Efeito de diferentes tempos de resfriamento pré-congelamento na viabilidade espermática do sêmen descongelado de caprino

Detalhes bibliográficos
Autor(a) principal: Oliveira, Giselle Dias de
Data de Publicação: 2013
Tipo de documento: Dissertação
Idioma: por
Título da fonte: LOCUS Repositório Institucional da UFV
Texto Completo: http://locus.ufv.br/handle/123456789/5148
Resumo: The experiment was conducted at the Animal Reproduction Section of Veterinary Department, UFV, Viçosa, MG. The aim of the study was develop a technique of cryopreservation in order to improve the viability of goat semen after thawing. Were used four treatments: T1, cooling time of 1 h; T2, cooling time of 2 h; T3, cooling time of 4 h; and T4, with cooling time of 6 h before freezing. The semen was collected from four adult goats with three years old, totaling five collections using as dummy an adult male and the artificial vagina method, with the collections being conducted during the natural breeding season (April and May 2012). Were evaluated physical characteristics of semen immediately after collection and after thawing. After thawing, were also performed four complementary tests: heat resistance (TTR), hyposmotic (HOST), membrane integrity (INT), and morphological. The average values obtained for the fresh semen as the volume (mL), motility (%), sperm vigor (0-5) and sperm concentration (x109 total) were within the standards set by the Brazilian College of Animal Reproduction (1998), 1,5; 85%, 3,78; 3,3 billion / ml, respectively. The postthaw sperm motility and sperm vigor in the T2 showed mot. (38.0 ± 3.3) and vigor (2.2 ± 0.1), T3 mot. (52.3 ± 4.7) vigor (2.4 ± 0.1) and T4 mot. (47.0 ± 5.0) and vigor (2.4 ± 0.1), also proved within the values recommended by CBRA (1998). It was observed that the semen had resistance until the time 180 minutes in all treatments throughout the TTR. However, semen samples in treatments 3 and 4 were the ones that obtained better results. Regression analysis was performed to strengthen the results of the TTR time zero, where a greater curve was observed on time 265 minutes cooling, in other words, around 4 h and 25 minutes. The complementary tests (HOST, morphological and INT) performed in this study with different cooling times showed differences (P <0.05) between treatments only in INT test (29,7±3,3; 39,8±4,6; 50,0±5,1 e 56,5±4,1). Positive correlation was observed between motility and sperm vigor, and between motility and test INT. It is concluded that the cooling time of goat semen in times of 4 and 6 h has promoted better sperm cell viability after thawing of semen, increasing longevity of the spermatozoa.
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spelling Oliveira, Giselle Dias deCosta, Eduardo Paulino dahttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787237D6Guimarães, José Domingoshttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4782270U6Benjamin, Laércio dos Anjoshttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4797917E7Torres, Ciro Alexandre Alveshttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787213D42015-03-26T13:47:16Z2013-11-072015-03-26T13:47:16Z2013-04-30OLIVEIRA, Giselle Dias de. Effect of different cooling times pre-frozen on the sperm viability of the thawed goat semen. 2013. 52 f. Dissertação (Mestrado em Biotecnologia, diagnóstico e controle de doenças; Epidemiologia e controle de qualidade de prod. de) - Universidade Federal de Viçosa, Viçosa, 2013.http://locus.ufv.br/handle/123456789/5148The experiment was conducted at the Animal Reproduction Section of Veterinary Department, UFV, Viçosa, MG. The aim of the study was develop a technique of cryopreservation in order to improve the viability of goat semen after thawing. Were used four treatments: T1, cooling time of 1 h; T2, cooling time of 2 h; T3, cooling time of 4 h; and T4, with cooling time of 6 h before freezing. The semen was collected from four adult goats with three years old, totaling five collections using as dummy an adult male and the artificial vagina method, with the collections being conducted during the natural breeding season (April and May 2012). Were evaluated physical characteristics of semen immediately after collection and after thawing. After thawing, were also performed four complementary tests: heat resistance (TTR), hyposmotic (HOST), membrane integrity (INT), and morphological. The average values obtained for the fresh semen as the volume (mL), motility (%), sperm vigor (0-5) and sperm concentration (x109 total) were within the standards set by the Brazilian College of Animal Reproduction (1998), 1,5; 85%, 3,78; 3,3 billion / ml, respectively. The postthaw sperm motility and sperm vigor in the T2 showed mot. (38.0 ± 3.3) and vigor (2.2 ± 0.1), T3 mot. (52.3 ± 4.7) vigor (2.4 ± 0.1) and T4 mot. (47.0 ± 5.0) and vigor (2.4 ± 0.1), also proved within the values recommended by CBRA (1998). It was observed that the semen had resistance until the time 180 minutes in all treatments throughout the