Reduction of seminal plasma concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa

Abstract This study was conducted to investigate the effect of different levels of seminal plasma (SP) and cold-shock on ram spermatozoa during 36 h storage at 5°C. In both ejaculated spermatozoa coated with egg yolk (second ejaculate; coated spermatozoa) and epididymal spermatozoa, samples were treated with 0, 50 and 100% seminal plasma. Different levels of seminal plasma were added on the basis of ram spermatocrit (32%). Then half of aliquots were suddenly put on ice water (cold-shock) and other half were gradually (0.25°C/min) chilled (non- cold shock). Sperm motility, viability and functional membrane integrity were determined in both aliquots at 0, 12, 24 and 36 h storage at 5°C. Under non- cold shock and cold-shock conditions, coated spermatozoa treated with 0% SP showed the highest motility compared to ejaculated spermatozoa (first ejaculate; uncoated spermatozoa) after 12, 24 and 36 h of storage at 5°C (P<0.05). Under non- cold shock and cold-shock conditions, viability and functional membrane integrity was higher in the coated spermatozoa treated with 0% SP than in the uncoated spermatozoa during 36 h storage (P<0.05). There was no significant difference between coated spermatozoa treated with 0 and 50% SP in the percentage of motility and viability after 24 and 36 h of storage (P>0.05). Under non- cold shock and cold-shock conditions, the percentage of motility of epididymal spermatozoa treated with 0% SP was significantly (P<0.05) higher than those treated with 100% SP after 36 h of storage at 5°C. In conclusion, removal of seminal plasma and/or reduction (up to 50%) of its concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa.

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Main Authors: Rajabi-Toustani,Reza, Mehr,Mohammad Roostaei-Ali, Motamedi-Mojdehi,Rasool
Format: Digital revista
Language:English
Published: Colégio Brasileiro de Reprodução Animal 2021
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1984-31432021000100206
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spelling oai:scielo:S1984-314320210001002062021-05-26Reduction of seminal plasma concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoaRajabi-Toustani,RezaMehr,Mohammad Roostaei-AliMotamedi-Mojdehi,Rasool coated spermatozoa cold-shock ram spermatozoa seminal plasma Abstract This study was conducted to investigate the effect of different levels of seminal plasma (SP) and cold-shock on ram spermatozoa during 36 h storage at 5°C. In both ejaculated spermatozoa coated with egg yolk (second ejaculate; coated spermatozoa) and epididymal spermatozoa, samples were treated with 0, 50 and 100% seminal plasma. Different levels of seminal plasma were added on the basis of ram spermatocrit (32%). Then half of aliquots were suddenly put on ice water (cold-shock) and other half were gradually (0.25°C/min) chilled (non- cold shock). Sperm motility, viability and functional membrane integrity were determined in both aliquots at 0, 12, 24 and 36 h storage at 5°C. Under non- cold shock and cold-shock conditions, coated spermatozoa treated with 0% SP showed the highest motility compared to ejaculated spermatozoa (first ejaculate; uncoated spermatozoa) after 12, 24 and 36 h of storage at 5°C (P<0.05). Under non- cold shock and cold-shock conditions, viability and functional membrane integrity was higher in the coated spermatozoa treated with 0% SP than in the uncoated spermatozoa during 36 h storage (P<0.05). There was no significant difference between coated spermatozoa treated with 0 and 50% SP in the percentage of motility and viability after 24 and 36 h of storage (P>0.05). Under non- cold shock and cold-shock conditions, the percentage of motility of epididymal spermatozoa treated with 0% SP was significantly (P<0.05) higher than those treated with 100% SP after 36 h of storage at 5°C. In conclusion, removal of seminal plasma and/or reduction (up to 50%) of its concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa.info:eu-repo/semantics/openAccessColégio Brasileiro de Reprodução AnimalAnimal Reproduction v.18 n.1 20212021-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1984-31432021000100206en10.1590/1984-3143-ar2020-0211
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country Brasil
countrycode BR
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access En linea
databasecode rev-scielo-br
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region America del Sur
libraryname SciELO
language English
format Digital
author Rajabi-Toustani,Reza
Mehr,Mohammad Roostaei-Ali
Motamedi-Mojdehi,Rasool
spellingShingle Rajabi-Toustani,Reza
Mehr,Mohammad Roostaei-Ali
Motamedi-Mojdehi,Rasool
Reduction of seminal plasma concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa
author_facet Rajabi-Toustani,Reza
Mehr,Mohammad Roostaei-Ali
Motamedi-Mojdehi,Rasool
author_sort Rajabi-Toustani,Reza
title Reduction of seminal plasma concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa
title_short Reduction of seminal plasma concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa
title_full Reduction of seminal plasma concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa
title_fullStr Reduction of seminal plasma concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa
title_full_unstemmed Reduction of seminal plasma concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa
title_sort reduction of seminal plasma concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa
description Abstract This study was conducted to investigate the effect of different levels of seminal plasma (SP) and cold-shock on ram spermatozoa during 36 h storage at 5°C. In both ejaculated spermatozoa coated with egg yolk (second ejaculate; coated spermatozoa) and epididymal spermatozoa, samples were treated with 0, 50 and 100% seminal plasma. Different levels of seminal plasma were added on the basis of ram spermatocrit (32%). Then half of aliquots were suddenly put on ice water (cold-shock) and other half were gradually (0.25°C/min) chilled (non- cold shock). Sperm motility, viability and functional membrane integrity were determined in both aliquots at 0, 12, 24 and 36 h storage at 5°C. Under non- cold shock and cold-shock conditions, coated spermatozoa treated with 0% SP showed the highest motility compared to ejaculated spermatozoa (first ejaculate; uncoated spermatozoa) after 12, 24 and 36 h of storage at 5°C (P<0.05). Under non- cold shock and cold-shock conditions, viability and functional membrane integrity was higher in the coated spermatozoa treated with 0% SP than in the uncoated spermatozoa during 36 h storage (P<0.05). There was no significant difference between coated spermatozoa treated with 0 and 50% SP in the percentage of motility and viability after 24 and 36 h of storage (P>0.05). Under non- cold shock and cold-shock conditions, the percentage of motility of epididymal spermatozoa treated with 0% SP was significantly (P<0.05) higher than those treated with 100% SP after 36 h of storage at 5°C. In conclusion, removal of seminal plasma and/or reduction (up to 50%) of its concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa.
publisher Colégio Brasileiro de Reprodução Animal
publishDate 2021
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1984-31432021000100206
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