4.7 Article

Combination of CNP, MT and FLI during IVM Significantly Improved the Quality and Development Abilities of Bovine Oocytes and IVF-Derived Embryos

Journal

ANTIOXIDANTS
Volume 12, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/antiox12040897

Keywords

bovine; oocytes; ovum pich up; C-type natriuretic peptide; melatonin; FLI (IGF plus FGF plus LIF)

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Oocyte maturation is crucial for female gametogenesis and subsequent fertilization and embryogenesis. This study investigated the effect of Pre-IVM with CNP, MT, and FLI on the developmental potential of bovine oocytes during in vitro maturation (IVM). The combination of CNP, MT, and FLI significantly improved the development of oocytes to blastocyst stage, as well as ATP content, GSH levels, TZP intensity, Delta psi m, cacline-AM fluorescence intensity, and reduced ROS levels. The survival and hatched rates after vitrification were also significantly higher in the CNP+MT+FLI group. Overall, targeting the combination of CNP, MT, and FLI can enhance the quality and developmental potential of bovine oocytes.
Oocyte maturation is a critical step in the completion of female gametogenesis in the ovary; thus, for subsequent fertilization and embryogenesis. Vitrification of embryo also has been shown to be closely associated with oocyte maturation. To improve the quality and developmental potential of bovine oocytes derived from in vitro maturation (IVM), Pre-IVM with C-type natriuretic peptide (CNP), melatonin (MT) and in combination, IGF1, FGF2, LIF (FLI) were supplemented in the IVM medium. In this current study, we cultured bovine oocytes in Pre-IVM with CNP for 6 h before transferring them to the IVM medium supplemented with MT and FLI. The developmental potential of bovine oocytes was then investigated by measuring the reactive oxygen species (ROS), the intracellular glutathione (GSH) and ATP levels, the transzonal projections (TZP), the mitochondrial membrane potential (Delta psi m), cacline-AM, and the expression of related genes (cumulus cells (CCs), oocytes, blastocysts). The results revealed that oocytes treated with a combination of CNP, MT, and FLI had dramatically improved the percentage of oocytes developed to blastocyst, ATP content, GSH levels, TZP intensity, the Delta psi m, cacline-AM fluorescence intensity, and considerably reduced ROS levels of oocytes. Furthermore, the survival rate and the hatched rate after vitrification of the CNP+MT+FLI group were significantly higher than those other groups. Thus, we speculated that CNP+MT+FLI increases the IVM of bovine oocytes. In conclusion, our findings deepen our understanding and provide new perspectives on targeting the combination of CNP, MT and FLI to enhance the quality and developmental potential of bovine oocytes.

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