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Reproductive performance of immobilized cryopreserved bovine semen used for timed artificial insemination
Contents The SpermVital® technology comprises embedding of spermatozoa within an alginate gel to facilitate release of sperm cells over a prolonged period in utero after AI. The aim of this study was to examine whether the survival time of spermatozoa is extended when applying this immobilization te...
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Published in: | Reproduction in domestic animals 2017-12, Vol.52 (6), p.1019-1024 |
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container_title | Reproduction in domestic animals |
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creator | Alm‐Kristiansen, AH Dalen, G Klinkenberg, G Bekk, L Thorkildsen, LT Waterhouse, KE Kommisrud, E |
description | Contents
The SpermVital® technology comprises embedding of spermatozoa within an alginate gel to facilitate release of sperm cells over a prolonged period in utero after AI. The aim of this study was to examine whether the survival time of spermatozoa is extended when applying this immobilization technology in combination with cryopreservation. Sperm cell survival (acrosome and plasma membrane integrity) was studied in vitro for 48 hr at physiological temperature. One dose of SpermVital® (SV) semen was compared with single doses of Biladyl® (B) processed semen as well as double doses of B (B double). B double was obtained by adding a second B dose the following day, thereby mimicking double AI. Furthermore, reproductive performance applying single early timed AI (TAI) with SV following oestrus synchronization was studied in a field trial. Double insemination (TAI on two consecutive days) with B semen served as control. Number of acrosome‐intact live sperm cells decreased over time in vitro for all treatments (p .05). However, after 48 hr, SV sperm cell survival was higher than B double (p .05). Likelihood of pregnancy and calving in the heifer group was higher than in the cow group (p |
doi_str_mv | 10.1111/rda.13017 |
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The SpermVital® technology comprises embedding of spermatozoa within an alginate gel to facilitate release of sperm cells over a prolonged period in utero after AI. The aim of this study was to examine whether the survival time of spermatozoa is extended when applying this immobilization technology in combination with cryopreservation. Sperm cell survival (acrosome and plasma membrane integrity) was studied in vitro for 48 hr at physiological temperature. One dose of SpermVital® (SV) semen was compared with single doses of Biladyl® (B) processed semen as well as double doses of B (B double). B double was obtained by adding a second B dose the following day, thereby mimicking double AI. Furthermore, reproductive performance applying single early timed AI (TAI) with SV following oestrus synchronization was studied in a field trial. Double insemination (TAI on two consecutive days) with B semen served as control. Number of acrosome‐intact live sperm cells decreased over time in vitro for all treatments (p < .05). There was no difference between SV sperm cell survival and B double after 24 hr (p > .05). However, after 48 hr, SV sperm cell survival was higher than B double (p < .05). Moreover, multivariate analysis showed that the outcome of single early TAI with SV was not significantly different from B double (p > .05). Likelihood of pregnancy and calving in the heifer group was higher than in the cow group (p < .05). These results imply that spermatozoa immobilized in alginate gel have prolonged survival.</description><identifier>ISSN: 0936-6768</identifier><identifier>EISSN: 1439-0531</identifier><identifier>DOI: 10.1111/rda.13017</identifier><identifier>PMID: 28691353</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>Acrosome - physiology ; Alginates ; Alginic acid ; animal breeding ; Animals ; Artificial insemination ; Cattle ; Cell Survival ; cryobiology ; Cryopreservation ; Cryopreservation - veterinary ; Embedding ; Female ; Immobilization ; Insemination, Artificial - methods ; Insemination, Artificial - veterinary ; Lymphocytes B ; Male ; Mimicry ; Multivariate analysis ; Pregnancy ; Reproduction ; Reproduction (biology) ; Semen ; Semen Preservation - methods ; Semen Preservation - veterinary ; Sperm ; Spermatozoa ; Spermatozoa - physiology ; Survival ; Synchronism ; Synchronization ; Technology ; Time Factors</subject><ispartof>Reproduction in domestic animals, 2017-12, Vol.52 (6), p.1019-1024</ispartof><rights>2017 Blackwell Verlag GmbH</rights><rights>2017 Blackwell Verlag GmbH.