Using CR1aa versus KSOM as the culture medium for in vitro embryo production of cattle

This research has been conducted at the laboratory of in vitro fertilization in the Department of Animal Science University of Wisconsin, USA. These embryos can be used for improving genetic value of Indonesian cattle. Oocytes were matured in TCM- 199 medium (in 5% CO2 incubator and at 390C) enriche...

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Main Authors: Endang Triwulaninngsih, M.R Toelihere, J.J Rutledge, T.L Yusuf, B Purwantara, K Diwyanto
Format: Article
Language:English
Published: Pusat Penelitian dan Pengembangan Peternakan 2002-03-01
Series:Jurnal Ilmu Ternak dan Veteriner
Subjects:
Online Access:http://medpub.litbang.pertanian.go.id/index.php/jitv/article/view/272/272
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spelling doaj-0503629db5324a0d8261b5d729b4f3a42020-11-24T22:34:36ZengPusat Penelitian dan Pengembangan PeternakanJurnal Ilmu Ternak dan Veteriner0853-73802252-696X2002-03-01713037Using CR1aa versus KSOM as the culture medium for in vitro embryo production of cattleEndang TriwulaninngsihM.R ToelihereJ.J RutledgeT.L YusufB PurwantaraK DiwyantoThis research has been conducted at the laboratory of in vitro fertilization in the Department of Animal Science University of Wisconsin, USA. These embryos can be used for improving genetic value of Indonesian cattle. Oocytes were matured in TCM- 199 medium (in 5% CO2 incubator and at 390C) enriched with follicle stimulating hormone (FSH) 10 μl/ml, oestradiol 17 β 1μl/ml and 10% Fetal Calf Serum (FCS). The oocytes were fertilized in vitro with motile sperm and incubation between sperm and oocytes in fertilization medium Tyroide Albumin Lactate Pyruvate (TALP) for 20 hours. All zygotes were cultured in CR1aa (n=1549) medium versus modification of protein-free pottasium simplex optimized medium (KSOM) (n=675) up to blastocyst stage and were fed FCS 5 μl/50 μl medium on day 6, as treatment A and B respectively. Data were analyzed by completely randomized design with SAS program. Percentages of cleavage, morula, blastocyst, expanded blastocyst, unfertilized and degenerated ova in this study were 91.4% vs 75.6 %; 75.6% vs 58.9%; 61.5% vs 38.5%; 31.2% vs 5.1%, 8.6% vs 24.4%, 15.7% vs 8% which were significantly different (P<0.01) for treatment CR1aa and KSOM respectively. Based on this study, CR1aa medium is better culture medium than KSOM for efficient in vitro production (IVP) of bovine embryos.http://medpub.litbang.pertanian.go.id/index.php/jitv/article/view/272/272Oocytesin vitro fertilizationembryoblastocystculture medium
collection DOAJ
language English
format Article
sources DOAJ
author Endang Triwulaninngsih
M.R Toelihere
J.J Rutledge
T.L Yusuf
B Purwantara
K Diwyanto
spellingShingle Endang Triwulaninngsih
M.R Toelihere
J.J Rutledge
T.L Yusuf
B Purwantara
K Diwyanto
Using CR1aa versus KSOM as the culture medium for in vitro embryo production of cattle
Jurnal Ilmu Ternak dan Veteriner
Oocytes
in vitro fertilization
embryo
blastocyst
culture medium
author_facet Endang Triwulaninngsih
M.R Toelihere
J.J Rutledge
T.L Yusuf
B Purwantara
K Diwyanto
author_sort Endang Triwulaninngsih
title Using CR1aa versus KSOM as the culture medium for in vitro embryo production of cattle
title_short Using CR1aa versus KSOM as the culture medium for in vitro embryo production of cattle
title_full Using CR1aa versus KSOM as the culture medium for in vitro embryo production of cattle
title_fullStr Using CR1aa versus KSOM as the culture medium for in vitro embryo production of cattle
title_full_unstemmed Using CR1aa versus KSOM as the culture medium for in vitro embryo production of cattle
title_sort using cr1aa versus ksom as the culture medium for in vitro embryo production of cattle
publisher Pusat Penelitian dan Pengembangan Peternakan
series Jurnal Ilmu Ternak dan Veteriner
issn 0853-7380
2252-696X
publishDate 2002-03-01
description This research has been conducted at the laboratory of in vitro fertilization in the Department of Animal Science University of Wisconsin, USA. These embryos can be used for improving genetic value of Indonesian cattle. Oocytes were matured in TCM- 199 medium (in 5% CO2 incubator and at 390C) enriched with follicle stimulating hormone (FSH) 10 μl/ml, oestradiol 17 β 1μl/ml and 10% Fetal Calf Serum (FCS). The oocytes were fertilized in vitro with motile sperm and incubation between sperm and oocytes in fertilization medium Tyroide Albumin Lactate Pyruvate (TALP) for 20 hours. All zygotes were cultured in CR1aa (n=1549) medium versus modification of protein-free pottasium simplex optimized medium (KSOM) (n=675) up to blastocyst stage and were fed FCS 5 μl/50 μl medium on day 6, as treatment A and B respectively. Data were analyzed by completely randomized design with SAS program. Percentages of cleavage, morula, blastocyst, expanded blastocyst, unfertilized and degenerated ova in this study were 91.4% vs 75.6 %; 75.6% vs 58.9%; 61.5% vs 38.5%; 31.2% vs 5.1%, 8.6% vs 24.4%, 15.7% vs 8% which were significantly different (P<0.01) for treatment CR1aa and KSOM respectively. Based on this study, CR1aa medium is better culture medium than KSOM for efficient in vitro production (IVP) of bovine embryos.
topic Oocytes
in vitro fertilization
embryo
blastocyst
culture medium
url http://medpub.litbang.pertanian.go.id/index.php/jitv/article/view/272/272
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