Combination of sugars, lipoproteins and centrifugation improve dairy goat sperm viability submitted to cryopreservation

Detalhes bibliográficos
Autor(a) principal: Queiros, Aline Francelina de
Data de Publicação: 2021
Outros Autores: Farias, Camilla Flávia Avelino de, Rique, Alex Souza, Tork, André Luiz Pereira, Clemente, Carlos Augusto Alanis, Guerra, Maria Madalena Pessoa, Silva, Sildivane Valcácia
Tipo de documento: Artigo
Idioma: por
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/21559
Resumo: Abstract The aim of the present study was to evaluate the effects of different cryoprotectants and semen centrifugation on the kinetic parameters and membrane integrity of cryopreserved goat semen. Four buck goats were used, and their semen was collected using an artificial vagina. After semen collection and approval, six pools were formed, and each pool was divided into eight aliquots. The plasma was removed from four aliquots by centrifugation (1200 g/10 min) and subsequently diluted; the remaining four aliquots were diluted in standard Tris-egg yolk (SYE), standard milk (SME), test Tris-egg yolk (TYE) and test milk (TME) extenders without removing the seminal plasma. After dilution, samples were loaded into straws (0.25 mL), frozen and stored at -196 °C. The samples were thawed (37 °C/30 s) and evaluated immediately and two hours after thawing to determine the kinetics and integrity of plasma and mitochondrial membranes. A difference (p< 0.05) in the maintenance of sperm kinetics, plasma membrane integrity and mitochondrial potential was observed between the centrifuged and non-centrifuged groups and between the extenders at different time points. We concluded that the use of centrifugation to remove seminal plasma positively affects the semen evaluation parameters and that the yolk extender is more efficient when applied with different cryopreservation techniques, preserving the desirable traits after the cryopreservation of goat semen.
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spelling Combination of sugars, lipoproteins and centrifugation improve dairy goat sperm viability submitted to cryopreservationLa combinación de azúcares, lipoproteinas y centrifugación mejora la viabilidad de los espermatozoides de macho cabrio lechera pos-congelácionCombinação de açúcares, lipoproteínas e centrifugação melhoram a viabilidade de espermatozoides de caprinos leiteiros pós-criopreservaçãocongelaciónCongelaciónFosfolipasa Afosfolipasa AmitocondriaMitocondriaplasma seminalPlasma seminal.FreezingfreezingMitochondriaphospholipase APhospholipase AmitochondriaSeminal plasma.seminal plasmacongelaçãoCongelaçãoFosfolipase Afosfolipase AmitocôndriaMitocôndriaPlasma seminal.plasma seminalAbstract The aim of the present study was to evaluate the effects of different cryoprotectants and semen centrifugation on the kinetic parameters and membrane integrity of cryopreserved goat semen. Four buck goats were used, and their semen was collected using an artificial vagina. After semen collection and approval, six pools were formed, and each pool was divided into eight aliquots. The plasma was removed from four aliquots by centrifugation (1200 g/10 min) and subsequently diluted; the remaining four aliquots were diluted in standard Tris-egg yolk (SYE), standard milk (SME), test Tris-egg yolk (TYE) and test milk (TME) extenders without removing the seminal plasma. After dilution, samples were loaded into straws (0.25 mL), frozen and stored at -196 °C. The samples were thawed (37 °C/30 s) and evaluated immediately and two hours after thawing to determine the kinetics and integrity of plasma and mitochondrial membranes. A difference (p< 0.05) in the maintenance of sperm kinetics, plasma membrane integrity and mitochondrial potential was observed between the centrifuged and non-centrifuged groups and between the extenders at different time points. We concluded that the use of centrifugation to remove seminal plasma positively affects the semen evaluation parameters and that the yolk extender is more efficient when applied with different cryopreservation techniques, preserving the desirable traits after the cryopreservation of goat semen.El objetivo de este estudio fue evaluar los efectos de diferentes crioprotectores y la centrifugación del semen sobre los parámetros cinéticos y la integridad de la membrana del semen del macho cabrio criopreservado. Se utilizaron cuatro machos y el semen se recogió a través de una vagina artificial. Después de la recolección y aprobación