Buffalo cumulus oocytes were cultured in a serum-free medium in the in vivo bovine vagina using empty CIDR and semen straws. The culture was successful yet a lower proportion of oocytes matured in the in vivo vagina compared to conventional culture in an incubator.
Original Title
In Vitro Maturation of Buffalo Oocytes in Bovine Vagina in a serum free medium
Buffalo cumulus oocytes were cultured in a serum-free medium in the in vivo bovine vagina using empty CIDR and semen straws. The culture was successful yet a lower proportion of oocytes matured in the in vivo vagina compared to conventional culture in an incubator.
Buffalo cumulus oocytes were cultured in a serum-free medium in the in vivo bovine vagina using empty CIDR and semen straws. The culture was successful yet a lower proportion of oocytes matured in the in vivo vagina compared to conventional culture in an incubator.
738 Therioganology f
_IN VITRO MATURATION OF BUBALINE
UM-
OOCYTES INTHE BOVINE VAGINA IN
MEDIUM.
GN, Purohit and 8. Sharnia
Department of Veterinary Obstetrics & Gynaecology, Vely Coll
Bikaner, Rajasthan, |
pe, Rajasthan Agric, University,
In an silempt to find out simpler-cos
L-effective means of in vitro fertilization, a technique of
intra-vagiial culture for in vitro maturation of buffalo follicular oocytes in the bovine vagina was
Weveloped. Ovaries were collected from the skiughterhouse in v
plemented with 50-1U of pea and 50 Ug.steptomye
Oocytes recovered by aspiration of ov:
25. mM Hepes, 0.25 mM pyruvat
in 100 ul droplets under oil
rm, normal saline solution sup- 2
vil withit hours of slaughter. £3
ss were cultured in'TCM 199 medium supplemented with “3
Sup/inl FSH, Sug/ml LU, Lug/il estradiol libiotics either
4 CO2 incubator for 24h or loaded in pre-sterilized emply semea
straws which were scaled and then loaded in the groove of an empty commercial plastic proges-
Xerone implant, CIDR-B (Controlled Internal Drug Release-Bovine, Inter-Ag Hamilton NJ). The
CIDR:B was. loaded in its applicator and placed in the vagina of a cow. The irnplant was with-
drawn after 24h of culture, the straws taken out and oocytes with medium emptied in-a petri dish...
Oocytes were freed from the cumulus cells by vortexing and fixed with acetic methanol for 248.
* Oocytes were stained with 1% aceto-oreein and examined for nuclear maturation. The proportion
4, of oocytes reaching M-Il in the laboratory culture and intra-vaginal culture was 68.88% (31/45) and
} 52.70% (58/111) respectively. The proportion of oocytes not resuming meiosis and remaining at 7
"GV was 8.88% (4/45) and 25.22% (28/111), whereas, those arrested at AT-1 were 22.22% (10/45) “#
“and 13.51% (15/111) in the two cultures, respectively. ‘The percentage comparisons for the two ‘$
cultures was done by Chi-square test. Preliminary results show a lower effi
cultuig, however, the technique has a field application and needs experiment:
ture,
a
3
4
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