Neuropathological Differences Between Rats and Mice After Spinal Cord Injury

被引:66
作者
Byrnes, Kimberly R. [1 ]
Fricke, Stanley T. [1 ,2 ]
Faden, Alan I. [1 ]
机构
[1] Georgetown Univ, Med Ctr, Dept Neurosci, Washington, DC 20007 USA
[2] Childrens Natl Med Ctr, Ctr Genet Med, Washington, DC 20010 USA
基金
美国国家卫生研究院;
关键词
blood-spinal cord-barrier; cavitation; lesion volume; MRI; SIGNAL PATTERNS; MRI; BARRIER; RECOVERY; LESION; MOUSE; MODEL; PERMEABILITY; CONTRAST; SERIAL;
D O I
10.1002/jmri.22323
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
100231 [临床病理学]; 100902 [航空航天医学];
摘要
Purpose: To investigate the utility of noninvasive magnetic resonance imaging (MRI) protocols to demonstrate pathological differences between rats and mice after spinal cord injury (SCI). Rats and mice are commonly used to model SCI; however, histology and immunohistochemistry have shown differences in neuropathology between the two species, including cavity formation and scar/inflammatory responses. Materials and Methods: Moderate contusion SCI was performed on adult male rats and mice. At 28 days postinjury, animals underwent T1-weighted (T1W), with or without gadolinium contrast, or T2-weighted (T2W) magnetic resonance imaging (MRI), to be compared with histology at the same timepoint. Results: In both species, all MRI methods demonstrated changes in spinal cord anatomy. Immunohistochemistry indicated that T2W accurately reflected areas of inflammation and glial scar formation in rats and mice. Quantitation of lesion volume by histology and functional performance correlated best with T2W measurements in both species. Gadolinium contrast accurately reflected the blood-spinal cord-barrier permeability in both species, which appeared greater in rats than in mice. Conclusion: These data demonstrate that MRI, with either a T1W or T2W protocol, can effectively distinguish pathological differences between rats and mice.
引用
收藏
页码:836 / 846
页数:11
相关论文
共 43 条
[1]
MASCIS evaluation of open field locomotor scores: Effects of experience and teamwork on reliability [J].
Basso, DM ;
Beattie, MS ;
Bresnahan, JC ;
Anderson, DK ;
Faden, AI ;
Gruner, JA ;
Holford, TR ;
Hsu, CY ;
Noble, LJ ;
Nockels, R ;
Perot, PL ;
Salzman, SK ;
Young, W .
JOURNAL OF NEUROTRAUMA, 1996, 13 (07) :343-359
[2]
A reproducible model of an epidural mass lesion in rodents. Part II: Characterization by in vivo magnetic resonance imaging [J].
Bendszus, M ;
Burger, R ;
Vince, GH ;
Solymosi, L .
JOURNAL OF NEUROSURGERY, 2002, 97 (06) :1419-1423
[3]
Berens SA, 2005, AM J NEURORADIOL, V26, P1612
[4]
In vivo assessment of blood-spinal cord barrier permeability: serial dynamic contrastenhanced MRI of spinal cord injury [J].
Bilgen, M ;
Dogan, B ;
Narayana, PA .
MAGNETIC RESONANCE IMAGING, 2002, 20 (04) :337-341
[5]
Dynamic contrast-enhanced MRI of experimental spinal cord injury: In vivo serial studies [J].
Bilgen, M ;
Abbe, R ;
Narayana, PA .
MAGNETIC RESONANCE IN MEDICINE, 2001, 45 (04) :614-622
[6]
Longitudinal magnetic resonance imaging of spinal cord injury in mouse: changes in signal patterns associated with the inflammatory response [J].
Bilgen, Mehmet ;
Al-Hafez, Baraa ;
Alrefae, Tareq ;
He, Yong-Yu ;
Smimova, Irina V. ;
Aldur, M. Mustafa ;
Festoff, Barry W. .
MAGNETIC RESONANCE IMAGING, 2007, 25 (05) :657-664
[7]
ACUTE SPINAL-CORD INJURY - A STUDY USING PHYSICAL-EXAMINATION AND MAGNETIC-RESONANCE-IMAGING [J].
BONDURANT, FJ ;
COTLER, HB ;
KULKARNI, MV ;
MCARDLE, CB ;
HARRIS, JH .
SPINE, 1990, 15 (03) :161-168
[8]
NEUROANATOMICAL ANALYSIS OF SPINAL-CORD INJURY IN RHESUS-MONKEY (MACACA-MULATTA) [J].
BRESNAHAN, JC ;
KING, JS ;
MARTIN, GF ;
YASHON, D .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1976, 28 (04) :521-542
[9]
Brightman MW, 1995, CURR TOP MICROBIOL, V202, P63
[10]
Cell cycle activation contributes to post-mitotic cell death and secondary damage after spinal cord injury [J].
Byrnes, Kimberly R. ;
Stoica, Bogdan A. ;
Fricke, Stanley ;
Di Giovanni, Simone ;
Faden, Alan I. .
BRAIN, 2007, 130 :2977-2992