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Embryonic diapause in humans: time to consider?

BACKGROUND: When a competent blastocyst stage embryo finds itself in an unreceptive uterus, it delays development. In around one hundred species representing various orders, this delay is known to be reversible, but this phenomenon - termed embryonic diapause (ED) - is not considered a general chara...

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Detalles Bibliográficos
Autores principales: Ptak, Grazyna E, Modlinski, Jacek A, Loi, Pasqualino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848826/
https://www.ncbi.nlm.nih.gov/pubmed/24044744
http://dx.doi.org/10.1186/1477-7827-11-92
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author Ptak, Grazyna E
Modlinski, Jacek A
Loi, Pasqualino
author_facet Ptak, Grazyna E
Modlinski, Jacek A
Loi, Pasqualino
author_sort Ptak, Grazyna E
collection PubMed
description BACKGROUND: When a competent blastocyst stage embryo finds itself in an unreceptive uterus, it delays development. In around one hundred species representing various orders, this delay is known to be reversible, but this phenomenon - termed embryonic diapause (ED) - is not considered a general characteristic of all mammals. PRESENTATION OF THE HYPOTHESIS: Recently, however, we demonstrated that a non-diapausing species, the sheep, is capable of ED, suggesting the hypothesis that this is in fact an ancestral trait common to all mammals, including humans. TESTING THE HYPOTHESIS: In spite of the obvious difficulties in testing this idea, we propose a combination of indirect observations on human fertility patients, and direct study of the embryos of non-human primates. IMPLICATIONS OF THE HYPOTHESIS: Support for our hypothesis would require revision of obstetric interventions routinely performed when a human pregnancy extends beyond the due date.
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spelling pubmed-38488262013-12-04 Embryonic diapause in humans: time to consider? Ptak, Grazyna E Modlinski, Jacek A Loi, Pasqualino Reprod Biol Endocrinol Hypothesis BACKGROUND: When a competent blastocyst stage embryo finds itself in an unreceptive uterus, it delays development. In around one hundred species representing various orders, this delay is known to be reversible, but this phenomenon - termed embryonic diapause (ED) - is not considered a general characteristic of all mammals. PRESENTATION OF THE HYPOTHESIS: Recently, however, we demonstrated that a non-diapausing species, the sheep, is capable of ED, suggesting the hypothesis that this is in fact an ancestral trait common to all mammals, including humans. TESTING THE HYPOTHESIS: In spite of the obvious difficulties in testing this idea, we propose a combination of indirect observations on human fertility patients, and direct study of the embryos of non-human primates. IMPLICATIONS OF THE HYPOTHESIS: Support for our hypothesis would require revision of obstetric interventions routinely performed when a human pregnancy extends beyond the due date. BioMed Central 2013-09-17 /pmc/articles/PMC3848826/ /pubmed/24044744 http://dx.doi.org/10.1186/1477-7827-11-92 Text en Copyright © 2013 Ptak et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Hypothesis
Ptak, Grazyna E
Modlinski, Jacek A
Loi, Pasqualino
Embryonic diapause in humans: time to consider?
title Embryonic diapause in humans: time to consider?
title_full Embryonic diapause in humans: time to consider?
title_fullStr Embryonic diapause in humans: time to consider?
title_full_unstemmed Embryonic diapause in humans: time to consider?
title_short Embryonic diapause in humans: time to consider?
title_sort embryonic diapause in humans: time to consider?
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848826/
https://www.ncbi.nlm.nih.gov/pubmed/24044744
http://dx.doi.org/10.1186/1477-7827-11-92
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