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5. | | RITTERBUSCH, G. A.; ZANELLA, E. L.; VIANCELLI, A.; SIMON, N.; DAHMER, A.; CIACCI-ZANELLA, J. R. Análise da morfologia espermática e detecção de PCV2 em amostras de sêmen de reprodutores suínos. In: CONGRESSO BRASILEIRO DE VETERINÁRIOS ESPECIALISTAS EM SUÍNOS, 13., 2007, Florianópolis. Anais... Concórdia: Embrapa Suínos e Aves, 2007. 1 CD-ROM. Projeto n. 10.06.21.032-01. Biblioteca(s): Embrapa Suínos e Aves. |
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6. | | ZANELLA, E. L.; LEDUR, M. C.; SCHMIDT, G. S.; JAENISCH, F. R. F.; COUTINHO, L. L. Development of a new reference population for QTL detection in poultry. In: ANNUAL MEETING, 89., 2000, Montreal, Canadá. Abstracts... Montreal: PSA, 2000. p. 61 Biblioteca(s): Embrapa Suínos e Aves. |
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9. | | SILVEIRA, P. R. S. da, ZANELLA, E. L. BARIONI JUNIOR, W. ZANUZZO, A. CANDINI, P. H. Desempenho reprodutivo de porcas injetadas com Vitamina A. In: CONGRESSO BRASILEIRO DE VETERINARIOS ESPECIALISTAS EM SUINOS, 9., 1999, Belo Horizonte, MG. Anais... Concórdia : EMBRAPA-CNPSA, 1999. p.319-329. Parceria: CNPq/Sadia Concórdia S/A/USP Biblioteca(s): Embrapa Suínos e Aves. |
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12. | | ZANELLA, E. L. MESQUITA, F. S. SILVEIRA, P. R. S. da, COLDEBELLA, A. BARIONI JUNIOR, W. Avaliaçao morfológica de sêmen suíno no Estado de Santa Catarina, Brasil.\n In: CONGRESSO MERCOSUL DE PRODUÇAO SUINA, 2000, Buenos Aires, Argentina. Memória... Buenos Aires, 2000. p.R8. Parceria: CNPq / ESALQ-USP / Universidade de Passo Fundo. Biblioteca(s): Embrapa Suínos e Aves. |
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16. | | ZANELLA, J. R. C.; ZANELLA, E. L.; MORÉS, N.; SIMON, N.; ASCOLI, K.; RITTERBUSCH, G.; DAHMER, A.; GAVA, D. Absence of apoptosis and cellular changes in the reproductive system of boars naturally infected with porcine circovirus 2 (PCV2). In: INTERNATIONAL PIG VETERINARY SOCIETY, 20., 2008, Durban, South Africa. Proceedings. Durban: IPVS, 2008. p. 23 Projeto/Plano de Ação: 03.07.51.900-07. Biblioteca(s): Embrapa Suínos e Aves. |
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19. | | CONSALTER, A.; SILVA, A. P. da; GAIA, V. G.; ZANELLA, E. L.; SOUZA, G. N. de; FERREIRA, A. M. R. Seroprevalence and risk factors associated with Neospora caninum in commercial sheep from northwest of Rio Grande do Sul, Brazil. Semina. Ciências Agrárias, v. 41, n. 2, p. 705-710, mar./abr. 2020. Biblioteca(s): Embrapa Gado de Leite. |
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20. | | ALBRING, D. C.; SUPERTI, B. F. V.; SOUZA, A. P.; ZANELLA, E. L.; ZANELLA, R.; MARQUES, M. G. Effect of different melatonin concentration in integrity of acrosomal membrane in swine sperm cryopreserved. In: ANNUAL MEETING OF THE BRAZILIAN EMBRYO TECHNOLOGY SOCIETY (SBTE), 30., 2016, Foz do Iguaçu; MEETING OF THE EUROPEAN EMBRYO TRANSFER ASSOCIATION (AETE), 32., 2016, Barcelona. Proceedings... Animal Reproduction., v.13, n.3, p. 554, Jul./Sept. 2016. A180. 1 CD-Rom. Biblioteca(s): Embrapa Suínos e Aves. |
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Registros recuperados : 52 | |
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Registro Completo
Biblioteca(s): |
Embrapa Suínos e Aves. |
Data corrente: |
10/08/2021 |
Data da última atualização: |
10/08/2021 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
C - 0 |
Autoria: |
ROMERO TISOT, C. M.; ZANELLA, R.; SOUZA, A. P.; LÖF, L. M.; SOARES, J. C. M.; MARQUES, M. G.; ZANELLA, E. L. |
Afiliação: |
CÂNDIDA MALDANER ROMERO TISOT, UPF; RICARDO ZANELLA, UPF; UDESC/Lages; LUCAS MALLMANN LÖF, UPF; UFSM; MARIANA GROKE MARQUES, CNPSA; ERALDO LOURENSO ZANELLA, UPF. |
Título: |
Melatonin effect on cryopreserved sperm cells of crioulo stallions. |
Ano de publicação: |
2020 |
Fonte/Imprenta: |
Open Access Journal of Veterinary Science & Research, v. 5, n. 2, 2020. |
DOI: |
10.23880/oajvsr-16000202 |
Idioma: |
Inglês |
Conteúdo: |
Abstract: The freezing/thawing process of spermatozoa can cause cellular damage to the male gamete, decreasing the fertilization potential due to the increase in the production of reactive oxygen species (ROS). Melatonin is a potent endogenous antioxidant that protects the body against the damage caused by ROS. This study has evaluated different melatonin concentrations on the sperm viability of cryopreserved semen of Crioulo stallions. For that, three ejaculates were collected from five stallions diluted in a commercial extender followed by centrifugation and resuspension in a commercial freezing extender supplemented with 0; 1.25; 2.5. 