</rights><rights>Copyright © 2017 Blackwell Verlag GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3537-e68a8b2284e86ee24cf775807e126173fdc60354e1cfe6b8ab93d835054c073d3</citedby><cites>FETCH-LOGICAL-c3537-e68a8b2284e86ee24cf775807e126173fdc60354e1cfe6b8ab93d835054c073d3</cites><orcidid>0000-0002-0954-3525 ; 0000-0003-4350-1887</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28691353$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alm‐Kristiansen, AH</creatorcontrib><creatorcontrib>Dalen, G</creatorcontrib><creatorcontrib>Klinkenberg, G</creatorcontrib><creatorcontrib>Bekk, L</creatorcontrib><creatorcontrib>Thorkildsen, LT</creatorcontrib><creatorcontrib>Waterhouse, KE</creatorcontrib><creatorcontrib>Kommisrud, E</creatorcontrib><title>Reproductive performance of immobilized cryopreserved bovine semen used for timed artificial insemination</title><title>Reproduction in domestic animals</title><addtitle>Reprod Domest Anim</addtitle><description>Contents
The SpermVital® technology comprises embedding of spermatozoa within an alginate gel to facilitate release of sperm cells over a prolonged period in utero after AI. The aim of this study was to examine whether the survival time of spermatozoa is extended when applying this immobilization technology in combination with cryopreservation. Sperm cell survival (acrosome and plasma membrane integrity) was studied in vitro for 48 hr at physiological temperature. One dose of SpermVital® (SV) semen was compared with single doses of Biladyl® (B) processed semen as well as double doses of B (B double). B double was obtained by adding a second B dose the following day, thereby mimicking double AI. Furthermore, reproductive performance applying single early timed AI (TAI) with SV following oestrus synchronization was studied in a field trial. Double insemination (TAI on two consecutive days) with B semen served as control. Number of acrosome‐intact live sperm cells decreased over time in vitro for all treatments (p < .05). There was no difference between SV sperm cell survival and B double after 24 hr (p > .05). However, after 48 hr, SV sperm cell survival was higher than B double (p < .05). Moreover, multivariate analysis showed that the outcome of single early TAI with SV was not significantly different from B double (p > .05). Likelihood of pregnancy and calving in the heifer group was higher than in the cow group (p < .05). These results imply that spermatozoa immobilized in alginate gel have prolonged survival.</description><subject>Acrosome - physiology</subject><subject>Alginates</subject><subject>Alginic acid</subject><subject>animal breeding</subject><subject>Animals</subject><subject>Artificial insemination</subject><subject>Cattle</subject><subject>Cell Survival</subject><subject>cryobiology</subject><subject>Cryopreservation</subject><subject>Cryopreservation - veterinary</subject><subject>Embedding</subject><subject>Female</subject><subject>Immobilization</subject><subject>Insemination, Artificial - methods</subject><subject>Insemination, Artificial - veterinary</subject><subject>Lymphocytes B</subject><subject>Male</subject><subject>Mimicry</subject><subject>Multivariate analysis</subject><subject>Pregnancy</subject><subject>Reproduction</subject><subject>Reproduction (biology)</subject><subject>Semen</subject><subject>Semen Preservation - methods</subject><subject>Semen Preservation - veterinary</subject><subject>Sperm</subject><subject>Spermatozoa</subject><subject>Spermatozoa - physiology</subject><subject>Survival</subject><subject>Synchronism</subject><subject>Synchronization</subject><subject>Technology</subject><subject>Time Factors</subject><issn>0936-6768</issn><issn>1439-0531</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LxDAQhoMo7rp68A9IwYse6iZN89Hjsn7CgrDouaTpFLK0TU3alfXXG-3qQTCXyQxPXiYPQucE35Bw5q5UN4RiIg7QlKQ0izGj5BBNcUZ5zAWXE3Ti_QZjwqQQx2iSSJ4RyugUmTV0zpaD7s0Wog5cZV2jWg2RrSLTNLYwtfmAMtJuZzsHHtw2dIXdmhYiDw200eDDJLyLetOEm3K9qYw2qo5MGwjTqt7Y9hQdVar2cLavM_R6f_eyfIxXzw9Py8Uq1mEhEQOXShZJIlOQHCBJdSUEk1gASTgRtCo1x5SlQHQFvJCqyGgpKcMs1VjQks7Q1Zgb_vU2gO_zxngNda1asIPPSUYE55RlOKCXf9CNHVwbtgsUJ5RSJlmgrkdKO-u9gyrvnGmU2-UE51_-8-A___Yf2It94lAEF7_kj_AAzEfg3dSw-z8pX98uxshPY5KP8w</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Alm‐Kristiansen, AH</creator><creator>Dalen, G</creator><creator>Klinkenberg, G</creator><creator>Bekk, L</creator><creator>Thorkildsen, LT</creator><creator>Waterhouse, KE</creator><creator>Kommisrud, E</creator><general>Blackwell Publishing Ltd</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0954-3525</orcidid><orcidid>https://orcid.org/0000-0003-4350-1887</orcidid></search><sort><creationdate>201712</creationdate><title>Reproductive performance of immobilized cryopreserved bovine semen used for timed artificial insemination</title><author>Alm‐Kristiansen, AH ; Dalen, G ; Klinkenberg, G ; Bekk, L ; Thorkildsen, LT ; Waterhouse, KE ; Kommisrud, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3537-e68a8b2284e86ee24cf775807e126173fdc60354e1cfe6b8ab93d835054c073d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acrosome - physiology</topic><topic>Alginates</topic><topic>Alginic acid</topic><topic>animal breeding</topic><topic>Animals</topic><topic>Artificial insemination</topic><topic>Cattle</topic><topic>Cell Survival</topic><topic>cryobiology</topic><topic>Cryopreservation</topic><topic>Cryopreservation - veterinary</topic><topic>Embedding</topic><topic>Female</topic><topic>Immobilization</topic><topic>Insemination, Artificial - methods</topic><topic>Insemination, Artificial - veterinary</topic><topic>Lymphocytes B</topic><topic>Male</topic><topic>Mimicry</topic><topic>Multivariate analysis</topic><topic>Pregnancy</topic><topic>Reproduction</topic><topic>Reproduction (biology)</topic><topic>Semen</topic><topic>Semen Preservation - methods</topic><topic>Semen Preservation - veterinary</topic><topic>Sperm</topic><topic>Spermatozoa</topic><topic>Spermatozoa - physiology</topic><topic>Survival</topic><topic>Synchronism</topic><topic>Synchronization</topic><topic>Technology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alm‐Kristiansen, AH</creatorcontrib><creatorcontrib>Dalen, G</creatorcontrib><creatorcontrib>Klinkenberg, G</creatorcontrib><creatorcontrib>Bekk, L</creatorcontrib><creatorcontrib>Thorkildsen, LT</creatorcontrib><creatorcontrib>Waterhouse, KE</creatorcontrib><creatorcontrib>Kommisrud, E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Reproduction in domestic animals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alm‐Kristiansen, AH</au><au>Dalen, G</au><au>Klinkenberg, G</au><au>Bekk, L</au><au>Thorkildsen, LT</au><au>Waterhouse, KE</au><au>Kommisrud, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reproductive performance of immobilized cryopreserved bovine semen used for timed artificial insemination</atitle><jtitle>Reproduction in domestic animals</jtitle><addtitle>Reprod Domest Anim</addtitle><date>2017-12</date><risdate>2017</risdate><volume>52</volume><issue>6</issue><spage>1019</spage><epage>1024</epage><pages>1019-1024</pages><issn>0936-6768</issn><eissn>1439-0531</eissn><abstract>Contents
The SpermVital® technology comprises embedding of spermatozoa within an alginate gel to facilitate release of sperm cells over a prolonged period in utero after AI. The aim of this study was to examine whether the survival time of spermatozoa is extended when applying this immobilization technology in combination with cryopreservation. Sperm cell survival (acrosome and plasma membrane integrity) was studied in vitro for 48 hr at physiological temperature. One dose of SpermVital® (SV) semen was compared with single doses of Biladyl® (B) processed semen as well as double doses of B (B double). B double was obtained by adding a second B dose the following day, thereby mimicking double AI. Furthermore, reproductive performance applying single early timed AI (TAI) with SV following oestrus synchronization was studied in a field trial. Double insemination (TAI on two consecutive days) with B semen served as control. Number of acrosome‐intact live sperm cells decreased over time in vitro for all treatments (p < .05). There was no difference between SV sperm cell survival and B double after 24 hr (p > .05). However, after 48 hr, SV sperm cell survival was higher than B double (p < .05). Moreover, multivariate analysis showed that the outcome of single early TAI with SV was not significantly different from B double (p > .05). Likelihood of pregnancy and calving in the heifer group was higher than in the cow group (p < .05). These results imply that spermatozoa immobilized in alginate gel have prolonged survival.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>28691353</pmid><doi>10.1111/rda.13017</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-0954-3525</orcidid><orcidid>https://orcid.org/0000-0003-4350-1887</orcidid></addata></record> |
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subjects | Acrosome - physiology Alginates Alginic acid animal breeding Animals Artificial insemination Cattle Cell Survival cryobiology Cryopreservation Cryopreservation - veterinary Embedding Female Immobilization Insemination, Artificial - methods Insemination, Artificial - veterinary Lymphocytes B Male Mimicry Multivariate analysis Pregnancy Reproduction Reproduction (biology) Semen Semen Preservation - methods Semen Preservation - veterinary Sperm Spermatozoa Spermatozoa - physiology Survival Synchronism Synchronization Technology Time Factors |
title | Reproductive performance of immobilized cryopreserved bovine semen used for timed artificial insemination |
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