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Habilitation Improves Mouse Gait Development Following Neonatal Brain Injury
OBJECTIVES: Neonatal brain injury during gait development disrupts neural circuits and causes permanent gait dysfunction. Rehabilitation as an intervention to improve impaired gait function has been used in adults as a treatment for stroke and spinal cord injury. However, although neonates have grea...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JARM
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706041/ https://www.ncbi.nlm.nih.gov/pubmed/36479304 http://dx.doi.org/10.2490/prm.20220061 |
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author | Tsuboi, Yoshiaki Ito, Akira Otsuka, Takanobu Murakami, Hideki Sawada, Masato Sawamoto, Kazunobu |
author_facet | Tsuboi, Yoshiaki Ito, Akira Otsuka, Takanobu Murakami, Hideki Sawada, Masato Sawamoto, Kazunobu |
author_sort | Tsuboi, Yoshiaki |
collection | PubMed |
description | OBJECTIVES: Neonatal brain injury during gait development disrupts neural circuits and causes permanent gait dysfunction. Rehabilitation as an intervention to improve impaired gait function has been used in adults as a treatment for stroke and spinal cord injury. However, although neonates have greater neuroplasticity and regenerative capacity than adults, normal gait development and the effects of habilitation on gait function following neonatal brain injury are largely unknown. METHODS: In this study, we generated cryogenic injury in mice at postnatal day 2 and subsequently performed habilitative training to promote autonomous limb movement for 4 weeks. We also quantitatively analyzed the gait acquisition process in developing mice using the Catwalk XT system. RESULTS: Using quantitative gait analyses, we showed that during normal gait development in mice, stance phase function matures later than swing phase function. We also demonstrated that habilitation in which active limb movements were enhanced by suspending mice with a rubber band with no floor grounding promotes motor learning, including gait function, in mice with impaired acquisition of gait function resulting from neonatal brain injury. CONCLUSIONS: Our findings provide a basis for research on gait development in mice and suggest new habilitation strategies for patients with impaired gait development caused by perinatal brain diseases such as hypoxic–ischemic encephalopathy and periventricular leukomalacia. |
format | Online Article Text |
id | pubmed-9706041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | JARM |
record_format | MEDLINE/PubMed |
spelling | pubmed-97060412022-12-06 Habilitation Improves Mouse Gait Development Following Neonatal Brain Injury Tsuboi, Yoshiaki Ito, Akira Otsuka, Takanobu Murakami, Hideki Sawada, Masato Sawamoto, Kazunobu Prog Rehabil Med Original Article OBJECTIVES: Neonatal brain injury during gait development disrupts neural circuits and causes permanent gait dysfunction. Rehabilitation as an intervention to improve impaired gait function has been used in adults as a treatment for stroke and spinal cord injury. However, although neonates have greater neuroplasticity and regenerative capacity than adults, normal gait development and the effects of habilitation on gait function following neonatal brain injury are largely unknown. METHODS: In this study, we generated cryogenic injury in mice at postnatal day 2 and subsequently performed habilitative training to promote autonomous limb movement for 4 weeks. We also quantitatively analyzed the gait acquisition process in developing mice using the Catwalk XT system. RESULTS: Using quantitative gait analyses, we showed that during normal gait development in mice, stance phase function matures later than swing phase function. We also demonstrated that habilitation in which active limb movements were enhanced by suspending mice with a rubber band with no floor grounding promotes motor learning, including gait function, in mice with impaired acquisition of gait function resulting from neonatal brain injury. CONCLUSIONS: Our findings provide a basis for research on gait development in mice and suggest new habilitation strategies for patients with impaired gait development caused by perinatal brain diseases such as hypoxic–ischemic encephalopathy and periventricular leukomalacia. JARM 2022-12-01 /pmc/articles/PMC9706041/ /pubmed/36479304 http://dx.doi.org/10.2490/prm.20220061 Text en 2022 The Japanese Association of Rehabilitation Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND) 4.0 License. |
spellingShingle | Original Article Tsuboi, Yoshiaki Ito, Akira Otsuka, Takanobu Murakami, Hideki Sawada, Masato Sawamoto, Kazunobu Habilitation Improves Mouse Gait Development Following Neonatal Brain Injury |
title | Habilitation Improves Mouse Gait Development Following Neonatal Brain
Injury |
title_full | Habilitation Improves Mouse Gait Development Following Neonatal Brain
Injury |
title_fullStr | Habilitation Improves Mouse Gait Development Following Neonatal Brain
Injury |
title_full_unstemmed | Habilitation Improves Mouse Gait Development Following Neonatal Brain
Injury |
title_short | Habilitation Improves Mouse Gait Development Following Neonatal Brain
Injury |
title_sort | habilitation improves mouse gait development following neonatal brain
injury |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706041/ https://www.ncbi.nlm.nih.gov/pubmed/36479304 http://dx.doi.org/10.2490/prm.20220061 |
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