CC BY-NC-ND 4.0 · Journal of Morphological Sciences 2017; 34(04): 241-246
DOI: 10.4322/jms.111117
Original Article
Thieme Revinter Publicações Ltda Rio de Janeiro, Brazil

Evaluation of changes in the locomotion and histology of sciatic nerve following experimental autoimmune encephalomyelitis

S. M. W. Chang
1   Department of Anatomy, School of Medicine, Taylor's University, Subang Jaya 47500, Selangor, Malaysia
,
S. X. Wai
1   Department of Anatomy, School of Medicine, Taylor's University, Subang Jaya 47500, Selangor, Malaysia
,
P. Y. Chin
1   Department of Anatomy, School of Medicine, Taylor's University, Subang Jaya 47500, Selangor, Malaysia
,
J. T. Lim
1   Department of Anatomy, School of Medicine, Taylor's University, Subang Jaya 47500, Selangor, Malaysia
,
N. K. Mitra
2   Department of Human Biology, School of Medicine, International Medical University, Bukit Jalil 57000, Kuala Lumpur, Malaysia
› Author Affiliations
Further Information

Publication History

27 February 2017

07 November 2017

Publication Date:
18 October 2018 (online)

Abstract

Introduction: Involvement of peripheral nerves in the experimental model of multiple sclerosis (MS) is rarely observed. The objective of this study was to investigate the changes in the locomotion in a mouse model of experimental autoimmune encephalomyelitis (EAE) and correlate with histological changes, if any, in the sections of sciatic nerve and lumbar part of spinal cord. Material and Methods: C57BL/6 mice (10 weeks, n = 8) were immunized with single subcutaneous injection of 300 μg of MOG35-55 and 200 μL of complete Freund's adjuvant (CFA) to produce EAE models. Limp tail with weakness of hindlimb was observed on day 10 and improvement in the weakness was observed on day 20 onwards. Footprint analysis was done to evaluate the impairment in the locomotion on day 0, 5, 10, 15 and 20 of the experiment. Results: One way repeated measure ANOVA found significant reduction in the mean hindlimb stride length on day 10 and 15 (left) and on day 15 and day 20 (right) when compared to mean stride length in day 0 (p<0.05). Histological analysis showed evidence of macrophage infiltration around the dilated blood vessels in the epineurium of sciatic nerve and evidence of damage in the myelinated white matter of lateral funiculus of the lumbar sections of the spinal cord in EAE mice. Conclusion: It is concluded that in mouse model of EAE, the impairment oflocomotion due to damage in the lumbar part of spinal cord can be associated with inflammatory changes in the sciatic nerve.