Please use this identifier to cite or link to this item:
https://ir.swu.ac.th/jspui/handle/123456789/13474
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Krityakiarana W. | |
dc.contributor.author | Zhao P.M. | |
dc.contributor.author | Nguyen K. | |
dc.contributor.author | Gomez-Pinilla F. | |
dc.contributor.author | Kotchabhakdi N. | |
dc.contributor.author | De Vellis J. | |
dc.contributor.author | Espinosa-Jeffrey A. | |
dc.date.accessioned | 2021-04-05T03:24:10Z | - |
dc.date.available | 2021-04-05T03:24:10Z | - |
dc.date.issued | 2016 | |
dc.identifier.issn | 3643190 | |
dc.identifier.other | 2-s2.0-84958751578 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/13474 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84958751578&doi=10.1007%2fs11064-016-1850-z&partnerID=40&md5=8d3d558d572c97d4921f430836c45792 | |
dc.description.abstract | Trophic factor treatment has been shown to improve the recovery of brain and spinal cord injury (SCI). In this study, we examined the effects of TSC1 (a combination of insulin-like growth factor 1 and transferrin) 4 and 8 h after SCI at the thoracic segment level (T12) in nestin- GFP transgenic mice. TSC1 treatment for 4 and 8 h increased the number of nestin-expressing cells around the lesion site and prevented Wallerian degeneration. Treatment with TSC1 for 4 h significantly increased heat shock protein (HSP)-32 and HSP-70 expression 1 and 2 mm from lesion site (both, caudal and rostral). Conversely, the number of HSP-32 positive cells decreased after an 8-h TSC1 treatment, although it was still higher than in both, non-treated SCI and intact spinal cord animals. Furthermore, TSC1 increased NG2 expressing cell numbers and preserved most axons intact, facilitating remyelination and repair. These results support our hypothesis that TSC1 is an effective treatment for cell and tissue neuroprotection after SCI. An early intervention is crucial to prevent secondary damage of the injured SC and, in particular, to prevent Wallerian degeneration. © Springer Science+Business Media New York 2016. | |
dc.subject | brain derived neurotrophic factor | |
dc.subject | epidermal growth factor receptor | |
dc.subject | glial cell line derived neurotrophic factor | |
dc.subject | green fluorescent protein | |
dc.subject | heat shock protein 70 | |
dc.subject | heme oxygenase 1 | |
dc.subject | hybrid protein | |
dc.subject | intermediate filament protein | |
dc.subject | nestin | |
dc.subject | recombinant growth factor | |
dc.subject | somatomedin C | |
dc.subject | transferrin | |
dc.subject | TSC1 | |
dc.subject | unclassified drug | |
dc.subject | nestin | |
dc.subject | neuroprotective agent | |
dc.subject | animal cell | |
dc.subject | animal experiment | |
dc.subject | animal model | |
dc.subject | animal tissue | |
dc.subject | Article | |
dc.subject | axon | |
dc.subject | cell count | |
dc.subject | cell regeneration | |
dc.subject | controlled study | |
dc.subject | cytoarchitecture | |
dc.subject | demyelination | |
dc.subject | early intervention | |
dc.subject | gray matter | |
dc.subject | immunohistochemistry | |
dc.subject | mitochondrion | |
dc.subject | motoneuron | |
dc.subject | mouse | |
dc.subject | neural stem cell | |
dc.subject | neuroprotection | |
dc.subject | nonhuman | |
dc.subject | oxidative stress | |
dc.subject | priority journal | |
dc.subject | protein expression | |
dc.subject | protein phosphorylation | |
dc.subject | remyelinization | |
dc.subject | spinal cord | |
dc.subject | spinal cord injury | |
dc.subject | stem cell niche | |
dc.subject | Wallerian degeneration | |
dc.subject | white matter | |
dc.subject | animal | |
dc.subject | metabolism | |
dc.subject | pathophysiology | |
dc.subject | spinal cord injury | |
dc.subject | stem cell | |
dc.subject | transgenic mouse | |
dc.subject | Animals | |
dc.subject | Mice | |
dc.subject | Mice, Transgenic | |
dc.subject | Nestin | |
dc.subject | Neuroprotective Agents | |
dc.subject | Spinal Cord Injuries | |
dc.subject | Stem Cells | |
dc.title | Proof-of concept that an acute trophic factors intervention after spinal cord injury provides an adequate niche for neuroprotection, recruitment of nestin-expressing progenitors and regeneration | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Neurochemical Research. Vol 41, (2016), p.431-449 | |
dc.identifier.doi | 10.1007/s11064-016-1850-z | |
Appears in Collections: | Scopus 1983-2021 |
Files in This Item:
There are no files associated with this item.
Items in SWU repository are protected by copyright, with all rights reserved, unless otherwise indicated.