Abstract
Introduction
Spinal cord injury is a complex cascade of reactions secondary to the initial mechanical trauma that puts into action the innate properties of the injured cells, the circulatory, inflammatory, and chemical status around them, into a non-permissive and destructive environment for neuronal function and regeneration. Priming means putting a cell, in a state of “arousal” towards better function. Priming can be mechanical as trauma is known to enhance activity in cells.
Materials and methods
A comprehensive review of the literature was performed to better understand the possible chemical primers used for spinal cord injuries.
Conclusions
Taken together, many studies have shown various promising results using the substances outlined herein for treating SCI.
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References
Spencer T, Filbin MT (2004) A role for cAMP in regeneration of the adult mammalian CNS. J Anat 204:49–55
Bradbury EJ, Khemani S, Von R, King PJV, McMahon SB (1999) NT-3 promotes growth of lesioned adult rat sensory axons ascending in the dorsal columns of the spinal cord. Eur J Neurosci 11:3873–3883
Nakahara Y, Gage FH, Tuszynski MH (1996) Grafts of firoblasts genetically modified to secrete NGF, BDNF, NT-3, or basic FGF elicit differential responses in the adult spinal cord. Cell Transplant 5:191–204
Grill R, Murai K, Blesch A, Gage FH, Tuszynski MH (1997) Cellular delivery of neurotrophin-3 promotes corticospinal axonal growth and partial functional recovery after spinal cord injury. J Neurosci 17:5560–5572
Himes BT, Liu Y, Solowska JM, Snyder EY, Fischer I, Tessler A (2001) Transplants of cells genetically modified to express neurotrophin-3 rescue axotomized Clarke’s nucleus neurons after spinal cord hemisection in adult rats. J Neurosci Res 65:549–564
Schnell L, Schneider R, Kolbeck R, Barde YA, Schwab ME (1994) Neurotrophin-3 enhances sprouting of corticospinal tract during development and after adult spinal cord lesion. Nature 367:170–173
Jones LL, Oudega M, Bunge MB, Tuszynski MH (2001) Neurotrophic factors, cellular bridges and gene therapy for spinal cord injury. J Physiol 83:533-Pt 1
Koshinaga M, Sanon HR, Whittemore SR (1993) Altered acidic and basic fibroblast growth factor expression following spinal cord injury. Exp Neurol 120:32–48
Madiai F, Hussain SR, Goettl VM, Burry RW, Stephens RL, Hackshaw KV (2003) Upregulation of FGF-2 in reactive spinal cord astrocytes following unilateral lumbar spinal nerve ligation. Exp Brain Res 148:366–376
Tassi E, Walter S, Aigner A, Cabal-Manzano RH, Ray R, Reier PJ, Wellstein A (2007) Effects on neurite outgrowth and cell survival of a secreted fibroblast growth factor binding protein upregulated during spinal cord injury. Am J Physiol Regul Integr Comp Physiol 293:R775–R783
Cuevas P, Giménez-Gallego G (1997) Role of fibroblast growth factors in neural trauma. Neurol Res 19:254–256
Teng YD, Mocchetti I, Wrathall JR (1998) Basic and acidic fibroblast growth factors protect spinal motor neurones in vivo after experimental spinal cord injury. Eur J Neurosci 10:798–802
Laird JM, Mason GS, Thomas KA, Hargreaves RJ, Hill RG (1995) Acidic fibroblast growth factor stimulates motor and sensory axon regeneration after sciatic nerve crush in the rat. Neuroscience 65:209–216
Rabchevsky AG, Fugaccia I, Turner AF, Blades DA, Mattson MP, Scheff SW (2000) Basic fibroblast growth factor (bFGF) enhances functional recovery following severe spinal cord injury to the rat. Exp Neurol 164:280–291
