Literature DB >> 28963684

Possible effects of melatonin against rat uterus exposure to bisphenol A during neonatal period.

Damla Dernek1, Suna Ömeroğlu2, Neslihan Coşkun Akçay3, Bahar Kartal4, Saadet Özen Akarca Dizakar5, İsmail Türkoğlu2, Vildan Aydin2.   

Abstract

The aim of this study was to investigate the possible effects of melatonin on rat uterine tissue against exposure with bisphenol A (BPA) in the neonatal period. Twenty-four female rats were divided into four groups, (n=6) per group. Group I was used as a control (sesame oil + ethanol), group II was injected daily with (100 mg/kg) BPA by subcutaneously (sc) daily postnatal days (PND 0-10), group III was injected daily with (10 mg/kg) melatonin by sc for 10 days (PND 20-30), and group IV was injected daily with (100 mg/kg) BPA (PND 0-10) and (10 mg/kg) melatonin (PND 20-30). All rats were sacrificed in the same day of metestrus cycle, approximately PND 70. Histological analyses, immunostaining of B cell lymphoma 2 (Bcl-2), and cytochrome c and TUNEL assays were performed. According to our results, neonatal exposure to BPA accelerates onset of puberty, causes degenerative and morphometric changes on rat uterus, and increases apoptotic reaction rates. The immunoreactivity of Bcl-2 was decreased after BPA administration. In addition, immunoreactivity of Bcl-2 showed an increase after melatonin treatment. However, cytochrome c immunoreactivity was decreased after melatonin administration. Our results suggest that melatonin may have positive effects against BPA-induced degenerative changes on rat uterus.

Entities:  

Keywords:  Apostosis; Bisphenol A; Histology; Melatonin; Neonatal period; Uterus

Mesh:

Substances:

Year:  2017        PMID: 28963684     DOI: 10.1007/s11356-017-0187-8

Source DB:  PubMed          Journal:  Environ Sci Pollut Res Int        ISSN: 0944-1344            Impact factor:   4.223


  29 in total

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4.  The activity of bisphenol A depends on both the estrogen receptor subtype and the cell type.

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6.  Long-term effects of fetal exposure to low doses of the xenoestrogen bisphenol-A in the female mouse genital tract.

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Journal:  Environ Health Perspect       Date:  2014-06-04       Impact factor: 9.031

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