Efeito de diferentes tempos de equilíbrio, taxas de congelamento e concentrações espermáticas na fertilidade do sêmen eqüino

Detalhes bibliográficos
Ano de defesa: 2006
Autor(a) principal: Fürst, Rogério
Orientador(a): Carvalho, Giovanni Ribeiro de lattes
Banca de defesa: Guimarães, José Domingos lattes, Fonseca, Jeferson Ferreira da lattes
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Viçosa
Programa de Pós-Graduação: Doutorado em Zootecnia
Departamento: Genética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e Forragicul
País: BR
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://locus.ufv.br/handle/123456789/1811
Resumo: The freezing process cause damages the structural integrity, biochemist and biophysical the plasmatic membrane of the spermatozoon, leading a reduction in the fertility of the semen after the unfreeze. These damages are in consequence the imperfections in the freezing process that it understands since the collection until speed and time of centrifugation; curve of cooling and freezing; balance time; spermatic concentration for inseminated dose and frequency of insemination. The objective of this study was to evaluate the efficiency of alternative method equine semen freezing, as different times of balance, curves of freezing and unfreeze on the fertility of the equine semen. In Experiment 1, five ejaculates of three had been used sires of the race Mangalarga Marchador where the experimental group was divided in three treatments: T1 = time of balance of 25; T2 minutes = 1 time of balance and 25 minutes; and T3 = time of balance with 2 hours 25 minutes, where tests had been evaluated as survival, hypostatic test motilities and vigor in the TTR. The total motilities evaluated by the TTR in the times of 0, 20 and 40 minutes did not differ (P > 0.05) between the T1 and the evaluated semen the cool one. It did not have difference (P > 0.05) enter the treatments how much the evaluated motilities in the different times of the TTR, and evaluated vigor inside of each time. It approximately had a reduction of 33% number of reactive spermatozoa to the Host in the unfreeze, comparison to the results found in the cool semen. The structural integrity of the plasmatic membranes was evaluated using the survival test, being the dead spermatozoa had been approximately 36.15% superior in the frozen semen when compared with the cool semen. In Experiment 2 for fertility test one used five ejaculates ones of six sires of the race Mangalarga Marchador and two of the race Breton. Where a curve of freezing T1 was tested and two spermatic concentrations for inseminated dose T1 = 300 million and T2 = 150 million. The tax of gestation gotten in 95 cycles was analyzed getting tax of 54.7% fertility (T1 = 35/64 cycles) e 51.6% (T2 = 16/31 cycles). It did not have difference (P > 0.05) between treatments between the treatments. In Experiment 3 five ejaculates of three sires of the race Mangalarga Marchador had been used where it was tested two protocols of freezing, CH (horizontal curve) with one tax of freezing of -60 oC/minute and CV (vertical curve) with one tax of freezing of -100 oC/minute (extreme-fast) and two protocols of unfreeze 37 oC/30 and 75 oC/7 . Comparing it mobile percentage of spermatozoa after unfreeze with the cool semen, had observed losses of next motilities to 28.6% in the T0 of the TTR, to the end of the TTR (90 minutes) this value did not exceed to 50%, independently of the procedure of freezing and unfreeze. However, a fall accented in the motilities and vigor after unfreeze for CH when compared with the 40, 60 and 90 minutes of the TTR with the CV (39.7% versus 50.23% and 40.2% versus 50%), (36.7% versus 43.7% and 36.3 versus 43.9) e (27.8 versus 35.9 and 25.44 versus 40.86) in such a way in the unfreeze the 37 oC and 75 oC respectively (P < 0.05). Superior results had been gotten for the vigor. The tax of gestation gotten in 25 cycles for the CV was of 81.8% for the concentration 300 71.4% and million for 150 million viable spermatozoa in the unfreeze.
