» Articles » PMID: 15731326

Obesity Reduces the Expression of GLUT4 in the Endometrium of Normoinsulinemic Women Affected by the Polycystic Ovary Syndrome

Overview
Specialty Science
Date 2005 Feb 26
PMID 15731326
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

GLUT4 is the most important glucose transporter in insulin-dependent tissues. A decrease of its expression by the adipocytes was reported in polycystic ovary syndrome (PCOS), regardless of obesity and glucose tolerance. In PCOS, abnormal menstrual cycles, abnormal insulin secretory patterns, and obesity, which are risk factors for endometrial diseases, frequently coexist. The endometrial effects of insulin are direct through specific insulin receptors. However, it is unknown whether the endometrium expresses GLUT4 and can be considered an insulin-regulated tissue. In this study, we investigated this question, and we investigated whether obesity modulates this expression in PCOS normoinsulinemic patients. We assayed GLUT4 in the endometrial samples from 18 normoinsulinemic PCOS patients and 9 controls in the advanced follicular phase of the cycle; 10 patients were lean and 8 obese, and all were aged between 23 and 32 years. Most tissue was immediately frozen for RT-PCR; some tissue was saved for histology and immunohistochemistry. GLUT4 mRNA expression was measured in three samples for every patient and expressed as mean +/- SE of an arbitrary unit. In obese PCOS subjects, endometrial GLUT4 expression was significantly lower than in the lean ones (24.0 +/- 6.8 vs. 65.2 +/- 24.4; P < 0.005) and the controls (53.2 +/- 10.7). Lean PCOS and control subjects showed similar values. GLUT4 immunostaining was strong in the epithelial and absent in the stromal cells. We demonstrated endometrial GLUT4 expression. The similar results in lean PCOS and control subjects suggest that endometrial GLUT4 expression is not affected by PCOS itself, whereas it is reduced by obesity in PCOS patients.

Citing Articles

Glucose metabolism and endometrium decidualization.

Huang Y, Zhu Q, Sun Y Front Endocrinol (Lausanne). 2025; 16:1546335.

PMID: 40034230 PMC: 11872720. DOI: 10.3389/fendo.2025.1546335.


Do Androgenic Pattern, Insulin State and Growth Hormone Affect Cardiorespiratory Fitness and Strength in Young Women with PCOS?.

Baioccato V, Quinto G, Rovai S, Conte F, Dassie F, Neunhaeuserer D Biomedicines. 2022; 10(9).

PMID: 36140277 PMC: 9496105. DOI: 10.3390/biomedicines10092176.


Role of metformin in functional endometrial hyperplasia and polycystic ovary syndrome involves the regulation of MEG3/miR‑223/GLUT4 and SNHG20/miR‑4486/GLUT4 signaling.

Liu J, Zhao Y, Chen L, Li R, Ning Y, Zhu X Mol Med Rep. 2022; 26(1).

PMID: 35552758 PMC: 9175273. DOI: 10.3892/mmr.2022.12734.


Endometrial Glucose Transporters in Health and Disease.

Vrhovac Madunic I, Karin-Kujundzic V, Madunic J, Sola I, Serman L Front Cell Dev Biol. 2021; 9:703671.

PMID: 34552924 PMC: 8450505. DOI: 10.3389/fcell.2021.703671.


Hyperandrogenic Milieu Dysregulates the Expression of Insulin Signaling Factors and Glucose Transporters in the Endometrium of Patients With Polycystic Ovary Syndrome.

Lee M, Yoon J, Kim H, Kim Y, Lyu S, Lee B Reprod Sci. 2020; 27(8):1637-1647.

PMID: 32430710 DOI: 10.1007/s43032-020-00194-7.