Effects of fetal calf serum in culture medium on development of bovine oocytes matured and fertilized in vitro

Bovine oocytes matured and fertilized in vitro were cultured in a chemically defined bovine embryo culture medium (BECM) or polyvinylalcohol (PVA)-free BECM supplemented with 10% heat-treated or unheated fetal calf serum (FCS). When PVA in BECM was replaced with FCS 8 h postinsemination, the proport...

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Veröffentlicht in:Theriogenology 1994, Vol.41 (5), p.1091-1098
Hauptverfasser: Lim, J.M., Okitsu, O., Okuda, K., Niwa, K.
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container_end_page 1098
container_issue 5
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container_title Theriogenology
container_volume 41
creator Lim, J.M.
Okitsu, O.
Okuda, K.
Niwa, K.
description Bovine oocytes matured and fertilized in vitro were cultured in a chemically defined bovine embryo culture medium (BECM) or polyvinylalcohol (PVA)-free BECM supplemented with 10% heat-treated or unheated fetal calf serum (FCS). When PVA in BECM was replaced with FCS 8 h postinsemination, the proportion of ≥-cell-stage embryos 48 h postinsemination was significantly lower in heat-treated FCS (74%) than in PVA (91%) medium, but the value (84%) in unheated FCS was not different from the values in PVA and heat-treated FCS. However, the addition of either heat-treated FCS or unheated FCS to PVA-free BECM did not depress or increase the proportions (63 to 70%) of ≥-cell-stage embryos 96 h postinsemination and stimulated blastocyst formation 144 (21 to 28%) and 192 (47 to 54%) h postinsemination. Blastocyst formation was also stimulated when heattreated FCS or unheated FCS was added to PVA-free BECM 120 h postinsemination. The mean cell number of blastocysts developed in PVA-free BECM with heat-treated FCS (150 cells) or unheated FCS (152 cells) significantly increased compared with that (119 cells) developed without FCS. These results indicate that, although BECM can support bovine embryo development, a high proportion (about 50%) of morphologically normal blastocysts can be produced from oocytes matured and fertilized in vitro when they are cultured in PVA-free BECM containing FCS.
doi_str_mv 10.1016/S0093-691X(05)80032-9
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When PVA in BECM was replaced with FCS 8 h postinsemination, the proportion of ≥-cell-stage embryos 48 h postinsemination was significantly lower in heat-treated FCS (74%) than in PVA (91%) medium, but the value (84%) in unheated FCS was not different from the values in PVA and heat-treated FCS. However, the addition of either heat-treated FCS or unheated FCS to PVA-free BECM did not depress or increase the proportions (63 to 70%) of ≥-cell-stage embryos 96 h postinsemination and stimulated blastocyst formation 144 (21 to 28%) and 192 (47 to 54%) h postinsemination. Blastocyst formation was also stimulated when heattreated FCS or unheated FCS was added to PVA-free BECM 120 h postinsemination. The mean cell number of blastocysts developed in PVA-free BECM with heat-treated FCS (150 cells) or unheated FCS (152 cells) significantly increased compared with that (119 cells) developed without FCS. 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When PVA in BECM was replaced with FCS 8 h postinsemination, the proportion of ≥-cell-stage embryos 48 h postinsemination was significantly lower in heat-treated FCS (74%) than in PVA (91%) medium, but the value (84%) in unheated FCS was not different from the values in PVA and heat-treated FCS. However, the addition of either heat-treated FCS or unheated FCS to PVA-free BECM did not depress or increase the proportions (63 to 70%) of ≥-cell-stage embryos 96 h postinsemination and stimulated blastocyst formation 144 (21 to 28%) and 192 (47 to 54%) h postinsemination. Blastocyst formation was also stimulated when heattreated FCS or unheated FCS was added to PVA-free BECM 120 h postinsemination. The mean cell number of blastocysts developed in PVA-free BECM with heat-treated FCS (150 cells) or unheated FCS (152 cells) significantly increased compared with that (119 cells) developed without FCS. These results indicate that, although BECM can support bovine embryo development, a high proportion (about 50%) of morphologically normal blastocysts can be produced from oocytes matured and fertilized in vitro when they are cultured in PVA-free BECM containing FCS.</description><subject>body fluids</subject><subject>bovin</subject><subject>bovine</subject><subject>cattle</subject><subject>cultivo de embriones</subject><subject>culture d' embryon</subject><subject>culture media</subject><subject>desarrollo embrionario</subject><subject>developpement embryonnaire</subject><subject>duracion</subject><subject>duration</subject><subject>duree</subject><subject>embryo culture</subject><subject>embryonic development</subject><subject>embryos</subject><subject>experimentacion in vitro</subject><subject>experimentation in vitro</subject><subject>fecondation</subject><subject>fecundacion</subject><subject>fertilization</subject><subject>fetal calf serum</subject><subject>ganado bovino</subject><subject>gestacion</subject><subject>gestation</subject><subject>in vitro experimentation</subject><subject>liquide biologique</subject><subject>liquidos corporales</subject><subject>medio de cultivo</subject><subject>milieu de culture</subject><subject>ova</subject><subject>ovule</subject><subject>ovulo</subject><subject>pregnancy</subject><subject>preimplantation development</subject><issn>0093-691X</issn><issn>1879-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNqFkc1q3DAUhUVoSSZpHyFFuzYLt_oZydaqlJCfQqCLNNCdkK-vgoptTSV5IH36ajJDsuxKXPGdc8UnQs45-8wZ11_uGTOy0Yb_-sTURceYFI05IivetaaRQvI3ZPWCnJDTnH-zCmnNj8kJ161o11qsyHzlPULJNHrqsbiRghs9zZiWiYaZwjKWJSGdcAj1Js50wC2OcTPhXHahPm7DjDRGeCqY6eR2-EDdPNS-VMIY_taxNm1DSfEdeevdmPH94TwjD9dXPy9vm7sfN98vv901sFa8NB2TRnoJbjDKM2688qBV35nOO1ADrFuHygnOALpeI-97DqITg--wyhEgz8jHfe8mxT8L5mKnkAHH0c0Yl2xbueaslUJUUu1JSDHnhN5uUphcerKc2Z1p-2za7jRapuyzaWtq7sNhw9JXOa-pg9pXwLto3WMK2T7cc2MUY9oIrSvwdQ9gFbENmGyGgDNU06l-iR1i-M8b_gEk05kF</recordid><startdate>1994</startdate><enddate>1994</enddate><creator>Lim, J.M.