Transvaginal aspiration of oocytes from hormone-treated pregnant beef cattle for in vitro fertilization.

1995 
The ability to produce oocytes from genetically valuable, pregnant donors in a safe, repeatable manner would broaden the application of in vitro fertilization (IVF) procedures for beef and dairy cattle. The objectives of this study were to evaluate two gonadotropin treatment schedules for follicle stimulation of pregnant donor cattle and to determine the efficacy and safety of the repeated oocyte aspiration procedure from pregnant cattle. In Exp. 1, pregnant donors at 60 to 90 d of gestation were randomly allotted to three treatment groups. Cows in Treatment A received a total dose of 40 mg of FSH. Cows in Treatment B were administered a total of 20 mg of FSH, and females in Treatment C served as pregnant vehicle-treated controls. A group of luteal phase cows received a total of 40 mg of FSH and served as nonpregnant controls (Treatment D). Ultrasound-guided transvaginal oocyte aspiration was performed 12 h following the last FSH or saline injection. Following follicle aspiration, oocytes were matured for 24 h and then entered a standard bovine IVF procedure. Experiment 2 was conducted to determine the repeatability of this procedure on first trimester cows. Cows in Exp. 2 were selected (after a 20-d recovery period) from each of the three pregnant treatment groups in Exp. 1 and each given 40 mg of FSH before a second oocyte aspiration procedure. The number of follicles aspirated per cow in treatment groups receiving the high FSH dose treatment (40 mg of FSH total dose) was not different (Treatment A, Treatment D, and cows in Exp. 2). The oocyte recovery rate for cows in Treatments A and D (also for cows in Exp. 2) given the high FSH dose was greater (P<.05) than for cows in both Treatments B (low FSH dose) and C (no FSH). The percentage of viable oocytes recovered from pregnant donors in Treatment A was greater (P<.05) than from similar pregnant females aspirated in Treatment B. This procedure proved to be effective and repeatable for viable oocyte recovery and safe for pregnant donors, because luteal function was maintained and no fetal loss resulted during pregnancy
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