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Başlık: Replacement of fetal calf serum with synthetic serum substitute in the in vitro maturation medium: Effects on maturation, fertilization and subsequent development of cattle oocytes in vitro
Diğer Başlıklar: In vitro olgulaştırma medyumunda fötal buzağı serumu yerine sentetik serumun kullanılması: Sığır oositlerinin in vitro maturasyon, fertilizasyon ve sonraki gelişimleri üzerindeki etkileri
Yazarlar: Uludağ Üniversitesi/Veteriner Fakültesi/Dölerme ve Suni Tohumlama Anabilim Dalı.
Sağırkaya, Hakan
Yağmur, Mehmet
Soylu, Mustafa Kemal
Nur, Zekariya
AAH-8821-2021
6602400461
57223684553
7003293300
6508060684
Anahtar kelimeler: Veterinary sciences
Animalia
Bos taurus
Bovinae
In vitro maturation
Cattle oocytes
Fetal calf serum
Synthetic serum substitute
Embryo
Bovine follicular oocytes
Epidermal growth-factor
Invitro fertilization
IGF-I
Golden-hamster
Culture media
Embryos
Hormone
Gonadotropins
Complexes
Yayın Tarihi: 2004
Yayıncı: TÜBİTAK
Atıf: Sağırkaya, H. vd. (2004). “Replacement of fetal calf serum with synthetic serum substitute in the in vitro maturation medium: Effects on maturation, fertilization and subsequent development of cattle oocytes in vitro”. Turkish Journal Of Veterinary and Animal Sciences, 28(4), 779-784.
Özet: The aim of this study was to investigate the possibility of using synthetic serum substitute (SSS) instead of fetal calf serum (FCS) in maturation medium to stimulate in vitro maturation (IVM). fertilization (IVF) and subsequent development of bovine oocytes. Ovaries were obtained from a local slaughterhouse. Selected oocytes were matured in tissue culture medium 199 (M-199) supplemented with 2 mM glutamine + 0.25 mM Na-pyruvate + 0.5 mug/ml of FSH + 5 mug/ml of LH + 25 mug/ml of gentamycin and 10% FCS or 10% SSS (FCS and SSS groups, respectively) for 22 h. Matured oocytes were fertilized in vitro using frozen bull sperm. Fertilization day was taken as day 0 in the present study. Forty-eight h after IVF, the numbers of 2-4-cell stage embryos were recorded and they were transferred into CR1aa culture medium for in vitro culture until day 8. In addition, blastocyst numbers were recorded on day 8. A total of 255 and 250 oocytes were used for the FCS and SSS groups, respectively. The cleavage rate of the FCS group (73.7%; 188/255) was significantly higher (P < 0.001) than that of the SSS group (30.0%; 75/250). While the blastocyst formation rate of the FCS group was 16.1% (41/255), no blastocyst development was observed in the SSS group. The difference between the groups in terms of blastocyst formation was also significant (P < 0.001). These results show that serum supplementation of the IVM medium is necessary to obtain a higher cleavage rate and development rate to the blastocyst stage of immature bovine oocytes recovered from ovaries obtained from slaughterhouses. In conclusion, further studies are required to replace FCS with SSS in the maturation medium, and supplementation with growth factors might improve cleavage and development rates in maturation medium supplemented with SSS.
URI: http://hdl.handle.net/11452/29486
ISSN: 1300-0128
Koleksiyonlarda Görünür:Scopus
Web of Science

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