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The feasibility of in vivo imaging of infiltrating blood cells for predicting the functional prognosis after spinal cord injury

After a spinal cord injury (SCI), a reliable prediction of the potential functional outcome is essential for determining the optimal treatment strategy. Despite recent advances in the field of neurological assessment, there is still no satisfactory methodology for predicting the functional outcome a...

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Autores principales: Yokota, Kazuya, Saito, Takeyuki, Kobayakawa, Kazu, Kubota, Kensuke, Hara, Masamitsu, Murata, Masaharu, Ohkawa, Yasuyuki, Iwamoto, Yukihide, Okada, Seiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4860707/
https://www.ncbi.nlm.nih.gov/pubmed/27156468
http://dx.doi.org/10.1038/srep25673
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author Yokota, Kazuya
Saito, Takeyuki
Kobayakawa, Kazu
Kubota, Kensuke
Hara, Masamitsu
Murata, Masaharu
Ohkawa, Yasuyuki
Iwamoto, Yukihide
Okada, Seiji
author_facet Yokota, Kazuya
Saito, Takeyuki
Kobayakawa, Kazu
Kubota, Kensuke
Hara, Masamitsu
Murata, Masaharu
Ohkawa, Yasuyuki
Iwamoto, Yukihide
Okada, Seiji
author_sort Yokota, Kazuya
collection PubMed
description After a spinal cord injury (SCI), a reliable prediction of the potential functional outcome is essential for determining the optimal treatment strategy. Despite recent advances in the field of neurological assessment, there is still no satisfactory methodology for predicting the functional outcome after SCI. We herein describe a novel method to predict the functional outcome at 12 hours after SCI using in vivo bioluminescence imaging. We produced three groups of SCI mice with different functional prognoses: 50 kdyn (mild), 70 kdyn (moderate) and 90 kdyn (severe). Only the locomotor function within 24 hours after SCI was unable to predict subsequent functional recovery. However, both the number of infiltrating neutrophils and the bioluminescence signal intensity from infiltrating blood cells were found to correlate with the severity of the injury at 12 hours after SCI. Furthermore, a strong linear relationship was observed among the number of infiltrating neutrophils, the bioluminescence signal intensity, and the severity of the injury. Our findings thus indicate that in vivo bioluminescence imaging is able to accurately predict the long-term functional outcome in the hyperacute phase of SCI, thereby providing evidence that this imaging modality could positively contribute to the future development of tailored therapeutic approaches for SCI.
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spelling pubmed-48607072016-05-20 The feasibility of in vivo imaging of infiltrating blood cells for predicting the functional prognosis after spinal cord injury Yokota, Kazuya Saito, Takeyuki Kobayakawa, Kazu Kubota, Kensuke Hara, Masamitsu Murata, Masaharu Ohkawa, Yasuyuki Iwamoto, Yukihide Okada, Seiji Sci Rep Article After a spinal cord injury (SCI), a reliable prediction of the potential functional outcome is essential for determining the optimal treatment strategy. Despite recent advances in the field of neurological assessment, there is still no satisfactory methodology for predicting the functional outcome after SCI. We herein describe a novel method to predict the functional outcome at 12 hours after SCI using in vivo bioluminescence imaging. We produced three groups of SCI mice with different functional prognoses: 50 kdyn (mild), 70 kdyn (moderate) and 90 kdyn (severe). Only the locomotor function within 24 hours after SCI was unable to predict subsequent functional recovery. However, both the number of infiltrating neutrophils and the bioluminescence signal intensity from infiltrating blood cells were found to correlate with the severity of the injury at 12 hours after SCI. Furthermore, a strong linear relationship was observed among the number of infiltrating neutrophils, the bioluminescence signal intensity, and the severity of the injury. Our findings thus indicate that in vivo bioluminescence imaging is able to accurately predict the long-term functional outcome in the hyperacute phase of SCI, thereby providing evidence that this imaging modality could positively contribute to the future development of tailored therapeutic approaches for SCI. Nature Publishing Group 2016-05-09 /pmc/articles/PMC4860707/ /pubmed/27156468 http://dx.doi.org/10.1038/srep25673 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yokota, Kazuya
Saito, Takeyuki
Kobayakawa, Kazu
Kubota, Kensuke
Hara, Masamitsu
Murata, Masaharu
Ohkawa, Yasuyuki
Iwamoto, Yukihide
Okada, Seiji
The feasibility of in vivo imaging of infiltrating blood cells for predicting the functional prognosis after spinal cord injury
title The feasibility of in vivo imaging of infiltrating blood cells for predicting the functional prognosis after spinal cord injury
title_full The feasibility of in vivo imaging of infiltrating blood cells for predicting the functional prognosis after spinal cord injury
title_fullStr The feasibility of in vivo imaging of infiltrating blood cells for predicting the functional prognosis after spinal cord injury
title_full_unstemmed The feasibility of in vivo imaging of infiltrating blood cells for predicting the functional prognosis after spinal cord injury
title_short The feasibility of in vivo imaging of infiltrating blood cells for predicting the functional prognosis after spinal cord injury
title_sort feasibility of in vivo imaging of infiltrating blood cells for predicting the functional prognosis after spinal cord injury
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4860707/
https://www.ncbi.nlm.nih.gov/pubmed/27156468
http://dx.doi.org/10.1038/srep25673
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