Holtzer CA, Marani E, Lakke EA, et a/. Repair of ventral root avulsions of the brachial plexus: A review. J Peripher Nerv Syst 2002; 7: 233–242
  • Haller FR, Low FN. The fine structure of the peripheral nerve root sheath in the subarachnoid space in the rat and other laboratory animals. Am] Anat 1971; 131: 1–19
  • Berthold CH, Carlstedt T. Observations on the morphology at the transition between the peripheral and the central nervous system in the cat. III. Myelinated fibres in Si dorsal rootlets. Acta Physiol Scand Suppl 1977; 446: 43–60
  • Schlaepfer VVVV, Freeman LA, Eng LE. Studies of human and bovine spinal nerve roots and the outgrowth of CNS tissues into the nerve root entry zone. Brain Res 1979; 177: 219–229
  • Griffiths IR. Avulsion of the brachial plexus-1. Neuropathology of the spinal cord and peripheral nerves. 1 Small Anim Pract 1974; 15: 165–176
  • Cul lheim S, Kellerth JO. A morphological study of the axons and recurrent axon col laterals of cat sciatic alpha-motoneurons after intracellular staining with horseradish peroxidase. J Comp Neurol 1978; 178: 537-557
  • Scheibe! ME, Scheibe! AB. The organization of the ventral anterior nucleus of the thalamus. A Golgi study. Brain Res 1966; 1: 250–268
  • Inciong JG, Marrocco WC, Terzis JK. Efficacy of intervention strategies in a brachial plexus global avulsion model in the rat. Plast Reconstr Surg 2000; 105: 2059–2071
  • Terzis JK, Maragh H. Strategies in the microsurgical management of brachial plexus injuries. Clin Plast Surg 1989; 16: 605–616
  • Bertelli JA, Ghizoni ME. Brachial plexus avulsion injury repairs with nerve transfers and nerve grafts directly implanted into the spinal cord yield partial recovery of shoulder and elbow move-ments. Neurosurgery 2003; 52: 1385–1390
  • Cullheim S, Carlstedt T, Risling M. Axon regeneration of spinal motoneurons following a lesion at the cord-ventral root interface. Spinal Cord 1999; 37: 811–819
  • Carlstedt T. Functional recovery after ventral root avulsion and implantation in the spinal cord. Clin Neurol Neurosurg 1993; 95 (Suppl.): S109—S111
  • Brushart TM. Motor axons preferentially reinnervate motor path-ways. J Neurosci 1993; 13: 2730–2738
  • Carlstedt T, Grane P, Hallin RG, et al. Return of function after spinal cord implantation of avulsed spinal nerve roots. Lancet 1995; 346: 1323–1325
  • Selles-Navarro I, El lezam B, Fajardo R, et al. Retinal ganglion cell and nonneuronal cell responses to a microcrush lesion of adult rat optic nerve. Exp Neurol 2001; 167: 282–289
  • David S, Aguayo AJ. Axonal elongation into peripheral nervous system “bridges” after central nervous system injury in adult rats. Science 1981; 214: 931–933
  • Filbin MT. Myelin-associated inhibitors of axonal regeneration in the adult mammalian CNS. Nat Rev Neurosci 2003; 4: 703–713
  • Yiu G, He Z. Signaling mechanisms of the myelin inhibitors of axon regeneration. Curr Opin Neurobiol 2003; 13: 545–551
  • He Z, Koprivica V. The Nogo signaling pathway for regeneration block. Annu Rev Neurosci 2004; 27: 341–368
  • Fitch MT, Doller C, Combs CK, et al. Cellular and molecular mechanisms of glial scarring and progressive cavitation: In vivo and in vitro analysis of inflammation-induced secondary injury after CNS trauma. J Neurosci 1999; 19: 8182-8198
  • Becker T, Anliker B, Becker CG, et a/. Tenascin-R inhibits regrowth of optic fibers in vitro and persists in the optic nerve of mice after injury. Glia 2000; 29: 330–346
  • McKeon RJ, Schreiber RC, Rudge JS, et al. Reduction of neurite outgrowth in a model of glial scarring following CNS injury is correlated with the expression of inhibitory molecules on reactive astrocytes. J Neurosci 1991; 11: 3398–3411
  • Snow DM, Lemmon V, Carrino DA, etal. Sulfated proteoglycans in astroglial barriers inhibit neurite outgrowth in vitro. Exp Neurol 1990; 109:111–130
  • McKerracher L, David S, Jackson DL, et al. Identification of myelin-associated glycoprotein as a major myelin-derived inhi-bitor of neurite growth. Neuron 1994; 13: 805–811