Teng YD, Mocchetti I, Taveira-DaSilva AM, Gillis RA, Wrathall JR (1999) Basic fibroblast growth factor increases long-term survival of spinal motor neurons and improves respiratory function after experimental spinal cord injury. J Neurosci 19:7037–7047
Mocchetti I, Wrathall JR (1995) Neurotrophic factors in central nervous system trauma. J Neurotrauma 12:853–870
Zhang Z, Coomans C, David G (2001) Membrane heparan sulfate proteoglycan-supported FGF2-FGFR1 signaling: evidence in support of the “cooperative end structures” model. J Biol Chem 276:41921–41929
Oudega M, Hagg T (1996) Nerve growth factor promotes regeneration of sensory axons into adult rat spinal cord. Exp Neurol 140:218–229
Oudega M, Hagg T (1999) Neurotrophins promote regeneration of sensory axons in the adult rat spinal cord. Brain Res 818:431–438
Tobias CA, Shumsky JS, Shibata M, Tuszynski MH, Fischer I, Tessler A, Murray M (2003) Delayed grafting of BDNF and NT-3 producing fibroblasts into the injured spinal cord stimulates sprouting, partially rescues axotomized red nucleus neurons from loss and atrophy, and provides limited regeneration. Exp Neurol 184:97–113
Sharma HS (2006) Post-traumatic application of brain-derived neurotrophic factor and glia-derived neurotrophic factor on the rat spinal cord enhances neuroprotection and improves motor function. Acta Neurochir Suppl 96:329–334
Ramer MS, Priestley JV, Mcmahon SB (2000) Functional regeneration of sensory axons into the adult spinal cord. Nature 403:312–316
Tuszynski MH, Murai K, Blesch A, Grill R, Miller I (1997) Functional characterization of NGF-secreting cell grafts to the acutely injured spinal cord. Cell Transplant 6:361–368
Satake K, Matsuyama Y, Kamiya M, Kawakami H, Iwata H, Adachi K, Kiuchi K (2000) Up-regulation of glial cell line-derived neurotrophic factor (GDNF) following traumatic spinal cord injury. NeuroReport 11:3877–3881
Dolbeare D, Houle JD (2003) Restriction of axonal retraction and promotion of axonal regeneration by chronically injured neurons after intraspinal treatment with glial cell line-derived neurotrophic factor (GDNF). J Neurotrauma 20:1251–1261
Iannotti C, Li H, Yan P, Lu X, Wirthlin L, Xu XM (2003) Glial cell line-derived neurotrophic factor-enriched bridging transplants promote propriospinal axonal regeneration and enhance myelination after spinal cord injury. Exp Neurol 183:379–393
Nakashima S, Matsuyama Y, Yu Y, Katayama Y, Ito Z, Ishiguro N (2004) Expression of GDNF in spinal cord injury and its repression by ONO-1714. NeuroReport 16:17–20
Hashimoto M, Nitta A, Fukumitsu H, Nomoto H, Shen L, Furukawa S (2005) Inflammation-induced GDNF improves locomotor function after spinal cord injury. NeuroReport 16:99–102
Novikova L, Novikov L, Kellerth JO (1996) Brain-derived neurotrophic factor reduces necrotic zone and supports neuronal survival after spinal cord hemisection in adult rats. Neurosci Lett 220:203–206
Vavrek R, Girgis J, Tetzlaff W, Hiebert GW, Fouad K (2006) BDNF promotes connections of corticospinal neurons onto spared descending interneurons in spinal cord injured rats. Brain 129:1534–1545
Lu P, Jones LL, Tuszynski MH (2005) BDNF-expressing marrow stromal cells support extensive axonal growth at sites of spinal cord injury. Exp Neurol 191:344–360
