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Moderate caloric restriction initiated in rodents during adulthood sustains function of the female reproductive axis into advanced chronological age

Age-related ovarian failure in women heralds the transition into postmenopausal life, which is characterized by a loss of fertility and increased risk for cardiovascular disease, osteoporosis and cognitive dysfunction. Unfortunately, there are no options available for delaying loss of ovarian functi...

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Autores principales: Selesniemi, Kaisa, Lee, Ho-Joon, Tilly, Jonathan L
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990913/
https://www.ncbi.nlm.nih.gov/pubmed/18549458
http://dx.doi.org/10.1111/j.1474-9726.2008.00409.x
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author Selesniemi, Kaisa
Lee, Ho-Joon
Tilly, Jonathan L
author_facet Selesniemi, Kaisa
Lee, Ho-Joon
Tilly, Jonathan L
author_sort Selesniemi, Kaisa
collection PubMed
description Age-related ovarian failure in women heralds the transition into postmenopausal life, which is characterized by a loss of fertility and increased risk for cardiovascular disease, osteoporosis and cognitive dysfunction. Unfortunately, there are no options available for delaying loss of ovarian function with age in humans. Rodent studies have shown that caloric restriction (CR) can extend female fertile lifespan; however, much of this work initiated CR at weaning, which causes stunted adolescent growth and a delayed onset of sexual maturation. Herein we tested in mice if CR initiated in adulthood could delay reproductive aging. After 4 months of CR, the ovarian follicle reserve was doubled compared to ad libitum (AL)-fed age-matched controls, which in mating trials exhibited a loss of fertility by 15.5 months of age. In CR females returned to AL feeding at 15.5 months of age, approximately one-half remained fertile for 6 additional months and one-third continued to deliver offspring through 23 months of age. Notably, fecundity of CR-then-AL-fed females and postnatal offspring survival rates were dramatically improved compared with aging AL-fed controls. For example, between 10 and 23 months of age, only 22% of the 54 offspring delivered by AL-fed females survived. In contrast, over 73% of the 94 pups delivered by 15.5- to 23-month-old CR-then-AL-fed mice survived without any overt complications. These data indicate that in mice adult-onset CR maintains function of the female reproductive axis into advanced age and dramatically improves postnatal survival of offspring delivered by aged females.
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spelling pubmed-29909132010-12-06 Moderate caloric restriction initiated in rodents during adulthood sustains function of the female reproductive axis into advanced chronological age Selesniemi, Kaisa Lee, Ho-Joon Tilly, Jonathan L Aging Cell Original Articles Age-related ovarian failure in women heralds the transition into postmenopausal life, which is characterized by a loss of fertility and increased risk for cardiovascular disease, osteoporosis and cognitive dysfunction. Unfortunately, there are no options available for delaying loss of ovarian function with age in humans. Rodent studies have shown that caloric restriction (CR) can extend female fertile lifespan; however, much of this work initiated CR at weaning, which causes stunted adolescent growth and a delayed onset of sexual maturation. Herein we tested in mice if CR initiated in adulthood could delay reproductive aging. After 4 months of CR, the ovarian follicle reserve was doubled compared to ad libitum (AL)-fed age-matched controls, which in mating trials exhibited a loss of fertility by 15.5 months of age. In CR females returned to AL feeding at 15.5 months of age, approximately one-half remained fertile for 6 additional months and one-third continued to deliver offspring through 23 months of age. Notably, fecundity of CR-then-AL-fed females and postnatal offspring survival rates were dramatically improved compared with aging AL-fed controls. For example, between 10 and 23 months of age, only 22% of the 54 offspring delivered by AL-fed females survived. In contrast, over 73% of the 94 pups delivered by 15.5- to 23-month-old CR-then-AL-fed mice survived without any overt complications. These data indicate that in mice adult-onset CR maintains function of the female reproductive axis into advanced age and dramatically improves postnatal survival of offspring delivered by aged females. Blackwell Publishing Ltd 2008-10 /pmc/articles/PMC2990913/ /pubmed/18549458 http://dx.doi.org/10.1111/j.1474-9726.2008.00409.x Text en Journal compilation © 2008 Blackwell Publishing Ltd/The Anatomical Society of Great Britain and Ireland http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Articles
Selesniemi, Kaisa
Lee, Ho-Joon
Tilly, Jonathan L
Moderate caloric restriction initiated in rodents during adulthood sustains function of the female reproductive axis into advanced chronological age
title Moderate caloric restriction initiated in rodents during adulthood sustains function of the female reproductive axis into advanced chronological age
title_full Moderate caloric restriction initiated in rodents during adulthood sustains function of the female reproductive axis into advanced chronological age
title_fullStr Moderate caloric restriction initiated in rodents during adulthood sustains function of the female reproductive axis into advanced chronological age
title_full_unstemmed Moderate caloric restriction initiated in rodents during adulthood sustains function of the female reproductive axis into advanced chronological age
title_short Moderate caloric restriction initiated in rodents during adulthood sustains function of the female reproductive axis into advanced chronological age
title_sort moderate caloric restriction initiated in rodents during adulthood sustains function of the female reproductive axis into advanced chronological age
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990913/
https://www.ncbi.nlm.nih.gov/pubmed/18549458
http://dx.doi.org/10.1111/j.1474-9726.2008.00409.x
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