TTR. However, semen samples in treatments 3 and 4 were the ones that obtained better results. Regression analysis was performed to strengthen the results of the TTR time zero, where a greater curve was observed on time 265 minutes cooling, in other words, around 4 h and 25 minutes. The complementary tests (HOST, morphological and INT) performed in this study with different cooling times showed differences (P <0.05) between treatments only in INT test (29,7±3,3; 39,8±4,6; 50,0±5,1 e 56,5±4,1). Positive correlation was observed between motility and sperm vigor, and between motility and test INT. It is concluded that the cooling time of goat semen in times of 4 and 6 h has promoted better sperm cell viability after thawing of semen, increasing longevity of the spermatozoa.O experimento foi realizado no Setor de Reprodução Animal do Departamento de Veterinária da UFV, Viçosa-MG. O objetivo do estudo foi desenvolver uma técnica de criopreservação visando melhorar a viabilidade do sêmen de caprino após descongelamento. Foram utilizados 4 tratamentos: T1, tempo de resfriamento de 1 h; T2, tempo de resfriamento de 2 h; T3, tempo de resfriamento de 4 h; e T4, com tempo de resfriamento de 6 h antes do congelamento. O sêmen foi coletado de quatro caprinos adultos com três anos idade, realizando-se cinco coletas/animal, utilizando um macho adulto como manequim e metodo de vagina artificial, com as coletas sendo realizadas durante a estação de monta natural (abril e maio de 2012. Foram avaliadas as características físicas do sêmen imediatamente após a coleta e após o descongelamento. Após o descongelamento, foram realizados também quatro testes complementares: termorresistência (TTR), hiposmótico (HOST), de integridade de membrana (INT), e morfológico. Os valores médios obtidos para o sêmen fresco quanto a volume (mL), motilidade espermática progressiva (%), vigor espermático (0-5) e concentração espermática (x109 totais), se encontraram dentro dos padrões preconizados pelo Colégio Brasileiro de Reprodução Animal (1998), respectivamente de 1,5; 85%, 3,78; 3,3 bilhões/mL. A motilidade espermática pós-descongelamento e o vigor espermático nos tratamentos T2 mot. (38,0±3,3) e vigor (2,2±0,1) , T3 mot. (52,3±4,7) vigor (2,4±0,1) e T4 mot. (47,0±5,0) e vigor (2,4±0,1), também se mostraram nos padrões recomendados pelo CBRA (1998). Foi observado que o sêmen teve resistência até o tempo de 180 minutos em todos os tratamentos ao longo do TTR. Porém, as amostras de sêmen nos tratamentos 3 e 4 foram os que obtiveram melhores resultados. Foi realizada análise de regressão para reforçar os resultados do tempo zero do TTR, onde se observou uma curva maior no tempo de 265 minutos de resfriamento, ou seja, por volta de 4hs e 25minutos. Os valores médios dos parâmetros seminais analisados nos testes complementares (HOST, morfológico e INT) realizados no presente estudo se mostraram diferentes (P<0,05) entre os tratamentos somente no teste INT (29,7±3,3; 39,8±4,6; 50,0±5,1 e 56,5±4,1). Foi observada correlação positiva entre motilidade e vigor espermático, e entre motilidade e teste INT. Conclui-se que o tempo de resfriamento do sêmen de caprino em tempos de 4 e 6 h promoveu melhor viabilidade da célula espermática após o descongelamento do sêmen, aumentado a longevidade do espermatozoide.application/pdfporUniversidade Federal de ViçosaMestrado em Medicina VeterináriaUFVBRBiotecnologia, diagnóstico e controle de doenças; Epidemiologia e controle de qualidade de prod. deEspermatozoidesCriopreservaçãoTempo de equilíbrioSpermCryopreservationBalancing timeCNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIAEfeito de diferentes tempos de resfriamento pré-congelamento na viabilidade espermática do sêmen descongelado de caprinoEffect of different cooling times pre-frozen on the sperm viability of the thawed goat semeninfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFVORIGINALtexto completo.pdfapplication/pdf1148814https://locus.ufv.br//bitstream/123456789/5148/1/texto%20completo.pdffed3d8d370f810a216a50acab2db6ae6MD51TEXTtexto completo.pdf.txttexto completo.pdf.txtExtracted texttext/plain108734https://locus.ufv.br//bitstream/123456789/5148/2/texto%20completo.pdf.txtee32a347239da8d1dbe8e9fbbd79c1d1MD52THUMBNAILtexto completo.pdf.jpgtexto completo.pdf.jpgIM Thumbnailimage/jpeg3516https://locus.ufv.br//bitstream/123456789/5148/3/texto%20completo.pdf.jpg1a85a4ffad6b253a8ff75315cec4d186MD53123456789/51482016-04-11 23:09:32.675oai:locus.ufv.br:123456789/5148Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452016-04-12T02:09:32LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false
dc.title.por.fl_str_mv Efeito de diferentes tempos de resfriamento pré-congelamento na viabilidade espermática do sêmen descongelado de caprino
dc.title.alternative.eng.fl_str_mv Effect of different cooling times pre-frozen on the sperm viability of the thawed goat semen
title Efeito de diferentes tempos de resfriamento pré-congelamento na viabilidade espermática do sêmen descongelado de caprino