Jin Y, Fischer I, Tessler A, Houle JD (2002) Transplant of fibroblasts genetically modified to express BDNF promote axonal regeneration from supraspinal neurons following chronic spinal cord injury. Exp Neurol 177:265–275
Hiebert GW, Khodarahmi K, McGraw J, Steeves JD, Tetzlaff W (2002) Brain-derived neurotrophic factor applied to the motor cortex promotes sprouting of corticospinal fibers but not regeneration into a peripheral nerve transplant. J Neurosci Res 69:160–683
Namiki J, Kojima A, Tator CH (2002) Effect of brain-derived neurotrophic factor, nerve growth factor, and neurotrophin-3 on functional recovery and regeneration after spinal cord injury in adult rats. J Neurotrauma 17:1219–1231
Facchiano F, Fernandez E, Mancarella S et al (2002) Promotion of regeneration of corticospinal tract axons in rats with recombinant vascular endothelial growth factor alone and combined with adenovirus coding for this factor. J Neurosurg 97:161–168
Herdegen T, Skene P, Bahr M (1997) The c-Jun transcription factor—bipotential mediator of neuronal death, survival and regeneration. Trends Neurosci 20:227–231
Chong MS, Reynolds ML, Irwin N, Coggeshall RE, Emson PC, Benowitz LI, Woolf CJ (1994) GAP-43 expression in primary sensory neurons following central axotomy. J Neurosci 14:4375–4384
Spencer SA, Schuh SM, Liu WS, Willard MB (1992) GAP-43, a protein associated with axon growth, is phosphorylated at three sites in cultured neurons and rat brain. J Biol Chem 267:9059–9064
Ninomiya K, Ishimoto T, Taguchi T (2005) Subcellular localization of PMES-2 proteins regulated by their two cytoskeleton-associated domains. Cell Mol Neurobiol 25:899–911
Ye J, Cao L, Cui R, Huang A, Yan Z, Lu C, He C (2004) The effects of ciliary neurotrophic factor on neurological function and glial activity following contusive spinal cord injury in the rats. Brain Res 997:30–39
Ye JH, Houle JD (1997) Treatment of the chronically injured spinal cord with neurotrophic factors can promote axonal regeneration from supraspinal neurons. Exp Neurol 143:70–81
Ozdinler PH, Macklis JD (2006) IGF-I specifically enhances axon outgrowth of corticospinal motor neurons. Nat Neurosci 9:1371–1381
Hung KS, Tsai SH, Lee TC, Lin JW, Chang CK, Chiu WT (2007) Gene transfer of insulin-like growth factor-I providing neuroprotection after spinal cord injury in rats. J Neurosurg Spine 6:35–46
Bambakidis NC, Wang RZ, Franic L, Miller RH (2003) Sonic hedgehog-induced neural precursor proliferation after adult rodent spinal cord injury. J Neurosurg 99:70–75
Bambakidis NC, Miller RH (2004) Transplantation of oligodendrocyte precursors and sonic hedgehog results in improved function and white matter sparing in the spinal cords of adult rats after contusion. Spine J 4:16–26
Bambakidis NC, Theodore N, Nakaji P, Harvey A, Sonntag VK, Preul MC, Miller RH (2005) Endogenous stem cell proliferation after central nervous system injury: alternative therapeutic options. Neurosurg Focus 19:E1
Simonen M, Pedersen V, Weinmann O, Schnell L, Buss A, Ledermann B, Christ F, Sansig G, van der Putten H, Schwab ME (2003) Systemic deletion of the myelin-associated outgrowth inhibitor Nogo-A improves regenerative and plastic responses after spinal cord injury. Neuron 38:201–211
Ahmed Z, Suggate EL, Brown ER, Dent RG, Armstrong SJ, Barrett LB, Berry M, Logan A (2006) Schwann cell-derived factor-induced modulation of the NgR/p75NTR/EGFR axis disinhibits axon growth through CNS myelin in vivo and in vitro. Brain 129:1517–1533
