Please use this identifier to cite or link to this item: https://doi.org/10.3389/fneur.2011.00019
DC FieldValue
dc.titleLow level primary blast injury in rodent brain
dc.contributor.authorPun, P.B.L.
dc.contributor.authorKan, E.M.
dc.contributor.authorSalim, A.
dc.contributor.authorLi, Z.
dc.contributor.authorNg, K.C.
dc.contributor.authorMoochhala, S.M.
dc.contributor.authorLing, E.-A.
dc.contributor.authorHongTan, M.
dc.contributor.authorLu, J.
dc.date.accessioned2014-11-26T07:45:54Z
dc.date.available2014-11-26T07:45:54Z
dc.date.issued2011
dc.identifier.citationPun, P.B.L.,Kan, E.M.,Salim, A.,Li, Z.,Ng, K.C.,Moochhala, S.M.,Ling, E.-A.,HongTan, M.,Lu, J. (2011). Low level primary blast injury in rodent brain. Frontiers in Neurology APR : -. ScholarBank@NUS Repository. <a href="https://doi.org/10.3389/fneur.2011.00019" target="_blank">https://doi.org/10.3389/fneur.2011.00019</a>
dc.identifier.issn16642295
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/109446
dc.description.abstractThe incidence of blast attacks and resulting traumatic brain injuries has been on the rise in recent years. Primary blast is one of the mechanisms in which the blast wave can cause injury to the brain. The aim of this study was to investigate the effects of a single sub-lethal blast over pressure (BOP) exposure of either 48.9 kPa (7.1 psi) or 77.3 kPa (11.3 psi) to rodents in an open-field setting. Brain tissue from these rats was harvested for microarray and histopathological analyses. Gross histopathology of the brains showed that cortical neurons were "darkened" and shrunken with narrowed vasculature in the cerebral cor-tex day 1 after blast with signs of recovery at day 4 and day 7 after blast. TUNEL-positive cells were predominant in the white matter of the brain at day 1 after blast and double-labeling of brain tissue showed that these DNA-damaged cells were both oligodendrocytes and astrocytes but were mainly not apoptotic due to the low caspase-3 immunopositivity. There was also an increase in amyloid precursor protein immunoreactive cells in the white matter which suggests acute axonal damage. In contrast, Iba-1 staining for macrophages or microglia was not different from control post-blast. Blast exposure altered the expres-sion of over 5786 genes in the brain which occurred mostly at day 1 and day 4 post-blast. These genes were narrowed down to 10 overlapping genes after time-course evaluation and functional analyses. These genes pointed toward signs of repair at day 4 and day 7 post-blast. Our findings suggest that the BOP levels in the study resulted in mild cellu-lar injury to the brain as evidenced by acute neuronal, cerebrovascular, and white matter perturbations that showed signs of resolution. It is unclear whether these perturbations exist at a milder level or normalize completely and will need more investigation. Specific changes in gene expression may be further evaluated to understand the mechanism of blast-induced neurotrauma. © 2011 Pun, Kan, Salim, Li, Ng, Moochhala, Ling, Tan and Lu.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.3389/fneur.2011.00019
dc.sourceScopus
dc.subjectCentral nervous system
dc.subjectGene expression
dc.subjectHistopathology
dc.subjectImmunohistochemistry
dc.subjectPrimary blast injury
dc.typeArticle
dc.contributor.departmentEPIDEMIOLOGY & PUBLIC HEALTH
dc.description.doi10.3389/fneur.2011.00019
dc.description.sourcetitleFrontiers in Neurology
dc.description.volumeAPR
dc.description.page-
dc.identifier.isiutNOT_IN_WOS
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.