In vitro comparison of egg yolk–based and soybean lecithin–based extenders for cryopreservation of ram semen
Substitution of egg yolk with soybean lecithin may reduce hygienic risks in extenders. Though a few studies have been performed on the effect of soybean lecithin in bull, to date evaluation of ram semen in vitro fertility after cryopreservation with use of soybean lecithin has not been studied. This...
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creator | Forouzanfar, M. Sharafi, M. Hosseini, S.M. Ostadhosseini, S. Hajian, M. Hosseini, L. Abedi, P. Nili, N. Rahmani, H.R. Nasr-Esfahani, M.H. |
description | Substitution of egg yolk with soybean lecithin may reduce hygienic risks in extenders. Though a few studies have been performed on the effect of soybean lecithin in bull, to date evaluation of ram semen in vitro fertility after cryopreservation with use of soybean lecithin has not been studied. This study assessed the effect of 1% or 2% (wt/vol) soybean lecithin (L1 or L2) or 15% or 20% (vol/vol) egg yolk (E15 or E20) supplemented with 5% or 7% glycerol (G5 or G7) in a Tris-based medium for cryopreservation of ram (Oviss arries) semen. Although no significant difference was observed in pattern of capacitation, the best results in terms of sperm motility, viability postthaw, and cleavage rates were observed with L1G7 (51.9
±
4.8%, 48.1
±
3.5%, and 79.6
±
3.9%, respectively) and E20G7 (51.8
±
2.9%, 46.7
±
4.0%, and 72.9
±
6.4%, respectively). Our results also showed that 1% lecithin and 20% egg yolk was superior to 2% lecithin and 15% egg yolk. In terms of cleavage rate, 7% glycerol was superior to 5% glycerol. No significant difference was obtained between groups in terms of blastocysts rate per cleaved embryo. Therefore, we concluded that the optimal concentration of lecithin and egg yolk is 1% and 20%, respectively, along with 7% glycerol. In addition, our results suggest that lecithin can be used as a substitute for egg yolk. |
doi_str_mv | 10.1016/j.theriogenology.2009.10.005 |
format | Article |
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±
4.8%, 48.1
±
3.5%, and 79.6
±
3.9%, respectively) and E20G7 (51.8
±
2.9%, 46.7
±
4.0%, and 72.9
±
6.4%, respectively). Our results also showed that 1% lecithin and 20% egg yolk was superior to 2% lecithin and 15% egg yolk. In terms of cleavage rate, 7% glycerol was superior to 5% glycerol. No significant difference was obtained between groups in terms of blastocysts rate per cleaved embryo. Therefore, we concluded that the optimal concentration of lecithin and egg yolk is 1% and 20%, respectively, along with 7% glycerol. In addition, our results suggest that lecithin can be used as a substitute for egg yolk.</description><identifier>ISSN: 0093-691X</identifier><identifier>EISSN: 1879-3231</identifier><identifier>DOI: 10.1016/j.theriogenology.2009.10.005</identifier><identifier>PMID: 20022626</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acrosome Reaction - physiology ; Animals ; capacitation ; Capacitation status ; cell cleavage ; Cryopreservation ; Cryopreservation - methods ; Cryopreservation - veterinary ; Cryoprotective Agents ; Egg Yolk ; Extenders ; Fertilization in Vitro - veterinary ; Glycine max - chemistry ; in vitro studies ; IVF ; Lecithins ; Male ; phosphatidylcholines ; Ram semen ; rams ; semen ; semen extenders ; Semen Preservation - methods ; Semen Preservation - veterinary ; Sheep ; soybean lecithin ; soybean products ; sperm motility ; Sperm Motility - physiology ; sperm viability ; Spermatozoa ; viability</subject><ispartof>Theriogenology, 2010-03, Vol.73 (4), p.480-487</ispartof><rights>2010 Elsevier Inc.</rights><rights>Copyright 2010 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-73ba30eb622c7b935fed18ea76c49b968f9144a2a1cad66379f7cf4bb9538f163</citedby><cites>FETCH-LOGICAL-c475t-73ba30eb622c7b935fed18ea76c49b968f9144a2a1cad66379f7cf4bb9538f163</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.theriogenology.2009.10.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3554,27933,27934,46004</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20022626$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Forouzanfar, M.</creatorcontrib><creatorcontrib>Sharafi, M.</creatorcontrib><creatorcontrib>Hosseini, S.M.</creatorcontrib><creatorcontrib>Ostadhosseini, S.</creatorcontrib><creatorcontrib>Hajian, M.</creatorcontrib><creatorcontrib>Hosseini, L.