Fournier AE, Takizawa BT, Strittmatter SM (2003) Rho kinase inhibition enhances axonal regeneration in the injured CNS. J Neurosci 23:1416–1423
Dubreuil CI, Winton MJ, McKerracher L (2003) Rho activation patterns after spinal cord injury and the role of activated Rho in apoptosis in the central nervous system. J Cell Biol 162:233–243
von Meyenburg J, Brosamle C, Metz GA, Schwab ME (1998) Regeneration and sprouting of chronically injured corticospinal tract fibers in adult rats promoted by NT-3 and the mAb IN-1, which neutralizes myelin-associated neurite growth inhibitors. Exp Neurol 154:583–594
Bradbury EJ, Moon LD, Popat RJ et al (2002) Chondroitinase ABC promotes functional recovery after spinal cord injury. Nature 416:636–640
Faden AI, Holaday JW (1981) A role for endorphins in the pathophysiology of spinal cord injury. Adv Biochem Psychopharmacol 28:435–446
McIntosh TK, Faden AI (1986) Opiate antagonist in traumatic shock. Ann Emerg Med 15:1462–1465
Benzel EC, Khare V, Fowler MR (1992) Effects of Naloxone and Nalmefene in rat spinal cord injury induced by ventral compression technique. J Spinal Disord 5:75–77
Akdemir H, Pasaoglu A, Ozturk F et al (1992) Histopathology of experimental spinal cord trauma. Comparison of treatment with TRH, naloxone, and dexamethasone. Res Exp Med (Berl) 192:177–183
Arias MJ (1987) Treatment of experimental spinal cord injury with TRH, naloxone, and dexamethasone. Surg Neurol 28:335–338
Faden AI, Jacobs TP, Holaday JW (1981) Opiate antagonist improves neurologic recovery after spinal injury. Science 211:493–494
Faden AI, Jacobs TP, Holaday JW (1981) Thyrotropin-releasing hormone improves neurologic recovery after spinal trauma in cats. New Engl J Med 305:1063–1067
Bracken MB, Shepard MJ, Collins WF et al (1990) A randomized, controlled trial of methyl-prednisolone or naloxone in the treatment of acute spinal cord injury. Reslts of the second NASCIS. New Engl J Med 322:1405–1411
Flamm ES, Young W, Collins WF et al (1985) A phase I trial of naloxone treatment in acute spinal cord injury. J Neurosurg 63:390–397
Guha A, Tator CH, Piper I (1987) Effect of a calcium channel blocker on posttraumatic spinal blood flow. J Neurosurg 66:423–430
Ross IB, Tator CH (1993) Spinal cord blood flow and evoked potential responses after treatment with nimodipine or methylprednisolone in spinal cord-injured rats. Neurosurgery 33:470–476
Imamura H, Tator CH (1998) Effect of intrathecal nimodipine on spinal cord blood flow and evoked potentials in the normal or injured cord. Spinal Cord 36:497–506
Holtz A, Nyström B, Gerdin B (1989) Spinal cord injury in rats: inability of nimodipine or anti-neutrophil serum to improve spinal cord blood flow or neurologic status. Acta Neurol Scand 79:460–467
Ford RW, Malm DN (1985) Failure of nimodipine to reverse acute experimental spinal cord injury. Cent Nerv Syst Trauma 2:9–17
Haghighi SS, Stiens T, Oro JJ, Madsen R (1993) Evaluation of the calcium channel antagonist nimodipine after experimental spinal cord injury. Surg Neurol 39:403–408
Agrawal SK, Nashmi R, Fehlings MG (2000) Role of L- and N-type calcium channels in the pathophysiolongy of traumatic psinal cord white matter injury. Neuroscience 99:179–188
Pointillart V, Gense D, Gross C et al (1993) Effects of nimodipine on posttraumatic spinal cord ischemia in baboons. J Neurotrauma 10:201–213
