References
- Balentine JD : Pathology of experimental spinal cord trauma. I. The necrotic lesion as a function of vascular injury. Lab Invest 39 : 236-253, 1978
- Balentine JD : Pathology of experimental spinal cord trauma. II. Ultrastructure of axons and myelin. Lab Invest 39 : 254-266, 1978
- Basso DM, Beattie MS, Bresnahan JC : Graded histological and locomotor outcomes after spinal cord contusion using the NYU weight-drop device versus transection. Exp Neurol 139 : 244-256, 1996 https://doi.org/10.1006/exnr.1996.0098
- Brederlau A, Correia AS, Anisimov SV, Elmi M, Paul G, Roybon L, et al. : Transplantation of human embryonic stem cell-derived cells to a rat model of Parkinson's disease : effect of in vitro differentiation on graft survival and teratoma formation. Stem Cells 24 : 1433-1440, 2006 https://doi.org/10.1634/stemcells.2005-0393
- Brustle O, Jones KN, Learish RD, Karram K, Choudhary K, Wiestler OD, et al. : Embryonic stem cell-derived glial precursors : a source of myelinating transplants. Science 285 : 754-756, 1999 https://doi.org/10.1126/science.285.5428.754
- Bug G, Gül H, Schwarz K, Pfeifer H, Kampfmann M, Zheng X, et al. : Valproic acid stimulates proliferation and self-renewal of hematopoietic stem cells. Cancer Res 65 : 2537-2541, 2005 https://doi.org/10.1158/0008-5472.CAN-04-3011
- Chen PS, Peng GS, Li G, Yang S, Wu X, Wang CC, et al. : Valproate protects dopaminergic neurons in midbrain neuron/glia cultures by stimulating the release of neurotrophic factors from astrocytes. Mol Psychiatry 11 : 1116-1125, 2006 https://doi.org/10.1038/sj.mp.4001893
- Chuang DM, Leng Y, Marinova Z, Kim HJ, Chiu CT : Multiple roles of HDAC inhibition in neurodegenerative conditions. Trends Neurosci 32 : 591-601, 2009 https://doi.org/10.1016/j.tins.2009.06.002
- Dash PK, Orsi SA, Zhang M, Grill RJ, Pati S, Zhao J, et al. : Valproate administered after traumatic brain injury provides neuroprotection and improves cognitive function in rats. PLoS One 5 : e11383, 2010 https://doi.org/10.1371/journal.pone.0011383
- Feng HL, Leng Y, Ma CH, Zhang J, Ren M, Chuang DM : Combined lithium and valproate treatment delays disease onset, reduces neurologionic cal deficits and prolongs survival in an amyotrophic lateral sclerosis mouse model. Neuroscience 155 : 567-572, 2008 https://doi.org/10.1016/j.neuroscience.2008.06.040
- Gage FH, Coates PW, Palmer TD, Kuhn HG, Fisher LJ, Suhonen JO, et al. : Survival and differentiation of adult neuronal progenitor cells transplanted to the adult brain. Proc Natl Acad Sci U S A 92 : 11879-11883, 1995 https://doi.org/10.1073/pnas.92.25.11879
-
Go HS, Kim KC, Choi CS, Jeon SJ, Kwon KJ, Han SH, et al. : Prenatal exposure to valproic acid increases the neural progenitor cell pool and induces macrocephaly in rat brain via a mechanism involving the GSK-
$3{\beta}/{\beta}$ -catenin pathway. Neuropharmacology 63 : 1028-1041, 2012 https://doi.org/10.1016/j.neuropharm.2012.07.028 - Gorio A, Gokmen N, Erbayraktar S, Yilmaz O, Madaschi L, Cichetti C, et al. : Recombinant human erythropoietin counteracts secondary injury and markedly enhances neurological recovery from experimental spinal cord trauma. Proc Natl Acad Sci U S A 99 : 9450-9455, 2002 https://doi.org/10.1073/pnas.142287899
- Imitola J, Raddassi K, Park KI, Mueller FJ, Nieto M, Teng YD, et al. : Directed migration of neural stem cells to sites of CNS injury by the stromal cell-derived factor 1alpha/CXC chemokine receptor 4 pathway. Proc Natl Acad Sci U S A 101 : 18117-18122, 2004 https://doi.org/10.1073/pnas.0408258102
- Inoue T, Kawaguchi S, Kurisu K : Spontaneous regeneration of the pyramidal tract after transection in young rats. Neurosci Lett 247 : 151-154, 1998 https://doi.org/10.1016/S0304-3940(98)00297-3
- Iseda T, Nishio T, Kawaguchi S, Yamanoto M, Kawasaki T, Wakisaka S : Spontaneous regeneration of the corticospinal tract after transection in young rats : a key role of reactive astrocytes in making favorable and unfavorable conditions for regeneration. Neuroscience 126 : 365-374, 2004 https://doi.org/10.1016/j.neuroscience.2004.03.056
- Johansson CB, Momma S, Clarke DL, Risling M, Lendahl U, Frisén J : Identification of a neural stem cell in the adult mammalian central nervous system. Cell 96 : 25-34, 1999 https://doi.org/10.1016/S0092-8674(00)80956-3
