Genetic rodent models of obesity-associated ovarian dysfunction and subfertility: insights into polycystic ovary syndrome

Polycystic ovary syndrome (PCOS) is the most common endocrinopathy affecting women, and a leading cause of female infertility worldwide. Defined clinically by the presence of hyperandrogenemia and oligomenorrhoea, PCOS represents a state of hormonal dysregulation, disrupted ovarian follicle dynamics...

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Main Authors: Isabel eHuang-Doran, Stephen eFranks
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-06-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fendo.2016.00053/full
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spelling doaj-ad02dab1eb6940b2af3b605ad01f075f2020-11-25T00:29:55ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922016-06-01710.3389/fendo.2016.00053202961Genetic rodent models of obesity-associated ovarian dysfunction and subfertility: insights into polycystic ovary syndromeIsabel eHuang-Doran0Isabel eHuang-Doran1Stephen eFranks2University of CambridgeImperial College LondonImperial College LondonPolycystic ovary syndrome (PCOS) is the most common endocrinopathy affecting women, and a leading cause of female infertility worldwide. Defined clinically by the presence of hyperandrogenemia and oligomenorrhoea, PCOS represents a state of hormonal dysregulation, disrupted ovarian follicle dynamics, and subsequent oligo- or anovulation. The syndrome’s prevalence is attributed at least partly to a well-established association with obesity and insulin resistance (IR). Indeed, the presence of severe PCOS in human genetic obesity and IR syndromes supports a causal role for IR in the pathogenesis of PCOS. The molecular mechanisms underlying this causality, however, as well as the important role of hyperandrogenemia, remain poorly elucidated. As such, treatment of PCOS is necessarily empirical, focusing on symptom alleviation. The generation of knockout and transgenic rodent models of obesity and IR offer a promising platform in which to address mechanistic questions about reproductive dysfunction in the context of metabolic disease. The impact of primary perturbations in rodent gonadotrophin or androgen signaling has been similarly interrogated. The insights gained from such models, however, have been limited by the relatively poor fidelity of rodent models to human PCOS. In this minireview we evaluate the ovarian phenotypes associated with rodent models of obesity and IR, including the extent of endocrine disturbance, ovarian dysmorphology and subfertility. We compare them to both human PCOS and other animal models of the syndrome (genetic and hormonal), explore reasons for their discordance and consider the new opportunities that are emerging to better understand and treat this important condition.http://journal.frontiersin.org/Journal/10.3389/fendo.2016.00053/fullFertilityInsulin ResistanceObesitymouse modelsandrogenpcos
collection DOAJ
language English
format Article
sources DOAJ
author Isabel eHuang-Doran
Isabel eHuang-Doran
Stephen eFranks
spellingShingle Isabel eHuang-Doran
Isabel eHuang-Doran
Stephen eFranks
Genetic rodent models of obesity-associated ovarian dysfunction and subfertility: insights into polycystic ovary syndrome
Frontiers in Endocrinology
Fertility
Insulin Resistance
Obesity
mouse models
androgen
pcos
author_facet Isabel eHuang-Doran
Isabel eHuang-Doran
Stephen eFranks
author_sort Isabel eHuang-Doran
title Genetic rodent models of obesity-associated ovarian dysfunction and subfertility: insights into polycystic ovary syndrome
title_short Genetic rodent models of obesity-associated ovarian dysfunction and subfertility: insights into polycystic ovary syndrome
title_full Genetic rodent models of obesity-associated ovarian dysfunction and subfertility: insights into polycystic ovary syndrome
title_fullStr Genetic rodent models of obesity-associated ovarian dysfunction and subfertility: insights into polycystic ovary syndrome
title_full_unstemmed Genetic rodent models of obesity-associated ovarian dysfunction and subfertility: insights into polycystic ovary syndrome
title_sort genetic rodent models of obesity-associated ovarian dysfunction and subfertility: insights into polycystic ovary syndrome
publisher Frontiers Media S.A.
series Frontiers in Endocrinology
issn 1664-2392
publishDate 2016-06-01
description Polycystic ovary syndrome (PCOS) is the most common endocrinopathy affecting women, and a leading cause of female infertility worldwide. Defined clinically by the presence of hyperandrogenemia and oligomenorrhoea, PCOS represents a state of hormonal dysregulation, disrupted ovarian follicle dynamics, and subsequent oligo- or anovulation. The syndrome’s prevalence is attributed at least partly to a well-established association with obesity and insulin resistance (IR). Indeed, the presence of severe PCOS in human genetic obesity and IR syndromes supports a causal role for IR in the pathogenesis of PCOS. The molecular mechanisms underlying this causality, however, as well as the important role of hyperandrogenemia, remain poorly elucidated. As such, treatment of PCOS is necessarily empirical, focusing on symptom alleviation. The generation of knockout and transgenic rodent models of obesity and IR offer a promising platform in which to address mechanistic questions about reproductive dysfunction in the context of metabolic disease. The impact of primary perturbations in rodent gonadotrophin or androgen signaling has been similarly interrogated. The insights gained from such models, however, have been limited by the relatively poor fidelity of rodent models to human PCOS. In this minireview we evaluate the ovarian phenotypes associated with rodent models of obesity and IR, including the extent of endocrine disturbance, ovarian dysmorphology and subfertility. We compare them to both human PCOS and other animal models of the syndrome (genetic and hormonal), explore reasons for their discordance and consider the new opportunities that are emerging to better understand and treat this important condition.
topic Fertility
Insulin Resistance
Obesity
mouse models
androgen
pcos
url http://journal.frontiersin.org/Journal/10.3389/fendo.2016.00053/full
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