Liquid storage of dromedary camel semen in different extenders

•Suitability of extenders for liquid storage of dromedary camel semen was examined.•Better semen quality was observed in Triladyl than Green buffer or OPTIXcell.•Semen quality was not affected by storage temperature (4 versus 15 °C). This study was conducted to assess the effects of commercial exten...

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Veröffentlicht in:Animal reproduction science 2019-08, Vol.207, p.95-106
Hauptverfasser: Al-Bulushi, Samir, Manjunatha, B.M., Bathgate, R., Rickard, J.P., de Graaf, S.P.
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container_issue
container_start_page 95
container_title Animal reproduction science
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creator Al-Bulushi, Samir
Manjunatha, B.M.
Bathgate, R.
Rickard, J.P.
de Graaf, S.P.
description •Suitability of extenders for liquid storage of dromedary camel semen was examined.•Better semen quality was observed in Triladyl than Green buffer or OPTIXcell.•Semen quality was not affected by storage temperature (4 versus 15 °C). This study was conducted to assess the effects of commercial extenders and storage temperature on dromedary camel sperm quality during liquid preservation. In Experiment 1, ejaculates (n = five males; replicated seven times) were split and diluted with synthetic (OPTIXcell, EquiPlus, INRA96, Bioxcell or AndroMed; Experiment 1a) or egg-yolk based (Biladyl, Green buffer or Triladyl; Experiment 1b) extenders and stored for 48 h at 4 °C. In Experiment 2, split ejaculates (n = five males; replicated six times) were used to directly compare Green buffer, OPTIXcell and Triladyl extenders over 48 h of storage at 4 °C. Ejaculates collected in Experiment 3 (n = five males; replicated five times) were diluted with Green buffer or Triladyl before chilled storage for 48 h at 4 or 15 °C. Sperm kinematics, viability and acrosome integrity were assessed during liquid storage. In Experiment 1a, there was the greatest total sperm motility (TM) in the OPTIXcell group following 24 and 48 h of storage, while in Experiment 1b, there was the greatest TM after 48 h of storage with Triladyl and Green buffer. In Experiment 2, there were greater TM and viable acrosome intact spermatozoa in the Triladyl and Green buffer than with OPTIXcell group. In Experiment 3, there was a greater TM in the Triladyl than Green buffer group at 24 and 48 h of storage regardless of storage temperature (which had no effect on sperm quality). In conclusion, camel sperm have greater viability when preserved in liquid form for 48 h following dilution with Triladyl and storage at either 4 or 15 °C.
doi_str_mv 10.1016/j.anireprosci.2019.06.008
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This study was conducted to assess the effects of commercial extenders and storage temperature on dromedary camel sperm quality during liquid preservation. In Experiment 1, ejaculates (n = five males; replicated seven times) were split and diluted with synthetic (OPTIXcell, EquiPlus, INRA96, Bioxcell or AndroMed; Experiment 1a) or egg-yolk based (Biladyl, Green buffer or Triladyl; Experiment 1b) extenders and stored for 48 h at 4 °C. In Experiment 2, split ejaculates (n = five males; replicated six times) were used to directly compare Green buffer, OPTIXcell and Triladyl extenders over 48 h of storage at 4 °C. Ejaculates collected in Experiment 3 (n = five males; replicated five times) were diluted with Green buffer or Triladyl before chilled storage for 48 h at 4 or 15 °C. Sperm kinematics, viability and acrosome integrity were assessed during liquid storage. In Experiment 1a, there was the greatest total sperm motility (TM) in the OPTIXcell group following 24 and 48 h of storage, while in Experiment 1b, there was the greatest TM after 48 h of storage with Triladyl and Green buffer. In Experiment 2, there were greater TM and viable acrosome intact spermatozoa in the Triladyl and Green buffer than with OPTIXcell group. In Experiment 3, there was a greater TM in the Triladyl than Green buffer group at 24 and 48 h of storage regardless of storage temperature (which had no effect on sperm quality). 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In conclusion, camel sperm have greater viability when preserved in liquid form for 48 h following dilution with Triladyl and storage at either 4 or 15 °C.</description><subject>Animals</subject><subject>Buffers</subject><subject>Camelid</subject><subject>Camelus</subject><subject>CASA</subject><subject>Cell Survival - drug effects</subject><subject>Egg Yolk - physiology</subject><subject>Extenders</subject><subject>Isotonic Solutions - pharmacology</subject><subject>Liquid storage</subject><subject>Male</subject><subject>Organ Preservation Solutions - chemistry</subject><subject>Organ Preservation Solutions - pharmacology</subject><subject>Refrigeration - methods</subject><subject>Refrigeration - veterinary</subject><subject>Semen - drug effects</subject><subject>Semen Analysis</subject><subject>Semen Preservation - methods</subject><subject>Semen Preservation - veterinary</subject><subject>Spermatozoa</subject><subject>Spermatozoa - drug effects</subject><subject>Spermatozoa - physiology</subject><subject>Temperature</subject><subject>Time Factors</subject><issn>0378-4320</issn><issn>1873-2232</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkD1PwzAURS0EoqXwF1DYWBKe7cR2FiRU8SVVYoHZcu0X5KpJWjtB8O9x1YIYmd5y3r26h5ArCgUFKm5Whel8wE3oo_UFA1oXIAoAdUSmVEmeM8bZMZkClyovOYMJOYtxBQBSiPqUTDhloFSppuR24bejd1kc-mDeMeubzIW-RWfCV2ZNi-ssYotd5rvM-abBgN2Q4eeAncMQz8lJY9YRLw53Rt4e7l_nT_ni5fF5frfILZdyyIUqOa9AVJJKYXmFlaUAHMulatByIU0lStc0qgabiJI5YMLI0lFXM0WXfEau97lp83bEOOjWR4vrtemwH6NmrExcLZVKaL1HbdITAzZ6E3yb5mgKeqdPr_QffXqnT4PQSV_6vTzUjMvk4Pfzx1cC5nsA09gPj0GnCOwsuhRoB-16_4-ab7UIhg8</recordid><startdate>201908</startdate><enddate>201908</enddate><creator>Al-Bulushi, Samir</creator><creator>Manjunatha, B.M.