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Understanding Reproductive Aging in Wildlife to Improve Animal Conservation and Human Reproductive Health

Similar to humans and laboratory animals, reproductive aging is observed in wild species-from small invertebrates to large mammals. Aging issues are also prevalent in rare and endangered species under human care as their life expectancy is longer than in the wild. The objectives of this review are t...

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Autores principales: Comizzoli, Pierre, Ottinger, Mary Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170016/
https://www.ncbi.nlm.nih.gov/pubmed/34095152
http://dx.doi.org/10.3389/fcell.2021.680471
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author Comizzoli, Pierre
Ottinger, Mary Ann
author_facet Comizzoli, Pierre
Ottinger, Mary Ann
author_sort Comizzoli, Pierre
collection PubMed
description Similar to humans and laboratory animals, reproductive aging is observed in wild species-from small invertebrates to large mammals. Aging issues are also prevalent in rare and endangered species under human care as their life expectancy is longer than in the wild. The objectives of this review are to (1) present conserved as well as distinctive traits of reproductive aging in different wild animal species (2) highlight the value of comparative studies to address aging issues in conservation breeding as well as in human reproductive medicine, and (3) suggest next steps forward in that research area. From social insects to mega-vertebrates, reproductive aging studies as well as observations in the wild or in breeding centers often remain at the physiological or organismal scale (senescence) rather than at the germ cell level. Overall, multiple traits are conserved across very different species (depletion of the ovarian reserve or no decline in testicular functions), but unique features also exist (endless reproductive life or unaltered quality of germ cells). There is a broad consensus about the need to fill research gaps because many cellular and molecular processes during reproductive aging remain undescribed. More research in male aging is particularly needed across all species. Furthermore, studies on reproductive aging of target species in their natural habitat (sentinel species) are crucial to define more accurate reproductive indicators relevant to other species, including humans, sharing the same environment. Wild species can significantly contribute to our general knowledge of a crucial phenomenon and provide new approaches to extend the reproductive lifespan.
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spelling pubmed-81700162021-06-03 Understanding Reproductive Aging in Wildlife to Improve Animal Conservation and Human Reproductive Health Comizzoli, Pierre Ottinger, Mary Ann Front Cell Dev Biol Cell and Developmental Biology Similar to humans and laboratory animals, reproductive aging is observed in wild species-from small invertebrates to large mammals. Aging issues are also prevalent in rare and endangered species under human care as their life expectancy is longer than in the wild. The objectives of this review are to (1) present conserved as well as distinctive traits of reproductive aging in different wild animal species (2) highlight the value of comparative studies to address aging issues in conservation breeding as well as in human reproductive medicine, and (3) suggest next steps forward in that research area. From social insects to mega-vertebrates, reproductive aging studies as well as observations in the wild or in breeding centers often remain at the physiological or organismal scale (senescence) rather than at the germ cell level. Overall, multiple traits are conserved across very different species (depletion of the ovarian reserve or no decline in testicular functions), but unique features also exist (endless reproductive life or unaltered quality of germ cells). There is a broad consensus about the need to fill research gaps because many cellular and molecular processes during reproductive aging remain undescribed. More research in male aging is particularly needed across all species. Furthermore, studies on reproductive aging of target species in their natural habitat (sentinel species) are crucial to define more accurate reproductive indicators relevant to other species, including humans, sharing the same environment. Wild species can significantly contribute to our general knowledge of a crucial phenomenon and provide new approaches to extend the reproductive lifespan. Frontiers Media S.A. 2021-05-19 /pmc/articles/PMC8170016/ /pubmed/34095152 http://dx.doi.org/10.3389/fcell.2021.680471 Text en Copyright © 2021 Comizzoli and Ottinger. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Comizzoli, Pierre
Ottinger, Mary Ann
Understanding Reproductive Aging in Wildlife to Improve Animal Conservation and Human Reproductive Health
title Understanding Reproductive Aging in Wildlife to Improve Animal Conservation and Human Reproductive Health
title_full Understanding Reproductive Aging in Wildlife to Improve Animal Conservation and Human Reproductive Health
title_fullStr Understanding Reproductive Aging in Wildlife to Improve Animal Conservation and Human Reproductive Health
title_full_unstemmed Understanding Reproductive Aging in Wildlife to Improve Animal Conservation and Human Reproductive Health
title_short Understanding Reproductive Aging in Wildlife to Improve Animal Conservation and Human Reproductive Health
title_sort understanding reproductive aging in wildlife to improve animal conservation and human reproductive health
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170016/
https://www.ncbi.nlm.nih.gov/pubmed/34095152
http://dx.doi.org/10.3389/fcell.2021.680471
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