Literature DB >> 12614586

Physical size does not determine the unique histopathological response seen in the injured mouse spinal cord.

Denise M Inman1, Oswald Steward.   

Abstract

Mice display a wound healing process after spinal cord injury that has not been seen in any other species. Rather than exhibiting progressive necrosis and cavitation at the injury site, the mouse lesion site fills in with connective tissue. The connective tissue matrix then undergoes a remodeling in which it contracts, drawing the two ends of the injured spinal cord closer together. One possible explanation for this unique wound healing response is that the spinal cord is much smaller in mice than in rats or other species that have been analyzed. To evaluate this possibility, we compared the histopathological response to spinal cord injury in mice, hamsters (in which the spinal cord is similar in size to that in mice), and rats. Crush injuries were produced at T9, and lesion area and cavitation were assessed using quantitative morphometry at 1, 3, and 8 weeks post-injury. Both hamsters and rats exhibited large lesions and areas of cavitation that increased from 1 to 3 weeks and then stabilized. In mice, the lesion site contained compact meshworks of cells and connective tissue that decreased in size over time. In rats, the cavities contained substantial degeneration debris, whereas in hamsters, cavities were fluid-filled cysts with minimal debris. Hamsters had the largest lesions relative to the cross-sectional area of the spinal cord, despite having a spinal cord similar in size to the mouse. These results indicate that the physical size of the spinal cord does not determine the unique histopathological responses after spinal cord injury in mice.

Entities:  

Mesh:

Year:  2003        PMID: 12614586     DOI: 10.1089/08977150360517164

Source DB:  PubMed          Journal:  J Neurotrauma        ISSN: 0897-7151            Impact factor:   5.269


  17 in total

1.  Schwann cell coculture improves the therapeutic effect of bone marrow stromal cells on recovery in spinal cord-injured mice.

Authors:  Xiaoyun Xu; Nicole Geremia; Feng Bao; Anna Pniak; Melissa Rossoni; Arthur Brown
Journal:  Cell Transplant       Date:  2010-11-19       Impact factor: 4.064

2.  Batroxobin protects against spinal cord injury in rats by promoting the expression of vascular endothelial growth factor to reduce apoptosis.

Authors:  Hui Yu; Bin Lin; Yongzhi He; Wenbin Zhang; Yang Xu
Journal:  Exp Ther Med       Date:  2015-03-17       Impact factor: 2.447

3.  Neuropathological differences between rats and mice after spinal cord injury.

Authors:  Kimberly R Byrnes; Stanley T Fricke; Alan I Faden
Journal:  J Magn Reson Imaging       Date:  2010-10       Impact factor: 4.813

4.  Chronic spinal cord injury impairs primary antibody responses but spares existing humoral immunity in mice.

Authors:  Michael A Oropallo; Katherine S Held; Radhika Goenka; Sifat A Ahmad; Patrick J O'Neill; Oswald Steward; Thomas E Lane; Michael P Cancro
Journal:  J Immunol       Date:  2012-04-20       Impact factor: 5.422

5.  Axonal thinning and extensive remyelination without chronic demyelination in spinal injured rats.

Authors:  Berit E Powers; Jurate Lasiene; Jason R Plemel; Larry Shupe; Steve I Perlmutter; Wolfram Tetzlaff; Philip J Horner
Journal:  J Neurosci       Date:  2012-04-11       Impact factor: 6.167

Review 6.  Translational spinal cord injury research: preclinical guidelines and challenges.

Authors:  Paul J Reier; Michael A Lane; Edward D Hall; Y D Teng; Dena R Howland
Journal:  Handb Clin Neurol       Date:  2012

Review 7.  The glial scar in spinal cord injury and repair.

Authors:  Yi-Min Yuan; Cheng He
Journal:  Neurosci Bull       Date:  2013-07-16       Impact factor: 5.203

Review 8.  Translational Challenges of Rat Models of Upper Extremity Dysfunction After Spinal Cord Injury.

Authors:  Laura Krisa; Madeline Runyen; Megan Ryan Detloff
Journal:  Top Spinal Cord Inj Rehabil       Date:  2018

Review 9.  Aquaporins in spinal cord injury: the janus face of aquaporin 4.

Authors:  O Nesic; J D Guest; D Zivadinovic; P A Narayana; J J Herrera; R J Grill; V U L Mokkapati; B B Gelman; J Lee
Journal:  Neuroscience       Date:  2010-01-28       Impact factor: 3.590

10.  Evaluating regional blood spinal cord barrier dysfunction following spinal cord injury using longitudinal dynamic contrast-enhanced MRI.

Authors:  Ilkan Tatar; Peter Cheng-te Chou; Mohamed Mokhtar Desouki; Hanaa El Sayed; Mehmet Bilgen
Journal:  BMC Med Imaging       Date:  2009-06-11       Impact factor: 1.930

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