</creatorcontrib><creatorcontrib>Abedi, P.</creatorcontrib><creatorcontrib>Nili, N.</creatorcontrib><creatorcontrib>Rahmani, H.R.</creatorcontrib><creatorcontrib>Nasr-Esfahani, M.H.</creatorcontrib><title>In vitro comparison of egg yolk–based and soybean lecithin–based extenders for cryopreservation of ram semen</title><title>Theriogenology</title><addtitle>Theriogenology</addtitle><description>Substitution of egg yolk with soybean lecithin may reduce hygienic risks in extenders. Though a few studies have been performed on the effect of soybean lecithin in bull, to date evaluation of ram semen in vitro fertility after cryopreservation with use of soybean lecithin has not been studied. This study assessed the effect of 1% or 2% (wt/vol) soybean lecithin (L1 or L2) or 15% or 20% (vol/vol) egg yolk (E15 or E20) supplemented with 5% or 7% glycerol (G5 or G7) in a Tris-based medium for cryopreservation of ram (Oviss arries) semen. Although no significant difference was observed in pattern of capacitation, the best results in terms of sperm motility, viability postthaw, and cleavage rates were observed with L1G7 (51.9
±
4.8%, 48.1
±
3.5%, and 79.6
±
3.9%, respectively) and E20G7 (51.8
±
2.9%, 46.7
±
4.0%, and 72.9
±
6.4%, respectively). Our results also showed that 1% lecithin and 20% egg yolk was superior to 2% lecithin and 15% egg yolk. In terms of cleavage rate, 7% glycerol was superior to 5% glycerol. No significant difference was obtained between groups in terms of blastocysts rate per cleaved embryo. Therefore, we concluded that the optimal concentration of lecithin and egg yolk is 1% and 20%, respectively, along with 7% glycerol. In addition, our results suggest that lecithin can be used as a substitute for egg yolk.</description><subject>Acrosome Reaction - physiology</subject><subject>Animals</subject><subject>capacitation</subject><subject>Capacitation status</subject><subject>cell cleavage</subject><subject>Cryopreservation</subject><subject>Cryopreservation - methods</subject><subject>Cryopreservation - veterinary</subject><subject>Cryoprotective Agents</subject><subject>Egg Yolk</subject><subject>Extenders</subject><subject>Fertilization in Vitro - veterinary</subject><subject>Glycine max - chemistry</subject><subject>in vitro studies</subject><subject>IVF</subject><subject>Lecithins</subject><subject>Male</subject><subject>phosphatidylcholines</subject><subject>Ram semen</subject><subject>rams</subject><subject>semen</subject><subject>semen extenders</subject><subject>Semen Preservation - methods</subject><subject>Semen Preservation - veterinary</subject><subject>Sheep</subject><subject>soybean lecithin</subject><subject>soybean products</subject><subject>sperm motility</subject><subject>Sperm Motility - physiology</subject><subject>sperm viability</subject><subject>Spermatozoa</subject><subject>viability</subject><issn>0093-691X</issn><issn>1879-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMFu1DAQhi1ERZfCK4APSJyytePEjiUuqKJQqVIPUImb5Tjj1EtiBzu7am68A2_Ik-BVSqXeOM3h__6Z0YfQO0q2lFB-vtvOdxBd6MGHIfTLtiRE5mhLSP0MbWgjZMFKRp-jTQ5YwSX9fopeprQjhDDO6Qt0mitlyUu-QdOVxwc3x4BNGCcdXQoeB4uh7_EShh9_fv1udYIOa9_hFJYWtMcDGDffOf8Ywv0MvoOYsA0Rm7iEKUKCeNCzW_dFPeIEI_hX6MTqIcHrh3mGbi8_fbv4UlzffL66-HhdmErUcyFYqxmBlpelEa1ktYWONqAFN5VsJW-spFWlS02N7jhnQlphbNW2smaNpZydoffr3imGn3tIsxpdMjAM2kPYJyUYqyljjczkh5U0MaQUwaopulHHRVGijsrVTj1Vro7Kj2lWnutvHg7t2xG6x_I_xxl4uwJWB6X7rFjdfi0JZYQKKSVhmbhcCchCDg6iSsaBN9C5CGZWXXD_98tfD3ypGQ</recordid><startdate>20100301</startdate><enddate>20100301</enddate><creator>Forouzanfar, M.</creator><creator>Sharafi, M.</creator><creator>Hosseini, S.M.</creator><creator>Ostadhosseini, S.</creator><creator>Hajian, M.</creator><creator>Hosseini, L.</creator><creator>Abedi, P.</creator><creator>Nili, N.</creator><creator>Rahmani, H.R.</creator><creator>Nasr-Esfahani, M.H.</creator><general>Elsevier Inc</general><general>[Oxford]: Butterworth-Heinemann; [New York]: Elsevier Science</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>20100301</creationdate><title>In vitro comparison of egg yolk–based and soybean lecithin–based extenders for cryopreservation of ram semen</title><author>Forouzanfar, M. ; Sharafi, M. ; Hosseini, S.M. ; Ostadhosseini, S. ; Hajian, M. ; Hosseini, L. ; Abedi, P. ; Nili, N. ; Rahmani, H.R. ; Nasr-Esfahani, M.