  • Mukhopadhyay G, Doherty P, Walsh FS, et al. A novel role for myelin-associated glycoprotein as an inhibitor of axonal regenera-tion. Neuron 1994; 13: 757–767
  • Caroni P, Schwab ME. Two membrane protein fractions from rat central myelin with inhibitory properties for neurite growth and fibroblast spreading. J Cell Biol 1988; 106: 1281–1288
  • Wang KC, Koprivica V, Kim JA, et al. Oligodendrocyte-myelin glycoprotein is a Nogo receptor ligand that inhibits neurite outgrowth. Nature 2002; 417: 941–944
  • Fournier AE, Strittmatter SM. Repulsive factors and axon regenera-tion in the CNS. Curr Opin Neurobiol 2001; 11: 89–94
  • Bradbury Et Moon LD, Popat RJ, et al. Chondroitinase ABC promotes functional recovery after spinal cord injury. Nature 2002; 416: 636–640
  • Moon LD, Asher RA, Rhodes KE, et al. Regeneration of CNS axons back to their target following treatment of adult rat brain with chondroitinase ABC. Nat Neurosci 2001; 4: 465–466
  • GrandPre T, Li S, Strittmatter SM. Nogo-66 receptor antagonist peptide promotes axonal regeneration. Nature 2002; 417: 547–551
  • Li M, Shibata A, Li C, etal. Myelin-associated glycoprotein inhibits neurite/axon growth and causes growth cone collapse. J Neurosci Res 1996; 46: 404–414
  • Trapp BD, Andrews SB, Cootauco C, et al. The myelin-associated glycoprotein is enriched in multivesicular bodies and periaxonal membranes of actively myelinating oligodendrocytes. J Cell Biol 1989; 109: 2417–2426
  • Schnaar RL. Glycolipid-mediated cell—cell recognition in inflam-mation and nerve regeneration. Arch Biochem Biophys 2004; 426: 163–172
  • Sadoul R, Fahrig T, Bartsch U, et al. Binding properties of liposomes containing the myelin-associated glycoprotein MAG to neural cell cultures. J Neurosci Res 1990; 25: 1–13
  • Bartsch S, Montag D, Schachner M, et al. Increased number of unmyelinated axons in optic nerves of adult mice deficient in the myelin-associated glycoprotein (MAG). Brain Res 1997; 762: 231–234
  • Fruttiger M, Montag D, Schachner M, et al. Crucial role for the myelin-associated glycoprotein in the maintenance of axon—myelin integrity. Eur J Neurosci 1995; 7: 511–515
  • Fujita N, Kemper A, Dupree J, et al. The cytoplasmic domain of the large myelin-associated glycoprotein isoform is needed for proper CNS but not peripheral nervous system myelination. J Neurosci 1998; 18: 1970–1978
  • Yin X, Crawford TO, Griffin JW, et al. Myelin-associated glycoprotein is a myelin signal that modulates the caliber of myel inated axons. J Neurosci 1998; 18: 1953–1962
  • Prinjha R, Moore SE, Vinson M, et a/. Inhibitor of neurite outgrowth in humans. Nature 2000; 403: 383–384
  • Shen YJ, DeBel lard ME, Salzer JL, etal. Myelin-associated glycopro-tein in myelin and expressed by Schwann cells inhibits axonal regeneration and branching. Mol Cell Neurosci 1998; 12: 79–91
  • Schafer M, Fruttiger M, Montag D, et al. Disruption of the gene for the myelin-associated glycoprotein improves axonal regrowth along myelin in C57BUVVIds mice. Neuron 1996; 16:1107–1113
  • Torigoe K, Lundborg G. Selective inhibition of early axonal regeneration by myelin-associated glycoprotein. Exp Neurol 1998; 150: 254–262
  • Hansson GC, Karlsson KA, Larson G, et al. Carbohydrate-specific adhesion of bacteria to thin-layer chromatograms: A rationalized approach to the study of host cell glycolipid receptors. Anal Biochem 1985; 146: 158–163
  • Krivan HC, Ginsburg V, Roberts DD. Pseudomonas aeruginosa and Pseudomonas cepacia isolated from cystic fibrosis patients bind specifically to gangliotetraosylceramide (asialo GM1) and gangliotriaosylceramide (asialo GM2). Arch Biochem Biophys 1988; 260: 493–496
  • Magnani JL, Brockhaus M, Smith DF, etal. Detection of glycolipid ligands by direct binding of carbohydrate-binding proteins to thin-layer chromatograms. Methods Enzymol 1982; 83: 235–241
  • Yang Li, Zeller CB, Schnaar RL. Detection and isolation of lectin-transfected COS cells based on cell adhesion to immobilized glycosphingolipids. Anal Biochem 1996; 236: 161–167
  • Collins BE, Yang Li, Mukhopadhyay G, et al. Sialic acid specificity of myelin-associated glycoprotein binding.] Biol Chem 1997; 272: 1248–1255
