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Time course of recovery of different motor functions following a reproducible cortical infarction in non-human primates

A major challenge in human stroke research is interpatient variability in the extent of sensorimotor deficits and determining the time course of recovery following stroke. Although the relationship between the extent of the lesion and the degree of sensorimotor deficits is well established, the fact...

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Autores principales: Kosugi, Akito, Saga, Yosuke, Kudo, Moeko, Koizumi, Masashi, Umeda, Tatsuya, Seki, Kazuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947718/
https://www.ncbi.nlm.nih.gov/pubmed/36846141
http://dx.doi.org/10.3389/fneur.2023.1094774
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author Kosugi, Akito
Saga, Yosuke
Kudo, Moeko
Koizumi, Masashi
Umeda, Tatsuya
Seki, Kazuhiko
author_facet Kosugi, Akito
Saga, Yosuke
Kudo, Moeko
Koizumi, Masashi
Umeda, Tatsuya
Seki, Kazuhiko
author_sort Kosugi, Akito
collection PubMed
description A major challenge in human stroke research is interpatient variability in the extent of sensorimotor deficits and determining the time course of recovery following stroke. Although the relationship between the extent of the lesion and the degree of sensorimotor deficits is well established, the factors determining the speed of recovery remain uncertain. To test these experimentally, we created a cortical lesion over the motor cortex using a reproducible approach in four common marmosets, and characterized the time course of recovery by systematically applying several behavioral tests before and up to 8 weeks after creation of the lesion. Evaluation of in-cage behavior and reach-to-grasp movement revealed consistent motor impairments across the animals. In particular, performance in reaching and grasping movements continued to deteriorate until 4 weeks after creation of the lesion. We also found consistent time courses of recovery across animals for in-cage and grasping movements. For example, in all animals, the score for in-cage behaviors showed full recovery at 3 weeks after creation of the lesion, and the performance of grasping movement partially recovered from 4 to 8 weeks. In addition, we observed longer time courses of recovery for reaching movement, which may rely more on cortically initiated control in this species. These results suggest that different recovery speeds for each movement could be influenced by what extent the cortical control is required to properly execute each movement.
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spelling pubmed-99477182023-02-24 Time course of recovery of different motor functions following a reproducible cortical infarction in non-human primates Kosugi, Akito Saga, Yosuke Kudo, Moeko Koizumi, Masashi Umeda, Tatsuya Seki, Kazuhiko Front Neurol Neurology A major challenge in human stroke research is interpatient variability in the extent of sensorimotor deficits and determining the time course of recovery following stroke. Although the relationship between the extent of the lesion and the degree of sensorimotor deficits is well established, the factors determining the speed of recovery remain uncertain. To test these experimentally, we created a cortical lesion over the motor cortex using a reproducible approach in four common marmosets, and characterized the time course of recovery by systematically applying several behavioral tests before and up to 8 weeks after creation of the lesion. Evaluation of in-cage behavior and reach-to-grasp movement revealed consistent motor impairments across the animals. In particular, performance in reaching and grasping movements continued to deteriorate until 4 weeks after creation of the lesion. We also found consistent time courses of recovery across animals for in-cage and grasping movements. For example, in all animals, the score for in-cage behaviors showed full recovery at 3 weeks after creation of the lesion, and the performance of grasping movement partially recovered from 4 to 8 weeks. In addition, we observed longer time courses of recovery for reaching movement, which may rely more on cortically initiated control in this species. These results suggest that different recovery speeds for each movement could be influenced by what extent the cortical control is required to properly execute each movement. Frontiers Media S.A. 2023-02-09 /pmc/articles/PMC9947718/ /pubmed/36846141 http://dx.doi.org/10.3389/fneur.2023.1094774 Text en Copyright © 2023 Kosugi, Saga, Kudo, Koizumi, Umeda and Seki. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Kosugi, Akito
Saga, Yosuke
Kudo, Moeko
Koizumi, Masashi
Umeda, Tatsuya
Seki, Kazuhiko
Time course of recovery of different motor functions following a reproducible cortical infarction in non-human primates
title Time course of recovery of different motor functions following a reproducible cortical infarction in non-human primates
title_full Time course of recovery of different motor functions following a reproducible cortical infarction in non-human primates
title_fullStr Time course of recovery of different motor functions following a reproducible cortical infarction in non-human primates
title_full_unstemmed Time course of recovery of different motor functions following a reproducible cortical infarction in non-human primates
title_short Time course of recovery of different motor functions following a reproducible cortical infarction in non-human primates
title_sort time course of recovery of different motor functions following a reproducible cortical infarction in non-human primates
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947718/
https://www.ncbi.nlm.nih.gov/pubmed/36846141
http://dx.doi.org/10.3389/fneur.2023.1094774
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