Article ID Journal Published Year Pages File Type
2582921 Environmental Toxicology and Pharmacology 2015 10 Pages PDF
Abstract

•Dependent on corpus luteum development expression of metabolizing enzymes.•Inhibitory action on CYP2B1/2, but no effect on SULT1A or COMT expression.•Opposite actions of BDE-47 on estrogen secretion in MLP and in LLP, and no effect on progesterone secretion.•Metabolites inhibited progesterone, but had no effect on estradiol secretion.

In this study we determined the effects of BDE-47 on the expression and activity of phase I (CYP2B1/2) and phase II (SULT1A and COMT) enzymes, and assessed the actions of BDE-47 and its metabolites on luteal steroidogenesis. Luteal cells collected during early (ELP), middle (MLP) and late (LLP) luteal phase were exposed to BDE-47 (0.5, 25, and 50 ng/ml) or metabolites (2.5, 5 and 25 ng/ml). BDE-47 decreased CYP2B1/2 activity and expression but had no effect on SULT1A or COMT. BDE-47 exerted a stimulatory action on estrogen secretion in MLP and an inhibitory in LLP, but had no effect on progesterone secretion. 5-OH-BDE-47 and 6-OH-BDE-47 decreased progesterone, but had no effect on estrogen secretion.ConclusionsThe inhibitory effect of BDE-47 on CYP2B1/2 suggests the possibility of BDE-47 accumulation in the corpus luteum; by affecting steroid secretion and steroidogenesis enzymes, BDE-47 and its metabolites can be responsible for shortening luteal phase.

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