Ejaculate and type of freezing extender affect rates of fertilization of horse oocytes in vitro

Abstract

In vitro fertilization (IVF) was performed on in vitro-matured equine oocytes in three experiments. Frozen–thawed sperm were prepared using swim-up separation and heparin treatment. In Experiment 1, fertilization was achieved with sperm from only one frozen ejaculate of four obtained from the same stallion. Within this ejaculate, fertilization rates were higher with fresh media, as compared to media held for 6–8 days before use (39.6% versus 7.3%, respectively; P < 0.001). The type of bovine serum albumin used affected fertilization rates (4% versus 39.6%; P < 0.001). To determine if IVF rates were influenced by factors associated with the freezing process (Experiment 2), a single ejaculate from a second stallion was frozen using eight variations in timing of steps in the freezing protocol. There were no differences among treatments in fertilization rates (range, 0–3%). In Experiment 3, fertilization rates of semen frozen in an extender containing 21.5% egg yolk were lower than fertilization rates of semen from the same ejaculate but frozen with a 3% egg-yolk extender (0% versus 15%, respectively; P < 0.01). We inferred that rates of equine IVF with frozen–thawed sperm were influenced by ejaculate, the composition and age of the media used, and freezing extender. To our knowledge, this is the first report of ejaculate or extender differences affecting in vitro fertilization in this species. These factors may help to explain the great variability in fertilization rates reported with equine IVF, both among and within laboratories.