4.5 Article

Effects of estrogen and estrogenic compounds, 4-tert-octylphenol, and bisphenol A on the uterine contraction and contraction-associated proteins in rats

Journal

MOLECULAR AND CELLULAR ENDOCRINOLOGY
Volume 375, Issue 1-2, Pages 27-34

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.mce.2013.04.025

Keywords

Myometrium; Endocrine disrupting chemicals; Estradiol; Prostaglandins; Oxytocin

Funding

  1. National Research Foundation of Korea (NRF)
  2. Korea government (MEST) [2012R1A1A2041975]
  3. National Research Foundation of Korea [2012R1A1A2041975] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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We examined the effects of estradiol (E2), 4-tert-octylphenol (OP), and bisphenol A (BPA) on uterine contractions in immature rats. The expression and localization of contraction-associated proteins (CAPs), and contractility of rat uterus with a collagen gel contraction assay were analyzed. E2, OP, and BPA all increased oxytocin (OT)-related pathway, while the prostaglandin-related signaling was reduced. Interestingly, E2 and estrogenic compounds showed distinct effects on the contractile activity of uterine cells. E2 enhanced the contractility, while OP and BPA significantly decreased it. Immunohistochemical analysis of CAPs showed distinct regulation of prostaglandin F receptor localization by E2 and estrogenic compounds, which may explain the different contractile activities of those reagents. In summary, we demonstrate that E2, OP, and BPA regulate CAP expression in a similar manner in the immature rat uterus, however, the effects on contractile activity were modulated differently. These findings suggest that OP and BPA interfere with uterine contractility. (C) 2013 Elsevier Ireland Ltd. All rights reserved.

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