The effects of duration of in vitro maturation of bovine oocytes on subsequent development, quality and transfer of embryos

We examined the effects of IVM duration on rates of Korean Native Cow (KNC) first polar body extrusion, embryo development and offspring. Cumulus oocytes complexes were cultured in vitro for up to 24 h. Extrusion of the first polar body was highest at 16 h. At selected times during IVM, oocytes were...

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Veröffentlicht in:Theriogenology 2005-07, Vol.64 (1), p.123-134
Hauptverfasser: Park, Yong-Soo, Kim, So-Seob, Kim, Jae-Myeoung, Park, Hum-Dai, Byun, Myung-Dae
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creator Park, Yong-Soo
Kim, So-Seob
Kim, Jae-Myeoung
Park, Hum-Dai
Byun, Myung-Dae
description We examined the effects of IVM duration on rates of Korean Native Cow (KNC) first polar body extrusion, embryo development and offspring. Cumulus oocytes complexes were cultured in vitro for up to 24 h. Extrusion of the first polar body was highest at 16 h. At selected times during IVM, oocytes were fertilized and in vitro development was compared to blastocysts collected from superovulated KNC. After fertilization, the cleavage rate did not differ for oocytes with different durations of IVM, but the development rates of the 8-cell and blastocyst stages were significantly higher in IVM 18-h than other durations. The mean inner cell mass, trophectoderm and total cell numbers of in vivo blastocysts (40.0 ± 3.8, 87.5 ± 3.5 and 127.5 ± 1.6, respectively) were similar to those for IVM 18-h group. When in vitro- and in vivo-derived blastocysts were transferred to Holstein heifer recipients, pregnancy and abortion rates did not differ among treatments. Mean gestation length was significantly shorter for in vivo-derived blastocysts than those derived from oocytes with 24 h of IVM. Birth weight produced by the IVM 24-h group (32.0 ± 2.2 kg) was significantly higher than that of in vivo and IVM 18-h groups. The sex ratio of calves was similar between the in vivo and the IVM 24-h group, but all calves derived from the IVM 18-h group were males. Therefore, duration of bovine oocyte IVM played a critical role in embryo development and blastocyst cell number. In addition, it also affected birth weight and sex ratio.
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Cumulus oocytes complexes were cultured in vitro for up to 24 h. Extrusion of the first polar body was highest at 16 h. At selected times during IVM, oocytes were fertilized and in vitro development was compared to blastocysts collected from superovulated KNC. After fertilization, the cleavage rate did not differ for oocytes with different durations of IVM, but the development rates of the 8-cell and blastocyst stages were significantly higher in IVM 18-h than other durations. The mean inner cell mass, trophectoderm and total cell numbers of in vivo blastocysts (40.0 ± 3.8, 87.5 ± 3.5 and 127.5 ± 1.6, respectively) were similar to those for IVM 18-h group. When in vitro- and in vivo-derived blastocysts were transferred to Holstein heifer recipients, pregnancy and abortion rates did not differ among treatments. Mean gestation length was significantly shorter for in vivo-derived blastocysts than those derived from oocytes with 24 h of IVM. Birth weight produced by the IVM 24-h group (32.0 ± 2.2 kg) was significantly higher than that of in vivo and IVM 18-h groups. The sex ratio of calves was similar between the in vivo and the IVM 24-h group, but all calves derived from the IVM 18-h group were males. Therefore, duration of bovine oocyte IVM played a critical role in embryo development and blastocyst cell number. 