Ceylan S, Ilbay K, Baykal S, Ceylan S, Senser U, Ozmenoğlu M, Kalelioğlu M, Aktürk F, Komsuoğlu SS, Ozoran A (1992) Treatment of acute spinal cord injuries: comparison of thyrotropin-releasing hormone and nimodipine. Res Exp Med (Berl) 192:23–33
Kaynar MY, Erdinçler P, Tadayyon E, Belce A, Gümüstas K, Ciplak N (1998) Effect of nimodipine and N-acetylcysteine on lipid peroxidation after experimental spinal cord injury. Neurosurg Rev 21:260–264
Shi RY, Lucas JH, Wolf A, Gross GW (1989) Calcium antagonists fail to protect mammalian spinal neurons after physical injury. J Neurotrauma 6(261–76):277–278
Petitjean ME, Pointillart V, Dixmerias F et al (1998) Medical treatment of spinal cord injury in the acute stage. Ann Fr Anesth Rèanim 17:114–122
Scheller C, Richter HP, Engelhardt M, Köenig R, Antoniadis G (2007) The influence of prophylactic vasoactive treatment on cochlear and facial nerve functions after vestibular schwannoma surgery: a prospective and open-label randomized pilot study. Neurosurgery 61:92–97
Wrathall JR, Teng YD, Choiniere D (1996) Amelioration of functional deficits from spinal cord trauma with systemically administered NBQX, an antagonist of non-N-methyl-D-aspartate receptors. Exp Neurol 137:119–126
Kinuta Y, Kimura M, Itokawa Y et al (1989) Changes in Xanthine oxidase in ischemic rat brain. J Neurosurg 71:417–420
Farooque M, Hillered L, Holtz A et al (1996) Changes of extracellular levels of amino acids after graded compression trauma to the spinal cord: an experimental study in the rat using microdialysis. J Neurotrauma 13:537–548
Wrathall JR, Choiniere D, Teng YD (1994) Dose-dependent reduction of tissue loss and functional impairment after spinal cord trauma with the AMPA/kainate antagonist NBQX. J Neurosci 14:6598–6607
Lang-Luzdunski L, Heurteaux C, Vaillant N et al (1999) Riluzole prevents ischemic spinal cord injury casued by aortic crossclamping. J Thorac Cardiovasc Surg 117:881–889
Mitha AP, Maynard KI (2001) Gacyclidine (Beaufour-Ipsen). Curr Opin Investig Drugs 2:814–819
Nesathurai S (1998) Steroids and spinal cord injury: revisiting the NASCIS 2 and NASCIS 3 trials. J Trauma 45:1088–1093
Bracken MB, Shepard MJ, Holford TR et al (1998) Methylprednisolone or trilazad mesylate administration after acute spinal cord injury: 1-year follow-up. Results of the third NSCIS randomized controlled trial. J Neurosurg 8:699–706
Qiao F, Atkinson C, Song H, Pannu R, Singh I, Tomlinson S (2006) Complement plays an important role in spinal cord injury and represents a therapeutic target for improving recovery following trauma. Am J Pathol 169:1039–1047
Rapalino O, Lazarov-Spiegler O, Agranov E, Velan GJ, Yoles E, Fraidakis M, Solomon A, Gepstein R, Katz A, Belkin M, Hadani M, Schwartz M (1998) Implantation of stimulated homologous macrophages results in partial recovery of paraplegic rats. Nat Med 4:814–821
Franzen R, Schoenen J, Leprince P, Joosten E, Moonen G, Martin D (1998) Effects of macrophage transplantation in the injured adult rat spinal cord: a combined immunocytochemical and biochemical study. J Neurosci Res 51:316–327
Bomstein Y, Marder JB, Vitner K, Smirnov I, Lisaey G, Butovsky O, Fulga V, Yoles E (2003) Features of skin-coincubated macrophages that promote recovery from spinal cord injury. J Neuroimmunol 142:10–16
Knoller N, Auerbach G, Fulga V, Zelig G, Attias J, Bakimer R, Marder JB, Yoles E, Belkin M, Schwartz M, Hadani M (2005) Clinical experience using incubated autologous macrophages as a treatment for complete spinal cord injury: phase I study results. J Neurosurg Spine 3:173–181
