2019
DOI: 10.1210/en.2018-00966
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A Hyperandrogenic Environment Causes Intrinsic Defects That Are Detrimental to Follicular Dynamics in a PCOS Mouse Model

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Cited by 38 publications
(23 citation statements)
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“…Our data show that the PCOS traits of acyclicity and anovulation can be rescued by a specific dietary macronutrient balance, supporting the use of dietary manipulation as a potential viable strategy to be used to assist in restoration of ovulatory dysfunction in women with PCOS. In agreement with previous studies 25,26,34 , ovulatory function is aberrant in the hyperandrogenic mouse model of PCOS as corpora lutea populations are diminished. However, ovulatory function was restored in PCOS females on a tightly defined intake range of protein, carbohydrate and fat, indicated by the presence of corpora lutea in their ovaries (8/35), which conclusively confirms the occurrence of recent ovulations.…”
Section: Discussionsupporting
confidence: 92%
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“…Our data show that the PCOS traits of acyclicity and anovulation can be rescued by a specific dietary macronutrient balance, supporting the use of dietary manipulation as a potential viable strategy to be used to assist in restoration of ovulatory dysfunction in women with PCOS. In agreement with previous studies 25,26,34 , ovulatory function is aberrant in the hyperandrogenic mouse model of PCOS as corpora lutea populations are diminished. However, ovulatory function was restored in PCOS females on a tightly defined intake range of protein, carbohydrate and fat, indicated by the presence of corpora lutea in their ovaries (8/35), which conclusively confirms the occurrence of recent ovulations.…”
Section: Discussionsupporting
confidence: 92%
“…The pattern of PCOS females being unable to regulate adiponectin and cholesterol across various diets, also extended to their inability to regulate serum glucose levels. In our study, as per our previous publications 26 , 34 , impaired glucose homeostasis was observed in PCOS females. This finding is consistent with studies in humans where women with PCOS have increased levels of steady state plasma glucose and fasting glucose compared to non-PCOS women 32 .…”
Section: Discussionsupporting
confidence: 90%
“…While this model has been reported to not have a strong metabolic PCOS phenotype and may be most representative of the lean PCOS phenotype, it has been reported that adipocyte hypertrophy and impaired glucose tolerance are still present, inferring that metabolic function is still aberrant (Roland et al 2010, Caldwell et al 2014. Early postnatal DHT exposure induces a robust mouse PCOS model with a wide range of PCOS traits including irregular cycles, ovulatory dysfunction, PCOM, adiposity, adipocyte hypertrophy, dyslipidemia, hepatic steatosis and altered glucose and insulin homeostasis (Caldwell et al 2014, Bertoldo et al 2019. In sheep and nonhuman primate PCOS models, prenatal exposure to testosterone generates the closest simulation to the clinical features of PCOS, with both models also displaying a breadth of endocrine, reproductive and metabolic PCOS traits, including irregular cycles, oligo-or anovulation, PCOM, LH hypersecretion, lipid abnormalities and insulin resistance (Padmanabhan & Veiga-Lopez 2013, Abbott et al 2016.…”
Section: Evidence From Hyperandrogenized Preclinical Animal Pcos Modementioning
confidence: 99%
“…The different effects observed between treatments are summarised in Figure 1. However, interventions that reduce levels of excess androgens may still not be effective in patients desiring children as it appears hyperandrogenism may impart adverse legacies on fertility, even after follicles and oocytes have been removed from the hyperandrogenic environment [31].…”
Section: Clinical Targeting Of Androgen Excess—potential For Mitigmentioning
confidence: 99%