Mechanism of the adverse effect of hyaluronidase used for oocyte denudation on early development of bovine embryos

Hyaluronidase is widely used in animal and human assisted reproductive technologies (ARTs) to remove cumulus cells around oocytes. However, adverse effects of hyaluronidase treatment, such as increased rates of degeneration and parthenogenesis, have been found after treatment of human and mouse oocytes. Currently, the mechanism(s) of the detrimental effects are unclear. The present study was initiated to identify the mechanism of adverse responses to hyaluronidase treatment in bovine oocytes and early embryos. Cumulus cells were removed from cumulus-oocyte complexes (COCs) with or without hyaluronidase and the oocytes were subjected to intracytoplasmic sperm injection (ICSI) or in vitro fertilization (IVF). Significantly lower rates of blastocyst formation were obtained in the hyaluronidase treatment group after ICSI (22.4%) and IVF (21.2%) compared with the non-hyaluronidase control groups: 36.1% after ICSI and 30.4% after IVF. Next, we examined the effect of hyaluronidase on parthenogenetic development rates and on the cytoplasmic levels of free calciumions (Ca2thorn), reactive oxygen species (ROS) and reduced glutathione (GSH). No differences in parthenogenesis rates were found between treated and untreated groups. Ca2thorn levels in oocytes from the hyaluronidase treatment group indicated using mean fluorescence intensity were significantly higher (68.8 +/- 5.3) compared with in the control group (45.0 +/- 2.5). No differences were found in the levels of ROS or GSH between the treated and untreated groups. We conclude that hyaluronidase might trigger an increase in Ca2thorn levels in oocytes, resulting in a decreased potential for normal embryonic development.

Automated summary

This study investigated the mechanism of adverse effects of hyaluronidase treatment in bovine oocytes and early embryos. The results showed a significantly lower blastocyst formation rate in the hyaluronidase treatment group, and an increase in intracellular calcium ion levels, potentially inhibiting normal embryonic development. No differences were found in parthenogenetic development rates, reactive oxygen species, or reduced glutathione levels between treated and untreated groups.