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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7941173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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