Department of Animal Reproduction, Gynaecology and Obstetrics College of Veterinary Science, Assam Agricultural University, Khanapara, Guwahati-781 022, Assam
*E-mail address: bcdeka@gmail.com
Online published on 13 September, 2012.
Goat follicular oocytes recovered by dissection of ovaries obtained from abattoir immediately after slaughter were incubated in vitro at 39° C for 28 h in humidified carbon -di -oxide atmosphere using Dulbecco's Phosphate Buffer Saline (DPBS) and Tissue Culture Medium-199 (TCM-199) - based culture media containing non-hormonal additives to record the extent of oocyte maturation. The incidences of metaphase I and metaphase II in oocytes were significantly (P<0.05) higher in TCM-199 (58.19%, 31.08%, 61.18%, 36.47%) than in DPBS medium (39.39%, 15.15%, 41.33%, 18.67%) when both contained 1 or 3% Bovine Serum Albumin (BSA), granulosa cells and 500 μg sodium pyruvate, 125 μg sodium lactate and 200 μg heparin/ml of media. Replacing BSA with heat-inactivated 20% non-oestrous or oestrous goat serum had no significant effect on the rate of in vitro maturation (IVM) of oocytes. It was concluded that the rate of IVM of goat oocytes could be enhanced by 1 or 3% BSA, granulosa cells, sodium pyruvate (500 μg), sodium lactate (125 μg) and heparin (200 μg)/ml of medium in TCM-199.
Culture media, Follicular oocytes, Goat, In vitro maturation