Hauben E, Gothilf A, Cohen A, Butovsky O, Nevo U, Smirnov I, Yoles E, Akselrod S, Schwartz M (2003) Vaccination with dendritic cells pulsed with peptides of myelin basic protein promotes functional recovery from spinal cord injury. J Neurosci 23:8808–8819
Mikami Y, Okano H, Sakaguchi M, Nakamura M, Shimazaki T, Okano HJ, Kawakami Y, Toyama Y, Toda M (2004) Implantation of dendritic cells in injured adult spinal cord results in activation of endogenous neural stem/progenitor cells leading to de novo neurogenesis and functional recovery. J Neurosci Res 76:453–465
Geisler FH, Dorsey FC, Coleman WP (1991) Recovery of motor function after spinal cord injury—a randomized, placebo-controlled trial with GM-1 ganglioside. New Engl J Med 324:1829–1838
Geisler FH, Coleman WP, Grieco G (2001) The sygen multicenter acute spinal cord injury study. Spine 26:S87–S98
Pannu R, Barbosa E, Singh AK, Singh I (2005) Attenuation of acute inflammatory response by atorvastatin after spinal cord injury in rats. J Neurosci Res 79:340–350
Holmberg E, Nordstrom T, Gross M, Kluge B, Zhang SX, Doolen S (2006) Simvastatin promotes neurite outgrowth in the presence of inhibitory molecules found in central nervous system injury. J Neurotrauma 23:1366–1378
Pannu R, Christie DK, Barbosa E, Singh I, Singh AK (2007) Post-trauma Lipitor treatment prevents endothelial dysfunction, facilitates neuroprotection, and promotes locomotor recovery following spinal cord injury. J Neurochem 101:182–200
Scott GS, Cuzzocrea S, Genovese T, Koprowski H, Hooper DC (2005) Uric acid protects against secondary damage after spinal cord injury. Proc Natl Acad Sci USA 102:3483–3488
Su H (2007) Lithium enhances proliferation and neuronal differentiation of neural progenitor cells in vitro and after transplantation into the adult rat spinal cord. Exp Neurol 206:296–307
Galandiuk S, Raque G, Appel S, Polk HC (1993) The two-edged sword of large-dose steroids for spinal cord trauma. Ann Surg 218:419–425
Raineteau O, Fouad K, Noth P, Thallmair M, Schwab ME (2001) Functional switch between motor tracts in the presence of the mAb IN-1 in the adult rat. Proc Natl Acad Sci USA 98:6929–6934
Mi S, Lee X, Shao Z, Thill G, Ji B, Relton J, Levesque M, Allaire N, Perrin S, Sands B, Crowell T, Cate RL, McCoy JM, Pepinsky RB (2004) LINGO-1 is a component of the Nogo-66 receptor/p75 signaling complex. Nat Neurosci 7:221–228
Laurén J (2007) Characterization of LRRTM and NGR gene families: expression and functions. Dissertation, University of Helsinki
Park JB, Yiu G, Kaneko S, Wang J, Chang J, He XL, Garcia KC, He Z (2005) A TNF receptor family member, TROY, is a coreceptor with Nogo receptor in mediating the inhibitory activity of myelin inhibitors. Neuron 45:345–351
Shao Z, Browning JL, Lee X, Scott ML, Shulga-Morskaya S, Allaire N, Thill G (2005) TAJ/TROY, an orphan TNF receptor family member, binds Nogo-66 receptor 1 and regulates axonal regeneration. Neuron 45:353–359
Ahmed Z, Mazibrada G, Seabright RJ, Dent RG, Berry M, Logan A (2006) TACE-induced cleavage of NgR and p75NTR in dorsal root ganglion cultures disinhibits outgrowth and promotes branching of neurites in the presence of inhibitory CNS myelin. FASEB J 20:1939–1941