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spelling Fürst, Rogériohttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4728419J7Costa, Eduardo Paulino dahttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787237D6Torres, Ciro Alexandre Alveshttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787213D4Carvalho, Giovanni Ribeiro dehttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4723068Z6Guimarães, José Domingoshttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4782270U6Fonseca, Jeferson Ferreira dahttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4703690H82015-03-26T12:54:45Z2007-04-172015-03-26T12:54:45Z2006-09-18FÜRST, Rogério. Effect of different times of balance, freezing rates and concentrations espermatics in the fertility of the semen equine. 2006. 114 f. Tese (Doutorado em Genética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e Forragicul) - Universidade Federal de Viçosa, Viçosa, 2006.http://locus.ufv.br/handle/123456789/1811The freezing process cause damages the structural integrity, biochemist and biophysical the plasmatic membrane of the spermatozoon, leading a reduction in the fertility of the semen after the unfreeze. These damages are in consequence the imperfections in the freezing process that it understands since the collection until speed and time of centrifugation; curve of cooling and freezing; balance time; spermatic concentration for inseminated dose and frequency of insemination. The objective of this study was to evaluate the efficiency of alternative method equine semen freezing, as different times of balance, curves of freezing and unfreeze on the fertility of the equine semen. In Experiment 1, five ejaculates of three had been used sires of the race Mangalarga Marchador where the experimental group was divided in three treatments: T1 = time of balance of 25; T2 minutes = 1 time of balance and 25 minutes; and T3 = time of balance with 2 hours 25 minutes, where tests had been evaluated as survival, hypostatic test motilities and vigor in the TTR. The total motilities evaluated by the TTR in the times of 0, 20 and 40 minutes did not differ (P > 0.05) between the T1 and the evaluated semen the cool one. It did not have difference (P > 0.05) enter the treatments how much the evaluated motilities in the different times of the TTR, and evaluated vigor inside of each time. It approximately had a reduction of 33% number of reactive spermatozoa to the Host in the unfreeze, comparison to the results found in the cool semen. The structural integrity of the plasmatic membranes was evaluated using the survival test, being the dead spermatozoa had been approximately 36.15% superior in the frozen semen when compared with the cool semen. In Experiment 2 for fertility test one used five ejaculates ones of six sires of the race Mangalarga Marchador and two of the race Breton. Where a curve of freezing T1 was tested and two spermatic concentrations for inseminated dose T1 = 300 million and T2 = 150 million. The tax of gestation gotten in 95 cycles was analyzed getting tax of 54.7% fertility (T1 = 35/64 cycles) e 51.6% (T2 = 16/31 cycles). It did not have difference (P > 0.05) between treatments between the treatments. In Experiment 3 five ejaculates of three sires of the race Mangalarga Marchador had been used where it was tested two protocols of freezing, CH (horizontal curve) with one tax of freezing of -60 oC/minute and CV (vertical curve) with one tax of freezing of -100 oC/minute (extreme-fast) and two protocols of unfreeze 37 oC/30 and 75 oC/7 . Comparing it mobile percentage of spermatozoa after unfreeze with the cool semen, had observed losses of next motilities to 28.6% in the T0 of the TTR, to the end of the TTR (90 minutes) this value did not exceed to 50%, independently of the procedure of freezing and unfreeze. However, a fall accented in the motilities and vigor after unfreeze for CH when compared with the 40, 60 and 90 minutes of the TTR with the CV (39.7% versus 50.23% and 