The effects of cryoprotectants on chilled pirapitinga (Piaractus brachypomus) embryos at various ontogenetic stages
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Revista brasileira de higiene e sanidade animal |
Texto Completo: | http://www.higieneanimal.ufc.br/seer/index.php/higieneanimal/article/view/189 |
Resumo: | Cryopreservation has not been successfully used to preserve fish embryos, although chilling techniques have been used with good results. The aim of this study was to chill Piaractus brachypomus embryos at different stages of development in some cryoprotectants and for various periods of chilling. Embryos at the following ontogenetic stages were used: blastoderm – 1.2 hours post-fertilization (hpf); epiboly – 5 hpf; blastopore closure – 8 hpf; and appearance of optic vesicle – 13 hpf. One hundred embryos were selected from each of the four stages and chilled in methanol, methylglycol or dimethylsulfoxide (DMSO) for 6, 8, 10 or 12 hours, at 2ºC. The total number of treatments was 4 stages x 3 cryoprotectants x 4 periods of chilling. The highest percentage of normal and live larvae (30.6%) was observed when embryos were chilled at 13-hpf in methanol for 6 hours. In general, larvae chilled at a more developed stages (8 and 13 hpf), in methanol and for shorter periods could survive chilling and develop normally, compared to the other treatments. Therefore, P. brachypomus embryos at the optical vesicle appearance stage (13 hpf) should be chilled in a solution containing 17.5% glucose and 10% methanol for up to eight six at 2°C. |
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The effects of cryoprotectants on chilled pirapitinga (Piaractus brachypomus) embryos at various ontogenetic stagesaquaculture; South American fish; embryonic stage; Larval survivalCryopreservation has not been successfully used to preserve fish embryos, although chilling techniques have been used with good results. The aim of this study was to chill Piaractus brachypomus embryos at different stages of development in some cryoprotectants and for various periods of chilling. Embryos at the following ontogenetic stages were used: blastoderm – 1.2 hours post-fertilization (hpf); epiboly – 5 hpf; blastopore closure – 8 hpf; and appearance of optic vesicle – 13 hpf. One hundred embryos were selected from each of the four stages and chilled in methanol, methylglycol or dimethylsulfoxide (DMSO) for 6, 8, 10 or 12 hours, at 2ºC. The total number of treatments was 4 stages x 3 cryoprotectants x 4 periods of chilling. The highest percentage of normal and live larvae (30.6%) was observed when embryos were chilled at 13-hpf in methanol for 6 hours. In general, larvae chilled at a more developed stages (8 and 13 hpf), in methanol and for shorter periods could survive chilling and develop normally, compared to the other treatments. Therefore, P. brachypomus embryos at the optical vesicle appearance stage (13 hpf) should be chilled in a solution containing 17.5% glucose and 10% methanol for up to eight six at 2°C.Revista Brasileira de Higiene e Sanidade Animal2014-09-30info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://www.higieneanimal.ufc.br/seer/index.php/higieneanimal/article/view/18910.5935/rbhsa.v8i3.189Revista Brasileira de Higiene e Sanidade Animal; v. 8, n. 3 (2014); 27-46reponame:Revista brasileira de higiene e sanidade animalinstname:Universidade Federal do Ceará (UFC)instacron:UFCporhttp://www.higieneanimal.ufc.br/seer/index.php/higieneanimal/article/view/189/2008Pessoa, Nathalie Ommundsen; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, BrazilViveiros, Ana Tereza de Mendonça; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, BrazilBarbosa, Thales Cordeiro; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, BrazilSouza Filho, Francisco Gerson Mendes de; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, BrazilFilho, Aldeney Andrade Soares; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, BrazilSousa, Míriam Luiza Nogueira Martins de; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, BrazilLourenço, Athur Vinícius; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, BrazilSampaio, Célia Maria Souza; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazilinfo:eu-repo/semantics/openAccess2015-09-26T00:42:31Zoai:ojs.www.higieneanimal.ufc.br:article/189Revistahttp://www.higieneanimal.ufc.br/PUBhttp://www.higieneanimal.ufc.br/seer/index.php/higieneanimal/oaiwesleylyeverton@yahoo.com.br||ronaldo.sales@ufc.br1981-29651981-2965opendoar:2015-09-26T00:42:31Revista brasileira de higiene e sanidade animal - Universidade Federal do Ceará (UFC)false |
dc.title.none.fl_str_mv |
The effects of cryoprotectants on chilled pirapitinga (Piaractus brachypomus) embryos at various ontogenetic stages |
title |
The effects of cryoprotectants on chilled pirapitinga (Piaractus brachypomus) embryos at various ontogenetic stages |
spellingShingle |
The effects of cryoprotectants on chilled pirapitinga (Piaractus brachypomus) embryos at various ontogenetic stages Pessoa, Nathalie Ommundsen; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil aquaculture; South American fish; embryonic stage; Larval survival |
title_short |
The effects of cryoprotectants on chilled pirapitinga (Piaractus brachypomus) embryos at various ontogenetic stages |
title_full |
The effects of cryoprotectants on chilled pirapitinga (Piaractus brachypomus) embryos at various ontogenetic stages |