</creator><creator>Okitsu, O.</creator><creator>Okuda, K.</creator><creator>Niwa, K.</creator><general>Elsevier Inc</general><scope>FBQ</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>1994</creationdate><title>Effects of fetal calf serum in culture medium on development of bovine oocytes matured and fertilized in vitro</title><author>Lim, J.M. ; Okitsu, O. ; Okuda, K. ; Niwa, K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-80393f3cad95f019f5fc65b898fac5dc47ae5a210cc8b6e1bb1c282df8e1012c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>body fluids</topic><topic>bovin</topic><topic>bovine</topic><topic>cattle</topic><topic>cultivo de embriones</topic><topic>culture d' embryon</topic><topic>culture media</topic><topic>desarrollo embrionario</topic><topic>developpement embryonnaire</topic><topic>duracion</topic><topic>duration</topic><topic>duree</topic><topic>embryo culture</topic><topic>embryonic development</topic><topic>embryos</topic><topic>experimentacion in vitro</topic><topic>experimentation in vitro</topic><topic>fecondation</topic><topic>fecundacion</topic><topic>fertilization</topic><topic>fetal calf serum</topic><topic>ganado bovino</topic><topic>gestacion</topic><topic>gestation</topic><topic>in vitro experimentation</topic><topic>liquide biologique</topic><topic>liquidos corporales</topic><topic>medio de cultivo</topic><topic>milieu de culture</topic><topic>ova</topic><topic>ovule</topic><topic>ovulo</topic><topic>pregnancy</topic><topic>preimplantation development</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lim, J.M.</creatorcontrib><creatorcontrib>Okitsu, O.</creatorcontrib><creatorcontrib>Okuda, K.</creatorcontrib><creatorcontrib>Niwa, K.</creatorcontrib><creatorcontrib>Selskostopanska Akademiya, Sofia (Bulgaria)</creatorcontrib><collection>AGRIS</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>Lim, J.M.</au><au>Okitsu, O.</au><au>Okuda, K.</au><au>Niwa, K.</au><aucorp>Selskostopanska Akademiya, Sofia (Bulgaria)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of fetal calf serum in culture medium on development of bovine oocytes matured and fertilized in vitro</atitle><jtitle>Theriogenology</jtitle><addtitle>Theriogenology</addtitle><date>1994</date><risdate>1994</risdate><volume>41</volume><issue>5</issue><spage>1091</spage><epage>1098</epage><pages>1091-1098</pages><issn>0093-691X</issn><eissn>1879-3231</eissn><abstract>Bovine oocytes matured and fertilized in vitro were cultured in a chemically defined bovine embryo culture medium (BECM) or polyvinylalcohol (PVA)-free BECM supplemented with 10% heat-treated or unheated fetal calf serum (FCS). When PVA in BECM was replaced with FCS 8 h postinsemination, the proportion of ≥-cell-stage embryos 48 h postinsemination was significantly lower in heat-treated FCS (74%) than in PVA (91%) medium, but the value (84%) in unheated FCS was not different from the values in PVA and heat-treated FCS. However, the addition of either heat-treated FCS or unheated FCS to PVA-free BECM did not depress or increase the proportions (63 to 70%) of ≥-cell-stage embryos 96 h postinsemination and stimulated blastocyst formation 144 (21 to 28%) and 192 (47 to 54%) h postinsemination. Blastocyst formation was also stimulated when heattreated FCS or unheated FCS was added to PVA-free BECM 120 h postinsemination. The mean cell number of blastocysts developed in PVA-free BECM with heat-treated FCS (150 cells) or unheated FCS (152 cells) significantly increased compared with that (119 cells) developed without FCS. These results indicate that, although BECM can support bovine embryo development, a high proportion (about 50%) of morphologically normal blastocysts can be produced from oocytes matured and fertilized in vitro when they are cultured in PVA-free BECM containing FCS.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16727462</pmid><doi>10.1016/S0093-691X(05)80032-9</doi><tpages>8</tpages></addata></record>
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source Elsevier ScienceDirect Journals
subjects body fluids
bovin
bovine
cattle
cultivo de embriones
culture d' embryon
culture media
desarrollo embrionario
developpement embryonnaire
duracion
duration
duree
embryo culture
embryonic development
embryos
experimentacion in vitro
experimentation in vitro
fecondation
fecundacion
fertilization
fetal calf serum
ganado bovino
gestacion
gestation
in vitro experimentation
liquide biologique
liquidos corporales
medio de cultivo
milieu de culture
ova
ovule
ovulo
pregnancy
preimplantation development
title Effects of fetal calf serum in culture medium on development of bovine oocytes matured and fertilized in vitro
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