40.2% versus 50%), (36.7% versus 43.7% and 36.3 versus 43.9) e (27.8 versus 35.9 and 25.44 versus 40.86) in such a way in the unfreeze the 37 oC and 75 oC respectively (P < 0.05). Superior results had been gotten for the vigor. The tax of gestation gotten in 25 cycles for the CV was of 81.8% for the concentration 300 71.4% and million for 150 million viable spermatozoa in the unfreeze.O objetivo deste estudo foi avaliar a eficiência de diferentes tempos de equilíbrio, as curvas de congelamento e descongelamento e a concentração espermática por dose inseminante sobre a fertilidade do sêmen eqüino. No Experimento 1, foram utilizados cinco ejaculados de três garanhões da raça Mangalarga Marchador, sendo o grupo experimental dividido em três tratamentos: T1 = tempo de equilíbrio de 25 minutos, T2 = tempo de equilíbrio 1h25 min e T3 = tempo de equilíbrio com 2h25 min, em que a qualidade seminal foi avaliada por testes como supravital, teste hiposmótico (Host), motilidade e vigor espermático progressivo no TTR. A motilidade espermática progressiva avaliada no TTR nos tempos de 0, 20 e 40 minutos não diferiu. Não houve diferença na qualidade do sêmen nos diferentes tempos do TTR (P > 0,05). Houve redução de aproximadamente 33% de espermatozóides reativos ao Host após o descongelamento, em comparação aos resultados registrados no sêmen in natura, de onde se conclui que o tempo de equilíbrio não tem nenhuma influência na qualidade espermática do sêmen congelado. No Experimento 2, para teste de fertilidade, foram utilizados cinco ejaculados de seis garanhões da raça Mangalarga Marchador e dois garanhões da raça Bretão-Postier e foram testadas duas concentrações espermáticas por dose inseminante, em que T1 = 300 milhões e T2 = 150 milhões. A taxa de prenhez obtida em 95 estros foi de 54,7% (T1 = 35/64 estros) e 51,6% (T2 = 16/31 estros), e não diferiu das taxas de prenhez registradas nos dois tratamentos (P > 0,05). No Experimento 3 foram utilizados cinco ejaculados de três garanhões da raça Mangalarga Marchador, em que foram testados dois protocolos de congelamento, sendo curva horizontal (CH) com taxa de congelamento de -60 oC/minuto e curva vertical (CV) com taxa de congelamento de -100 oC/minuto e dois protocolos de descongelamento, sendo 37 oC/30 e 75 oC/7 . Comparando-se a porcentagem de espermatozóides móveis pós-descongelamento com o sêmen fresco, observaram-se perdas de motilidades progressiva de 28,6% no T0 do TTR; ao final do TTR (90 minutos) este valor não ultrapassou 50%, independentemente dos protocolos de congelamento e descongelamento. Entretanto, queda acentuada na motilidade espermática e no vigor espermático pós-descongelamento para CH, quando comparada aos 40, 60 e 90 minutos do TTR com a CV (39,7% vs 50,23% e 40,2% vs 50%), (36,7% vs 43,7% e 36,3 vs 43,9) e (27,8 vs 35,9 e 25,44 vs 40,86) tanto no descongelamento quanto a 37 oC e 75 oC, respectivamente (P < 0,05). Resultados superiores foram obtidos para o vigor. A taxa de prenhez obtida em 25 ciclos para a CV foi de 81,8% para a concentração 300 milhões e de 71,4% para 150 milhões de espermatozóides viáveis no descongelamento.Conselho Nacional de Desenvolvimento Científico e Tecnológicoapplication/pdfporUniversidade Federal de ViçosaDoutorado em ZootecniaUFVBRGenética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e ForragiculEquinoSêmenCriopreservaçãoEquineSemenCryopreservationCNPQ::CIENCIAS AGRARIAS::ZOOTECNIA::PRODUCAO ANIMALEfeito de diferentes tempos de equilíbrio, taxas de congelamento e concentrações espermáticas na fertilidade do sêmen eqüinoEffect of different times of balance, freezing rates and concentrations espermatics in the fertility of the semen equineinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/openAccessreponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFVORIGINALtexto completo.pdfapplication/pdf820899https://locus.ufv.br//bitstream/123456789/1811/1/texto%20completo.pdf9d5c37f00182c95ec34e9e0e9bb4c730MD51TEXTtexto completo.pdf.txttexto completo.pdf.txtExtracted texttext/plain278208https://locus.ufv.br//bitstream/123456789/1811/2/texto%20completo.pdf.txt56643db1851cf2841302dcf048582689MD52THUMBNAILtexto completo.pdf.jpgtexto completo.pdf.jpgIM Thumbnailimage/jpeg3750https://locus.ufv.br//bitstream/123456789/1811/3/texto%20completo.pdf.jpg2b7183f64f36708fb84e724506d78614MD53123456789/18112016-04-07 23:13:35.14oai:locus.ufv.br:123456789/1811Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452016-04-08T02:13:35LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false
