4.6 Article

Effects of fatty acid supplementation during vitrification and warming on the developmental competence of mouse, bovine and human oocytes and embryos

Journal

REPRODUCTIVE BIOMEDICINE ONLINE
Volume 43, Issue 1, Pages 14-25

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.rbmo.2021.03.022

Keywords

Embryo development; Fatty acid; Human embryo outgrowth; Oocyte development; Vitrification; beta-oxidation

Funding

  1. Japan Agency for Medical Research and Development (AMED) [JP 18gk0110014]

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The study demonstrates that fatty acid supplementation in vitrification and warming media can enhance the developmental competence of mouse and bovine embryos, as well as improve the morphological characteristics of human embryos.
Research question: Does fatty acid supplementation in vitrification and warming media influence developmental competence in oocytes after vitrification and warming? Design: Mouse oocytes and four-cell embryos were vitrified and warmed with solutions supplemented with fatty acid and cultured to the blastocyst stage. To study lipid metabolism after vitrification, quantitative real-time polymerase chain reaction was used to analyse the expression of genes related to beta oxidation in mouse embryos vitrified and warmed with or without fatty acids. The effects of fatty acid supplementation in the warming solutions on the developmental competence of bovine and human embryos were analysed. Blastocyst outgrowth assay was used to evaluate the potential of human blastocysts for adhesion to fibronectin. Results: The neutral lipid content of mouse oocytes in the fatty acid 1% supplementation group was significantly higher than in the fatty acid 0% group (P = 0.0032). The developmental rate to the blastocyst stage was significantly higher in the fatty acid 1% group than in the fatty acid 0% group in mice (P = 0.0345). Fatty acid supplementation in warming solution upregulated Acaa2 and Hadha in mouse embryos. Fatty acids significantly improved the developmental ability of bovine embryos to the blastocyst stage (P = 0.0048). Warming with 1% fatty acid supplementation significantly increased the proportion of human blastocysts with morphological grade A inner cell mass (P = 0.0074) and trophectoderm (P = 0.0323). Conclusions: Fatty acid supplementation in the warming solutions improved the developmental competence of vitrified-warmed mouse oocytes by activating the beta-oxidation pathway. Fatty acid supplementation enhanced the developmental rate of bovine embryos to the blastocyst stage and improved morphological characteristics of human embryos vitrified at the cleavage stage.

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