Effect of seminal plasma removal before cryopreservation of bovine semen obtained by electroejaculation on semen quality and in vitro fertility

Detalhes bibliográficos
Autor(a) principal: Campanholi, Suzane Peres [UNESP]
Data de Publicação: 2017
Outros Autores: Monteiro, Fabio Morato, Ribeiro Dias, Erika Aline, Mercadante, Maria Eugênia Zerlotti, de Paz, Claudia Cristina Paro, Dell'Aqua Junior, José Antonio [UNESP], Papa, Frederico Ozanam [UNESP], Dell'Aqua, Camila de Paula Freitas [UNESP], Vantini, Roberta [UNESP], Garcia, Joaquim Mansano [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.theriogenology.2016.10.008
http://hdl.handle.net/11449/173807
Resumo: Cryopreservation of bull semen is a common biotechnology procedure in cattle breeding. However, when the ejaculate is obtained by electroejaculation, wide variation is observed in the sperm/seminal plasma (SP) ratio that can affect the freezability of semen in this species. The removal of SP may improve the quality of frozen bull semen. The objective of this study was to evaluate the effect of SP removal from the ejaculate on the cryopreservation of semen from 38 Nellore bulls collected by electroejaculation. After collection, the ejaculate was divided into three aliquots: (1) control (N) diluted to a concentration of 60 × 106 spermatozoa/mL and frozen with SP; (2) centrifugation (C) at ×600g for 10 minutes and the pellet resuspended and frozen at the same concentration as N; and (3) filtration (F) through SpermFilter and sperm recovered and frozen at the same concentration as N. After thawing, sperm kinetics, plasma and acrosome membrane integrity, mitochondrial membrane potential, oxidative stress, and in vitro fertility were evaluated. Statistical analysis was performed using the SAS 9.2 package, and differences were considered significant when P < 0.05. Higher average path velocity and straight-line velocity were observed in the groups submitted to SP removal compared to the control group (P < 0.01). In contrast, filtered samples exhibited higher beat cross frequency, straightness, and linearity compared to the other groups. Plasma membrane integrity was reduced when SP was removed, but lower oxidative stress was observed in groups C and F (34.91 ± 2.95% and 31.63 ± 2.95%, respectively) compared to group N (57.39 ± 2.95%). However, the percentage of hatched blastocysts was similar in the N and F groups (21.22 ± 1.05% and 24.00 ± 1.05%, respectively) and higher compared to group C (18.83 ± 1.05%). In conclusion, removal of SP by centrifugation for bull semen freezing reduced the rate of in vitro–produced embryos, whereas filtration of prefrozen semen was found to be an efficient alternative in terms of semen freezability and in vitro production of bovine embryos.
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spelling Effect of seminal plasma removal before cryopreservation of bovine semen obtained by electroejaculation on semen quality and in vitro fertilityBullCentrifugationCryopreservationFiltrationSemenSeminal plasmaCryopreservation of bull semen is a common biotechnology procedure in cattle breeding. However, when the ejaculate is obtained by electroejaculation, wide variation is observed in the sperm/seminal plasma (SP) ratio that can affect the freezability of semen in this species. The removal of SP may improve the quality of frozen bull semen. The objective of this study was to evaluate the effect of SP removal from the ejaculate on the cryopreservation of semen from 38 Nellore bulls collected by electroejaculation. After collection, the ejaculate was divided into three aliquots: (1) control (N) diluted to a concentration of 60 × 106 spermatozoa/mL and frozen with SP; (2) centrifugation (C) at ×600g for 10 minutes and the pellet resuspended and frozen at the same concentration as N; and (3) filtration (F) through SpermFilter and sperm recovered and frozen at the same concentration as N. After thawing, sperm kinetics, plasma and acrosome membrane integrity, mitochondrial membrane