  • Yang Li, Zeller CB, Shaper NL, et al. Gangliosides are neuronal ligands for myelin-associated glycoprotein. Proc Natl Acad Sci USA 1996; 93: 814–818
  • Collins BE, Kiso M, Hasegawa A, et al. Binding specificities of the sialoadhesin family of I-type lectins. Sialic acid linkage and substructure requirements for binding of myelin-associated glyco-protein, Schwann cell myelin protein, and sialoadhesin. I Biol Chem 1997; 272: 16889–16895
  • Takamiya K, Yamamoto A, Furukawa K, et al. Mice with disrupted GM2/GD2 synthase gene lack complex gangliosides but exhibit only subtle defects in their nervous system. Proc Natl Acad Sci USA 1996; 93: 10662–10667
  • Sheikh KA, Sun J, Liu Y, et al. Mice lacking complex gangliosides develop Wallerian degeneration and myelination defects. Proc Natl Acad Sci USA 1999; 96: 7532–7537
  • Vyas AA, Patel HV, Fromholt SE, et al. Gangliosides are functional nerve cell ligands for myelin-associated glycoprotein (MAG), an inhibitor of nerve regeneration. Proc Natl Acad Sci USA 2002; 99: 8412–8417
  • Yang LJ, Lorenzini I, Vajn K, et al. Sialidase enhances spinal axon outgrowth in vivo. Proc Natl Acad Sci USA 2006; 103: 11057–11062
  • Jivan S, Novikova LN, Wiberg M, et al. The effects of delayed nerve repair on neuronal survival and axonal regeneration after seventh cervical spinal nerve axotomy in adult rats. Exp Brain Res 2006; 170: 245–254
  • Carlstedt T, Linda H, Cullheim S, et al. Reinnervation of hind limb muscles after ventral root avulsion and implantation in the lumbar spinal cord of the adult rat. Acta Physiol Scand 1986; 128: 645-646
  • Hoang TX, Havton LA. A single re-implanted ventral root exerts neurotropic effects over multiple spinal cord segments in the adult rat. Exp Brain Res 2006; 169: 208–217
  • Vinson M, Strijbos PJ, Rowles A, et al. Myelin-associated glycoprotein interacts with ganglioside GT1b. A mechanism for neurite outgrowth inhibition. I Biol Chem 2001; 276: 20280–20285
  • DeBel lard ME, Tang S, Mukhopadhyay G, et al. Myelin-associated glycoprotein inhibits axonal regeneration from a variety of neurons via interaction with a sialoglycoprotein. Mol Cell Neurosci 1996; 7: 89–101
  • Cassidy JT, Jourdian GW, Roseman S. The sialic acids. VI. Purification and properties of sialidase from Clostridium perfrin-gens. I Biol Chem 1965; 240: 3501–3506
  • Wu G, Lu ZH, Wang J, et al. Enhanced susceptibility to kainate-induced seizures, neuronal apoptosis, and death in mice lacking gangliotetraose gangliosides: Protection with LIGA 20, a mem-brane-permeant analog of GM1. I Neurosci 2005; 25: 11014–11022
  • Bartsch U, Bandtlow CE, Schnell L, et al. Lack of evidence that myelin-associated glycoprotein is a major inhibitor of axonal regeneration in the CNS. Neuron 1995; 15: 1375–1381
  • McGee AW, Strittmatter SM. The Nogo-66 receptor: Focusing myelin inhibition of axon regeneration. Trends Neurosci 2003; 26: 193–198
  • Zheng B, Atwal J, Ho C, et al. Genetic deletion of the Nogo receptor does not reduce neurite inhibition in vitro or promote corticospinal tract regeneration in vivo. Proc Natl Acad Sci U S A 2005; 102: 1205–1210
  • Zheng B, Ho C, Li S, et al. Lack of enhanced spinal regeneration in Nogo-deficient mice. Neuron 2003; 38: 213–224
  • Schwab ME. Repairing the injured spinal cord. Science 2002; 295: 1029–1031
  • Sicotte M, Tsatas 0, Jeong SY, etal. Immunization with myelin or recombinant Nogo-66/MAG in alum promotes axon regeneration and sprouting after corticospinal tract lesions in the spinal cord. Mol Cell Neurosci 2003; 23: 251–263
  • Dergham P, Ellezam B, Essagian C, et al. Rho signaling pathway targeted to promote spinal cord repair.] Neurosci 2002; 22: 6570–6577
  • Spencer T, Filbin MT. A role for cAMP in regeneration of the adult mammalian CNS. J Anat 2004; 204: 49–55
  • Mehta NR, Lopez PH, Vyas AA, et al. Gangliosides and Nogo receptors independently mediate myelin-associated glycoprotein inhibition of neurite outgrowth in different nerve cells.] Biol Chem 2007; 282: 27875–27886

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