del semen, se formaron seis grupos y cada grupo se dividió en alícuotas. O se extrajo plasma de cuatro alícuotas por centrifugación (1200 g/10 min) y se diluyó adicionalmente; Las cuatro alícuotas restantes se diluyen en Tris-yema de huevo estándar, Leche, Tris-yema de huevo de prueba y diluyente a base de leche, sin eliminar el plasma seminal. Después de la dilución, las muestras se colocaron en paletas (0.25 mL), se congelaron y se pelaron a -196 °C. Las muestras se descongelaron (37 °C/30 s) y se evaluaron inmediatamente durante dos horas después de la descongelación para determinar la cinética y la integridad del plasma y las mitocondrias. membranas. Se observaron diferencias (p <0,05) en el mantenimiento de la cinética de los espermatozoides, la integridad de la membrana plasmática y el potencial mitocondrial entre los grupos centrifugado y no centrifugado y entre los dilutores en diferentes momentos. Concluimos que el uso de la centrifugación para eliminar el plasma seminal afecta positivamente los parámetros de evaluación del semen y que el dilutor de yema es más eficiente cuando se aplica con diferentes técnicas de criopreservación, conservando las características de criopreservación del semen caprino.O objetivo do presente estudo foi avaliar os efeitos de diferentes crioprotetores e da centrifugação do sêmen sobre os parâmetros cinéticos e integridade da membrana do sêmen caprino criopreservado. Quatro bodes foram utilizados, e o sêmen foi colhido por meio de uma vagina artificial. Após colheita e aprovação do sêmen, seis pools foram formados, e cada pool foi dividido em oito alíquotas. O plasma foi retirado de quatro alíquotas por centrifugação (1200 g/10 min) e posteriormente diluído; as quatro alíquotas restantes foram diluídas em Tris-gema de ovo padrão, leite padrão, Tris-gema de ovo teste e diluente a base de leite, sem remoção do plasma seminal. Após a diluição, as amostras foram colocadas em palhetas (0,25 mL), congeladas e armazenadas a -196 °C. As amostras foram descongeladas (37 °C/30 s) e avaliadas imediatamente e duas horas pós-descongelação para determinar a cinética e integridade das membranas plasmática e mitocondrial. Foi observada diferença (p <0,05) na manutenção da cinética espermática, integridade da membrana plasmática e potencial mitocondrial entre os grupos centrifugados e não centrifugados e entre os extensores em diferentes momentos. Concluímos que o uso da centrifugação para remoção do plasma seminal afeta positivamente os parâmetros de avaliação do sêmen e que o extensor de gema é mais eficiente quando aplicado com diferentes técnicas de criopreservação, preservando as características desejáveis após a criopreservação do sêmen caprino.Research, Society and Development2021-10-16info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/2155910.33448/rsd-v10i13.21559Research, Society and Development; Vol. 10 No. 13; e358101321559Research, Society and Development; Vol. 10 Núm. 13; e358101321559Research, Society and Development; v. 10 n. 13; e3581013215592525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/21559/18989Copyright (c) 2021 Aline Francelina de Queiros; Camilla Flávia Avelino de Farias; Alex Souza Rique; André Luiz Pereira Tork; Carlos Augusto Alanis Clemente; Maria Madalena Pessoa Guerra; Sildivane Valcácia Silvahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessQueiros, Aline Francelina deFarias, Camilla Flávia Avelino de Rique, Alex SouzaTork, André Luiz Pereira Clemente, Carlos Augusto Alanis Guerra, Maria Madalena PessoaSilva, Sildivane Valcácia2021-11-21T18:26:28Zoai:ojs.pkp.sfu.ca:article/21559Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:40:57.181556Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Combination of sugars, lipoproteins and centrifugation improve dairy goat sperm viability submitted to cryopreservation
La combinación de azúcares, lipoproteinas y centrifugación mejora la viabilidad de los espermatozoides de macho cabrio lechera pos-congelácion
Combinação de açúcares, lipoproteínas e centrifugação melhoram a viabilidade de espermatozoides de caprinos leiteiros pós-criopreservação
title Combination of sugars, lipoproteins and centrifugation improve dairy goat sperm viability submitted to cryopreservation
spellingShingle Combination of sugars, lipoproteins and centrifugation improve dairy goat sperm viability submitted to cryopreservation
Queiros, Aline Francelina de
congelación
Congelación
Fosfolipasa A
fosfolipasa A
mitocondria
Mitocondria
plasma seminal
Plasma seminal.
