Nobiletin enhances the development and quality of bovine embryos in vitro during two key periods of embryonic genome activation

In vitro culture can alter the development and quality of bovine embryos. Therefore, we aimed to evaluate whether nobiletin supplementation during EGA improves embryonic development and blastocyst quality and if it affects PI3K/AKT signaling pathway. In vitro zygotes were cultured in SOF + 5% FCS (C...

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Veröffentlicht in:Scientific reports 2021-06, Vol.11 (1), p.11796-11796, Article 11796
Hauptverfasser: Cañón-Beltrán, Karina, Cajas, Yulia N., Peréz-Cerezales, Serafín, Leal, Claudia L. V., Agirregoitia, Ekaitz, Gutierrez-Adán, Alfonso, González, Encina M., Rizos, Dimitrios
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Sprache:eng
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Zusammenfassung:In vitro culture can alter the development and quality of bovine embryos. Therefore, we aimed to evaluate whether nobiletin supplementation during EGA improves embryonic development and blastocyst quality and if it affects PI3K/AKT signaling pathway. In vitro zygotes were cultured in SOF + 5% FCS (Control) or supplemented with 5, 10 or 25 µM nobiletin (Nob5, Nob10, Nob25) or with 0.03% dimethyl-sulfoxide (C DMSO ) during minor (2 to 8-cell stage; MN EGA ) or major (8 to 16-cell stage; MJ EGA ) EGA phase. Blastocyst yield on Day 8 was higher in Nob5 (42.7 ± 1.0%) and Nob10 (44.4 ± 1.3%) for MN EGA phase and in Nob10 (61.0 ± 0.8%) for MJ EGA phase compared to other groups. Mitochondrial activity was higher and lipid content was reduced in blastocysts produced with nobiletin, irrespective of EGA phase. The mRNA abundance of CDK2, H3-3B, H3-3A, GPX1, NFE2L2 and PPARα transcripts was increased in 8-cells, 16-cells and blastocysts from nobiletin groups. Immunofluorescence analysis revealed immunoreactive proteins for p-AKT forms (Thr308 and Ser473) in bovine blastocysts produced with nobiletin. In conclusion, nobiletin supplementation during EGA has a positive effect on preimplantation bovine embryonic development in vitro and corroborates on the quality improvement of the produced blastocysts which could be modulated by the activation of AKT signaling pathway.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-021-91158-7