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Cholecalciferol (Vitamin D(3)) Improves Myelination and Recovery after Nerve Injury
Previously, we demonstrated i) that ergocalciferol (vitamin D(2)) increases axon diameter and potentiates nerve regeneration in a rat model of transected peripheral nerve and ii) that cholecalciferol (vitamin D3) improves breathing and hyper-reflexia in a rat model of paraplegia. However, before bri...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669361/ https://www.ncbi.nlm.nih.gov/pubmed/23741446 http://dx.doi.org/10.1371/journal.pone.0065034 |
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author | Chabas, Jean-Francois Stephan, Delphine Marqueste, Tanguy Garcia, Stephane Lavaut, Marie-Noelle Nguyen, Catherine Legre, Regis Khrestchatisky, Michel Decherchi, Patrick Feron, Francois |
author_facet | Chabas, Jean-Francois Stephan, Delphine Marqueste, Tanguy Garcia, Stephane Lavaut, Marie-Noelle Nguyen, Catherine Legre, Regis Khrestchatisky, Michel Decherchi, Patrick Feron, Francois |
author_sort | Chabas, Jean-Francois |
collection | PubMed |
description | Previously, we demonstrated i) that ergocalciferol (vitamin D(2)) increases axon diameter and potentiates nerve regeneration in a rat model of transected peripheral nerve and ii) that cholecalciferol (vitamin D3) improves breathing and hyper-reflexia in a rat model of paraplegia. However, before bringing this molecule to the clinic, it was of prime importance i) to assess which form – ergocalciferol versus cholecalciferol – and which dose were the most efficient and ii) to identify the molecular pathways activated by this pleiotropic molecule. The rat left peroneal nerve was cut out on a length of 10 mm and autografted in an inverted position. Animals were treated with either cholecalciferol or ergocalciferol, at the dose of 100 or 500 IU/kg/day, or excipient (Vehicle), and compared to unlesioned rats (Control). Functional recovery of hindlimb was measured weekly, during 12 weeks, using the peroneal functional index. Ventilatory, motor and sensitive responses of the regenerated axons were recorded and histological analysis was performed. In parallel, to identify the genes regulated by vitamin D in dorsal root ganglia and/or Schwann cells, we performed an in vitro transcriptome study. We observed that cholecalciferol is more efficient than ergocalciferol and, when delivered at a high dose (500 IU/kg/day), cholecalciferol induces a significant locomotor and electrophysiological recovery. We also demonstrated that cholecalciferol increases i) the number of preserved or newly formed axons in the proximal end, ii) the mean axon diameter in the distal end, and iii) neurite myelination in both distal and proximal ends. Finally, we found a modified expression of several genes involved in axogenesis and myelination, after 24 hours of vitamin supplementation. Our study is the first to demonstrate that vitamin D acts on myelination via the activation of several myelin-associated genes. It paves the way for future randomised controlled clinical trials for peripheral nerve or spinal cord repair. |
format | Online Article Text |
id | pubmed-3669361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36693612013-06-05 Cholecalciferol (Vitamin D(3)) Improves Myelination and Recovery after Nerve Injury Chabas, Jean-Francois Stephan, Delphine Marqueste, Tanguy Garcia, Stephane Lavaut, Marie-Noelle Nguyen, Catherine Legre, Regis Khrestchatisky, Michel Decherchi, Patrick Feron, Francois PLoS One Research Article Previously, we demonstrated i) that ergocalciferol (vitamin D(2)) increases axon diameter and potentiates nerve regeneration in a rat model of transected peripheral nerve and ii) that cholecalciferol (vitamin D3) improves breathing and hyper-reflexia in a rat model of paraplegia. However, before bringing this molecule to the clinic, it was of prime importance i) to assess which form – ergocalciferol versus cholecalciferol – and which dose were the most efficient and ii) to identify the molecular pathways activated by this pleiotropic molecule. The rat left peroneal nerve was cut out on a length of 10 mm and autografted in an inverted position. Animals were treated with either cholecalciferol or ergocalciferol, at the dose of 100 or 500 IU/kg/day, or excipient (Vehicle), and compared to unlesioned rats (Control). Functional recovery of hindlimb was measured weekly, during 12 weeks, using the peroneal functional index. Ventilatory, motor and sensitive responses of the regenerated axons were recorded and histological analysis was performed. In parallel, to identify the genes regulated by vitamin D in dorsal root ganglia and/or Schwann cells, we performed an in vitro transcriptome study. We observed that cholecalciferol is more efficient than ergocalciferol and, when delivered at a high dose (500 IU/kg/day), cholecalciferol induces a significant locomotor and electrophysiological recovery. We also demonstrated that cholecalciferol increases i) the number of preserved or newly formed axons in the proximal end, ii) the mean axon diameter in the distal end, and iii) neurite myelination in both distal and proximal ends. Finally, we found a modified expression of several genes involved in axogenesis and myelination, after 24 hours of vitamin supplementation. Our study is the first to demonstrate that vitamin D acts on myelination via the activation of several myelin-associated genes. It paves the way for future randomised controlled clinical trials for peripheral nerve or spinal cord repair. Public Library of Science 2013-05-31 /pmc/articles/PMC3669361/ /pubmed/23741446 http://dx.doi.org/10.1371/journal.pone.0065034 Text en © 2013 Chabas et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chabas, Jean-Francois Stephan, Delphine Marqueste, Tanguy Garcia, Stephane Lavaut, Marie-Noelle Nguyen, Catherine Legre, Regis Khrestchatisky, Michel Decherchi, Patrick Feron, Francois Cholecalciferol (Vitamin D(3)) Improves Myelination and Recovery after Nerve Injury |
title | Cholecalciferol (Vitamin D(3)) Improves Myelination and Recovery after Nerve Injury |
title_full | Cholecalciferol (Vitamin D(3)) Improves Myelination and Recovery after Nerve Injury |
title_fullStr | Cholecalciferol (Vitamin D(3)) Improves Myelination and Recovery after Nerve Injury |
title_full_unstemmed | Cholecalciferol (Vitamin D(3)) Improves Myelination and Recovery after Nerve Injury |
title_short | Cholecalciferol (Vitamin D(3)) Improves Myelination and Recovery after Nerve Injury |
title_sort | cholecalciferol (vitamin d(3)) improves myelination and recovery after nerve injury |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669361/ https://www.ncbi.nlm.nih.gov/pubmed/23741446 http://dx.doi.org/10.1371/journal.pone.0065034 |
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