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-73ba30eb622c7b935fed18ea76c49b968f9144a2a1cad66379f7cf4bb9538f163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acrosome Reaction - physiology</topic><topic>Animals</topic><topic>capacitation</topic><topic>Capacitation status</topic><topic>cell cleavage</topic><topic>Cryopreservation</topic><topic>Cryopreservation - methods</topic><topic>Cryopreservation - veterinary</topic><topic>Cryoprotective Agents</topic><topic>Egg Yolk</topic><topic>Extenders</topic><topic>Fertilization in Vitro - veterinary</topic><topic>Glycine max - chemistry</topic><topic>in vitro studies</topic><topic>IVF</topic><topic>Lecithins</topic><topic>Male</topic><topic>phosphatidylcholines</topic><topic>Ram semen</topic><topic>rams</topic><topic>semen</topic><topic>semen extenders</topic><topic>Semen Preservation - methods</topic><topic>Semen Preservation - veterinary</topic><topic>Sheep</topic><topic>soybean lecithin</topic><topic>soybean products</topic><topic>sperm motility</topic><topic>Sperm Motility - physiology</topic><topic>sperm viability</topic><topic>Spermatozoa</topic><topic>viability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Forouzanfar, M.</creatorcontrib><creatorcontrib>Sharafi, M.</creatorcontrib><creatorcontrib>Hosseini, S.M.</creatorcontrib><creatorcontrib>Ostadhosseini, S.</creatorcontrib><creatorcontrib>Hajian, M.</creatorcontrib><creatorcontrib>Hosseini, L.</creatorcontrib><creatorcontrib>Abedi, P.</creatorcontrib><creatorcontrib>Nili, N.</creatorcontrib><creatorcontrib>Rahmani, H.R.</creatorcontrib><creatorcontrib>Nasr-Esfahani, M.H.</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>Forouzanfar, M.</au><au>Sharafi, M.</au><au>Hosseini, S.M.</au><au>Ostadhosseini, S.</au><au>Hajian, M.</au><au>Hosseini, L.</au><au>Abedi, P.</au><au>Nili, N.</au><au>Rahmani, H.R.</au><au>Nasr-Esfahani, M.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro comparison of egg yolk–based and soybean lecithin–based extenders for cryopreservation of ram semen</atitle><jtitle>Theriogenology</jtitle><addtitle>Theriogenology</addtitle><date>2010-03-01</date><risdate>2010</risdate><volume>73</volume><issue>4</issue><spage>480</spage><epage>487</epage><pages>480-487</pages><issn>0093-691X</issn><eissn>1879-3231</eissn><abstract>Substitution of egg yolk with soybean lecithin may reduce hygienic risks in extenders. Though a few studies have been performed on the effect of soybean lecithin in bull, to date evaluation of ram semen in vitro fertility after cryopreservation with use of soybean lecithin has not been studied. This study assessed the effect of 1% or 2% (wt/vol) soybean lecithin (L1 or L2) or 15% or 20% (vol/vol) egg yolk (E15 or E20) supplemented with 5% or 7% glycerol (G5 or G7) in a Tris-based medium for cryopreservation of ram (Oviss arries) semen. Although no significant difference was observed in pattern of capacitation, the best results in terms of sperm motility, viability postthaw, and cleavage rates were observed with L1G7 (51.9
±
4.8%, 48.1
±
3.5%, and 79.6
±
3.9%, respectively) and E20G7 (51.8
±
2.9%, 46.7
±
4.0%, and 72.9
±
6.4%, respectively). Our results also showed that 1% lecithin and 20% egg yolk was superior to 2% lecithin and 15% egg yolk. In terms of cleavage rate, 7% glycerol was superior to 5% glycerol. No significant difference was obtained between groups in terms of blastocysts rate per cleaved embryo. Therefore, we concluded that the optimal concentration of lecithin and egg yolk is 1% and 20%, respectively, along with 7% glycerol. In addition, our results suggest that lecithin can be used as a substitute for egg yolk.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>20022626</pmid><doi>10.1016/j.theriogenology.2009.10.005</doi><tpages>8</tpages></addata></record> |
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subjects | Acrosome Reaction - physiology Animals capacitation Capacitation status cell cleavage Cryopreservation Cryopreservation - methods Cryopreservation - veterinary Cryoprotective Agents Egg Yolk Extenders Fertilization in Vitro - veterinary Glycine max - chemistry in vitro studies IVF Lecithins Male phosphatidylcholines Ram semen rams semen semen extenders Semen Preservation - methods Semen Preservation - veterinary Sheep soybean lecithin soybean products sperm motility Sperm Motility - physiology sperm viability Spermatozoa viability |
title | In vitro comparison of egg yolk–based and soybean lecithin–based extenders for cryopreservation of ram semen |
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