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Association of Vitamin E with Rapid Thawing on Goat Semen
The aim of this study was to evaluate the effects of vitamin E associated with rapid thawing on cryopreserved goat semen. Two bucks were used and eight ejaculates per animal were collected using artificial vagina. Semen was diluted with the following treatments: BIOXCELL (control), BIOXCELL + Equex...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037631/ https://www.ncbi.nlm.nih.gov/pubmed/24955428 http://dx.doi.org/10.1155/2014/964172 |
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author | Penitente-Filho, Jurandy Mauro Oliveira, Fabrício Albani Jimenez, Carolina Rodriguez Carrascal, Erly Dias, Júlio César Oliveira Oliveira, Gisele Dias Silveira, Renata Gomes Silveira, Camila Oliveira Torres, Ciro Alexandre Alves |
author_facet | Penitente-Filho, Jurandy Mauro Oliveira, Fabrício Albani Jimenez, Carolina Rodriguez Carrascal, Erly Dias, Júlio César Oliveira Oliveira, Gisele Dias Silveira, Renata Gomes Silveira, Camila Oliveira Torres, Ciro Alexandre Alves |
author_sort | Penitente-Filho, Jurandy Mauro |
collection | PubMed |
description | The aim of this study was to evaluate the effects of vitamin E associated with rapid thawing on cryopreserved goat semen. Two bucks were used and eight ejaculates per animal were collected using artificial vagina. Semen was diluted with the following treatments: BIOXCELL (control), BIOXCELL + Equex (sodium lauryl sulphate) and BIOXCELL + vitamin E 100 μM. Semen was packaged into 0.25 mL straws and cooled at 5°C for 1 hour. Freezing was performed in liquid nitrogen vapor (−155°C) during 15 minutes. Then, the straws were immersed in liquid nitrogen (−196°C). Straws were thawed at 38°C/60 seconds or at 60°C/7 seconds with immediate sperm analysis. Hypoosmotic swelling test was performed adding a 20 μL aliquot of thawed semen to 1 mL of hypoosmotic solution (100 mOsm·Kg(−1)) followed by incubation during 60 minutes in water bath (38°C). Vitamin E did not affect any studied parameters (P > 0.05). Nevertheless, defrosting rate of 60°C/7 seconds improved sperm membrane functional integrity (P < 0.05). Current knowledge about goat semen cryopreservation is not sufficient to ensure high post-thawing recovery rates; thus, this study brings important data about using antioxidants and different thawing rates on cryopreservation process. |
format | Online Article Text |
id | pubmed-4037631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40376312014-06-22 Association of Vitamin E with Rapid Thawing on Goat Semen Penitente-Filho, Jurandy Mauro Oliveira, Fabrício Albani Jimenez, Carolina Rodriguez Carrascal, Erly Dias, Júlio César Oliveira Oliveira, Gisele Dias Silveira, Renata Gomes Silveira, Camila Oliveira Torres, Ciro Alexandre Alves ScientificWorldJournal Research Article The aim of this study was to evaluate the effects of vitamin E associated with rapid thawing on cryopreserved goat semen. Two bucks were used and eight ejaculates per animal were collected using artificial vagina. Semen was diluted with the following treatments: BIOXCELL (control), BIOXCELL + Equex (sodium lauryl sulphate) and BIOXCELL + vitamin E 100 μM. Semen was packaged into 0.25 mL straws and cooled at 5°C for 1 hour. Freezing was performed in liquid nitrogen vapor (−155°C) during 15 minutes. Then, the straws were immersed in liquid nitrogen (−196°C). Straws were thawed at 38°C/60 seconds or at 60°C/7 seconds with immediate sperm analysis. Hypoosmotic swelling test was performed adding a 20 μL aliquot of thawed semen to 1 mL of hypoosmotic solution (100 mOsm·Kg(−1)) followed by incubation during 60 minutes in water bath (38°C). Vitamin E did not affect any studied parameters (P > 0.05). Nevertheless, defrosting rate of 60°C/7 seconds improved sperm membrane functional integrity (P < 0.05). Current knowledge about goat semen cryopreservation is not sufficient to ensure high post-thawing recovery rates; thus, this study brings important data about using antioxidants and different thawing rates on cryopreservation process. Hindawi Publishing Corporation 2014 2014-05-11 /pmc/articles/PMC4037631/ /pubmed/24955428 http://dx.doi.org/10.1155/2014/964172 Text en Copyright © 2014 Jurandy Mauro Penitente-Filho et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Penitente-Filho, Jurandy Mauro Oliveira, Fabrício Albani Jimenez, Carolina Rodriguez Carrascal, Erly Dias, Júlio César Oliveira Oliveira, Gisele Dias Silveira, Renata Gomes Silveira, Camila Oliveira Torres, Ciro Alexandre Alves Association of Vitamin E with Rapid Thawing on Goat Semen |
title | Association of Vitamin E with Rapid Thawing on Goat Semen |
title_full | Association of Vitamin E with Rapid Thawing on Goat Semen |
title_fullStr | Association of Vitamin E with Rapid Thawing on Goat Semen |
title_full_unstemmed | Association of Vitamin E with Rapid Thawing on Goat Semen |
title_short | Association of Vitamin E with Rapid Thawing on Goat Semen |
title_sort | association of vitamin e with rapid thawing on goat semen |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037631/ https://www.ncbi.nlm.nih.gov/pubmed/24955428 http://dx.doi.org/10.1155/2014/964172 |
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