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Cumulus oocytes complexes were cultured in vitro for up to 24 h. Extrusion of the first polar body was highest at 16 h. At selected times during IVM, oocytes were fertilized and in vitro development was compared to blastocysts collected from superovulated KNC. After fertilization, the cleavage rate did not differ for oocytes with different durations of IVM, but the development rates of the 8-cell and blastocyst stages were significantly higher in IVM 18-h than other durations. The mean inner cell mass, trophectoderm and total cell numbers of in vivo blastocysts (40.0 ± 3.8, 87.5 ± 3.5 and 127.5 ± 1.6, respectively) were similar to those for IVM 18-h group. When in vitro- and in vivo-derived blastocysts were transferred to Holstein heifer recipients, pregnancy and abortion rates did not differ among treatments. Mean gestation length was significantly shorter for in vivo-derived blastocysts than those derived from oocytes with 24 h of IVM. Birth weight produced by the IVM 24-h group (32.0 ± 2.2 kg) was significantly higher than that of in vivo and IVM 18-h groups. The sex ratio of calves was similar between the in vivo and the IVM 24-h group, but all calves derived from the IVM 18-h group were males. Therefore, duration of bovine oocyte IVM played a critical role in embryo development and blastocyst cell number. In addition, it also affected birth weight and sex ratio.</description><subject>Animals</subject><subject>Birth Weight</subject><subject>Blastocyst</subject><subject>calves</subject><subject>Cattle</subject><subject>Cattle - embryology</subject><subject>Cattle - physiology</subject><subject>Cell Count</subject><subject>Cell number</subject><subject>Cells, Cultured</subject><subject>embryo culture</subject><subject>Embryo development</subject><subject>Embryo transfer</subject><subject>Embryo Transfer - veterinary</subject><subject>Embryo, Mammalian - physiology</subject><subject>embryogenesis</subject><subject>Embryonic Development</subject><subject>Female</subject><subject>Fertilization in Vitro - veterinary</subject><subject>In vitro maturation</subject><subject>Male</subject><subject>Oocytes - growth &amp; development</subject><subject>Pregnancy</subject><subject>Pregnancy Outcome</subject><subject>Sex Ratio</subject><subject>Time Factors</subject><subject>Tissue and Organ Harvesting - methods</subject><subject>Tissue and Organ Harvesting - veterinary</subject><issn>0093-691X</issn><issn>1879-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU-LFDEQxYMo7uzqV9AcxJM9pjqd_gNeZHFXYcGDu-AtpNOV2QzdyWySHmj88qaZAfXmKUV479XjV4S8A7YFBvXH_TY9YrB-h86PfrdsS8aqLcCWQfmMbKBtuoKXHJ6TDWMdL-oOfl6Qyxj3jDFe1_CSXIDouGirdkN-3T8iRWNQp0i9ocMcVLLerbN19GhT8HRS6a_v3h-tQ-q9XhJmk6Nx7iM-zegSHfCIoz9Mef5An2Y12rRQ5QaagnLRYFgTcOrD4uMr8sKoMeLr83tFHm6-3F9_Le6-3367_nxX6KqpUqEUG4QWvBWt0azFpi61qqu6RGEabqAaGkAUgnfQtVXHFccW-0EIzaHThvMr8v6Uewg-t4xJTjZqHEfl0M9R1k3HyopBFn46CXXwMQY08hDspMIigckVvtzLf-HLFb4EkBl-tr8575n7CYc_5jPtLHh7EhjlpdoFG-XDjzIvZjm8BL42uDkpMPM4WgwyaotO42BDPpEcvP2_Lr8BhpCqxw</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Park, Yong-Soo</creator><creator>Kim, So-Seob</creator><creator>Kim, Jae-Myeoung</creator><creator>Park, Hum-Dai</creator><creator>Byun, Myung-Dae</creator><general>Elsevier Inc</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20050701</creationdate><title>The effects of duration of in vitro maturation of bovine oocytes on subsequent development, quality and transfer of embryos</title><author>Park, Yong-Soo ; Kim, So-Seob ; Kim, Jae-Myeoung ; Park, Hum-Dai ; Byun, Myung-Dae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-aa0d5c53858fc08e762ca6462e5f73f14d71ee5539198493a3e8ebd55c319cf33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Birth Weight</topic><topic>Blastocyst</topic><topic>calves</topic><topic>Cattle</topic><topic>Cattle - embryology</topic><topic>Cattle - physiology</topic><topic>Cell Count</topic><topic>Cell number</topic><topic>Cells, Cultured</topic><topic>embryo culture</topic><topic>Embryo development</topic><topic>Embryo