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

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.

[1]  T. Strowitzki,et al.  Glucose transporter proteins (GLUT) in human endometrium: expression, regulation, and function throughout the menstrual cycle and in early pregnancy. , 2003, The Journal of clinical endocrinology and metabolism.

[2]  Jinfang Lin,et al.  The influence of insulin on secretion of IGF-I and IGFBP-I in cultures of human endometrial stromal cells. , 2003, Chinese Medical Journal.

[3]  H. Lodish,et al.  Nomenclature of the GLUT/SLC2A family of sugar/polyol transport facilitators. , 2002, American journal of physiology. Endocrinology and metabolism.

[4]  R. Rosenfield,et al.  Polycystic ovary syndrome and insulin-resistant hyperinsulinemia. , 2001, Journal of the American Academy of Dermatology.

[5]  B. Çakır,et al.  Insulin Resistance in Nonobese Patients with Polycystic Ovary Syndrome , 2001, Hormone Research in Paediatrics.

[6]  M. Mueckler,et al.  Insulin resistance and the disruption of Glut4 trafficking in skeletal muscle. , 2001, The Journal of clinical investigation.

[7]  E. Capp,et al.  Expression of glucose transporter 1 in human endometrial and decidual tissue , 2001, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

[8]  M. Matsuda,et al.  Insulin sensitivity indices obtained from oral glucose tolerance testing: comparison with the euglycemic insulin clamp. , 1999, Diabetes care.

[9]  M. Palacín,et al.  Insulin-Induced Redistribution of GLUT4 Glucose Carriers in the Muscle Fiber: In Search of GLUT4 Trafficking Pathways , 1996, Diabetes.

[10]  H. Haring,et al.  Tyrosine kinase activity of insulin‐like growth factor I and insulin receptors in human endometrium during the menstrual cycle: Cyclic variation of insulin receptor expression , 1993, Fertility and sterility.

[11]  J. Olefsky,et al.  Insulin-responsive human adipocytes express two glucose transporter isoforms and target them to different vesicles. , 1993, The Journal of clinical endocrinology and metabolism.

[12]  D. Rosenbaum,et al.  Insulin resistance in polycystic ovary syndrome: decreased expression of GLUT-4 glucose transporters in adipocytes. , 1993, The American journal of physiology.

[13]  H. Häring,et al.  Tyrosine kinase activity of insulin-like growth factor I and insulin receptors in human endometrium during the menstrual cycle: cyclic variation of insulin receptor expression , 1993 .

[14]  J. Olefsky,et al.  Cellular mechanisms of insulin resistance in polycystic ovarian syndrome. , 1992, The Journal of clinical endocrinology and metabolism.

[15]  A. Marette,et al.  Abundance, localization, and insulin-induced translocation of glucose transporters in red and white muscle. , 1992, The American journal of physiology.

[16]  N. Ferrara,et al.  Molecular and biological properties of the vascular endothelial growth factor family of proteins. , 1992, Endocrine reviews.

[17]  S. Roy,et al.  In vitro effects of epidermal growth factor, insulin-like growth factor-I, fibroblast growth factor, and follicle-stimulating hormone on hamster follicular deoxyribonucleic acid synthesis and steroidogenesis. , 1991, Biology of reproduction.

[18]  M. Mueckler Family of Glucose-Transporter Genes: Implications for Glucose Homeostasis and Diabetes , 1990, Diabetes.

[19]  K. Segal,et al.  Profound Peripheral Insulin Resistance, Independent of Obesity, in Polycystic Ovary Syndrome , 1989, Diabetes.

[20]  S. Franks POLYCYSTIC OVARY SYNDROME: A CHANGING PERSPECTIVE , 1989, Clinical endocrinology.

[21]  A. Dunaif,et al.  Characterization of groups of hyperandrogenic women with acanthosis nigricans, impaired glucose tolerance, and/or hyperinsulinemia. , 1987, The Journal of clinical endocrinology and metabolism.

[22]  M. Hollenberg,et al.  Basal, oxytocin-, and insulin-stimulated glucose oxidation in human endometrium. , 1987, Canadian journal of physiology and pharmacology.

[23]  E. Sheets,et al.  In vitro binding of insulin and epidermal growth factor to human endometrium and endocervix. , 1985, American journal of obstetrics and gynecology.

[24]  D. Straus Growth-stimulatory actions of insulin in vitro and in vivo. , 1984, Endocrine reviews.