potential, oxidative stress, and in vitro fertility were evaluated. Statistical analysis was performed using the SAS 9.2 package, and differences were considered significant when P < 0.05. Higher average path velocity and straight-line velocity were observed in the groups submitted to SP removal compared to the control group (P < 0.01). In contrast, filtered samples exhibited higher beat cross frequency, straightness, and linearity compared to the other groups. Plasma membrane integrity was reduced when SP was removed, but lower oxidative stress was observed in groups C and F (34.91 ± 2.95% and 31.63 ± 2.95%, respectively) compared to group N (57.39 ± 2.95%). However, the percentage of hatched blastocysts was similar in the N and F groups (21.22 ± 1.05% and 24.00 ± 1.05%, respectively) and higher compared to group C (18.83 ± 1.05%). In conclusion, removal of SP by centrifugation for bull semen freezing reduced the rate of in vitro–produced embryos, whereas filtration of prefrozen semen was found to be an efficient alternative in terms of semen freezability and in vitro production of bovine embryos.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Departamento de Reprodução Animal Universidade Estadual Paulista FCAV/UNESPCentro APTA Bovinos de Corte IZ-APTADepartamento de Reprodução Animal e Radiologia Veterinária Universidade Estadual Paulista FMVZ/UNESPDepartamento de Reprodução Animal Universidade Estadual Paulista FCAV/UNESPDepartamento de Reprodução Animal e Radiologia Veterinária Universidade Estadual Paulista FMVZ/UNESPFAPESP: 2012/05555-8FAPESP: 2014/02659-2Universidade Estadual Paulista (Unesp)IZ-APTACampanholi, Suzane Peres [UNESP]Monteiro, Fabio MoratoRibeiro Dias, Erika AlineMercadante, Maria Eugênia Zerlottide Paz, Claudia Cristina ParoDell'Aqua Junior, José Antonio [UNESP]Papa, Frederico Ozanam [UNESP]Dell'Aqua, Camila de Paula Freitas [UNESP]Vantini, Roberta [UNESP]Garcia, Joaquim Mansano [UNESP]2018-12-11T17:07:50Z2018-12-11T17:07:50Z2017-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article114-121application/pdfhttp://dx.doi.org/10.1016/j.theriogenology.2016.10.008Theriogenology, v. 89, p. 114-121.0093-691Xhttp://hdl.handle.net/11449/17380710.1016/j.theriogenology.2016.10.0082-s2.0-849957836832-s2.0-84995783683.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengTheriogenologyinfo:eu-repo/semantics/openAccess2023-11-06T06:06:27Zoai:repositorio.unesp.br:11449/173807Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-11-06T06:06:27Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Effect of seminal plasma removal before cryopreservation of bovine semen obtained by electroejaculation on semen quality and in vitro fertility
title Effect of seminal plasma removal before cryopreservation of bovine semen obtained by electroejaculation on semen quality and in vitro fertility
spellingShingle Effect of seminal plasma removal before cryopreservation of bovine semen obtained by electroejaculation on semen quality and in vitro fertility
Campanholi, Suzane Peres [UNESP]
Bull
Centrifugation
Cryopreservation
Filtration
Semen
Seminal plasma
title_short Effect of seminal plasma removal before cryopreservation of bovine semen obtained by electroejaculation on semen quality and in vitro fertility
title_full Effect of seminal plasma removal before cryopreservation of bovine semen obtained by electroejaculation on semen quality and in vitro fertility
title_fullStr Effect of seminal plasma removal before cryopreservation of bovine semen obtained by electroejaculation on semen quality and in vitro fertility
title_full_unstemmed Effect of seminal plasma removal before cryopreservation of bovine semen obtained by electroejaculation on semen quality and in vitro fertility
title_sort Effect of seminal plasma removal before cryopreservation of bovine semen obtained by electroejaculation on semen quality and in vitro fertility
author Campanholi, Suzane Peres [UNESP]
author_facet Campanholi, Suzane Peres [UNESP]
Monteiro, Fabio Morato
Ribeiro Dias, Erika Aline
