The DOI matches its Crossref record; 70 of the 70 references it cites were found in a registry or an index.
Progesterone and nestorone promote myelin regeneration in chronic demyelinating lesions of corpus callosum and cerebral cortex: Progesterone Receptor and Myelin Repair
Open accessAbstract
Multiple Sclerosis affects mainly women and consists in intermittent or chronic damages to the myelin sheaths, focal inflammation, and axonal degeneration. Current therapies are limited to immunomodulators and antiinflammatory drugs, but there is no efficient treatment for stimulating the endogenous capacity of myelin repair. Progesterone and synthetic progestins have been shown in animal models of demyelination to attenuate myelin loss, reduce clinical symptoms severity, modulate inflammatory responses and partially reverse the age-dependent decline in remyelination. Moreover, progesterone has been demonstrated to promote myelin formation in organotypic cultures of cerebellar slices. In the present study, we show that progesterone and the synthetic 19-nor-progesterone derivative Nestorone® promote the repair of severe chronic demyelinating lesions induced by feeding cuprizone to female mice for up to 12 weeks. Progesterone and Nestorone increase the density of NG2(+) oligodendrocyte progenitor cells and CA II(+) mature oligodendrocytes and enhance the formation of myelin basic protein (MBP)- and proteolipid protein (PLP)-immunoreactive myelin. However, while demyelination in response to cuprizone was less marked in corpus callosum than in cerebral cortex, remyelination appeared earlier in the former. The remyelinating effect of progesterone was progesterone receptor (PR)-dependent, as it was absent in PR-knockout mice. Progesterone and Nestorone also decreased (but did not suppress) neuroinflammatory responses, specifically astrocyte and microglial cell activation. Therefore, some progestogens are promising therapeutic candidates for promoting the regeneration of myelin.
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“and recently, the same group has shown that administration of progesterone promotes myelin regeneration in chronic demyelinated lesions in the corpus callosum of mice after being fed with cuprizone51.”
From Tamoxifen accelerates the repair of demyelinated lesions in the central nervous system (2016) · cites this paper as [51]
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Mice lacking progesterone receptor exhibit pleiotropic reproductive abnormalities.Preprint
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Mechanisms of neurodegeneration and axonal dysfunction in multiple sclerosis
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ProTECT: A Randomized Clinical Trial of Progesterone for Acute Traumatic Brain Injury
Wright, D. W., Kellermann, A. L., Hertzberg, V., Clark, P. L., Frankel, M., Goldstein, F. C., Salomone, J. P., Dent, L. L., Harris, O. A., Ander, D. S., et al. (2006) · Annals of Emergency Medicine · doi:10.1016/j.annemergmed.2006.07.932 · Cited by 599
The cuprizone animal model: new insights into an old story
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Progesterone synthesis and myelin formation by Schwann cells
Koenig, H. L., Schumacher, M., Ferzaz, B., Thi, A. N. D., Ressouches, A., Guennoun, R., Jung-Testas, I., Robel, P., Akwa, Y., & Baulieu, E.-E. (1995) · Science · doi:10.1126/science.7770777 · Cited by 480
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Steroid hormone receptor expression and function in microglia
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Regenerating CNS myelin — from mechanisms to experimental medicines
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Brites, D., & Fernandes, A. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00476 · Cited by 599
“Magnetic resonance imaging findings in the chronic mild stress (CMS) rodent animal, a model of depression, showed demyelination signs at the bilateral frontal cortex, hippocampus and hypothalamus, which revealed to be associated with brain oedema and inflammation (El-Etr et al., 2015).”
BackgroundRole of Estrogen and Other Sex Hormones in Brain Aging. Neuroprotection and DNA Repair
Zárate, S., Stevnsner, T., & Gredilla, R. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00430 · Cited by 299
Neurosteroids as regulators of neuroinflammation
Yılmaz, C., Karali, K., Fodelianaki, G., Gravanis, A., Chavakis, T., Charalampopoulos, I., & Alexaki, V. I. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100788 · Cited by 261
Progesterone in the Brain: Hormone, Neurosteroid and Neuroprotectant
Guennoun, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155271 · Cited by 167
Metadata
- Authors
- El-Etr, M., Rame, M., Boucher, C., Ghoumari, A. M., Kumar, N., Liere, P., Pianos, A., Schumacher, M., & Sitruk-Ware, R.
- Affiliations
- UMR 788 Inserm and University Paris-Sud; 94276 Kremlin-Bicêtre France
- Inserm (FR)
- Population Council (US)
- Venue
- Glia
- Publisher
- Wiley
- Published
- 2014-08-04
- Volume
- 63
- Issue
- 1
- Pages
- 104-117
- ISSN
- 0894-1491 (ISSN-L)
- PMC
- PMC4237628
- OpenAlex
- W1494051921
- Cited by
- 116
- References
- 70
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 9 · 2023: 7 · 2022: 12 · 2021: 8 · 2020: 10 · 2019: 8 · 2018: 13 · 2017: 10 · 2016: 14 · 2015: 10
- FWCI
- 8.41
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Glia (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion)
- Funders
- National Institute of Child Health and Human Development (U54)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- progesterone, Nestorone, remyelination, demyelination, multiple sclerosis, cuprizone, corpus callosum, cerebral cortex, oligodendrocyte precursor cells, oligodendrocytes, myelin basic protein, proteolipid protein, progesterone receptor, neuroinflammation, astrocyte activation, microglial activation, progestogens
- MeSH terms
- Animals, Cerebral Cortex, Corpus Callosum, Cuprizone, Demyelinating Diseases, Disease Models, Animal, Myelin Basic Protein, Female, Mice, Inbred C57BL, Multiple Sclerosis, Myelin Sheath, Oligodendroglia, Progesterone, Stem Cells, Mice, Knockout, Myelin Proteolipid Protein
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