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Sensorimotor plasticity after spinal cord injury: a longitudinal and translational study

OBJECTIVE: The objective was to track and compare the progression of neuroplastic changes in a large animal model and humans with spinal cord injury. METHODS: A total of 37 individuals with acute traumatic spinal cord injury were followed over time (1, 3, 6, and 12 months post‐injury) with repeated...

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Autores principales: Jutzeler, Catherine R., Streijger, Femke, Aguilar, Juan, Shortt, Katelyn, Manouchehri, Neda, Okon, Elena, Hupp, Markus, Curt, Armin, Kwon, Brian K., Kramer, John L. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331953/
https://www.ncbi.nlm.nih.gov/pubmed/30656185
http://dx.doi.org/10.1002/acn3.679
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author Jutzeler, Catherine R.
Streijger, Femke
Aguilar, Juan
Shortt, Katelyn
Manouchehri, Neda
Okon, Elena
Hupp, Markus
Curt, Armin
Kwon, Brian K.
Kramer, John L. K.
author_facet Jutzeler, Catherine R.
Streijger, Femke
Aguilar, Juan
Shortt, Katelyn
Manouchehri, Neda
Okon, Elena
Hupp, Markus
Curt, Armin
Kwon, Brian K.
Kramer, John L. K.
author_sort Jutzeler, Catherine R.
collection PubMed
description OBJECTIVE: The objective was to track and compare the progression of neuroplastic changes in a large animal model and humans with spinal cord injury. METHODS: A total of 37 individuals with acute traumatic spinal cord injury were followed over time (1, 3, 6, and 12 months post‐injury) with repeated neurophysiological assessments. Somatosensory and motor evoked potentials were recorded in the upper extremities above the level of injury. In a reverse‐translational approach, similar neurophysiological techniques were examined in a porcine model of thoracic spinal cord injury. Twelve Yucatan mini‐pigs underwent a contusive spinal cord injury at T10 and tracked with somatosensory and motor evoked potentials assessments in the fore‐ and hind limbs pre‐ (baseline, post‐laminectomy) and post‐injury (10 min, 3 h, 12 weeks). RESULTS: In both humans and pigs, the sensory responses in the cranial coordinates of upper extremities/forelimbs progressively increased from immediately post‐injury to later time points. Motor responses in the forelimbs increased immediately after experimental injury in pigs, remaining elevated at 12 weeks. In humans, motor evoked potentials were significantly higher at 1‐month (and remained so at 1 year) compared to normative values. CONCLUSIONS: Despite notable differences between experimental models and the human condition, the brain's response to spinal cord injury is remarkably similar between humans and pigs. Our findings further underscore the utility of this large animal model in translational spinal cord injury research.
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spelling pubmed-63319532019-01-17 Sensorimotor plasticity after spinal cord injury: a longitudinal and translational study Jutzeler, Catherine R. Streijger, Femke Aguilar, Juan Shortt, Katelyn Manouchehri, Neda Okon, Elena Hupp, Markus Curt, Armin Kwon, Brian K. Kramer, John L. K. Ann Clin Transl Neurol Research Articles OBJECTIVE: The objective was to track and compare the progression of neuroplastic changes in a large animal model and humans with spinal cord injury. METHODS: A total of 37 individuals with acute traumatic spinal cord injury were followed over time (1, 3, 6, and 12 months post‐injury) with repeated neurophysiological assessments. Somatosensory and motor evoked potentials were recorded in the upper extremities above the level of injury. In a reverse‐translational approach, similar neurophysiological techniques were examined in a porcine model of thoracic spinal cord injury. Twelve Yucatan mini‐pigs underwent a contusive spinal cord injury at T10 and tracked with somatosensory and motor evoked potentials assessments in the fore‐ and hind limbs pre‐ (baseline, post‐laminectomy) and post‐injury (10 min, 3 h, 12 weeks). RESULTS: In both humans and pigs, the sensory responses in the cranial coordinates of upper extremities/forelimbs progressively increased from immediately post‐injury to later time points. Motor responses in the forelimbs increased immediately after experimental injury in pigs, remaining elevated at 12 weeks. In humans, motor evoked potentials were significantly higher at 1‐month (and remained so at 1 year) compared to normative values. CONCLUSIONS: Despite notable differences between experimental models and the human condition, the brain's response to spinal cord injury is remarkably similar between humans and pigs. Our findings further underscore the utility of this large animal model in translational spinal cord injury research. John Wiley and Sons Inc. 2018-12-01 /pmc/articles/PMC6331953/ /pubmed/30656185 http://dx.doi.org/10.1002/acn3.679 Text en © 2018 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Jutzeler, Catherine R.
Streijger, Femke
Aguilar, Juan
Shortt, Katelyn
Manouchehri, Neda
Okon, Elena
Hupp, Markus
Curt, Armin
Kwon, Brian K.
Kramer, John L. K.
Sensorimotor plasticity after spinal cord injury: a longitudinal and translational study
title Sensorimotor plasticity after spinal cord injury: a longitudinal and translational study
title_full Sensorimotor plasticity after spinal cord injury: a longitudinal and translational study
title_fullStr Sensorimotor plasticity after spinal cord injury: a longitudinal and translational study
title_full_unstemmed Sensorimotor plasticity after spinal cord injury: a longitudinal and translational study
title_short Sensorimotor plasticity after spinal cord injury: a longitudinal and translational study
title_sort sensorimotor plasticity after spinal cord injury: a longitudinal and translational study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331953/
https://www.ncbi.nlm.nih.gov/pubmed/30656185
http://dx.doi.org/10.1002/acn3.679
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