Freezing
freezing
Mitochondria
phospholipase A
Phospholipase A
mitochondria
Seminal plasma.
seminal plasma
congelação
Congelação
Fosfolipase A
fosfolipase A
mitocôndria
Mitocôndria
Plasma seminal.
plasma seminal
title_short Combination of sugars, lipoproteins and centrifugation improve dairy goat sperm viability submitted to cryopreservation
title_full Combination of sugars, lipoproteins and centrifugation improve dairy goat sperm viability submitted to cryopreservation
title_fullStr Combination of sugars, lipoproteins and centrifugation improve dairy goat sperm viability submitted to cryopreservation
title_full_unstemmed Combination of sugars, lipoproteins and centrifugation improve dairy goat sperm viability submitted to cryopreservation
title_sort Combination of sugars, lipoproteins and centrifugation improve dairy goat sperm viability submitted to cryopreservation
author Queiros, Aline Francelina de
author_facet Queiros, Aline Francelina de
Farias, Camilla Flávia Avelino de
Rique, Alex Souza
Tork, André Luiz Pereira
Clemente, Carlos Augusto Alanis
Guerra, Maria Madalena Pessoa
Silva, Sildivane Valcácia
author_role author
author2 Farias, Camilla Flávia Avelino de
Rique, Alex Souza
Tork, André Luiz Pereira
Clemente, Carlos Augusto Alanis
Guerra, Maria Madalena Pessoa
Silva, Sildivane Valcácia
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Queiros, Aline Francelina de
Farias, Camilla Flávia Avelino de
Rique, Alex Souza
Tork, André Luiz Pereira
Clemente, Carlos Augusto Alanis
Guerra, Maria Madalena Pessoa
Silva, Sildivane Valcácia
dc.subject.por.fl_str_mv congelación
Congelación
Fosfolipasa A
fosfolipasa A
mitocondria
Mitocondria
plasma seminal
Plasma seminal.
Freezing
freezing
Mitochondria
phospholipase A
Phospholipase A
mitochondria
Seminal plasma.
seminal plasma
congelação
Congelação
Fosfolipase A
fosfolipase A
mitocôndria
Mitocôndria
Plasma seminal.
plasma seminal
topic congelación
Congelación
Fosfolipasa A
fosfolipasa A
mitocondria
Mitocondria
plasma seminal
Plasma seminal.
Freezing
freezing
Mitochondria
phospholipase A
Phospholipase A
mitochondria
Seminal plasma.
seminal plasma
congelação
Congelação
Fosfolipase A
fosfolipase A
mitocôndria
Mitocôndria
Plasma seminal.
plasma seminal
description Abstract The aim of the present study was to evaluate the effects of different cryoprotectants and semen centrifugation on the kinetic parameters and membrane integrity of cryopreserved goat semen. Four buck goats were used, and their semen was collected using an artificial vagina. After semen collection and approval, six pools were formed, and each pool was divided into eight aliquots. The plasma was removed from four aliquots by centrifugation (1200 g/10 min) and subsequently diluted; the remaining four aliquots were diluted in standard Tris-egg yolk (SYE), standard milk (SME), test Tris-egg yolk (TYE) and test milk (TME) extenders without removing the seminal plasma. After dilution, samples were loaded into straws (0.25 mL), frozen and stored at -196 °C. The samples were thawed (37 °C/30 s) and evaluated immediately and two hours after thawing to determine the kinetics and integrity of plasma and mitochondrial membranes. A difference (p< 0.05) in the maintenance of sperm kinetics, plasma membrane integrity and mitochondrial potential was observed between the centrifuged and non-centrifuged groups and between the extenders at different time points. We concluded that the use of centrifugation to remove seminal plasma positively affects the semen evaluation parameters and that the yolk extender is more efficient when applied with different cryopreservation techniques, preserving the desirable traits after the cryopreservation of goat semen.
publishDate 2021
dc.date.none.fl_str_mv 2021-10-16
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/21559
10.33448/rsd-v10i13.21559
url https://rsdjournal.org/index.php/rsd/article/view/21559
identifier_str_mv 10.33448/rsd-v10i13.21559
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/21559/18989
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 10 No. 13; e358101321559
Research, Society and Development; Vol. 10 Núm. 13; e358101321559
Research, Society and Development; v. 10 n. 13; e358101321559
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
instname_str Universidade Federal de Itajubá (UNIFEI)
instacron_str UNIFEI
institution UNIFEI
reponame_str Research, Society and Development
collection Research, Society and Development
repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
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