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Nestorone(®), a 19nor‐progesterone derivative boosts remyelination in an animal model of demyelination

INTRODUCTION: We previously showed that Nestorone(®) (NES), a synthetic progestin structurally related to progesterone, stimulated remyelination of the corpus callosum in a Cuprizone (CUP) mouse model of demyelination in intact females by promoting replenishment with mature oligodendrocytes (OL) (Gl...

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Autores principales: El‐Etr, Martine, Akwa, Yvette, Rame, Marion, Schumacher, Michael, Sitruk‐Ware, Regine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941173/
https://www.ncbi.nlm.nih.gov/pubmed/33369182
http://dx.doi.org/10.1111/cns.13538
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author El‐Etr, Martine
Akwa, Yvette
Rame, Marion
Schumacher, Michael
Sitruk‐Ware, Regine
author_facet El‐Etr, Martine
Akwa, Yvette
Rame, Marion
Schumacher, Michael
Sitruk‐Ware, Regine
author_sort El‐Etr, Martine
collection PubMed
description INTRODUCTION: We previously showed that Nestorone(®) (NES), a synthetic progestin structurally related to progesterone, stimulated remyelination of the corpus callosum in a Cuprizone (CUP) mouse model of demyelination in intact females by promoting replenishment with mature oligodendrocytes (OL) (Glia. 2015;63:104‐117). Here, we further investigated the underlying mechanisms of this promyelinating effect. METHODS: We explored whether NES, applied subcutaneously through Alzet mini‐osmotic pumps, regulates specific transcription factors involved in oligodendrocyte progenitor cell (OPC) proliferation and their differentiation into mature OL, using RT‐qPCR and Western Blot analysis. RESULTS: Our present data show that in comparison to controls, a one‐week treatment with NES, through Alzet mini‐osmotic pumps, enhanced the production of three relevant transcription factor mRNAs encoding Olig2, Myt1, and Sox17. After 3 weeks, NES treatment reversed the effect of CUP on the levels of corresponding Olig2, Myt1, and Sox17 proteins. Moreover, in mice receiving NES + Estradiol (E2) co‐treatment, levels of Olig2, Myt1, and Sox17 proteins did not change as compared to NES alone. CONCLUSION: NES alone or with E2 increased the levels of transcription factors, essential for myelin synthesis.
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spelling pubmed-79411732021-03-16 Nestorone(®), a 19nor‐progesterone derivative boosts remyelination in an animal model of demyelination El‐Etr, Martine Akwa, Yvette Rame, Marion Schumacher, Michael Sitruk‐Ware, Regine CNS Neurosci Ther Original Articles INTRODUCTION: We previously showed that Nestorone(®) (NES), a synthetic progestin structurally related to progesterone, stimulated remyelination of the corpus callosum in a Cuprizone (CUP) mouse model of demyelination in intact females by promoting replenishment with mature oligodendrocytes (OL) (Glia. 2015;63:104‐117). Here, we further investigated the underlying mechanisms of this promyelinating effect. METHODS: We explored whether NES, applied subcutaneously through Alzet mini‐osmotic pumps, regulates specific transcription factors involved in oligodendrocyte progenitor cell (OPC) proliferation and their differentiation into mature OL, using RT‐qPCR and Western Blot analysis. RESULTS: Our present data show that in comparison to controls, a one‐week treatment with NES, through Alzet mini‐osmotic pumps, enhanced the production of three relevant transcription factor mRNAs encoding Olig2, Myt1, and Sox17. After 3 weeks, NES treatment reversed the effect of CUP on the levels of corresponding Olig2, Myt1, and Sox17 proteins. Moreover, in mice receiving NES + Estradiol (E2) co‐treatment, levels of Olig2, Myt1, and Sox17 proteins did not change as compared to NES alone. CONCLUSION: NES alone or with E2 increased the levels of transcription factors, essential for myelin synthesis. John Wiley and Sons Inc. 2020-12-24 /pmc/articles/PMC7941173/ /pubmed/33369182 http://dx.doi.org/10.1111/cns.13538 Text en © 2020 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
El‐Etr, Martine
Akwa, Yvette
Rame, Marion
Schumacher, Michael
Sitruk‐Ware, Regine
Nestorone(®), a 19nor‐progesterone derivative boosts remyelination in an animal model of demyelination
title Nestorone(®), a 19nor‐progesterone derivative boosts remyelination in an animal model of demyelination
title_full Nestorone(®), a 19nor‐progesterone derivative boosts remyelination in an animal model of demyelination
title_fullStr Nestorone(®), a 19nor‐progesterone derivative boosts remyelination in an animal model of demyelination
title_full_unstemmed Nestorone(®), a 19nor‐progesterone derivative boosts remyelination in an animal model of demyelination
title_short Nestorone(®), a 19nor‐progesterone derivative boosts remyelination in an animal model of demyelination
title_sort nestorone(®), a 19nor‐progesterone derivative boosts remyelination in an animal model of demyelination
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941173/
https://www.ncbi.nlm.nih.gov/pubmed/33369182
http://dx.doi.org/10.1111/cns.13538
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