Fertility after different artificial insemination methods using a synthetic semen extender in sheep

• Published in: Journal of Reproduction and Development 2009, Vol.55(1), pp.50-54
• Main Authors: Hiwasa, M.(Obihiro Univ. of Agriculture and Veterinary Medicine, Hokkaido (Japan)), Kohno, H, Togari, T, Okabe, K, Fukui, Y
• Format: Article
• Language: English
• Subjects: Animals; ARTIFICIAL INSEMINATION; Artificial insemination (AI); Breeding seasons; Cervix; Chorionic gonadotropin; CONSERVACION DEL SEMEN; CONSERVATION DU SPERME; Cryopreservation - methods; Cryoprotective Agents - pharmacology; Embryos; Estrus; Experiments; FECONDATION; FECUNDACION; Female; Fertility; Fertility - drug effects; Fertility - physiology; FERTILIZATION; Follicle-stimulating hormone; GESTACION; GESTATION; Gonadotropins; INSEMINACION ARTIFICIAL; INSEMINATION ARTIFICIELLE; Insemination, Artificial - methods; Insemination, Artificial - veterinary; Laparoscopy; Male; METHODE; METHODS; METODOS; Ova; OVIN; OVINOS; Ovulation; Pituitary (anterior); PREGNANCY; Pregnancy Rate; Progesterone; Semen; Semen extender; SEMEN PRESERVATION; Semen Preservation - methods; Semen Preservation - veterinary; SHEEP; Sheep - physiology; Uterus
• ISSN: 0916-8818; 1348-4400
• DOI: 10.1262/jrd.20062

The present study aimed to investigate the fertility of ewes artificially inseminated with three different methods using a synthetic semen extender, AndroMed. The three methods of artificial insemination (AI) were cervical AI with fresh-diluted or frozen-diluted semen at observed estrus, and an intrauterine AI with, frozen-thawed semen. A total of 80 ewes were treated with a controlled internal drug release (CIDR) containing 0.3 g progesterone per device for 12 days. In Experiment 1 (26 Suffolk ewes), superovulation was induced with 20 mg follicle-stimulating hormone and 250 IU equine chorionic gonadotropin (eCG) two days and one day before CIDR removal, respectively, during the nonbreeding season. In Experiment 2 (54 Suffolk and Suffolk crossbred ewes), an intramuscular injection of 500 IU eCG was administered one day before CIDR removal to synchronize estrus and ovulation during the breeding season. In Experiment 1, fresh-diluted or frozen-thawed semen was deposited into the cervical orifice after estrus detection, and an intrauterine AI with frozen-thawed semen was performed by laparoscopy at a fixed-time basis without estrus detection. Embryos were recovered by uterine flushing 6 days after AI, and the rates of recovered, fertilized (cleaved) ova and embryos at the morula or blastocyst stage were compared among the three AI methods. In Experiment 2, the pregnancy rates after the three AI methods were compared. In Experiment 1, the rates of recovered ova were not significantly different among the three AI methods (52.5-56.7%). The rate of fertilized ova (81.0%) by laparoscopic AI with frozen-thawed semen was significantly higher compared with cervical AI of fresh-diluted (25.5%) or frozen-thawed (3.5%) semen, but the rate of embryos at the morula or blastocyst stage (17.6%) was significantly lower than that of the cervical AI with fresh-diluted semen (69.2%). The rates of ewes yielding fertilized ova were not significantly different among the three groups (44.4. 11.1 and 62.5% for cervical AI with fresh-diluted and frozen-thawed semen and intrauterine AI with frozen-thawed semen). In Experiment 2, the pregnancy rate of ewes intrauterinally inseminated with frozen-thawed semen (72.2%) was significantly higher than those of ewes inseminated cervically with fresh-diluted (5.5%) or frozen-thawed (0.0%) semen. The present results showed that acceptable fertilization and pregnancy rates could be obtained by an intrauterine AI with frozen-thawed semen using a