Ankara Üniversitesi Veteriner Fakültesi Dergisi

Öz

In this study, in vitro fertilization of rabbit ova was
investigated. For this purpose, 42 females and 6 male rabbits (New
Zealand) were used during the research. The experimental animals
were divided into 12 groups. PMSG (150-250 LU) and HCG (75-100
LU) were injected for superfolliculation and superovulation. Totally
62 follicles and 616 ovulation places (corpus haemorrhagicum) were
counted in different times following administration of gonadotrophins.
Two hundredfiftyone (37.02 %) ova were collected by flushing oviducts
and ruptured follicles with the defined medium. Collected ova were identi/ied under stereo microscope and estimated as normal and degenerated. One Iıundred fourty five (57.76 %), 102 (40.63 %), and 4(1.59
%) of ova were covered with zona pellucida, corona radiata and cumulus oophorus, respectively. Totally 236 normalova were used for in
vitro fertilization. These normalova were incubated witlı capacitated
spermatozoa in tlıe in vitro fertilization medium under paraffin oif whiclı
had been equilibrated with 5 % COı + 95 % Nı at 37-38 oC in a incubator. Af ter 24-28 hours incubation, the ova were controlled under
stereo microscope and were classified as fertilized or unfertilized
According to the results, tlıe in vitro fertilization was observed in
47 (19.91 %) out of 236 ova and 34 of fertifized ova were normal and
the rest (13 ova) were abnormal. One hundred eightynine ova were foul/d as unfertilized and degenerated.