000 02979cam a2200325 a 4500
003 EG-GiCUC
008 160529s2016 ua dh f m 000 0 eng d
040 _aEG-GiCUC
_beng
_cEG-GiCUC
041 0 _aeng
049 _aDeposite
097 _aM.Sc
099 _aCai01.10.14.M.Sc.2016.Am.S
100 0 _aAmr Salah Mohamed Elshalofy
245 1 0 _aSome trials for cryobanking of Egyptian buffalo oocytes /
_cAmr Salah Mohamed Elshalofy ; Supervised Aly B. A. Badawy , Sayed T. Ismail , Gamal M. Darwish
246 1 5 _aبعض المحاولات لحفظ بويضات الجاموس المصرى عن طريق التجميد
260 _aCairo :
_bAmr Salah Mohamed Elshalofy ,
_c2016
300 _a120 P. :
_bcharts , facsimiles ;
_c25cm
502 _aThesis (M.Sc.) - Cairo University - Faculty of Veterinary Medicine - Department of Theriogenology
520 _aA total number of 2074 cumulus oocyte complexes (COCs) were aspirated from 1488 ovary collected from a local slaughterhouse (Cairo, Egypt) from January 2014 to October 2015, then COCs, with at least two to three compact layers of cumulus cells and a homogeneous cytoplasm, were selected under a stereomicroscope for the following experiments. Experiment 1, studied the effect of different CPAs and CPAs combinations on maturation of (GV) stage buffalo oocytes in vitro. The maturation rates of (GV) buffalo oocytes were accounted to be (38.10%, 32.00%, 26.51%, 24.07%and 22.00%) after exposure to EG40%, EG20% + GLY20%, EG20% + DMSO20%, EG20% and EG10% CPAs, respectively. Experiment 2, the removal of sucrose from these CPAs solutions has resulted in a significant (P < 0.05) increase in this criteria (59.74%, 51.85% and 40.26%) after exposure to EG20% + DMSO20%, EG20% + GLY20% and EG40%, respectively. Experiment 3, (GV) buffalo oocytes were vitrified after exposure to (20% EG + 20% GLY or 20% EG + 20% DMSO) in straw, open pulled straw or solid surface vitrification system. The highest cleavage and blastocyst rates were obtained in SSV with 20% EG + 20% DMSO group (47.06% and 24.00%, respectively). These values were comparable to those recorded in the control group (61.22% and 46.90%, respectively). Experiment 4, no significant difference was noted between sucrose and trehalose warming media in cleavage and blastocyst rates (44.89% and 20.41% vs. 28.89% and 8.89% respectively). In conclusion, vitrification of buffalo (GV) oocytes using vitrification solutions composed of 20% EG + 20 DMSO without sucrose using SSV, then warming in a stepwise manner using either sucrose or trehalose is the best method for vitrification of (GV) buffalo oocytes
530 _aIssued also as CD
653 4 _aBuffalo
653 4 _aOocyte
653 4 _aVitrification
700 0 _aAly Badawy Aly Badawy ,
_eSupervisor
700 0 _aGamal Moustafa Darwish ,
_eSupervisor
700 0 _aSayed Taha Ismail ,
_eSupervisor
905 _aNazla
_eRevisor
905 _aSamia
_eCataloger
942 _2ddc
_cTH
999 _c56687
_d56687