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- Developmental exposure to the endocrine disruptor tolylfluanid induces sex-specific later-life metabolic dysfunction.
Developmental exposure to the endocrine disruptor tolylfluanid induces sex-specific later-life metabolic dysfunction.
Citation | “Developmental Exposure To The Endocrine Disruptor Tolylfluanid Induces Sex-Specific Later-Life Metabolic Dysfunction.”. Reproductive Toxicology (Elmsford, N.y.), pp. 74-82. . |
Center | University of Chicago |
Author | Daniel Ruiz, Shane M Regnier, Andrew G Kirkley, Manami Hara, Fidel Haro, Hani Aldirawi, Michael P Dybala, Robert M Sargis |
Keywords | adipose, Endocrine disruptor, Glucocorticoid, Gluconeogenesis, glucose tolerance, insulin sensitivity, Perinatal, Sex differences, Tolylfluanid |
Abstract |
Endocrine-disrupting chemicals (EDCs) are implicated in the developmental mis-programming of energy metabolism. This study examined the impact of combined gestational and lactational exposure to the fungicide tolylfluanid (TF) on metabolic physiology in adult offspring. C57BL/6 J dams received standard rodent chow or the same diet containing 67 mg/kg TF. Offspring growth and metabolism were assessed up to 22 weeks of age. TF-exposed offspring exhibited reduced weaning weight. Body weight among female offspring remained low throughout the study, while male offspring matched controls by 17 weeks of age. Female offspring exhibited reduced glucose tolerance, markedly enhanced systemic insulin sensitivity, reduced adiposity, and normal gluconeogenic capacity during adulthood. In contrast, male offspring exhibited impaired glucose tolerance with unchanged insulin sensitivity, no differences in adiposity, and increased gluconeogenic capacity. These data indicate that developmental exposure to TF induces sex-specific metabolic disruptions that recapitulate key aspects of other in utero growth restriction models. |
Year of Publication |
2019
|
Journal |
Reproductive toxicology (Elmsford, N.Y.)
|
Volume |
89
|
Number of Pages |
74-82
|
Date Published |
12/2019
|
ISSN Number |
1873-1708
|
DOI |
10.1016/j.reprotox.2019.06.010
|
Alternate Journal |
Reprod. Toxicol.
|
PMID |
31260803
|
PMCID |
PMC6766412
|
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