title_fullStr |
The effects of cryoprotectants on chilled pirapitinga (Piaractus brachypomus) embryos at various ontogenetic stages |
title_full_unstemmed |
The effects of cryoprotectants on chilled pirapitinga (Piaractus brachypomus) embryos at various ontogenetic stages |
title_sort |
The effects of cryoprotectants on chilled pirapitinga (Piaractus brachypomus) embryos at various ontogenetic stages |
author |
Pessoa, Nathalie Ommundsen; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil |
author_facet |
Pessoa, Nathalie Ommundsen; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Viveiros, Ana Tereza de Mendonça; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Barbosa, Thales Cordeiro; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Souza Filho, Francisco Gerson Mendes de; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Filho, Aldeney Andrade Soares; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Sousa, Míriam Luiza Nogueira Martins de; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Lourenço, Athur Vinícius; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Sampaio, Célia Maria Souza; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil |
author_role |
author |
author2 |
Viveiros, Ana Tereza de Mendonça; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Barbosa, Thales Cordeiro; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Souza Filho, Francisco Gerson Mendes de; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Filho, Aldeney Andrade Soares; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Sousa, Míriam Luiza Nogueira Martins de; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Lourenço, Athur Vinícius; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Sampaio, Célia Maria Souza; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Pessoa, Nathalie Ommundsen; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Viveiros, Ana Tereza de Mendonça; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Barbosa, Thales Cordeiro; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Souza Filho, Francisco Gerson Mendes de; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Filho, Aldeney Andrade Soares; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Sousa, Míriam Luiza Nogueira Martins de; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Lourenço, Athur Vinícius; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil Sampaio, Célia Maria Souza; Dept of Biology, State University of Ceará, UECE, Fortaleza, CE, 60740-000, Brazil |
dc.subject.por.fl_str_mv |
aquaculture; South American fish; embryonic stage; Larval survival |
topic |
aquaculture; South American fish; embryonic stage; Larval survival |
description |
Cryopreservation has not been successfully used to preserve fish embryos, although chilling techniques have been used with good results. The aim of this study was to chill Piaractus brachypomus embryos at different stages of development in some cryoprotectants and for various periods of chilling. Embryos at the following ontogenetic stages were used: blastoderm – 1.2 hours post-fertilization (hpf); epiboly – 5 hpf; blastopore closure – 8 hpf; and appearance of optic vesicle – 13 hpf. One hundred embryos were selected from each of the four stages and chilled in methanol, methylglycol or dimethylsulfoxide (DMSO) for 6, 8, 10 or 12 hours, at 2ºC. The total number of treatments was 4 stages x 3 cryoprotectants x 4 periods of chilling. The highest percentage of normal and live larvae (30.6%) was observed when embryos were chilled at 13-hpf in methanol for 6 hours. In general, larvae chilled at a more developed stages (8 and 13 hpf), in methanol and for shorter periods could survive chilling and develop normally, compared to the other treatments. Therefore, P. brachypomus embryos at the optical vesicle appearance stage (13 hpf) should be chilled in a solution containing 17.5% glucose and 10% methanol for up to eight six at 2°C. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-09-30 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://www.higieneanimal.ufc.br/seer/index.php/higieneanimal/article/view/189 10.5935/rbhsa.v8i3.189 |
url |
http://www.higieneanimal.ufc.br/seer/index.php/higieneanimal/article/view/189 |
identifier_str_mv |
10.5935/rbhsa.v8i3.189 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
http://www.higieneanimal.ufc.br/seer/index.php/higieneanimal/article/view/189/2008 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
dc.publisher.none.fl_str_mv |
Revista Brasileira de Higiene e Sanidade Animal |
publisher.none.fl_str_mv |
Revista Brasileira de Higiene e Sanidade Animal |
dc.source.none.fl_str_mv |
Revista Brasileira de Higiene e Sanidade Animal; v. 8, n. 3 (2014); 27-46 reponame:Revista brasileira de higiene e sanidade animal instname:Universidade Federal do Ceará (UFC) instacron:UFC |
instname_str |
Universidade Federal do Ceará (UFC) |
instacron_str |
UFC |
institution |
UFC |
reponame_str |
Revista brasileira de higiene e sanidade animal |
collection |
Revista brasileira de higiene e sanidade animal |
repository.name.fl_str_mv |
Revista brasileira de higiene e sanidade animal - Universidade Federal do Ceará (UFC) |
repository.mail.fl_str_mv |
wesleylyeverton@yahoo.com.br||ronaldo.sales@ufc.br |
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1799695340568313856 |