TY - JOUR
T1 - Postnatal weaning to different diets leads to different reproductive phenotypes in female offspring following perinatal exposure to high levels of dietary advanced glycation end products
AU - Merhi, Zaher
AU - Du, Xiu Quan
AU - Charron, Maureen J.
N1 - Funding Information:
The authors thank Geralyn Messerlian, Ph.D. and Ms. Elizabeth Eklund for performing the enzyme-linked immunosorbent assays, Ms. Fengying Chen for performing the quantitative polymerase chain reactions, and Ashini Dias, Ph.D. for scoring the slides used in follicle counting. Supported by grants from the American Society for Reproductive Medicine and Society for Reproductive Investigation-Bayer to Z.M. and an American Diabetes Association grant (1-13-CE-06) to M.J.C. Additional support was provided by a grant from the Einstein-Mount Sinai Diabetes Research Center (P30 DK020541).
Funding Information:
Supported by grants from the American Society for Reproductive Medicine and Society for Reproductive Investigation-Bayer to Z.M. and an American Diabetes Association grant (1-13-CE-06) to M.J.C. Additional support was provided by a grant from the Einstein-Mount Sinai Diabetes Research Center (P30 DK020541).
Publisher Copyright:
© 2021 American Society for Reproductive Medicine
PY - 2022/2
Y1 - 2022/2
N2 - Objective: To examine, following perinatal exposure to a diet high in advanced glycation end products (AGEs), whether the use of standard AGE-free mouse chow during the postweaning period alters metabolism and reproduction differently than exposure to a diet low in AGEs. Design: Experimental animal study. Setting: University-based research laboratory. Animal(s): Female CD1 mice. Intervention(s): Seven-week-old mice were placed on a diet either low or high in AGEs perinatally, before mating and then during pregnancy and lactation. All offspring were weaned onto an AGE-free normal chow. Main Outcome Measure(s): Growth curve, liver and abdominal fat weight, insulin and glucose tolerance tests, vaginal opening, estrous cyclicity, and serum levels of antimüllerian hormone, leptin, and adiponectin were assessed. Ovarian histologic examination for follicular count and gene expression was also performed. Result(s): Compared with the mice exposed to a diet low in AGEs, the mice exposed to a diet high in AGEs showed lower body weight in pups, lower liver weight, delayed vaginal opening, higher serum antimüllerian hormone levels, lower primordial and secondary follicle pools, and higher ovarian Fshr messenger RNA levels. Conclusion(s): Following weaning, perinatal AGEs can target puberty onset and folliculogenesis differently to standard mouse chow.
AB - Objective: To examine, following perinatal exposure to a diet high in advanced glycation end products (AGEs), whether the use of standard AGE-free mouse chow during the postweaning period alters metabolism and reproduction differently than exposure to a diet low in AGEs. Design: Experimental animal study. Setting: University-based research laboratory. Animal(s): Female CD1 mice. Intervention(s): Seven-week-old mice were placed on a diet either low or high in AGEs perinatally, before mating and then during pregnancy and lactation. All offspring were weaned onto an AGE-free normal chow. Main Outcome Measure(s): Growth curve, liver and abdominal fat weight, insulin and glucose tolerance tests, vaginal opening, estrous cyclicity, and serum levels of antimüllerian hormone, leptin, and adiponectin were assessed. Ovarian histologic examination for follicular count and gene expression was also performed. Result(s): Compared with the mice exposed to a diet low in AGEs, the mice exposed to a diet high in AGEs showed lower body weight in pups, lower liver weight, delayed vaginal opening, higher serum antimüllerian hormone levels, lower primordial and secondary follicle pools, and higher ovarian Fshr messenger RNA levels. Conclusion(s): Following weaning, perinatal AGEs can target puberty onset and folliculogenesis differently to standard mouse chow.
KW - Advanced glycation end products
KW - folliculogenesis
KW - ovarian function
KW - puberty
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U2 - 10.1016/j.xfss.2021.12.001
DO - 10.1016/j.xfss.2021.12.001
M3 - Article
C2 - 35559999
AN - SCOPUS:85123603651
SN - 2666-335X
VL - 3
SP - 95
EP - 105
JO - F and S Science
JF - F and S Science
IS - 1
ER -