Literature DB >> 7940537

Mono-(2-ethylhexyl) phthalate suppresses estradiol production independent of FSH-cAMP stimulation in rat granulosa cells.

B J Davis1, R Weaver, L J Gaines, J J Heindel.   

Abstract

Di-(2-ethylhexyl) phthalate (DEHP) exposure suppressed preovulatory granulosa cell estradiol production in adult cycling rats. The active metabolite of DEHP, mono-(2-ethylhexyl) phthalate (MEHP), suppressed follicle-stimulating hormone (FSH)-stimulated cAMP and progesterone production in cultured rat granulosa cells. To examine how DEHP altered granulosa cell estradiol production, the effects of MEHP were studied in cultures of rat granulosa cells. Granulosa cells were obtained from DES-implanted 25-day-old female Fisher 344 rats and exposed in culture to various concentrations of MEHP (0 to 400 microM) in DMSO. Granulosa cells were stimulated with FSH, 8-bromo cyclic adenosine monophosphate (8br-cAMP), a stable cAMP analog, and various concentrations of testosterone. Estradiol production was measured by standard radioimmunoassays and normalized to cell protein. MEHP suppressed estradiol in a concentration-dependent manner whether granulosa cells were stimulated by FSH or 8-br cAMP. Therefore, MEHP suppressed estradiol independent of its suppression of the FSH-cAMP pathway and, thus, suppressed aromatase conversion of testosterone to estradiol. MEHP (100 microns) decreased the maximum velocity of aromatase in cells supplied with increasing concentrations of testosterone. However, MEHP did not alter the velocity or affinity of microsomal aromatase isolated from adult virgin Sprague-Dawley rat ovaries. Therefore, MEHP altered the absolute amount or availability of aromatase in granulosa cells. Decreased aromatase in granulosa cells would explain decreased estradiol concentrations from DEHP exposure in vivo.

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Year:  1994        PMID: 7940537     DOI: 10.1006/taap.1994.1201

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  30 in total

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Review 2.  Impact of environmental exposures on ovarian function and role of xenobiotic metabolism during ovotoxicity.

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4.  Di-(2-ethylhexyl) phthalate and mono-(2-ethylhexyl) phthalate inhibit growth and reduce estradiol levels of antral follicles in vitro.

Authors:  Rupesh K Gupta; Jeffery M Singh; Tracie C Leslie; Sharon Meachum; Jodi A Flaws; Humphrey H-C Yao
Journal:  Toxicol Appl Pharmacol       Date:  2009-10-27       Impact factor: 4.219

5.  Ovarian Toxicity and Epigenetic Mechanisms of Phthalates and Their Metabolites.

Authors:  Hua-Hua Jiang; Yao-Yao Du; Yu-Feng Li
Journal:  Curr Med Sci       Date:  2021-04-20

6.  Mono(2-ethylhexyl) phthalate accelerates early folliculogenesis and inhibits steroidogenesis in cultured mouse whole ovaries and antral follicles.

Authors:  Patrick R Hannon; Katherine E Brannick; Wei Wang; Jodi A Flaws
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7.  Ovarian Metabolism of an Environmentally Relevant Phthalate Mixture.

Authors:  Genoa R Warner; Zhong Li; Madeline L Houde; Cassandra E Atkinson; Daryl D Meling; Catheryne Chiang; Jodi A Flaws
Journal:  Toxicol Sci       Date:  2019-05-01       Impact factor: 4.849

8.  Urinary metabolites of di(2-ethylhexyl) phthalate are associated with decreased steroid hormone levels in adult men.

Authors:  John D Meeker; Antonia M Calafat; Russ Hauser
Journal:  J Androl       Date:  2008-12-04

9.  Association of exposure to phthalates with endometriosis and uterine leiomyomata: findings from NHANES, 1999-2004.

Authors:  Jennifer Weuve; Russ Hauser; Antonia M Calafat; Stacey A Missmer; Lauren A Wise
Journal:  Environ Health Perspect       Date:  2010-02-25       Impact factor: 9.031

10.  Transcriptional biomarkers of steroidogenesis and trophoblast differentiation in the placenta in relation to prenatal phthalate exposure.

Authors:  Jennifer J Adibi; Robin M Whyatt; Russ Hauser; Hari K Bhat; Barbara J Davis; Antonia M Calafat; Lori A Hoepner; Frederica P Perera; Deliang Tang; Paige L Williams
Journal:  Environ Health Perspect       Date:  2010-02       Impact factor: 9.031

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