Rosiglitazone and Pioglitazone Alter Aromatase Kinetic Properties in Human Granulosa Cells

Author:

Araki Takako1,Varadinova Miroslava1,Goldman Michael1,Rosenwaks Zev2,Poretsky Leonid1,Seto-Young Donna1

Affiliation:

1. Gerald J. Friedman Diabetes Institute and the Division of Endocrinology, Department of Medicine, Beth Israel Medical Center and Albert Einstein College of Medicine, New York, NY 10003, USA

2. Ronald O. Perelman and Cohen Center for Reproductive Medicine and Infertility, Weill Medical College of Cornell University, New York, NY 10021, USA

Abstract

We have previously reported that, in human granulosa cells, thiazolidinediones rosiglitazone and pioglitazone inhibit estrogen synthesis by interfering with androgen binding to aromatase, without an effect on aromatase mRNA or protein expression. In the current paper, we explore the effects of rosiglitazone and pioglitazone on the aromatase enzyme kinetic properties in human granulosa cells. The cells were incubated with various concentrations of testosterone or androstenedione, with or without rosiglitazone or pioglitazone. Estradiol and estrone concentrations in the conditioned tissue culture medium were measured by radioimmunoassay or immunosorbent assay. When testosterone was used as substrate, rosiglitazone or pioglitazone inhibited theVmaxby 35% (P<0.001) and 24% (P<0.001), respectively. When androstenedione was used as substrate, both rosiglitazone or pioglitazone inhibitedVmaxby 13% (P<0.007). We conclude that rosiglitazone or pioglitazone has no effect onKmbut inhibitsVmaxof aromatase in human granulosa cells, therefore, acting as noncompetitive inhibitors.

Funder

Gerald J. R. Friedman Foundation

Publisher

Hindawi Limited

Subject

Pharmacology (medical),Drug Discovery

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