» Articles » PMID: 18549458

Moderate Caloric Restriction Initiated in Rodents During Adulthood Sustains Function of the Female Reproductive Axis into Advanced Chronological Age

Overview
Journal Aging Cell
Specialties Cell Biology
Geriatrics
Date 2008 Jun 14
PMID 18549458
Citations 70
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Canagliflozin treatment prevents follicular exhaustion and attenuates hallmarks of ovarian aging in genetically heterogenous mice.

Isola J, Biswas S, Jayarathne H, Hubbart C, Hense J, Matsuzaki S Geroscience. 2024; .

PMID: 39672978 DOI: 10.1007/s11357-024-01465-w.


Hallmarks of female reproductive aging in physiologic aging mice.

Balough J, Dipali S, Velez K, Kumar T, Duncan F Nat Aging. 2024; 4(12):1711-1730.

PMID: 39672896 DOI: 10.1038/s43587-024-00769-y.


Emerging therapeutic strategies to mitigate female and male reproductive aging.

Winstanley Y, Stables J, Gonzalez M, Umehara T, Norman R, Robker R Nat Aging. 2024; 4(12):1682-1696.

PMID: 39672895 DOI: 10.1038/s43587-024-00771-4.


The role of cellular senescence in ovarian aging.

Hense J, Isola J, Garcia D, Magalhaes L, Masternak M, Stout M NPJ Aging. 2024; 10(1):35.

PMID: 39033161 PMC: 11271274. DOI: 10.1038/s41514-024-00157-1.


Reproductive Ageing: Inflammation, immune cells, and cellular senescence in the aging ovary.

Isola J, Hense J, Osorio C, Biswas S, Alberola-Ila J, Ocanas S Reproduction. 2024; 168(2).

PMID: 38744316 PMC: 11301429. DOI: 10.1530/REP-23-0499.


References
1.
Roth G, Ingram D, BLACK A, Lane M . Effects of reduced energy intake on the biology of aging: the primate model. Eur J Clin Nutr. 2000; 54 Suppl 3:S15-20. DOI: 10.1038/sj.ejcn.1601020. View

2.
Ventura S . Trends and variations in first births to older women, United States, 1970-86. Vital Health Stat 21. 1989; (47):1-27. View

3.
Martin B, Golden E, Carlson O, Egan J, Mattson M, Maudsley S . Caloric restriction: impact upon pituitary function and reproduction. Ageing Res Rev. 2008; 7(3):209-24. PMC: 2634963. DOI: 10.1016/j.arr.2008.01.002. View

4.
Tilly J, Rueda B . Minireview: stem cell contribution to ovarian development, function, and disease. Endocrinology. 2008; 149(9):4307-11. PMC: 2553384. DOI: 10.1210/en.2008-0458. View

5.
Lozano J, Lonergan P, Boland M, OCallaghan D . Influence of nutrition on the effectiveness of superovulation programmes in ewes: effect on oocyte quality and post-fertilization development. Reproduction. 2003; 125(4):543-53. View