Metformin directly inhibits androgen production in human thecal cells

Objective: To examine the direct effect of metformin on thecal cell androge n production. Setting: Basic science research laboratory, University of Texas Southwester n, Dallas, Texas. Intervention(s): Human ovarian theca-ne tumor cells were treated with vario us concentrations of metformin in the presence and absence of forskolin for 48 hours. Main Outcome Measure(s): Media were collected, and radioimmunoassay (RIA) f or progesterone, 17 alpha -hydroxyprogesterone (170HP), androstenedione, an d testosterone was performed. The effect of metformin on the expression of various enzymes involved in theca cell steroidogenesis was examined. Result(s): Metformin (50 muM and 200 muM) significantly inhibited androsten edione production from both forskolin-stimulated and unstimulated theca. ce lls. Testosterone production was also significantly inhibited in forskolin- treated cells in the presence of 200 muM of metformin-treated compared with forskolin-only-treated cells. Western blot analysis revealed that metformi n significantly inhibited the expression of steroidogenic acute regulatory (StAR) protein and 17 alpha -hydroxylase (CYP17) expression in cells stimul ated with forskolin compared with forskolin treatment alone. There was no s ignificant change in either 3 beta -hydroxysteroid dehydrogenase (3 beta HS D) or cholesterol side-chain cleavage (CY-P11A1) protein expression. Northe rn analysis revealed a significant decrease in the expression of CYP17 mRNA in forskolin-stimulated cells treated with metformin (200 muM) compared wi th forskolin-only-treated cells, however, there was no significant change i n steroidogenic acute regulatory protein mRNA expression. Conclusion(s): Our results suggest that metformin may have a direct effect on thecal cells' androgen production. (Fertil Steril(R) 2001;76:517-24. (C) 2001 by American Society for Reproductive Medicine.).