Mercadante, Maria Eugênia Zerlotti
de Paz, Claudia Cristina Paro
Dell'Aqua Junior, José Antonio [UNESP]
Papa, Frederico Ozanam [UNESP]
Dell'Aqua, Camila de Paula Freitas [UNESP]
Vantini, Roberta [UNESP]
Garcia, Joaquim Mansano [UNESP]
author_role author
author2 Monteiro, Fabio Morato
Ribeiro Dias, Erika Aline
Mercadante, Maria Eugênia Zerlotti
de Paz, Claudia Cristina Paro
Dell'Aqua Junior, José Antonio [UNESP]
Papa, Frederico Ozanam [UNESP]
Dell'Aqua, Camila de Paula Freitas [UNESP]
Vantini, Roberta [UNESP]
Garcia, Joaquim Mansano [UNESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
IZ-APTA
dc.contributor.author.fl_str_mv Campanholi, Suzane Peres [UNESP]
Monteiro, Fabio Morato
Ribeiro Dias, Erika Aline
Mercadante, Maria Eugênia Zerlotti
de Paz, Claudia Cristina Paro
Dell'Aqua Junior, José Antonio [UNESP]
Papa, Frederico Ozanam [UNESP]
Dell'Aqua, Camila de Paula Freitas [UNESP]
Vantini, Roberta [UNESP]
Garcia, Joaquim Mansano [UNESP]
dc.subject.por.fl_str_mv Bull
Centrifugation
Cryopreservation
Filtration
Semen
Seminal plasma
topic Bull
Centrifugation
Cryopreservation
Filtration
Semen
Seminal plasma
description Cryopreservation of bull semen is a common biotechnology procedure in cattle breeding. However, when the ejaculate is obtained by electroejaculation, wide variation is observed in the sperm/seminal plasma (SP) ratio that can affect the freezability of semen in this species. The removal of SP may improve the quality of frozen bull semen. The objective of this study was to evaluate the effect of SP removal from the ejaculate on the cryopreservation of semen from 38 Nellore bulls collected by electroejaculation. After collection, the ejaculate was divided into three aliquots: (1) control (N) diluted to a concentration of 60 × 106 spermatozoa/mL and frozen with SP; (2) centrifugation (C) at ×600g for 10 minutes and the pellet resuspended and frozen at the same concentration as N; and (3) filtration (F) through SpermFilter and sperm recovered and frozen at the same concentration as N. After thawing, sperm kinetics, plasma and acrosome membrane integrity, mitochondrial membrane potential, oxidative stress, and in vitro fertility were evaluated. Statistical analysis was performed using the SAS 9.2 package, and differences were considered significant when P < 0.05. Higher average path velocity and straight-line velocity were observed in the groups submitted to SP removal compared to the control group (P < 0.01). In contrast, filtered samples exhibited higher beat cross frequency, straightness, and linearity compared to the other groups. Plasma membrane integrity was reduced when SP was removed, but lower oxidative stress was observed in groups C and F (34.91 ± 2.95% and 31.63 ± 2.95%, respectively) compared to group N (57.39 ± 2.95%). However, the percentage of hatched blastocysts was similar in the N and F groups (21.22 ± 1.05% and 24.00 ± 1.05%, respectively) and higher compared to group C (18.83 ± 1.05%). In conclusion, removal of SP by centrifugation for bull semen freezing reduced the rate of in vitro–produced embryos, whereas filtration of prefrozen semen was found to be an efficient alternative in terms of semen freezability and in vitro production of bovine embryos.
publishDate 2017
dc.date.none.fl_str_mv 2017-02-01
2018-12-11T17:07:50Z
2018-12-11T17:07:50Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.theriogenology.2016.10.008
Theriogenology, v. 89, p. 114-121.
0093-691X
http://hdl.handle.net/11449/173807
10.1016/j.theriogenology.2016.10.008
2-s2.0-84995783683
2-s2.0-84995783683.pdf
url http://dx.doi.org/10.1016/j.theriogenology.2016.10.008
http://hdl.handle.net/11449/173807
identifier_str_mv Theriogenology, v. 89, p. 114-121.
0093-691X
10.1016/j.theriogenology.2016.10.008
2-s2.0-84995783683
2-s2.0-84995783683.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Theriogenology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 114-121
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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