dc.title.por.fl_str_mv Efeito de diferentes tempos de equilíbrio, taxas de congelamento e concentrações espermáticas na fertilidade do sêmen eqüino
dc.title.alternative.eng.fl_str_mv Effect of different times of balance, freezing rates and concentrations espermatics in the fertility of the semen equine
title Efeito de diferentes tempos de equilíbrio, taxas de congelamento e concentrações espermáticas na fertilidade do sêmen eqüino
spellingShingle Efeito de diferentes tempos de equilíbrio, taxas de congelamento e concentrações espermáticas na fertilidade do sêmen eqüino
Fürst, Rogério
Equino
Sêmen
Criopreservação
Equine
Semen
Cryopreservation
CNPQ::CIENCIAS AGRARIAS::ZOOTECNIA::PRODUCAO ANIMAL
title_short Efeito de diferentes tempos de equilíbrio, taxas de congelamento e concentrações espermáticas na fertilidade do sêmen eqüino
title_full Efeito de diferentes tempos de equilíbrio, taxas de congelamento e concentrações espermáticas na fertilidade do sêmen eqüino
title_fullStr Efeito de diferentes tempos de equilíbrio, taxas de congelamento e concentrações espermáticas na fertilidade do sêmen eqüino
title_full_unstemmed Efeito de diferentes tempos de equilíbrio, taxas de congelamento e concentrações espermáticas na fertilidade do sêmen eqüino
title_sort Efeito de diferentes tempos de equilíbrio, taxas de congelamento e concentrações espermáticas na fertilidade do sêmen eqüino
author Fürst, Rogério
author_facet Fürst, Rogério
author_role author
dc.contributor.authorLattes.por.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4728419J7
dc.contributor.author.fl_str_mv Fürst, Rogério
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 Torres, Ciro Alexandre Alves
dc.contributor.advisor-co2Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787213D4
dc.contributor.advisor1.fl_str_mv Carvalho, Giovanni Ribeiro de
dc.contributor.advisor1Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4723068Z6
dc.contributor.referee1.fl_str_mv Guimarães, José Domingos
dc.contributor.referee1Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4782270U6
dc.contributor.referee2.fl_str_mv Fonseca, Jeferson Ferreira da
dc.contributor.referee2Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4703690H8
contributor_str_mv Costa, Eduardo Paulino da
Torres, Ciro Alexandre Alves
Carvalho, Giovanni Ribeiro de
Guimarães, José Domingos
Fonseca, Jeferson Ferreira da
dc.subject.por.fl_str_mv Equino
Sêmen
Criopreservação
topic Equino
Sêmen
Criopreservação
Equine
Semen
Cryopreservation
CNPQ::CIENCIAS AGRARIAS::ZOOTECNIA::PRODUCAO ANIMAL
dc.subject.eng.fl_str_mv Equine
Semen
Cryopreservation
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS AGRARIAS::ZOOTECNIA::PRODUCAO ANIMAL
description The freezing process cause damages the structural integrity, biochemist and biophysical the plasmatic membrane of the spermatozoon, leading a reduction in the fertility of the semen after the unfreeze. These damages are in consequence the imperfections in the freezing process that it understands since the collection until speed and time of centrifugation; curve of cooling and freezing; balance time; spermatic concentration for inseminated dose and frequency of insemination. The objective of this study was to evaluate the efficiency of alternative method equine semen freezing, as different times of balance, curves of freezing and unfreeze on the fertility of the equine semen. In Experiment 1, five ejaculates of three had been used sires of the race Mangalarga