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Current Knowledge on the Multifactorial Regulation of Corpora Lutea Lifespan: The Rabbit Model
SIMPLE SUMMARY: Corpora lutea (CL) are temporary endocrine structures that secrete progesterone, which is essential for maintaining a healthy pregnancy. A variety of regulatory factors come into play in modulating the functional lifespan of CL, with luteotropic and luteolytic effects. Many aspects o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911389/ https://www.ncbi.nlm.nih.gov/pubmed/33503812 http://dx.doi.org/10.3390/ani11020296 |
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author | Zerani, Massimo Polisca, Angela Boiti, Cristiano Maranesi, Margherita |
author_facet | Zerani, Massimo Polisca, Angela Boiti, Cristiano Maranesi, Margherita |
author_sort | Zerani, Massimo |
collection | PubMed |
description | SIMPLE SUMMARY: Corpora lutea (CL) are temporary endocrine structures that secrete progesterone, which is essential for maintaining a healthy pregnancy. A variety of regulatory factors come into play in modulating the functional lifespan of CL, with luteotropic and luteolytic effects. Many aspects of luteal phase physiology have been clarified, yet many others have not yet been determined, including the molecular and/or cellular mechanisms that maintain the CL from the beginning of luteolysis during early CL development. This paper summarizes our current knowledge of the endocrine and cellular mechanisms involved in multifactorial CL lifespan regulation, using the pseudopregnant rabbit model. ABSTRACT: Our research group studied the biological regulatory mechanisms of the corpora lutea (CL), paying particular attention to the pseudopregnant rabbit model, which has the advantage that the relative luteal age following ovulation is induced by the gonadotrophin-releasing hormone (GnRH). CL are temporary endocrine structures that secrete progesterone, which is essential for maintaining a healthy pregnancy. It is now clear that, besides the classical regulatory mechanism exerted by prostaglandin E2 (luteotropic) and prostaglandin F2α (luteolytic), a considerable number of other effectors assist in the regulation of CL. The aim of this paper is to summarize our current knowledge of the multifactorial mechanisms regulating CL lifespan in rabbits. Given the essential role of CL in reproductive success, a deeper understanding of the regulatory mechanisms will provide us with valuable insights on various reproductive issues that hinder fertility in this and other mammalian species, allowing to overcome the challenges for new and more efficient breeding strategies. |
format | Online Article Text |
id | pubmed-7911389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79113892021-02-28 Current Knowledge on the Multifactorial Regulation of Corpora Lutea Lifespan: The Rabbit Model Zerani, Massimo Polisca, Angela Boiti, Cristiano Maranesi, Margherita Animals (Basel) Review SIMPLE SUMMARY: Corpora lutea (CL) are temporary endocrine structures that secrete progesterone, which is essential for maintaining a healthy pregnancy. A variety of regulatory factors come into play in modulating the functional lifespan of CL, with luteotropic and luteolytic effects. Many aspects of luteal phase physiology have been clarified, yet many others have not yet been determined, including the molecular and/or cellular mechanisms that maintain the CL from the beginning of luteolysis during early CL development. This paper summarizes our current knowledge of the endocrine and cellular mechanisms involved in multifactorial CL lifespan regulation, using the pseudopregnant rabbit model. ABSTRACT: Our research group studied the biological regulatory mechanisms of the corpora lutea (CL), paying particular attention to the pseudopregnant rabbit model, which has the advantage that the relative luteal age following ovulation is induced by the gonadotrophin-releasing hormone (GnRH). CL are temporary endocrine structures that secrete progesterone, which is essential for maintaining a healthy pregnancy. It is now clear that, besides the classical regulatory mechanism exerted by prostaglandin E2 (luteotropic) and prostaglandin F2α (luteolytic), a considerable number of other effectors assist in the regulation of CL. The aim of this paper is to summarize our current knowledge of the multifactorial mechanisms regulating CL lifespan in rabbits. Given the essential role of CL in reproductive success, a deeper understanding of the regulatory mechanisms will provide us with valuable insights on various reproductive issues that hinder fertility in this and other mammalian species, allowing to overcome the challenges for new and more efficient breeding strategies. MDPI 2021-01-25 /pmc/articles/PMC7911389/ /pubmed/33503812 http://dx.doi.org/10.3390/ani11020296 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Zerani, Massimo Polisca, Angela Boiti, Cristiano Maranesi, Margherita Current Knowledge on the Multifactorial Regulation of Corpora Lutea Lifespan: The Rabbit Model |
title | Current Knowledge on the Multifactorial Regulation of Corpora Lutea Lifespan: The Rabbit Model |
title_full | Current Knowledge on the Multifactorial Regulation of Corpora Lutea Lifespan: The Rabbit Model |
title_fullStr | Current Knowledge on the Multifactorial Regulation of Corpora Lutea Lifespan: The Rabbit Model |
title_full_unstemmed | Current Knowledge on the Multifactorial Regulation of Corpora Lutea Lifespan: The Rabbit Model |
title_short | Current Knowledge on the Multifactorial Regulation of Corpora Lutea Lifespan: The Rabbit Model |
title_sort | current knowledge on the multifactorial regulation of corpora lutea lifespan: the rabbit model |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911389/ https://www.ncbi.nlm.nih.gov/pubmed/33503812 http://dx.doi.org/10.3390/ani11020296 |
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