4.4 Article

Potential endocrine disrupting effect of ochratoxin A on human placental 3β-hydroxysteroid dehydrogenase/isomerase in JEG-3 cells at levels relevant to human exposure

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REPRODUCTIVE TOXICOLOGY
卷 38, 期 -, 页码 47-52

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.reprotox.2013.02.034

关键词

Ochratoxin A; 3 beta-Hydroxysteroid dehydrogenase/isomerase; Endocrine disruptor; JEG-3; Placenta; Steroidogenesis

资金

  1. University of Hong Kong, Hong Kong

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Ochratoxin A (OTA) is a common foodborne mycotoxin. Besides its classical toxicities, it is also associated with the impairment of steroidogenesis in rats. It is hypothesized that OTA may act as an endocrine disruptor by intervening 3 beta-hydroxysteroid dehydrogenase/isomerase (3 beta-HSD). To address this hypothesis, human placental cells JEG-3 were used in vitro to examine the effects of short- and long-term OTA exposures on expression levels of 3 beta-HSD1 and progesterone secretion at 24-96 h. Results showed that both cytotoxic and non-cytotoxic levels of OTA induced 3 beta-HSD1 mRNA expression by 281-378% at 72 and 96 h. A significant induction (43-316%) of 3 beta-HSD1 protein expression was observed at 48, 72 and 96 h, and the progesterone production with the involvement of 3 beta-HSD1 was significantly increased by 22-89% after 48-96 h. This is the first study to demonstrate OTA up-regulates 3 beta-HSD1 expression in human placental cells, indicating the potential endocrine-disrupting property of OTA. (c) 2013 Elsevier Inc. All rights reserved.

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