4.5 Article

Hyperandrogenism Induces Histo-Architectural Changes in the Rat Uterus

期刊

REPRODUCTIVE SCIENCES
卷 26, 期 5, 页码 657-668

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/1933719118783881

关键词

uterus; dehydroepiandrosterone; aquaporin; collagen; cell proliferation

资金

  1. Agencia Nacional de Promocion Cientifica y Tecnologica (ANPCyT) [2348, 1628, 0390]
  2. Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) [PIP 00397]
  3. Universidad Nacional del Litoral (UNL) [CAID 2016 PIC 50420150100088LI]

向作者/读者索取更多资源

The effects of androgens on the uterus have been poorly studied and they need to be clarified to understand why androgen excess, such as observed in women with polycystic ovary syndrome (PCOS), is a risk factor for the development of endometrial hyperplasia, cancer, and infertility. Thus, uterine histomorphology in a PCOS experimental model was evaluated. Beginning at weaning, female rats were injected daily with dehydroepiandrosterone (DHEA, 6 mg/100 g body weight) or vehicle (sesame oil) for 20 consecutive days. On postnatal day 41 (PND41), DHEA-treated animals showed high serum testosterone levels. In addition, uterine histological analysis showed a significant increase in luminal epithelial height and glandular density without changes in cell proliferation. The thickness of the subepithelial stroma and myometrium also increased in these animals. The effect of DHEA on uterine thickness was accompanied by a significant reduction in cell density in both tissue compartments (subepithelial stroma and myometrium). Cell proliferation was not altered in the myometrium, whereas a decrease in the proliferative activity was seen at PND41 in the subepithelial stroma of DHEA animals. The analysis of the extracellular space showed that the changes in the thickness of the subepithelial stroma and myometrium were related to an increase in the organization of collagen fibers and water imbibition. The latter was associated with higher aquaporin 3 and 8 expression. This study provides evidence to further the understanding of PCOS-associated hyperandrogenism effects on uterine architecture. This could have implications for the regulation of uterine function and the development of uterine lesions.

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