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Benzo(a)pyrene disrupts mouse preimplantation embryo development
Oleh:
Zhan, Shaoquan
;
Zhang, Xiya
;
Cao,, Shanbo
;
Huang, Junjiu
Jenis:
Article from Journal - ilmiah internasional
Dalam koleksi:
Fertility and Sterility (keterangan: ada di ClinicalKey) vol. 103 no. 03 (Mar. 2015)
,
page 815-825.
Topik:
Benzo(a)pyrene
;
preimplantation embryo
;
reactive oxygen species
;
DNA damage
;
telomere
Ketersediaan
Perpustakaan FK
Nomor Panggil:
F02.K
Non-tandon:
tidak ada
Tandon:
1
Lihat Detail Induk
Isi artikel
Objective To determine the effects of Benzo(a)pyrene (BaP) on the development of early preimplantation embryo by exposure to physiologic concentrations of BaP based on a previous report in human ovarian follicular fluid and serum. Design Zygotes were cultured in 5 nM or 50 nM BaP and then examined for development efficiency, embryo quality, and DNA damage. In addition, embryonic stem cells (ESCs) were used as a model to test the toxic effects of BaP on inner cell mass (ICM) of blastocysts. Setting Laboratory. Animal(s) CD1 mice. Intervention(s) Mouse zygotes and ESCs were cultured in medium with 5 nM or 50 nM BaP. Main Outcome Measure(s) The percentage (rate) of blastocyst development, reactive oxygen species level, and quality of embryos assessed by total cell number, cell apoptosis, Oct4- and Nanog-positive cell ratio, and DNA damage on genomic and telomeric DNA were compared between dimethyl sulfoxide control and BaP treatments. Result(s) The BaP-treated zygotes exhibited significantly higher reactive oxygen species activity, which might lead to more cell apoptosis, low ratio of Nanog- or Oct4-positive ICM cells, and increasing DNA damage in both genomic and telomeric DNA in blastocysts. By using mouse ESCs derived from ICM cells as a model, we showed that pluripotent cells might also show serious DNA damage after a brief exposure to BaP. Conclusion(s) Our data show that BaP could seriously disrupt cell growth and genomic DNA stability and increase cell apoptosis in mouse preimplantation embryo development.
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