Marchador where the experimental group was divided in three treatments: T1 = time of balance of 25; T2 minutes = 1 time of balance and 25 minutes; and T3 = time of balance with 2 hours 25 minutes, where tests had been evaluated as survival, hypostatic test motilities and vigor in the TTR. The total motilities evaluated by the TTR in the times of 0, 20 and 40 minutes did not differ (P > 0.05) between the T1 and the evaluated semen the cool one. It did not have difference (P > 0.05) enter the treatments how much the evaluated motilities in the different times of the TTR, and evaluated vigor inside of each time. It approximately had a reduction of 33% number of reactive spermatozoa to the Host in the unfreeze, comparison to the results found in the cool semen. The structural integrity of the plasmatic membranes was evaluated using the survival test, being the dead spermatozoa had been approximately 36.15% superior in the frozen semen when compared with the cool semen. In Experiment 2 for fertility test one used five ejaculates ones of six sires of the race Mangalarga Marchador and two of the race Breton. Where a curve of freezing T1 was tested and two spermatic concentrations for inseminated dose T1 = 300 million and T2 = 150 million. The tax of gestation gotten in 95 cycles was analyzed getting tax of 54.7% fertility (T1 = 35/64 cycles) e 51.6% (T2 = 16/31 cycles). It did not have difference (P > 0.05) between treatments between the treatments. In Experiment 3 five ejaculates of three sires of the race Mangalarga Marchador had been used where it was tested two protocols of freezing, CH (horizontal curve) with one tax of freezing of -60 oC/minute and CV (vertical curve) with one tax of freezing of -100 oC/minute (extreme-fast) and two protocols of unfreeze 37 oC/30 and 75 oC/7 . Comparing it mobile percentage of spermatozoa after unfreeze with the cool semen, had observed losses of next motilities to 28.6% in the T0 of the TTR, to the end of the TTR (90 minutes) this value did not exceed to 50%, independently of the procedure of freezing and unfreeze. However, a fall accented in the motilities and vigor after unfreeze for CH when compared with the 40, 60 and 90 minutes of the TTR with the CV (39.7% versus 50.23% and 40.2% versus 50%), (36.7% versus 43.7% and 36.3 versus 43.9) e (27.8 versus 35.9 and 25.44 versus 40.86) in such a way in the unfreeze the 37 oC and 75 oC respectively (P < 0.05). Superior results had been gotten for the vigor. The tax of gestation gotten in 25 cycles for the CV was of 81.8% for the concentration 300 71.4% and million for 150 million viable spermatozoa in the unfreeze.
publishDate 2006
dc.date.issued.fl_str_mv 2006-09-18
dc.date.available.fl_str_mv 2007-04-17
2015-03-26T12:54:45Z
dc.date.accessioned.fl_str_mv 2015-03-26T12:54:45Z
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dc.identifier.citation.fl_str_mv FÜRST, Rogério. Effect of different times of balance, freezing rates and concentrations espermatics in the fertility of the semen equine. 2006. 114 f. Tese (Doutorado em Genética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e Forragicul) - Universidade Federal de Viçosa, Viçosa, 2006.
dc.identifier.uri.fl_str_mv http://locus.ufv.br/handle/123456789/1811
identifier_str_mv FÜRST, Rogério. Effect of different times of balance, freezing rates and concentrations espermatics in the fertility of the semen equine. 2006. 114 f. Tese (Doutorado em Genética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e Forragicul) - Universidade Federal de Viçosa, Viçosa, 2006.
url http://locus.ufv.br/handle/123456789/1811
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dc.publisher.program.fl_str_mv Doutorado em Zootecnia
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dc.publisher.country.fl_str_mv BR
dc.publisher.department.fl_str_mv Genética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e Forragicul
publisher.none.fl_str_mv Universidade Federal de Viçosa
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