Literature DB >> 10912915

Spinal cord compression injury in the mouse: presentation of a model including assessment of motor dysfunction.

M Farooque1.   

Abstract

The purpose of this study was to develop a spinal cord injury model in the mouse. Various degrees of extradural compression were used to induce mild, moderate or severe compression injuries. Furthermore, a locomotor rating scale was developed by which the functional outcome of the spinal cord injury could be assessed. The introduction of such a model will be useful for further studies on the pathogenesis and treatment strategies of spinal cord injury. To assess hindlimb motor function, a 10-point scale was used. Initially, the animals were allowed to move freely in an open field and were rated 0-5, 0 being no movement and 5 being almost normal. Animals scoring a 5 were then assessed using steel bars with decreasing widths from 2 cm to 5 mm. For each bar successfully crossed over, they gained additional points. Before injury the hindlimb motor function score (MFS) in all the animals was 10. In mice with mild compression, MFS was decreased slightly on day 1 and recovered to 9 +/- 0.6 on day 14. For mice with moderate compression, the MFS decreased to 4.6 +/- 0.4 on day 1 after injury and gradually improved to 8.1 +/- 0.6 on day 14. Severe injury resulted in paraplegia of the hindlimbs day 1 after injury with a score of 0.6 +/- 0.2. By day 14 after injury, these animals gradually recovered to 3.9 +/- 0.1, could bear the weight on the hindlimbs and walk with a severe deficit. There was a 3%, 9% and 19% decrease in the total cross-sectional area of the spinal cord 14 days after mild, moderate and severe injury, respectively. Microtubule-associated protein immunostaining revealed that the gray matter decreased to 61 +/- 7% in moderately injured animals, while severe compression resulted in a complete loss of gray matter. White matter decreased to 86 +/- 6% in moderately injured animals and 29 +/- 11% in severely injured animals. This study shows that the mouse can be used to achieve reproducible spinal cord compression injuries of various degrees of severity. The force of the impact correlates well with the neurological and light microscopic outcome. The motor function test presented in this paper and the computerized quantification of tissue damage can be used to evaluate the efficacy of different treatment strategies.

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Year:  2000        PMID: 10912915     DOI: 10.1007/s004010051187

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  13 in total

1.  Activation of STAT1 in neurons following spinal cord injury in mice.

Authors:  Koji Osuka; Yasuo Watanabe; Nobuteru Usuda; Kimie Atsuzawa; Muneyoshi Yasuda; Chihiro Aoshima; Toshihiko Wakabayashi; Masakazu Takayasu
Journal:  Neurochem Res       Date:  2011-07-22       Impact factor: 3.996

2.  Transplantation of neural stem cells clonally derived from embryonic stem cells promotes recovery after murine spinal cord injury.

Authors:  Ryan P Salewski; Robert A Mitchell; Carl Shen; Michael G Fehlings
Journal:  Stem Cells Dev       Date:  2015-01-01       Impact factor: 3.272

3.  Early response of endogenous adult neural progenitor cells to acute spinal cord injury in mice.

Authors:  Yan Ke; Liying Chi; Renshi Xu; Chun Luo; David Gozal; Rugao Liu
Journal:  Stem Cells       Date:  2005-12-08       Impact factor: 6.277

4.  Gait analysis in normal and spinal contused mice using the TreadScan system.

Authors:  Jason E Beare; Johnny R Morehouse; William H DeVries; Gaby U Enzmann; Darlene A Burke; David S K Magnuson; Scott R Whittemore
Journal:  J Neurotrauma       Date:  2009-11       Impact factor: 5.269

5.  Treadmill locomotion in the intact and spinal mouse.

Authors:  Hugues Leblond; Marion L'Esperance; Didier Orsal; Serge Rossignol
Journal:  J Neurosci       Date:  2003-12-10       Impact factor: 6.167

6.  Erythropoietin mediates tissue protection through an erythropoietin and common beta-subunit heteroreceptor.

Authors:  Michael Brines; Giovanni Grasso; Fabio Fiordaliso; Alessandra Sfacteria; Pietro Ghezzi; Maddalena Fratelli; Roberto Latini; Qiao-Wen Xie; John Smart; Chiao-Ju Su-Rick; Eileen Pobre; Deborah Diaz; Daniel Gomez; Carla Hand; Thomas Coleman; Anthony Cerami
Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-29       Impact factor: 11.205

7.  Anatomical and functional outcomes following a precise, graded, dorsal laceration spinal cord injury in C57BL/6 mice.

Authors:  Rachel L Hill; Yi Ping Zhang; Darlene A Burke; William H Devries; Yongjie Zhang; David S K Magnuson; Scott R Whittemore; Christopher B Shields
Journal:  J Neurotrauma       Date:  2009-01       Impact factor: 5.269

8.  Chronic pain following spinal cord injury: Current approaches to cellular and molecular mechanisms.

Authors:  Jessica R Yasko; Richard E Mains
Journal:  Trends Cell Mol Biol       Date:  2018

9.  Investigation of anti-oxidative stress in vitro and water apparent diffusion coefficient in MRI on rat after spinal cord injury in vivo with Tithonia diversifolia ethanolic extracts treatment.

Authors:  Chi-Long Juang; Fei Shish Yang; Ming Shuang Hsieh; Hu-Yi Tseng; Su-Chiu Chen; Hsiao-Chuan Wen
Journal:  BMC Complement Altern Med       Date:  2014-11-18       Impact factor: 3.659

10.  G-1 exerts neuroprotective effects through G protein-coupled estrogen receptor 1 following spinal cord injury in mice.

Authors:  Qiang Cheng; Jia Meng; Xin-Shang Wang; Wen-Bo Kang; Zhen Tian; Kun Zhang; Gang Liu; Jian-Ning Zhao
Journal:  Biosci Rep       Date:  2016-08-31       Impact factor: 3.840

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