Details

Autor(en) / Beteiligte

• Baillargeon, Jean-Patrice
• Iuorno, Maria J
• Jakubowicz, Daniela J
• Apridonidze, Teimuraz
• He, Na
• Nestler, John E

Titel

Metformin Therapy Increases Insulin-Stimulated Release of d-Chiro-Inositol-Containing Inositolphosphoglycan Mediator in Women with Polycystic Ovary Syndrome

Ist Teil von

• The journal of clinical endocrinology and metabolism, 2004-01, Vol.89 (1), p.242-249

Ort / Verlag

Bethesda, MD: Endocrine Society

Erscheinungsjahr

2004

Quelle

Oxford Journals 2020 Medicine

Beschreibungen/Notizen

• Some actions of insulin are mediated by putative inositolphosphoglycan mediators, and a deficiency in d-chiro-inositol-containing inositolphosphoglycan (DCI-IPG) may contribute to insulin resistance in women with polycystic ovary syndrome (PCOS). Furthermore, similar effects of DCI and metformin, an insulin-sensitizing drug, have been demonstrated in PCOS women. To determine whether metformin improves insulin actions by increasing biologically active DCI-IPG in women with PCOS, we analyzed DCI-IPG during an oral glucose tolerance test in 19 obese women with PCOS before and after 4–8 wk of metformin or placebo. After treatment, the mean (±se) area under the curve (AUC) during the oral glucose tolerance test of insulin (AUCinsulin) decreased significantly more in the metformin group, compared with the placebo group [−3574 ± 962 vs. +1367 ± 1021 μIU/min·ml (−26 ± 7 vs. +10 ± 7 nmol/min·liter), P = 0.003], but the AUC of DCI-IPG (AUCDCI-IPG) decreased similarly in both groups (−1452 ± 968 vs. −2207 ± 1021%/min, P = 0.60). However, the ratio of AUCDCI-IPG/AUCinsulin increased by 160% after metformin and decreased by 29% after placebo (P = 0.002 between groups). Moreover, metformin seemed to improve the positive correlation between AUCDCI-IPG and AUCinsulin but not placebo (r = 0.32, P = 0.68 at baseline; r = 0.52, P = 0.12 after metformin; and r = −0.39, P = 0.30 after placebo). We conclude that in obese women with PCOS, metformin may improve the action of insulin in part by improving insulin-mediated release of DCI-IPG mediators, as evidenced by increased bioactive DCI-IPG released per unit of insulin.