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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...

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Autores principales: Tsuboi, Yoshiaki, Ito, Akira, Otsuka, Takanobu, Murakami, Hideki, Sawada, Masato, Sawamoto, Kazunobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JARM 2022
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.
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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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