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Live Birth from Slow-Frozen Rabbit Oocytes after In Vivo Fertilisation
In vivo fertilisation techniques such as intraoviductal oocyte transfer have been considered as alternatives to bypass the inadequacy of conventional in vitro fertilisation in rabbit. There is only one study in the literature, published in 1989, that reports live offspring from cryopreserved rabbit...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866232/ https://www.ncbi.nlm.nih.gov/pubmed/24358281 http://dx.doi.org/10.1371/journal.pone.0083399 |
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author | Jiménez-Trigos, Estrella Vicente, José S. Marco-Jiménez, Francisco |
author_facet | Jiménez-Trigos, Estrella Vicente, José S. Marco-Jiménez, Francisco |
author_sort | Jiménez-Trigos, Estrella |
collection | PubMed |
description | In vivo fertilisation techniques such as intraoviductal oocyte transfer have been considered as alternatives to bypass the inadequacy of conventional in vitro fertilisation in rabbit. There is only one study in the literature, published in 1989, that reports live offspring from cryopreserved rabbit oocytes. The aim of the present study was to establish the in vivo fertilisation procedure to generate live offspring with frozen oocytes. First, the effect of two recipient models (i) ovariectomised or (ii) oviduct ligated immediately after transfer on the ability of fresh oocytes to fertilise were compared. Second, generation of live offspring from slow-frozen oocytes was carried out using the ligated oviduct recipient model. Throughout the experiment, recipients were artificially inseminated 9 hours prior to oocyte transfer. In the first experiment, two days after unilateral transfer of fresh oocytes, oviducts and uterine horns were flushed to assess embryo recovery rates. The embryo recovery rates were low compared to control in both ovariectomised and ligated oviduct groups. However, ligated oviduct recipient showed significantly (P<0.05) higher embryo recovery rates compared to ovariectomised and control-transferred. In the second experiment, using bilateral oviduct ligation model, all females that received slow-frozen oocytes became pregnant and delivered a total of 4 live young naturally. Thus, in vivo fertilisation is an effective technique to generate live offspring using slow-frozen oocytes in rabbits. |
format | Online Article Text |
id | pubmed-3866232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38662322013-12-19 Live Birth from Slow-Frozen Rabbit Oocytes after In Vivo Fertilisation Jiménez-Trigos, Estrella Vicente, José S. Marco-Jiménez, Francisco PLoS One Research Article In vivo fertilisation techniques such as intraoviductal oocyte transfer have been considered as alternatives to bypass the inadequacy of conventional in vitro fertilisation in rabbit. There is only one study in the literature, published in 1989, that reports live offspring from cryopreserved rabbit oocytes. The aim of the present study was to establish the in vivo fertilisation procedure to generate live offspring with frozen oocytes. First, the effect of two recipient models (i) ovariectomised or (ii) oviduct ligated immediately after transfer on the ability of fresh oocytes to fertilise were compared. Second, generation of live offspring from slow-frozen oocytes was carried out using the ligated oviduct recipient model. Throughout the experiment, recipients were artificially inseminated 9 hours prior to oocyte transfer. In the first experiment, two days after unilateral transfer of fresh oocytes, oviducts and uterine horns were flushed to assess embryo recovery rates. The embryo recovery rates were low compared to control in both ovariectomised and ligated oviduct groups. However, ligated oviduct recipient showed significantly (P<0.05) higher embryo recovery rates compared to ovariectomised and control-transferred. In the second experiment, using bilateral oviduct ligation model, all females that received slow-frozen oocytes became pregnant and delivered a total of 4 live young naturally. Thus, in vivo fertilisation is an effective technique to generate live offspring using slow-frozen oocytes in rabbits. Public Library of Science 2013-12-17 /pmc/articles/PMC3866232/ /pubmed/24358281 http://dx.doi.org/10.1371/journal.pone.0083399 Text en © 2013 Jiménez-Trigos et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Jiménez-Trigos, Estrella Vicente, José S. Marco-Jiménez, Francisco Live Birth from Slow-Frozen Rabbit Oocytes after In Vivo Fertilisation |
title | Live Birth from Slow-Frozen Rabbit Oocytes after In Vivo Fertilisation |
title_full | Live Birth from Slow-Frozen Rabbit Oocytes after In Vivo Fertilisation |
title_fullStr | Live Birth from Slow-Frozen Rabbit Oocytes after In Vivo Fertilisation |
title_full_unstemmed | Live Birth from Slow-Frozen Rabbit Oocytes after In Vivo Fertilisation |
title_short | Live Birth from Slow-Frozen Rabbit Oocytes after In Vivo Fertilisation |
title_sort | live birth from slow-frozen rabbit oocytes after in vivo fertilisation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866232/ https://www.ncbi.nlm.nih.gov/pubmed/24358281 http://dx.doi.org/10.1371/journal.pone.0083399 |
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