5mM of Melatonin before the cryopreservation process. After thawing, the evaluation was performed assessing motility and flow cytometry evaluations: the plasma membrane integrity (PI), the integrity of the acrosomal membrane (FITC-PNA), mitochondrial membrane potential (JC1), and ROS generation (DCF-DA). Our results showed that sperm motility in the group without Melatonin and the 1.25mM group did not show the difference; however, the groups 2.5mM and 5mM presented a reduction in sperm motility. The 1.25 mM concentration was able to protect the plasma membrane during the cryopreservation process, in addition to showing a significant reduction in the production of ROS and increasing the percentage of sperm with integral acrosome. It can also be seen that high concentrations of Melatonin did not show beneficial effects. In conclusion, the addition of 1.25 mM of the Melatonin in Crioulo sperm cells showed to have a protective effect on the sperm cell during cryopreservation. MenosAbstract: The freezing/thawing process of spermatozoa can cause cellular damage to the male gamete, decreasing the fertilization potential due to the increase in the production of reactive oxygen species (ROS). Melatonin is a potent endogenous antioxidant that protects the body against the damage caused by ROS. This study has evaluated different melatonin concentrations on the sperm viability of cryopreserved semen of Crioulo stallions. For that, three ejaculates were collected from five stallions diluted in a commercial extender followed by centrifugation and resuspension in a commercial freezing extender supplemented with 0; 1.25; 2.5. 5mM of Melatonin before the cryopreservation process. After thawing, the evaluation was performed assessing motility and flow cytometry evaluations: the plasma membrane integrity (PI), the integrity of the acrosomal membrane (FITC-PNA), mitochondrial membrane potential (JC1), and ROS generation (DCF-DA). Our results showed that sperm motility in the group without Melatonin and the 1.25mM group did not show the difference; however, the groups 2.5mM and 5mM presented a reduction in sperm motility. The 1.25 mM concentration was able to protect the plasma membrane during the cryopreservation process, in addition to showing a significant reduction in the production of ROS and increasing the percentage of sperm with integral acrosome. It can also be seen that high concentrations of Melatonin did not show beneficial effects. In conclusion, the addi... Mostrar Tudo |
Palavras-Chave: |
Melatonina. |
Thesagro: |
Criopreservação; Espermatozóide; Garanhão; Reprodução Animal. |
Thesaurus NAL: |
Animal reproduction; Cryopreservation; Melatonin; Reactive oxygen species; Spermatozoa; Stallions. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/225036/1/final9560.pdf
|
Marc: |
LEADER 02592naa a2200337 a 4500 001 2133434 005 2021-08-10 008 2020 bl uuuu u00u1 u #d 024 7 $a10.23880/oajvsr-16000202$2DOI 100 1 $aROMERO TISOT, C. M. 245 $aMelatonin effect on cryopreserved sperm cells of crioulo stallions.$h[electronic resource] 260 $c2020 520 $aAbstract: The freezing/thawing process of spermatozoa can cause cellular damage to the male gamete, decreasing the fertilization potential due to the increase in the production of reactive oxygen species (ROS). Melatonin is a potent endogenous antioxidant that protects the body against the damage caused by ROS. This study has evaluated different melatonin concentrations on the sperm viability of cryopreserved semen of Crioulo stallions. For that, three ejaculates were collected from five stallions diluted in a commercial extender followed by centrifugation and resuspension in a commercial freezing extender supplemented with 0; 1.25; 2.5. 5mM of Melatonin before the cryopreservation process. After thawing, the evaluation was performed assessing motility and flow cytometry evaluations: the plasma membrane integrity (PI), the integrity of the acrosomal membrane (FITC-PNA), mitochondrial membrane potential (JC1), and ROS generation (DCF-DA). Our results showed that sperm motility in the group without Melatonin and the 1.25mM group did not show the difference; however, the groups 2.5mM and 5mM presented a reduction in sperm motility. The 1.25 mM concentration was able to protect the plasma membrane during the cryopreservation process, in addition to showing a significant reduction in the production of ROS and increasing the percentage of sperm with integral acrosome. It can also be seen that high concentrations of Melatonin did not show beneficial effects. In conclusion, the addition of 1.25 mM of the Melatonin in Crioulo sperm cells showed to have a protective effect on the sperm cell during cryopreservation. 650 $aAnimal reproduction 650 $aCryopreservation 650 $aMelatonin 650 $aReactive oxygen species 650 $aSpermatozoa 650 $aStallions 650 $aCriopreservação 650 $aEspermatozóide 650 $aGaranhão 650 $aReprodução Animal 653 $aMelatonina 700 1 $aZANELLA, R. 700 1 $aSOUZA, A. P. 700 1 $aLÖF, L. M. 700 1 $aSOARES, J. C. M. 700 1 $aMARQUES, M. G. 700 1 $aZANELLA, E. L 773 $tOpen Access Journal of Veterinary Science & Research$gv. 5, n. 2, 2020.
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