Details

Autor(en) / Beteiligte

• Cajas, Yulia N
• Cañón-Beltrán, Karina
• Núñez-Puente, Carolina
• Gutierrez-Adán, Alfonso
• González, Encina M
• Agirregoitia, Ekaitz
• Rizos, Dimitrios

Titel

Nobiletin-induced partial abrogation of deleterious effects of AKT inhibition on preimplantation bovine embryo development in vitro

Ist Teil von

• Biology of reproduction, 2021-12, Vol.105 (6), p.1427-1442

Ort / Verlag

United States: Society for the Study of Reproduction

Erscheinungsjahr

2021

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• During preimplantational embryo development, PI3K/AKT regulates cell proliferation and differentiation and nobiletin modulates this pathway to promote cell survival. Therefore, we aimed to establish whether, when the AKT cascade is inhibited using inhibitors III and IV, nobiletin supplementation to in vitro culture media during the minor (2- to 8-cell stage, MNEGA) or major (8- to 16-cell stage, MJEGA) phases of EGA is able to modulate the development and quality of bovine embryos. In vitro zygotes were cultured during MNEGA or MJEGA phase in SOF + 5% FCS or supplemented with: 15 µM AKT-InhIII; 10 µM AKT-InhIV; 10 µM nobiletin; nobiletin + AKT-InhIII; nobiletin + AKT-InhIV; 0.03% DMSO. Embryo development was lower in treatments with AKT inhibitors, while combination of nobiletin with AKT inhibitors was able to recover their adverse developmental effect and also increase blastocyst cell number. The mRNA abundance of GPX1, NFE2L2, and POU5F1 was partially increased in 8- and 16-cell embryos from nobiletin with AKT inhibitors. Besides, nobiletin increased the p-rpS6 level whether or not AKT inhibitors were present. In conclusion, nobiletin promotes bovine embryo development and quality and partially recovers the adverse developmental effect of AKT inhibitors, which infers that nobiletin probably uses another signaling cascade that PI3K/AKT during early embryo development in bovine. Summary sentence Nobiletin supplementation: promotes bovine embryo development and quality in vitro, partially protects against deleterious effects of exogenous AKT inhibition, and increases rpS6 phosphorylation irrespective of AKT inhibitor presence. Graphical Abstract