The adverse effects of bisphenol A on male albino rats

afaf hendawy kamel; Heba M. Moussa; Mona A. Foaud;

Abstract


Background: Bisphenol A (BPA) is a monomer used in the production of a multitude of chemical products, including
epoxy resins and polycarbonates. The purpose of this study was to consider the biochemical, histological, genetic, and
molecular alterations induced by BPA in adult male albino rats. They were orally subjected to BPA (20 and 100 mg/kg
body weight) mixed in olive oil once a day for 30 days. At the end of the experiment, liver, testis, serum, and bone marrow
were collected.
Result: A significant increase in the level of malondialdehyde (MDA), with a significant decline in the content of superoxide
dismutase (SOD) and reduced glutathione (GSH) in rats’ livers and testes after administration of both doses of BPA occurred.
Also, there was a significant decrease in the testosterone activity in both treated groups. Histopathologic effects of bisphenol
A on livers and testes of male rats showed that the treatment with both doses of BPA resulted in deleterious effects on livers
and testes. The frequency of the micronucleus (MN) in polychromatic erythrocytes (PCEs) in bone marrow cells at both
doses was significantly increased as compared to control group, while no changes were observed in polychromatic
erythrocytes/normochromatic erythrocytes (PCEs/NCEs) ratio. Finally, BPA caused a suppressive effect on spermatogenesisassociated
7 (SPATA 7) gene in a dose-dependent manner.
Conclusion: Exposure of rats to both selective doses of BPA leads to many adverse effects on liver and testis tissues. Also,
an increase in frequency of the micronucleus in bone marrow cells was shown and suppression in the expression of SPATA
7 gene.


Other data

Title The adverse effects of bisphenol A on male albino rats
Authors afaf hendawy kamel ; Heba M. Moussa ; Mona A. Foaud 
Keywords Bisphenol A, DNA damage, Hepatotoxicity, SPATA 7 gene, Oxidative stress
Issue Date 2018
Journal The Journal of Basic and Applied Zoology 
DOI 10.1186/s41936-018-0015-9

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