Open AccessSimultaneous alterations in ovaries and bone as a result of Polycystic Ovary Syndrome
Author(s) -
Ana Lúcia de Oliveira Bonfá,
Eduardo Donato Alves,
Victor Fabrício,
Keico Okino aka,
Janete Aparecida Anselmo-Franci,
Jorge Alberto Achcar,
Luís Henrique Montrezor
Publication year - 2021
Publication title -
international journal of advances in medical biotechnology
Language(s) - English
Resource type - Journals
ISSN - 2595-3931
DOI - 10.25061/ijamb.v3i2.81
Subject(s) - polycystic ovary , endocrine system , endocrinology , ovary , medicine , anovulation , mesenchymal stem cell , hyperandrogenism , biology , infertility , diabetes mellitus , pathology , hormone , pregnancy , insulin resistance , genetics
Polycystic ovary syndrome (PCOS) is one of the most widely recognized endocrine disorders affecting reproductive-age women. The etiopathogenesis and mechanisms of this syndrome remain unclear. Diagnosis requires two of the following: polycystic ovaries, oligo- or anovulation, and hyperandrogenism. Most women with PCOS display conditions such as metabolic abnormalities, diabetes, obesity, cardiovascular disease, and/or bone dysfunction. Considering the ethical limitations of human studies, animal and cell culture models that reflect some features of PCOS are important for investigation of this syndrome. The aim of the present work was to study some of the endocrine relationships between ovaries and bone tissue in a polycystic ovary syndrome animal model. The study was performed using an estradiol valerate PCOS-induced rat model (n = 30) and bone mesenchymal stem cell cultured from bone marrow of those animals. It was hypothesized that changes of the endocrine relationship between ovaries and bones could be observed in from in vivo animal model and in vitro cell culture assays. The ovarian morphological and endocrine changes seem to be correlated with endocrine, biophysical, and biomechanical changes in bone properties. Mesenchymal stem cells obtained from PCOS-induced rats, cultured for up to 21 days and differentiated into osteoblasts, presented lower viability and reduced mineralization of the extracellular matrix. Taken together, these results indicate important endocrine and structural effects of PCOS in ovaries and bones, contributing to part of the understanding of the pathophysiological mechanisms of PCOS.