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Joint-specific changes in locomotor complexity in the absence of muscle atrophy following incomplete spinal cord injury

BACKGROUND: Following incomplete spinal cord injury (iSCI), descending drive is impaired, possibly leading to a decrease in the complexity of gait. To test the hypothesis that iSCI impairs gait coordination and decreases locomotor complexity, we collected 3D joint angle kinematics and muscle paramet...

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Autores principales: Hillen, Brian K, Yamaguchi, Gary T, Abbas, James J, Jung, Ranu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765129/
https://www.ncbi.nlm.nih.gov/pubmed/23947694
http://dx.doi.org/10.1186/1743-0003-10-97
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author Hillen, Brian K
Yamaguchi, Gary T
Abbas, James J
Jung, Ranu
author_facet Hillen, Brian K
Yamaguchi, Gary T
Abbas, James J
Jung, Ranu
author_sort Hillen, Brian K
collection PubMed
description BACKGROUND: Following incomplete spinal cord injury (iSCI), descending drive is impaired, possibly leading to a decrease in the complexity of gait. To test the hypothesis that iSCI impairs gait coordination and decreases locomotor complexity, we collected 3D joint angle kinematics and muscle parameters of rats with a sham or an incomplete spinal cord injury. METHODS: 12 adult, female, Long-Evans rats, 6 sham and 6 mild-moderate T8 iSCI, were tested 4 weeks following injury. The Basso Beattie Bresnahan locomotor score was used to verify injury severity. Animals had reflective markers placed on the bony prominences of their limb joints and were filmed in 3D while walking on a treadmill. Joint angles and segment motion were analyzed quantitatively, and complexity of joint angle trajectory and overall gait were calculated using permutation entropy and principal component analysis, respectively. Following treadmill testing, the animals were euthanized and hindlimb muscles removed. Excised muscles were tested for mass, density, fiber length, pennation angle, and relaxed sarcomere length. RESULTS: Muscle parameters were similar between groups with no evidence of muscle atrophy. The animals showed overextension of the ankle, which was compensated for by a decreased range of motion at the knee. Left-right coordination was altered, leading to left and right knee movements that are entirely out of phase, with one joint moving while the other is stationary. Movement patterns remained symmetric. Permutation entropy measures indicated changes in complexity on a joint specific basis, with the largest changes at the ankle. No significant difference was seen using principal component analysis. Rats were able to achieve stable weight bearing locomotion at reasonable speeds on the treadmill despite these deficiencies. CONCLUSIONS: Decrease in supraspinal control following iSCI causes a loss of complexity of ankle kinematics. This loss can be entirely due to loss of supraspinal control in the absence of muscle atrophy and may be quantified using permutation entropy. Joint-specific differences in kinematic complexity may be attributed to different sources of motor control. This work indicates the importance of the ankle for rehabilitation interventions following spinal cord injury.
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spelling pubmed-37651292013-09-10 Joint-specific changes in locomotor complexity in the absence of muscle atrophy following incomplete spinal cord injury Hillen, Brian K Yamaguchi, Gary T Abbas, James J Jung, Ranu J Neuroeng Rehabil Research BACKGROUND: Following incomplete spinal cord injury (iSCI), descending drive is impaired, possibly leading to a decrease in the complexity of gait. To test the hypothesis that iSCI impairs gait coordination and decreases locomotor complexity, we collected 3D joint angle kinematics and muscle parameters of rats with a sham or an incomplete spinal cord injury. METHODS: 12 adult, female, Long-Evans rats, 6 sham and 6 mild-moderate T8 iSCI, were tested 4 weeks following injury. The Basso Beattie Bresnahan locomotor score was used to verify injury severity. Animals had reflective markers placed on the bony prominences of their limb joints and were filmed in 3D while walking on a treadmill. Joint angles and segment motion were analyzed quantitatively, and complexity of joint angle trajectory and overall gait were calculated using permutation entropy and principal component analysis, respectively. Following treadmill testing, the animals were euthanized and hindlimb muscles removed. Excised muscles were tested for mass, density, fiber length, pennation angle, and relaxed sarcomere length. RESULTS: Muscle parameters were similar between groups with no evidence of muscle atrophy. The animals showed overextension of the ankle, which was compensated for by a decreased range of motion at the knee. Left-right coordination was altered, leading to left and right knee movements that are entirely out of phase, with one joint moving while the other is stationary. Movement patterns remained symmetric. Permutation entropy measures indicated changes in complexity on a joint specific basis, with the largest changes at the ankle. No significant difference was seen using principal component analysis. Rats were able to achieve stable weight bearing locomotion at reasonable speeds on the treadmill despite these deficiencies. CONCLUSIONS: Decrease in supraspinal control following iSCI causes a loss of complexity of ankle kinematics. This loss can be entirely due to loss of supraspinal control in the absence of muscle atrophy and may be quantified using permutation entropy. Joint-specific differences in kinematic complexity may be attributed to different sources of motor control. This work indicates the importance of the ankle for rehabilitation interventions following spinal cord injury. BioMed Central 2013-08-15 /pmc/articles/PMC3765129/ /pubmed/23947694 http://dx.doi.org/10.1186/1743-0003-10-97 Text en Copyright © 2013 Hillen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Hillen, Brian K
Yamaguchi, Gary T
Abbas, James J
Jung, Ranu
Joint-specific changes in locomotor complexity in the absence of muscle atrophy following incomplete spinal cord injury
title Joint-specific changes in locomotor complexity in the absence of muscle atrophy following incomplete spinal cord injury
title_full Joint-specific changes in locomotor complexity in the absence of muscle atrophy following incomplete spinal cord injury
title_fullStr Joint-specific changes in locomotor complexity in the absence of muscle atrophy following incomplete spinal cord injury
title_full_unstemmed Joint-specific changes in locomotor complexity in the absence of muscle atrophy following incomplete spinal cord injury
title_short Joint-specific changes in locomotor complexity in the absence of muscle atrophy following incomplete spinal cord injury
title_sort joint-specific changes in locomotor complexity in the absence of muscle atrophy following incomplete spinal cord injury
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765129/
https://www.ncbi.nlm.nih.gov/pubmed/23947694
http://dx.doi.org/10.1186/1743-0003-10-97
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