Publication:
Augmented locomotor recovery after spinal cord injury in the athymic nude rat

dc.contributor.author Potas, J en_US
dc.contributor.author Zheng, Yu en_US
dc.contributor.author Moussa, C en_US
dc.contributor.author Venn, Melinda en_US
dc.contributor.author Gorrie, Catherine en_US
dc.contributor.author Deng, C en_US
dc.contributor.author Waite, Phil en_US
dc.date.accessioned 2021-11-25T12:54:10Z
dc.date.available 2021-11-25T12:54:10Z
dc.date.issued 2006 en_US
dc.description.abstract The immune response contributes to ongoing secondary tissue destruction following spinal cord injury (SCI). Although infiltrating neutrophils and monocytes have been well studied in this process, T-cells have received less attention. The objective of this study was to assess locomotor recovery and tissue morphology after SCI in athymic (nude) rats, in which T-cell numbers are reduced. Results in athymic rats were compared with heterozygote littermates with normal T-cell profiles and with Sprague-Dawley rats from previous studies in our lab. Following transection of rat spinal cords at T10, we assessed the animals` locomotor recovery on a weekly basis for up to 11 weeks, using the Basso-Beattie-Bresnahan locomotor rating scale. Nude rats showed better locomotor recovery than did heterozygote or Sprague-Dawley rats, achieving scores of 5.6 +/- 0.8 versus 1.0 +/- 0.0, respectively (p = 0.002), at 4 weeks postinjury. The improved recovery of nude rats persisted for the 11-week postinjury assessment period, and was consistent with improved spinal reflexes rather than with recovery of descending motor pathways. Anatomical evaluation at 11 weeks indicated no difference in nude versus heterozygote rats in the size or distribution of cavities caudal to the transection site, but secondary damage was more severe rostral to the transection site in heterozygote rats. In neither group did cavities extend beyond 4 mm caudal to the transection site, and were therefore not directly responsible for the functional differences between the two groups. Cellular expression of the microglia/macrophage antigen ectodysplasin A (ED1) was reduced in nude rats as compared to heterozygotes, but no difference was observed in expression levels of 5-hydroxytryptamine, the 200-kDa neurofilament, or glial fibrillary acidic protein. The findings of the study show that a reduction in T-cell numbers significantly improves locomotor recovery after spinal cord transection, indicating a deleterious role fo en_US
dc.identifier.issn 0897-7151 en_US
dc.identifier.uri http://hdl.handle.net/1959.4/38497
dc.language English
dc.language.iso EN en_US
dc.rights CC BY-NC-ND 3.0 en_US
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/3.0/au/ en_US
dc.source Legacy MARC en_US
dc.subject.other BBB score en_US
dc.subject.other cavity en_US
dc.subject.other ED1 en_US
dc.subject.other immune system en_US
dc.subject.other macrophages en_US
dc.subject.other secondary injury en_US
dc.subject.other T-cell deficient en_US
dc.title Augmented locomotor recovery after spinal cord injury in the athymic nude rat en_US
dc.type Journal Article en
dcterms.accessRights metadata only access
dspace.entity.type Publication en_US
unsw.accessRights.uri http://purl.org/coar/access_right/c_14cb
unsw.identifier.doiPublisher http://dx.doi.org/10.1089/neu.2006.23.660 en_US
unsw.relation.faculty Medicine & Health
unsw.relation.ispartofissue 5 en_US
unsw.relation.ispartofjournal Journal of Neurotrauma en_US
unsw.relation.ispartofpagefrompageto 660-673 en_US
unsw.relation.ispartofvolume 23 en_US
unsw.relation.originalPublicationAffiliation Potas, J en_US
unsw.relation.originalPublicationAffiliation Zheng, Yu, Faculty of Medicine, UNSW en_US
unsw.relation.originalPublicationAffiliation Moussa, C en_US
unsw.relation.originalPublicationAffiliation Venn, Melinda, Faculty of Medicine, UNSW en_US
unsw.relation.originalPublicationAffiliation Gorrie, Catherine, Faculty of Medicine, UNSW en_US
unsw.relation.originalPublicationAffiliation Deng, C en_US
unsw.relation.originalPublicationAffiliation Waite, Phil, Faculty of Medicine, UNSW en_US
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