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Boron enhances early embryonic gene expressions and improves fetal development of rats.

Authors :
Ince, Sinan
Erdogan, Metin
Demirel, Hasan Huseyin
Agca, Yuksel
Dal, Gamze
Uguz, Cevdet
Source :
Journal of Trace Elements in Medicine & Biology; Dec2018, Vol. 50, p34-46, 13p
Publication Year :
2018

Abstract

Abstract Boron is present as several different components in nature. Besides its industrial use, it is an essential element and is playing a very important role in the metabolism. In this study, it was aimed to determine the in vivo effects of boron on mRNA expression of HEX, NANOG, and OCT-3/4 genes in embryo and histological changes during fetal development. Therefore, totally 60 female rats were allocated into 5 equal groups. Experimental groups are as the followings; positive control (fed with standart rat diet), negative control (fed with boron free diet), low boron group (fed with boron free diet and given 0.04 μg boron/ml via gastric gavage), marginal boron group (fed with boron free diet and given 0.3 μg boron/ml via gastric gavage) and normal boron group (fed with boron free diet and given 2 μg boron/ml via gastric gavage). Experimental period was performed for 14 days. Embryos were collected after 4 days of mating and the expression and protein levels of early embryonic genes namely HEX, NANOG, and OCT-3/4 were determined by using Real-Time PCR. Also, 10–20 day embryo and fetus development were histologically determined. According to the results, mRNA expression and protein levels of early embryonic genes were increased in boron groups while decreased in boron deficient group. Histopathologically, tissue and organ developments were definitely observed in the boron groups. In conclusion, mRNA expression levels of early embryonic genes decreased in boron deficient group and boron has an important role for fetal development. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0946672X
Volume :
50
Database :
Supplemental Index
Journal :
Journal of Trace Elements in Medicine & Biology
Publication Type :
Academic Journal
Accession number :
131946364
Full Text :
https://doi.org/10.1016/j.jtemb.2018.06.002