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A Review of Delayed Delivery Models and the Analysis Method in Mice
In humans, the incidence of post-term delivery is 1–10%. Post-term delivery significantly increases the risk of cesarean section or neonatal intensive care unit (NICU) admission. Despite these serious challenges, the cause of prolonged delivery remains unclear. Several common factors of delayed part...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9149829/ https://www.ncbi.nlm.nih.gov/pubmed/35645296 http://dx.doi.org/10.3390/jdb10020020 |
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author | Yomogita, Hiroshi Miyasaka, Naoyuki Kanai-Azuma, Masami |
author_facet | Yomogita, Hiroshi Miyasaka, Naoyuki Kanai-Azuma, Masami |
author_sort | Yomogita, Hiroshi |
collection | PubMed |
description | In humans, the incidence of post-term delivery is 1–10%. Post-term delivery significantly increases the risk of cesarean section or neonatal intensive care unit (NICU) admission. Despite these serious challenges, the cause of prolonged delivery remains unclear. Several common factors of delayed parturition between mice and humans will help elucidate the mechanisms of pregnancy and labor. At present, gene modification techniques are rapidly developing; however, there are limited reviews available describing the mouse phenotype analysis as a human model for post-term delivery. We classified the delayed-labor mice into nine types according to their causes. In mice, progesterone (P₄) maintains pregnancy, and the most common cause of delayed labor is luteolysis failure. Other contributing factors include humoral molecules in the fetus/placenta, uterine contractile dysfunction, poor cervical ripening, and delayed implantation. The etiology of delayed parturition is overexpression of the pregnancy maintenance mechanism or suppression of the labor induction mechanism. Here, we describe how to investigated their causes using mouse genetic analysis. In addition, we generated a list to identify the causes. Our review will help understand the findings obtained using the mouse model, providing a foundation for conducting more systematic research on delayed delivery. |
format | Online Article Text |
id | pubmed-9149829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91498292022-05-31 A Review of Delayed Delivery Models and the Analysis Method in Mice Yomogita, Hiroshi Miyasaka, Naoyuki Kanai-Azuma, Masami J Dev Biol Review In humans, the incidence of post-term delivery is 1–10%. Post-term delivery significantly increases the risk of cesarean section or neonatal intensive care unit (NICU) admission. Despite these serious challenges, the cause of prolonged delivery remains unclear. Several common factors of delayed parturition between mice and humans will help elucidate the mechanisms of pregnancy and labor. At present, gene modification techniques are rapidly developing; however, there are limited reviews available describing the mouse phenotype analysis as a human model for post-term delivery. We classified the delayed-labor mice into nine types according to their causes. In mice, progesterone (P₄) maintains pregnancy, and the most common cause of delayed labor is luteolysis failure. Other contributing factors include humoral molecules in the fetus/placenta, uterine contractile dysfunction, poor cervical ripening, and delayed implantation. The etiology of delayed parturition is overexpression of the pregnancy maintenance mechanism or suppression of the labor induction mechanism. Here, we describe how to investigated their causes using mouse genetic analysis. In addition, we generated a list to identify the causes. Our review will help understand the findings obtained using the mouse model, providing a foundation for conducting more systematic research on delayed delivery. MDPI 2022-05-20 /pmc/articles/PMC9149829/ /pubmed/35645296 http://dx.doi.org/10.3390/jdb10020020 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Yomogita, Hiroshi Miyasaka, Naoyuki Kanai-Azuma, Masami A Review of Delayed Delivery Models and the Analysis Method in Mice |
title | A Review of Delayed Delivery Models and the Analysis Method in Mice |
title_full | A Review of Delayed Delivery Models and the Analysis Method in Mice |
title_fullStr | A Review of Delayed Delivery Models and the Analysis Method in Mice |
title_full_unstemmed | A Review of Delayed Delivery Models and the Analysis Method in Mice |
title_short | A Review of Delayed Delivery Models and the Analysis Method in Mice |
title_sort | review of delayed delivery models and the analysis method in mice |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9149829/ https://www.ncbi.nlm.nih.gov/pubmed/35645296 http://dx.doi.org/10.3390/jdb10020020 |
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