FACTORS AFFECTING IN VITRO PRODUCTION OF BUFFALO EMBRYOS
ABDOON, A., KANDIL, O., OTOI, T., SUZUKI, T. (2001). FACTORS AFFECTING IN VITRO PRODUCTION OF BUFFALO EMBRYOS. EKB Journal Management System, 49(2), 189-198. doi: 10.21608/vmjg.2001.372090
A ABDOON; OMAIMA M KANDIL; T OTOI; T SUZUKI. "FACTORS AFFECTING IN VITRO PRODUCTION OF BUFFALO EMBRYOS". EKB Journal Management System, 49, 2, 2001, 189-198. doi: 10.21608/vmjg.2001.372090
ABDOON, A., KANDIL, O., OTOI, T., SUZUKI, T. (2001). 'FACTORS AFFECTING IN VITRO PRODUCTION OF BUFFALO EMBRYOS', EKB Journal Management System, 49(2), pp. 189-198. doi: 10.21608/vmjg.2001.372090
ABDOON, A., KANDIL, O., OTOI, T., SUZUKI, T. FACTORS AFFECTING IN VITRO PRODUCTION OF BUFFALO EMBRYOS. EKB Journal Management System, 2001; 49(2): 189-198. doi: 10.21608/vmjg.2001.372090

FACTORS AFFECTING IN VITRO PRODUCTION OF BUFFALO EMBRYOS

Veterinary Medical Journal (Giza)
Volume 49, Issue 2, April 2001, Page 189-198  XML PDF (2.97 MB)
Document Type: Original Article
DOI: 10.21608/vmjg.2001.372090
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Authors
A ABDOON* 1; OMAIMA M KANDIL1; T OTOI2; T SUZUKI2
1Department of Animal Reproductions & A.I. National Research Centre, Dokki, 12622 Giza, Egypt.
2Department of Theriogenology, United Graduate School of Veterinary Science, Yamaguchi University 753 Yamaguchi, Japan.
Abstract
The present study was designed to examine the influence of Oocyte quality, culture media and gonadotropins on cleavage rate and development of in vitro fertilized buffalo oocytes. Three experiments were conducted. In Experiment 1; Oocytes were classified by number of cumulus cell layers And morphology of the oopbsm as Good, Fair or Poor. Oocytes were cultured for IVM, IVF and IVC in CR1aa medium. In Experiment 2, good quality oocytes were cultured For maturation in: (1) CR1aa; (2) CR2aa; (3) TCM-199; (4) MEM and (5) RPMI-1640, and then fertilized using frozen Thawed buffalo spermatozoa in CR1aa. After fertilization, Oocytes were cultured in the same medium used for maturation. In Experiment 3, oocytes were classified into 3 groups:Group (1) without gonadotropin and served as control; Group (2) in which IVM medium was supplemented with 10 μg/ml FSH; Group (3) in which IVM medium was supplemented with 10 IU/ml PMSG. In all experiments, 00Cytes were kept at 38.5°C under 5% CO 2 for IVM, IVF,IVC and examined for cleavage and embryo development Rates on day 3 and 8, respectively. Good and fair quality oocytes produced a higher (P<0.01) cleavage rate than poor Quality oocytes. Morula production rate was also higher (P<0.01) for good as compared to fair quality oocytes. Embryo development with poor quality oocytes was arrested at The 2 to 16-cell stage. In Experiment 2. The cleavage rate Was significantly higher(P<0.05) in CR1aa than CR2aa, and Significantly higher (P<0.01) than TCM-199, MEM and RPMI-1640. The numbers of morulae and blastocysts were Higher (P<0.01) for oocytes cultured in CR1aa and CR2aa Media than TCM-199 or MEM. In Experiment 3. The addition of FSH or PMSG to the maturation medium significantly increased (P<0.01) cleavage and developmental rates of Buffalo embryo compared to control media. In conclusion, The IVM of good quality buffalo oocytes in CR1aa or CR2aa medium and the addition of FSH or PMSG in maturation medium produced higher cleavage and developmental rates of IVF buffalo embryos.
Keywords
Buffalo; IVF; oocyte quality; culture media. Gonadotropins; cleavage and embryo developmental rates
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