</creator><creator>Bathgate, R.</creator><creator>Rickard, J.P.</creator><creator>de Graaf, S.P.</creator><general>Elsevier B.V</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>7X8</scope></search><sort><creationdate>201908</creationdate><title>Liquid storage of dromedary camel semen in different extenders</title><author>Al-Bulushi, Samir ; Manjunatha, B.M. ; Bathgate, R. ; Rickard, J.P. ; de Graaf, S.P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-6843350657176c35e5c1003e4b8fec367a564dff890c17642d026a74d1d9281b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Buffers</topic><topic>Camelid</topic><topic>Camelus</topic><topic>CASA</topic><topic>Cell Survival - drug effects</topic><topic>Egg Yolk - physiology</topic><topic>Extenders</topic><topic>Isotonic Solutions - pharmacology</topic><topic>Liquid storage</topic><topic>Male</topic><topic>Organ Preservation Solutions - chemistry</topic><topic>Organ Preservation Solutions - pharmacology</topic><topic>Refrigeration - methods</topic><topic>Refrigeration - veterinary</topic><topic>Semen - drug effects</topic><topic>Semen Analysis</topic><topic>Semen Preservation - methods</topic><topic>Semen Preservation - veterinary</topic><topic>Spermatozoa</topic><topic>Spermatozoa - drug effects</topic><topic>Spermatozoa - physiology</topic><topic>Temperature</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Al-Bulushi, Samir</creatorcontrib><creatorcontrib>Manjunatha, B.M.</creatorcontrib><creatorcontrib>Bathgate, R.</creatorcontrib><creatorcontrib>Rickard, J.P.</creatorcontrib><creatorcontrib>de Graaf, S.P.</creatorcontrib><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>Animal reproduction science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Al-Bulushi, Samir</au><au>Manjunatha, B.M.</au><au>Bathgate, R.</au><au>Rickard, J.P.</au><au>de Graaf, S.P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Liquid storage of dromedary camel semen in different extenders</atitle><jtitle>Animal reproduction science</jtitle><addtitle>Anim Reprod Sci</addtitle><date>2019-08</date><risdate>2019</risdate><volume>207</volume><spage>95</spage><epage>106</epage><pages>95-106</pages><issn>0378-4320</issn><eissn>1873-2232</eissn><abstract>•Suitability of extenders for liquid storage of dromedary camel semen was examined.•Better semen quality was observed in Triladyl than Green buffer or OPTIXcell.•Semen quality was not affected by storage temperature (4 versus 15 °C). This study was conducted to assess the effects of commercial extenders and storage temperature on dromedary camel sperm quality during liquid preservation. In Experiment 1, ejaculates (n = five males; replicated seven times) were split and diluted with synthetic (OPTIXcell, EquiPlus, INRA96, Bioxcell or AndroMed; Experiment 1a) or egg-yolk based (Biladyl, Green buffer or Triladyl; Experiment 1b) extenders and stored for 48 h at 4 °C. In Experiment 2, split ejaculates (n = five males; replicated six times) were used to directly compare Green buffer, OPTIXcell and Triladyl extenders over 48 h of storage at 4 °C. Ejaculates collected in Experiment 3 (n = five males; replicated five times) were diluted with Green buffer or Triladyl before chilled storage for 48 h at 4 or 15 °C. Sperm kinematics, viability and acrosome integrity were assessed during liquid storage. In Experiment 1a, there was the greatest total sperm motility (TM) in the OPTIXcell group following 24 and 48 h of storage, while in Experiment 1b, there was the greatest TM after 48 h of storage with Triladyl and Green buffer. In Experiment 2, there were greater TM and viable acrosome intact spermatozoa in the Triladyl and Green buffer than with OPTIXcell group. In Experiment 3, there was a greater TM in the Triladyl than Green buffer group at 24 and 48 h of storage regardless of storage temperature (which had no effect on sperm quality). In conclusion, camel sperm have greater viability when preserved in liquid form for 48 h following dilution with Triladyl and storage at either 4 or 15 °C.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31208848</pmid><doi>10.1016/j.anireprosci.2019.06.008</doi><tpages>12</tpages></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Animals
Buffers
Camelid
Camelus
CASA
Cell Survival - drug effects
Egg Yolk - physiology
Extenders
Isotonic Solutions - pharmacology
Liquid storage
Male
Organ Preservation Solutions - chemistry
Organ Preservation Solutions - pharmacology
Refrigeration - methods
Refrigeration - veterinary
Semen - drug effects
Semen Analysis
Semen Preservation - methods
Semen Preservation - veterinary
Spermatozoa
Spermatozoa - drug effects
Spermatozoa - physiology
Temperature
Time Factors
title Liquid storage of dromedary camel semen in different extenders
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