Published August 15, 2009 | Version v1
Journal article

Effect of mono-(2-ethylhexyl) phthalate on steroid production of human granulosa cells

  • 1. Department of Gynecological Endocrinology and Reproductive Medicine, University of Bonn, Sigmund-Freud-Strasse 25, D-53127 Bonn (Germany)
  • 2. Department of Clinical Chemistry and Clinical Pharmacology, University of Bonn, Sigmund-Freud-Strasse 25, D-53127 Bonn (Germany)

Description

The phthalate ester mono-(2-ethylhexyl) phthalate (MEHP) is the active metabolite of di-(2-ethylhexyl) phthalate, a high-production-volume chemical used as a plasticizer and solvent in numerous consumer products. MEHP has been demonstrated to be a reproductive toxicant in rodents decreasing estradiol and progesterone production in preovulatory granulosa cells. In the present study, we examined the effect of MEHP on steroid production of human granulosa-lutein (GL) cells. Human GL cells collected from women undergoing in vitro fertilization were cultured in medium containing FSH, hCG and 8-Br-cAMP, respectively, together with various concentrations of MEHP (0-500 μmol L-1). After incubation for 48 h estradiol and progesterone were assayed in the spent culture medium. Furthermore, aromatase activity and mRNA levels of GL cells were determined. Basal as well as FSH-, hCG- and 8-Br-cAMP-stimulated estradiol production of GL cells was suppressed by MEHP in a dose-dependent manner (IC50 = 105 μmol L-1, 138 μmol L-1, 49 μmol L-1 and 78 μmol L-1). Furthermore aromatase activity and mRNA levels were reduced in GL cells cultured with MEHP. In contrast, MEHP did not alter the production of progesterone up to a concentration of 167 μmol L-1. The present data indicate that MEHP is a specific inhibitor of estradiol production in human GL cells with a post-cAMP site of action. The inhibition of estradiol production obviously results from a reduction of aromatase activity on the transcript level. As the in vitro effective doses of MEHP are within the range of real environmental exposure levels an inhibitory effect on estrogen production in vivo seems to be possible.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.taap.2009.05.022

Additional details

Identifiers

DOI
10.1016/j.taap.2009.05.022;
PII
S0041-008X(09)00222-1;

Publishing Information

Journal Title
Toxicology and Applied Pharmacology
Journal Volume
239
Journal Issue
1
Journal Page Range
p. 116-123
ISSN
0041-008X
CODEN
TXAPA9

Optional Information

Copyright
Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.