Li S, Liu BP, Budel S, Li M, Ji B, Walus L, Li W, Jirik A, Rabacchi S, Choi E, Worley D, Sah DW, Pepinsky B, Lee D, Relton J, Strittmatter SM (2004) Blockade of Nogo-66, myelin-associated glycoprotein, and oligodendrocyte myelin glycoprotein by soluble Nogo-66 receptor promotes axonal sprouting and recovery after spinal injury. J Neurosci 24:10511–10520
Shelke SV, Gao GP, Mesch S, Gathje H, Kelm S, Schwardt O, Ernst B (2007) Synthesis of sialic acid derivatives as ligands for the myelin-associated glycoprotein (MAG). Bioorg Med Chem 15:4951–4965
Laketa V, Simpson JC, Bechtel S, Wiemann S, Pepperkok R (2006) High-content microscopy identifies new neurite outgrowth regulators. Mol Biol 18:242–252
Alessi DR, Andjelkovic M, Caudwell B, Cron P, Morrice N, Cohen P, Hemmings BA (1996) Mechanism of activation of protein kinase B by insulin and IGF-1. EMBO J 15:6541–6551
Chen ZY, Sun C, Reuhl K, Bergemann A, Henkemeyer M, Zhou R (2004) Abnormal hippocampal axon bundling in EphB receptor mutant mice. J Neurosci 24:2366–2374
Kadison SR, Makinen T, Klein R, Henkemeyer M, Kaprielian Z (2006) EphB receptors and ephrin-B3 regulate axon guidance at the ventral midline of the embryonic mouse spinal cord. J Neurosci 26:8909–8914
Benson MD, Romero MI, Lush ME, Lu QR, Henkemeyer M, Prada LF (2005) Ephrin-B3 is a myelin-based inhibitor of neurite outgrowth. Proc Natl Acad Sci USA 102:10694–10699
Chrencik JE, Brooun A, Recht MI, Kraus ML, Koolpe M, Kolatkar AR, Bruce RH, Martiny-Baron G, Widmer H, Pasquale EB, Kuhn P (2006) Structure and thermodynamic characterization of the EphB4/Ephrin-B2 antagonist peptide complex reveals the determinants for receptor specificity. Structure 14:321–330
Guthrie S (2004) Axon guidance: mice and men need Rig and Robo. Curr Biol 14:R632–R634
Blein S, Ginham R, Uhrin D, Smith BO, Soares DC, Veltel S, McIlhinney RA, White JH, Barlow PN (2004) Structural analysis of the complement control protein (CCP) modules of GABA(B) receptor 1a: only one of the two CCP modules is compactly folded. J Biol Chem 279:48292–48306
Marillat V, Sabatier C, Failli V, Matsunaga E, Sotelo C, Tessier-Lavigne M, Chedotal A (2004) The slit receptor Rig-1/Robo3 controls midline crossing by hindbrain precerebellar neurons and axons. Neuron 43:69–79
Chalasani SH, Sabol A, Xu H, Gyda MA, Rasband K, Granato M, Chien CB, Raper JA (2007) Stromal cell-derived factor-1 antagonizes slit/robo signaling in vivo. J Neurosci 27:973–980
Bellamy TC, Garthwaite J (2001) Sub-second kinetics of the nitric oxide receptor, soluble guanylyl cyclase, in intact cerebellar cells. J Biol Chem 276:4287–4292
Takagi H, Asano Y, Yamakawa N, Matsumoto I, Kimata K (2002) Annexin 6 is a putative cell surface receptor for chondroitin sulfate chains. J Cell Sci 115:3309–3318
Rolls A, Avidan H, Cahalon L, Schori H, Bakalash S, Litvak V, Lev S, Lider O, Schwartz M (2004) A disaccharide derived from chondroitin sulphate proteoglycan promotes central nervous system repair in rats and mice. Eur J Neurosci 20(8):1973–1983
Geisler FH, Dorsey FC, Coleman WP (1991) Recovery of motor function after spinal-cord injury—a randomized, placebo-controlled trial with GM-1 ganglioside. N Engl J Med 324:1829–1838
Flamm ES, Young W, Collins WF, Piepmeier J, Clifton GL, Fischer B (1985) A phase I trial of naloxone treatment in acute spinal cord injury. J Neurosurg 63:390–397
Bracken MB (1990) Methylprednisolone in the management of acute spinal cord injuries. Med J Aust 153:368