- Keirstead HS, Nistor G, Bernal G, Totoiu M, Cloutier F, Sharp K, et al. : Human embryonic stem cell-derived oligodendrocyte progenitor cell transplants remyelinate and restore locomotion after spinal cord injury. J Neurosci 25 : 4694-4705, 2005 https://doi.org/10.1523/JNEUROSCI.0311-05.2005
- Kikukawa S, Kawaguchi S, Mizoguchi A, Ide C, Koshinaga M : Regeneration of dorsal column axons after spinal cord injury in young rats. Neurosci Lett 249 : 135-138, 1998 https://doi.org/10.1016/S0304-3940(98)00406-6
- Kim HJ, Rowe M, Ren M, Hong JS, Chen PS, Chuang DM : Histone deacetylase inhibitors exhibit anti-inflammatory and neuroprotective effects in a rat permanent ischemic model of stroke : multiple mechanisms of action. J Pharmacol Exp Ther 321 : 892-901, 2007 https://doi.org/10.1124/jpet.107.120188
- Lee H, Shamy GA, Elkabetz Y, Schofield CM, Harrsion NL, Panagiotakos G, et al. : Directed differentiation and transplantation of human embryonic stem cell-derived motoneurons. Stem Cells 25 : 1931-1939, 2007 https://doi.org/10.1634/stemcells.2007-0097
- Lee HJ, Wu J, Chung J, Wrathall JR : SOX2 expression is upregulated in adult spinal cord after contusion injury in both oligodendrocyte lineage and ependymal cells. J Neurosci Res 91 : 196-210, 2013 https://doi.org/10.1002/jnr.23151
- Lee SM, Yune TY, Kim SJ, Park DW, Lee YK, Kim YC, et al. : Minocycline reduces cell death and improves functional recovery after traumatic spinal cord injury in the rat. J Neurotrauma 20 : 1017-1027, 2003 https://doi.org/10.1089/089771503770195867
- Li S, Strittmatter SM : Delayed systemic Nogo-66 receptor antagonist promotes recovery from spinal cord injury. J Neurosci 23 : 4219-4227, 2003
- Maurer MH, Bromme JO, Feldmann RE Jr, Jarve A, Sabouri F, Bürgers HF, et al. : Glycogen synthase kinase 3beta (GSK3beta) regulates differentiation and proliferation in neural stem cells from the rat subventricular zone. J Proteome Res 6 : 1198-1208, 2007 https://doi.org/10.1021/pr0605825
- Nistor GI, Totoiu MO, Haque N, Carpenter MK, Keirstead HS : Human embryonic stem cells differentiate into oligodendrocytes in high purity and myelinate after spinal cord transplantation. Glia 49 : 385-396, 2005 https://doi.org/10.1002/glia.20127
- Qing H, He G, Ly PT, Fox CJ, Staufenbiel M, Cai F, et al. : Valproic acid inhibits Abeta production, neuritic plaque formation, and behavioral deficits in Alzheimer's disease mouse models. J Exp Med 205 : 2781-2789, 2008 https://doi.org/10.1084/jem.20081588
- Ren M, Leng Y, Jeong M, Leeds PR, Chuang DM : Valproic acid reduces brain damage induced by transient focal cerebral ischemia in rats : potential roles of histone deacetylase inhibition and heat shock protein induction. J Neurochem 89 : 1358-1367, 2004 https://doi.org/10.1111/j.1471-4159.2004.02406.x
- Rowland JW, Hawryluk GW, Kwon B, Fehlings MG : Current status of acute spinal cord injury pathophysiology and emerging therapies : promise on the horizon. Neurosurg Focus 25 : E2, 2008.
- Shibuya S, Miyamoto O, Auer RN, Itano T, Mori S, Norimatsu H : Embryonic intermediate filament, nestin, expression following traumatic spinal cord injury in adult rats. Neuroscience 114 : 905-916, 2002 https://doi.org/10.1016/S0306-4522(02)00323-8
- Sinn DI, Kim SJ, Chu K, Jung KH, Lee ST, Song EC, et al. : Valproic acid-mediated neuroprotection in intracerebral hemorrhage via histone deacetylase inhibition and transcriptional activation. Neurobiol Dis 26 : 464-472, 2007 https://doi.org/10.1016/j.nbd.2007.02.006
- Sugai F, Yamamoto Y, Miyaguchi K, Zhou Z, Sumi H, Hamasaki T, et al. : Benefit of valproic acid in suppressing disease progression of ALS model mice. Eur J Neurosci 20 : 3179-3183, 2004 https://doi.org/10.1111/j.1460-9568.2004.03765.x
- Sumner CJ, Huynh TN, Markowitz JA, Perhac JS, Hill B, Coovert DD, et al. : Valproic acid increases SMN levels in spinal muscular atrophy patient cells. Ann Neurol 54 : 647-654, 2003 https://doi.org/10.1002/ana.10743
- Wang Z, Leng Y, Tsai LK, Leeds P, Chuang DM : Valproic acid attenuates blood-brain barrier disruption in a rat model of transient focal cerebral ischemia : the roles of HDAC and MMP-9 inhibition. J Cereb Blood Flow Metab 31 : 52-57, 2011 https://doi.org/10.1038/jcbfm.2010.195
- Yu SH, Cho DC, Kim KT, Nam KH, Cho HJ, Sung JK : The neuroprotective effect of treatment of valproic Acid in acute spinal cord injury. J Korean Neurosurg Soc 51 : 191-198, 2012 https://doi.org/10.3340/jkns.2012.51.4.191
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