spellingShingle Efeito de diferentes tempos de resfriamento pré-congelamento na viabilidade espermática do sêmen descongelado de caprino
Oliveira, Giselle Dias de
Espermatozoides
Criopreservação
Tempo de equilíbrio
Sperm
Cryopreservation
Balancing time
CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA
title_short Efeito de diferentes tempos de resfriamento pré-congelamento na viabilidade espermática do sêmen descongelado de caprino
title_full Efeito de diferentes tempos de resfriamento pré-congelamento na viabilidade espermática do sêmen descongelado de caprino
title_fullStr Efeito de diferentes tempos de resfriamento pré-congelamento na viabilidade espermática do sêmen descongelado de caprino
title_full_unstemmed Efeito de diferentes tempos de resfriamento pré-congelamento na viabilidade espermática do sêmen descongelado de caprino
title_sort Efeito de diferentes tempos de resfriamento pré-congelamento na viabilidade espermática do sêmen descongelado de caprino
author Oliveira, Giselle Dias de
author_facet Oliveira, Giselle Dias de
author_role author
dc.contributor.author.fl_str_mv Oliveira, Giselle Dias de
dc.contributor.advisor-co1.fl_str_mv Costa, Eduardo Paulino da
dc.contributor.advisor-co1Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787237D6
dc.contributor.advisor-co2.fl_str_mv Guimarães, José Domingos
dc.contributor.advisor-co2Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4782270U6
dc.contributor.advisor1.fl_str_mv Benjamin, Laércio dos Anjos
dc.contributor.advisor1Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4797917E7
dc.contributor.referee1.fl_str_mv Torres, Ciro Alexandre Alves
dc.contributor.referee1Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787213D4
contributor_str_mv Costa, Eduardo Paulino da
Guimarães, José Domingos
Benjamin, Laércio dos Anjos
Torres, Ciro Alexandre Alves
dc.subject.por.fl_str_mv Espermatozoides
Criopreservação
Tempo de equilíbrio
topic Espermatozoides
Criopreservação
Tempo de equilíbrio
Sperm
Cryopreservation
Balancing time
CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA
dc.subject.eng.fl_str_mv Sperm
Cryopreservation
Balancing time
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA
description The experiment was conducted at the Animal Reproduction Section of Veterinary Department, UFV, Viçosa, MG. The aim of the study was develop a technique of cryopreservation in order to improve the viability of goat semen after thawing. Were used four treatments: T1, cooling time of 1 h; T2, cooling time of 2 h; T3, cooling time of 4 h; and T4, with cooling time of 6 h before freezing. The semen was collected from four adult goats with three years old, totaling five collections using as dummy an adult male and the artificial vagina method, with the collections being conducted during the natural breeding season (April and May 2012). Were evaluated physical characteristics of semen immediately after collection and after thawing. After thawing, were also performed four complementary tests: heat resistance (TTR), hyposmotic (HOST), membrane integrity (INT), and morphological. The average values obtained for the fresh semen as the volume (mL), motility (%), sperm vigor (0-5) and sperm concentration (x109 total) were within the standards set by the Brazilian College of Animal Reproduction (1998), 1,5; 85%, 3,78; 3,3 billion / ml, respectively. The postthaw sperm motility and sperm vigor in the T2 showed mot. (38.0 ± 3.3) and vigor (2.2 ± 0.1), T3 mot. (52.3 ± 4.7) vigor (2.4 ± 0.1) and T4 mot. (47.0 ± 5.0) and vigor (2.4 ± 0.1), also proved within the values recommended by CBRA (1998). It was observed that the semen had resistance until the time 180 minutes in all treatments throughout the TTR. However, semen samples in treatments 3 and 4 were the ones that obtained better results. Regression analysis was performed to strengthen the results of the TTR time zero, where a greater curve was observed on time 265 minutes cooling, in other words, around 4 h and 25 minutes. The complementary tests (HOST, morphological and INT) performed in this study with different cooling times showed differences (P <0.05) between treatments only in INT test (29,7±3,3; 39,8±4,6; 50,0±5,1 e 56,5±4,1). Positive correlation was observed between motility and sperm vigor, and between motility and test INT. It is concluded that the cooling time of goat semen in times of 4 and 6 h has promoted better sperm cell viability after thawing of semen, increasing longevity of the spermatozoa.
publishDate 2013
dc.date.available.fl_str_mv 2013-11-07
2015-03-26T13:47:16Z
dc.date.issued.fl_str_mv 2013-04-30
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identifier_str_mv OLIVEIRA, Giselle Dias de. Effect of different cooling times pre-frozen on the sperm viability of the thawed goat semen. 2013. 52 f. Dissertação (Mestrado em Biotecnologia, diagnóstico e controle de doenças; Epidemiologia e controle de qualidade de prod. de) - Universidade Federal de Viçosa, Viçosa, 2013.
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