Bracken MB, Shepard MJ, Collins WF Jr, Holford TR, Baskin DS, Eisenberg HM, Flamm E, Leo-Summers L, Maroon JC, Marshall LF et al (1992) Methylprednisolone or naloxone treatment after acute spinal cord injury: 1-year follow-up data. Results of the second National Acute Spinal Cord Injury Study. J Neurosurg 76:23–31
Pitts LH, Ross A, Chase GA, Faden AI (1995) Treatment with thyrotropin-releasing hormone (TRH) in patients with traumatic spinal cord injuries. J Neurotrauma 12:235–243
Tadié M, d’Arbigny P, Mathé JF et al (1999) Acute spinal cord injury: early care and treatment in a multicenter study with gacyclidine. Soc Neurosci Abstr 25:1090
Pointillart V, Petitjean ME, Wiart L, Vital JM, Lassié P, Thicoipé M, Dabadie P (2000) Pharmacological therapy of spinal cord injury during the acute phase. Spinal Cord 38:71–76
Bracken MB, Collins WF, Freeman DF, Shepard MJ, Wagner FW, Silten RM, Hellenbrand KG, Ransohoff J, Hunt WE, Perot PL Jr et al (1984) Efficacy of methylprednisolone in acute spinal cord injury. JAMA 251:45–52
Bracken MB, Shepard MJ, Holford TR, Leo-Summers L, Aldrich EF, Fazl M, Fehlings M, Herr DL, Hitchon PW, Marshall LF, Nockels RP, Pascale V, Perot PL Jr, Piepmeier J, Sonntag VK, Wagner F, Wilberger JE, Winn HR, Young W (1997) Administration of methylprednisolone for 24 or 48 hours or tirilazad mesylate for 48 hours in the treatment of acute spinal cord injury. Results of the Third National Acute Spinal Cord Injury Randomized Controlled Trial. National Acute Spinal Cord Injury Study. JAMA 277:1597–1604
Bracken MB, Shepard MJ, Holford TR, Leo-Summers L, Aldrich EF, Fazl M, Fehlings MG, Herr DL, Hitchon PW, Marshall LF, Nockels RP, Pascale V, Perot PL Jr, Piepmeier J, Sonntag VK, Wagner F, Wilberger JE, Winn HR, Young W (1998) Methylprednisolone or tirilazad mesylate administration after acute spinal cord injury: 1-year follow up. Results of the third National Acute Spinal Cord Injury randomized controlled trial. J Neurosurg 89:699–706
Otani K, Abe H, Kadoya S et al (1994) Beneficial effect of methylprednisolone sodium succinate in the treatment of acute spinal cord injury. Sekitsui Sekizui Janaru 7:633–647
George ER, Scholten DJ, Buechler CM, Jordan-Tibbs J, Mattice C, Albrecht RM (1995) Failure of methylprednisolone to improve the outcome of spinal cord injuries. Am Surg 61:659–663, discussion 663–4
Gerhart DZ, Leino RL, Borson ND, Taylor WE, Gronlund KM, McCall AL, Drewes LR (1995) Localization of glucose transporter GLUT 3 in brain: comparison of rodent and dog using species-specific carboxyl-terminal antisera. Neuroscience 66:237–246
Kiwerski JE (1993) Application of dexamethasone in the treatment of acute spinal cord injury. Injury 24:457–460
Poynton AR, O’Farrell DA, Shannon F, Murray P, McManus F, Walsh MG (1997) An evaluation of the factors affecting neurological recovery following spinal cord injury. Injury 28:545–548
Prendergast MR, Saxe JM, Ledgerwood AM, Lucas CE, Lucas WF (1994) Massive steroids do not reduce the zone of injury after penetrating spinal cord injury. J Trauma 37:576–579, discussion 579–580
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Mortazavi, M.M., Verma, K., Deep, A. et al. Chemical priming for spinal cord injury: a review of the literature part II—potential therapeutics. Childs Nerv Syst 27, 1307–1316 (2011). https://doi.org/10.1007/s00381-010-1365-x
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DOI: https://doi.org/10.1007/s00381-010-1365-x