Damage assessment of the equine sperm membranes by fluorimetric technique

Detalhes bibliográficos
Autor(a) principal: Celeghini,Eneiva Carla Carvalho
Data de Publicação: 2010
Outros Autores: Andrade,André Furugen Cesar de, Raphael,Cláudia Fernandes, Nascimento,Juliana, Ticianelli,Janahi Souza, Arruda,Rubens Paes de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Archives of Biology and Technology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132010000600004
Resumo: To validate a practical technique of simultaneous evaluation of the plasma, acrosomal and mitochondrial membranes in equine spermatozoa three fluorescent probes (PI, FITC-PSA and MITO) were associated. Four ejaculates from three stallions (n=12) were diluted in TALP medium and split into 2 aliquots, 1 aliquot was flash frozen in liquid nitrogen to induce damage in cellular membranes. Three treatments were prepared with the following fixed ratios of fresh semen: flash frozen semen: 100:0 (T100), 50:50 (T50), and 0:100 (T0). A 150-µL aliquot of diluted semen of each treatment was added of 2 µL of PI, 2 µL of MITO and 80 µL of FITC-PSA; incubated at 38.5ºC/8 min, and sperm cells were evaluated by epifluorescent microscopy. Based in regression analysis, this could be an efficient and practical technique to assess damage in equine spermatozoa, as it was able to determine the sperm percentage more representative of the potential to fertilize the oocyte.
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spelling Damage assessment of the equine sperm membranes by fluorimetric techniqueStallionacrosomeplasma membranemitochondriafluorescent probesTo validate a practical technique of simultaneous evaluation of the plasma, acrosomal and mitochondrial membranes in equine spermatozoa three fluorescent probes (PI, FITC-PSA and MITO) were associated. Four ejaculates from three stallions (n=12) were diluted in TALP medium and split into 2 aliquots, 1 aliquot was flash frozen in liquid nitrogen to induce damage in cellular membranes. Three treatments were prepared with the following fixed ratios of fresh semen: flash frozen semen: 100:0 (T100), 50:50 (T50), and 0:100 (T0). A 150-µL aliquot of diluted semen of each treatment was added of 2 µL of PI, 2 µL of MITO and 80 µL of FITC-PSA; incubated at 38.5ºC/8 min, and sperm cells were evaluated by epifluorescent microscopy. Based in regression analysis, this could be an efficient and practical technique to assess damage in equine spermatozoa, as it was able to determine the sperm percentage more representative of the potential to fertilize the oocyte.Instituto de Tecnologia do Paraná - Tecpar2010-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132010000600004Brazilian Archives of Biology and Technology v.53 n.6 2010reponame:Brazilian Archives of Biology and Technologyinstname:Instituto de Tecnologia do Paraná (Tecpar)instacron:TECPAR10.1590/S1516-89132010000600004info:eu-repo/semantics/openAccessCeleghini,Eneiva Carla CarvalhoAndrade,André Furugen Cesar deRaphael,Cláudia FernandesNascimento,JulianaTicianelli,Janahi SouzaArruda,Rubens Paes deeng2011-01-18T00:00:00Zoai:scielo:S1516-89132010000600004Revistahttps://www.scielo.br/j/babt/https://old.scielo.br/oai/scielo-oai.phpbabt@tecpar.br||babt@tecpar.br1678-43241516-8913opendoar:2011-01-18T00:00Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)false
dc.title.none.fl_str_mv Damage assessment of the equine sperm membranes by fluorimetric technique
title Damage assessment of the equine sperm membranes by fluorimetric technique
spellingShingle Damage assessment of the equine sperm membranes by fluorimetric technique
Celeghini,Eneiva Carla Carvalho
Stallion
acrosome
plasma membrane
mitochondria
fluorescent probes
title_short Damage assessment of the equine sperm membranes by fluorimetric technique
title_full Damage assessment of the equine sperm membranes by fluorimetric technique
title_fullStr Damage assessment of the equine sperm membranes by fluorimetric technique
title_full_unstemmed Damage assessment of the equine sperm membranes by fluorimetric technique
title_sort Damage assessment of the equine sperm membranes by fluorimetric technique
author Celeghini,Eneiva Carla Carvalho
author_facet Celeghini,Eneiva Carla Carvalho
Andrade,André Furugen Cesar de
Raphael,Cláudia Fernandes
Nascimento,Juliana
Ticianelli,Janahi Souza
Arruda,Rubens Paes de
author_role author
author2 Andrade,André Furugen Cesar de
Raphael,Cláudia Fernandes
Nascimento,Juliana
Ticianelli,Janahi Souza
Arruda,Rubens Paes de
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Celeghini,Eneiva Carla Carvalho
Andrade,André Furugen Cesar de
Raphael,Cláudia Fernandes
Nascimento,Juliana
Ticianelli,Janahi Souza
Arruda,Rubens Paes de
dc.subject.por.fl_str_mv Stallion
acrosome
plasma membrane
mitochondria
fluorescent probes
topic Stallion
acrosome
plasma membrane
mitochondria
fluorescent probes
description To validate a practical technique of simultaneous evaluation of the plasma, acrosomal and mitochondrial membranes in equine spermatozoa three fluorescent probes (PI, FITC-PSA and MITO) were associated. Four ejaculates from three stallions (n=12) were diluted in TALP medium and split into 2 aliquots, 1 aliquot was flash frozen in liquid nitrogen to induce damage in cellular membranes. Three treatments were prepared with the following fixed ratios of fresh semen: flash frozen semen: 100:0 (T100), 50:50 (T50), and 0:100 (T0). A 150-µL aliquot of diluted semen of each treatment was added of 2 µL of PI, 2 µL of MITO and 80 µL of FITC-PSA; incubated at 38.5ºC/8 min, and sperm cells were evaluated by epifluorescent microscopy. Based in regression analysis, this could be an efficient and practical technique to assess damage in equine spermatozoa, as it was able to determine the sperm percentage more representative of the potential to fertilize the oocyte.
publishDate 2010
dc.date.none.fl_str_mv 2010-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132010000600004
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132010000600004
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1516-89132010000600004
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Instituto de Tecnologia do Paraná - Tecpar
publisher.none.fl_str_mv Instituto de Tecnologia do Paraná - Tecpar
dc.source.none.fl_str_mv Brazilian Archives of Biology and Technology v.53 n.6 2010
reponame:Brazilian Archives of Biology and Technology
instname:Instituto de Tecnologia do Paraná (Tecpar)
instacron:TECPAR
instname_str Instituto de Tecnologia do Paraná (Tecpar)
instacron_str TECPAR
institution TECPAR
reponame_str Brazilian Archives of Biology and Technology
collection Brazilian Archives of Biology and Technology
repository.name.fl_str_mv Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)
repository.mail.fl_str_mv babt@tecpar.br||babt@tecpar.br
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