Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13474
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dc.contributor.authorKrityakiarana W.
dc.contributor.authorZhao P.M.
dc.contributor.authorNguyen K.
dc.contributor.authorGomez-Pinilla F.
dc.contributor.authorKotchabhakdi N.
dc.contributor.authorDe Vellis J.
dc.contributor.authorEspinosa-Jeffrey A.
dc.date.accessioned2021-04-05T03:24:10Z-
dc.date.available2021-04-05T03:24:10Z-
dc.date.issued2016
dc.identifier.issn3643190
dc.identifier.other2-s2.0-84958751578
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13474-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84958751578&doi=10.1007%2fs11064-016-1850-z&partnerID=40&md5=8d3d558d572c97d4921f430836c45792
dc.description.abstractTrophic 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.subjectbrain derived neurotrophic factor
dc.subjectepidermal growth factor receptor
dc.subjectglial cell line derived neurotrophic factor
dc.subjectgreen fluorescent protein
dc.subjectheat shock protein 70
dc.subjectheme oxygenase 1
dc.subjecthybrid protein
dc.subjectintermediate filament protein
dc.subjectnestin
dc.subjectrecombinant growth factor
dc.subjectsomatomedin C
dc.subjecttransferrin
dc.subjectTSC1
dc.subjectunclassified drug
dc.subjectnestin
dc.subjectneuroprotective agent
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectaxon
dc.subjectcell count
dc.subjectcell regeneration
dc.subjectcontrolled study
dc.subjectcytoarchitecture
dc.subjectdemyelination
dc.subjectearly intervention
dc.subjectgray matter
dc.subjectimmunohistochemistry
dc.subjectmitochondrion
dc.subjectmotoneuron
dc.subjectmouse
dc.subjectneural stem cell
dc.subjectneuroprotection
dc.subjectnonhuman
dc.subjectoxidative stress
dc.subjectpriority journal
dc.subjectprotein expression
dc.subjectprotein phosphorylation
dc.subjectremyelinization
dc.subjectspinal cord
dc.subjectspinal cord injury
dc.subjectstem cell niche
dc.subjectWallerian degeneration
dc.subjectwhite matter
dc.subjectanimal
dc.subjectmetabolism
dc.subjectpathophysiology
dc.subjectspinal cord injury
dc.subjectstem cell
dc.subjecttransgenic mouse
dc.subjectAnimals
dc.subjectMice
dc.subjectMice, Transgenic
dc.subjectNestin
dc.subjectNeuroprotective Agents
dc.subjectSpinal Cord Injuries
dc.subjectStem Cells
dc.titleProof-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.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationNeurochemical Research. Vol 41, (2016), p.431-449
dc.identifier.doi10.1007/s11064-016-1850-z
Appears in Collections:Scopus 1983-2021

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