کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2196139 | 1550904 | 2013 | 8 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Nonhuman primate models of polycystic ovary syndrome Nonhuman primate models of polycystic ovary syndrome](/preview/png/2196139.png)
With close genomic and phenotypic similarity to humans, nonhuman primate models provide comprehensive epigenetic mimics of polycystic ovary syndrome (PCOS), suggesting early life targeting for prevention. Fetal exposure to testosterone (T), of all nonhuman primate emulations, provides the closest PCOS-like phenotypes, with early-to-mid gestation T-exposed female rhesus monkeys exhibiting adult reproductive, endocrinological and metabolic dysfunctional traits that are co-pathologies of PCOS. Late gestational T exposure, while inducing adult ovarian hyperandrogenism and menstrual abnormalities, has less dysfunctional metabolic accompaniment. Fetal exposures to dihydrotestosterone (DHT) or diethylstilbestrol (DES) suggest androgenic and estrogenic aspects of fetal programming. Neonatal exposure to T produces no PCOS-like outcome, while continuous T treatment of juvenile females causes precocious weight gain and early menarche (high T), or high LH and weight gain (moderate T). Acute T exposure of adult females generates polyfollicular ovaries, while chronic T exposure induces subtle menstrual irregularities without metabolic dysfunction.
► Early-to-mid gestation testosterone excess recapitulates PCOS phenotypes in monkeys.
► Transient maternal and fetal hyperglycemia accompany testosterone exposure.
► Epigenetic changes in visceral fat implicate altered TGF-β signaling.
► T-exposed monkeys may provide a close, epigenetic molecular mimic of PCOS.
Journal: Molecular and Cellular Endocrinology - Volume 373, Issues 1–2, 5 July 2013, Pages 21–28