Correlation Between Neurological Deficits and Spinal Cord Pathological Changes in a Mouse Model of Multiple Sclerosis

被引:0
|
作者
Zarandi, Faegheh Baha'addini Beigi [1 ]
Geramizadeh, Bita [2 ]
Farjam, Mojtaba [3 ]
Farjadian, Shirin [4 ]
Alizadeh, Ali [5 ]
机构
[1] Shiraz Univ Med Sci, Sch Med, Dept Pharmacol, Shiraz, Iran
[2] Shiraz Univ Med Sci, Transplant Res Ctr, Dept Pathol, Shiraz, Iran
[3] Fasa Univ Med Sci, Noncommunicable Dis Res Ctr, Fasa, Iran
[4] Shiraz Univ Med Sci, Dept Immunol, Sch Med, Shiraz, Iran
[5] Shiraz Univ Med Sci, Dept Tissue Engn, Sch Adv Sci & Technol, Shiraz, Iran
来源
IRANIAN JOURNAL OF SCIENCE AND TECHNOLOGY TRANSACTION A-SCIENCE | 2017年 / 41卷 / A4期
关键词
Multiple sclerosis; Experimental autoimmune encephalomyelitis; Spinal cord; Pathological changes; Correlation; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; INTERFERON-BETA; NEURODEGENERATION; INFLAMMATION; TARGETS;
D O I
10.1007/s40995-017-0256-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multiple sclerosis (MS) is a common neuroin-flammatory disease causing a wide spectrum of clinical signs and symptoms. Neuropathological changes in MS including inflammation, demyelination and axonal degeneration are seen in the animal counterpart of MS, experimental autoimmune encephalomyelitis (EAE) and are biomarkers to follow the pathophysiology and any pharmacology of MS in experimental studies. To elucidate the pattern of these pathological abnormalities in EAE, different aspects of pathological findings and their correlations were studied in the model. EAE induction was done using myelin oligodendrocyte glycoprotein (MOG) 35-55 in C57BL/6 mice and hematoxylin and eosin, Luxol-fast-blue and Bielschowsky staining were used for histopatho-logical evaluation in the lumbar, thoracic and cervical spinal cord. There were significant positive correlations between neurological disease score in EAE mice and each of these pathological findings: inflammation score, demyelination score and axonal degeneration. These correlations were observed regardless of the anatomic regions studied. Inflammation and demyelination scores were significantly associated. Degeneration and demyelination scores were correlated positively also. However, no statistically significant correlation was found between scores of inflammation and degeneration in neither of the three anatomical regions of the spinal cords of EAE mice. This study optimizes the EAE model regarding pathological findings in correlation with neurological deficits in the model. The results will help in better utility of the model in MS research.
引用
收藏
页码:867 / 871
页数:5
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