transfer</topic><topic>Embryo Transfer - veterinary</topic><topic>Embryo, Mammalian - physiology</topic><topic>embryogenesis</topic><topic>Embryonic Development</topic><topic>Female</topic><topic>Fertilization in Vitro - veterinary</topic><topic>In vitro maturation</topic><topic>Male</topic><topic>Oocytes - growth &amp; development</topic><topic>Pregnancy</topic><topic>Pregnancy Outcome</topic><topic>Sex Ratio</topic><topic>Time Factors</topic><topic>Tissue and Organ Harvesting - methods</topic><topic>Tissue and Organ Harvesting - veterinary</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Yong-Soo</creatorcontrib><creatorcontrib>Kim, So-Seob</creatorcontrib><creatorcontrib>Kim, Jae-Myeoung</creatorcontrib><creatorcontrib>Park, Hum-Dai</creatorcontrib><creatorcontrib>Byun, Myung-Dae</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Theriogenology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Yong-Soo</au><au>Kim, So-Seob</au><au>Kim, Jae-Myeoung</au><au>Park, Hum-Dai</au><au>Byun, Myung-Dae</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effects of duration of in vitro maturation of bovine oocytes on subsequent development, quality and transfer of embryos</atitle><jtitle>Theriogenology</jtitle><addtitle>Theriogenology</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>64</volume><issue>1</issue><spage>123</spage><epage>134</epage><pages>123-134</pages><issn>0093-691X</issn><eissn>1879-3231</eissn><abstract>We examined the effects of IVM duration on rates of Korean Native Cow (KNC) first polar body extrusion, embryo development and offspring. Cumulus oocytes complexes were cultured in vitro for up to 24 h. Extrusion of the first polar body was highest at 16 h. At selected times during IVM, oocytes were fertilized and in vitro development was compared to blastocysts collected from superovulated KNC. After fertilization, the cleavage rate did not differ for oocytes with different durations of IVM, but the development rates of the 8-cell and blastocyst stages were significantly higher in IVM 18-h than other durations. The mean inner cell mass, trophectoderm and total cell numbers of in vivo blastocysts (40.0 ± 3.8, 87.5 ± 3.5 and 127.5 ± 1.6, respectively) were similar to those for IVM 18-h group. When in vitro- and in vivo-derived blastocysts were transferred to Holstein heifer recipients, pregnancy and abortion rates did not differ among treatments. Mean gestation length was significantly shorter for in vivo-derived blastocysts than those derived from oocytes with 24 h of IVM. Birth weight produced by the IVM 24-h group (32.0 ± 2.2 kg) was significantly higher than that of in vivo and IVM 18-h groups. The sex ratio of calves was similar between the in vivo and the IVM 24-h group, but all calves derived from the IVM 18-h group were males. Therefore, duration of bovine oocyte IVM played a critical role in embryo development and blastocyst cell number. In addition, it also affected birth weight and sex ratio.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15935848</pmid><doi>10.1016/j.theriogenology.2004.11.012</doi><tpages>12</tpages></addata></record>
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subjects Animals
Birth Weight
Blastocyst
calves
Cattle
Cattle - embryology
Cattle - physiology
Cell Count
Cell number
Cells, Cultured
embryo culture
Embryo development
Embryo transfer
Embryo Transfer - veterinary
Embryo, Mammalian - physiology
embryogenesis
Embryonic Development
Female
Fertilization in Vitro - veterinary
In vitro maturation
Male
Oocytes - growth & development
Pregnancy
Pregnancy Outcome
Sex Ratio
Time Factors
Tissue and Organ Harvesting - methods
Tissue and Organ Harvesting - veterinary
title The effects of duration of in vitro maturation of bovine oocytes on subsequent development, quality and transfer of embryos
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