Effect of catalase, superoxide dismutase and reduced glutathione in LDL extender on ovine cryopreserved sperm viability
The aim of this study was to evaluate the motility, kinetics and membrane integrity of ovine sperm cryopreserved in extenders containing 8% LDL with enzymatic antioxidants at different concentrations. Four Santa Inês rams were used to form four pools of semen (each pool containing ejaculates f...
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Universidade Estadual de Londrina
2015-08-01
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doaj-d3f08da792de49f19f820cadb52d103f2020-11-25T01:30:17ZengUniversidade Estadual de LondrinaSemina: Ciências Agrárias1676-546X1679-03592015-08-013642593260210.5433/1679-0359.2015v36n4p2593Effect of catalase, superoxide dismutase and reduced glutathione in LDL extender on ovine cryopreserved sperm viabilityPaola Pereira das Neves Snoeck 0Luís Cláudio Oliveira Moura 1Carlos Augusto Alanis Clemente 2 Ana Maria Loaiza-Echeverri 3Mariana Machado Neves 4Ivan Bezerra Allaman 5Marc Henry 6Universidade Estadual de Santa CruzUniversidade Estadual de Santa CruzUniversidade Federal de Minas GeraisUniversidade Federal de Minas GeraisUniversidade Federal de ViçosaUniversidade Estadual de Santa CruzUniversidade Federal de Minas Gerais The aim of this study was to evaluate the motility, kinetics and membrane integrity of ovine sperm cryopreserved in extenders containing 8% LDL with enzymatic antioxidants at different concentrations. Four Santa Inês rams were used to form four pools of semen (each pool containing ejaculates from four ram, totaling four ejaculates per animal). Each seminal pool was divided into eight aliquots for the following treatments: 1) Tris-glucose-glycerol (TGG) + (16%) egg yolk (control 1); 2) TGG + 8% (w/v) LDL (control 2); 3) TGG + 8% LDL + catalase 100 U/mL; 4) TGG + 8% LDL + catalase 200 U/mL; 5) TGG + 8% LDL + superoxide dismutase 100 U/mL; 6) TGG + 8% LDL + superoxide dismutase 200 U/mL; 7) TGG + 8% LDL + reduced glutathione 5 mM; and 8) TGG + 8% LDL + reduced glutathione 10 mM. The samples were packed into 0.25 mL straws, cooled (-0.25 °C/ min), maintained at 5 °C for 2 h and then frozen (-25 °C/ min) using a TK4000®. Immediately after thawing (38 °C/ 30 s), sperm motility and movement characteristics were assessed by computer sperm analysis (CASA). The structural integrity of the plasma and acrosomal membranes was analyzed using fluorescent dyes. The functional integrity of membranes was assessed using a hypoosmotic swelling test. As assessed by ANOVA, significant differences (P<0.05) among treatments were only observed for VCL, VSL and VAP. For the VCL variable, the 2, 3, 4, 5, 6 and 7 extenders were similar and higher than 1 and 8 extenders, the latter being similar to each other. For the VSL variable, the 3, 4, 5, 6 and 7 extenders were similar and higher than 1, 2 and 8 extenders, the latter being similar to each other. For the VAP variable, the 3, 4 and 6 extenders were similar and higher than 1, 2, 5, 7 and 8 extenders, the latter being similar to each other. In conclusion, enzymatic antioxidants as catalase e superoxide dismutase improve the protective activity of extenders containing LDL on frozen ovine sperm. http://www.uel.br/revistas/uel/index.php/semagrarias/editor/submission/18174Cryopreservation; Semen; Enzymatic antioxidants; Santa Inês |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Paola Pereira das Neves Snoeck Luís Cláudio Oliveira Moura Carlos Augusto Alanis Clemente Ana Maria Loaiza-Echeverri Mariana Machado Neves Ivan Bezerra Allaman Marc Henry |
spellingShingle |
Paola Pereira das Neves Snoeck Luís Cláudio Oliveira Moura Carlos Augusto Alanis Clemente Ana Maria Loaiza-Echeverri Mariana Machado Neves Ivan Bezerra Allaman Marc Henry Effect of catalase, superoxide dismutase and reduced glutathione in LDL extender on ovine cryopreserved sperm viability Semina: Ciências Agrárias Cryopreservation; Semen; Enzymatic antioxidants; Santa Inês |
author_facet |
Paola Pereira das Neves Snoeck Luís Cláudio Oliveira Moura Carlos Augusto Alanis Clemente Ana Maria Loaiza-Echeverri Mariana Machado Neves Ivan Bezerra Allaman Marc Henry |
author_sort |
Paola Pereira das Neves Snoeck |
title |
Effect of catalase, superoxide dismutase and reduced glutathione in LDL extender on ovine cryopreserved sperm viability |
title_short |
Effect of catalase, superoxide dismutase and reduced glutathione in LDL extender on ovine cryopreserved sperm viability |
title_full |
Effect of catalase, superoxide dismutase and reduced glutathione in LDL extender on ovine cryopreserved sperm viability |
title_fullStr |
Effect of catalase, superoxide dismutase and reduced glutathione in LDL extender on ovine cryopreserved sperm viability |
title_full_unstemmed |
Effect of catalase, superoxide dismutase and reduced glutathione in LDL extender on ovine cryopreserved sperm viability |
title_sort |
effect of catalase, superoxide dismutase and reduced glutathione in ldl extender on ovine cryopreserved sperm viability |
publisher |
Universidade Estadual de Londrina |
series |
Semina: Ciências Agrárias |
issn |
1676-546X 1679-0359 |
publishDate |
2015-08-01 |
description |
The aim of this study was to evaluate the motility, kinetics and membrane integrity of ovine sperm cryopreserved in extenders containing 8% LDL with enzymatic antioxidants at different concentrations. Four Santa Inês rams were used to form four pools of semen (each pool containing ejaculates from four ram, totaling four ejaculates per animal). Each seminal pool was divided into eight aliquots for the following treatments: 1) Tris-glucose-glycerol (TGG) + (16%) egg yolk (control 1); 2) TGG + 8% (w/v) LDL (control 2); 3) TGG + 8% LDL + catalase 100 U/mL; 4) TGG + 8% LDL + catalase 200 U/mL; 5) TGG + 8% LDL + superoxide dismutase 100 U/mL; 6) TGG + 8% LDL + superoxide dismutase 200 U/mL; 7) TGG + 8% LDL + reduced glutathione 5 mM; and 8) TGG + 8% LDL + reduced glutathione 10 mM. The samples were packed into 0.25 mL straws, cooled (-0.25 °C/ min), maintained at 5 °C for 2 h and then frozen (-25 °C/ min) using a TK4000®. Immediately after thawing (38 °C/ 30 s), sperm motility and movement characteristics were assessed by computer sperm analysis (CASA). The structural integrity of the plasma and acrosomal membranes was analyzed using fluorescent dyes. The functional integrity of membranes was assessed using a hypoosmotic swelling test. As assessed by ANOVA, significant differences (P<0.05) among treatments were only observed for VCL, VSL and VAP. For the VCL variable, the 2, 3, 4, 5, 6 and 7 extenders were similar and higher than 1 and 8 extenders, the latter being similar to each other. For the VSL variable, the 3, 4, 5, 6 and 7 extenders were similar and higher than 1, 2 and 8 extenders, the latter being similar to each other. For the VAP variable, the 3, 4 and 6 extenders were similar and higher than 1, 2, 5, 7 and 8 extenders, the latter being similar to each other. In conclusion, enzymatic antioxidants as catalase e superoxide dismutase improve the protective activity of extenders containing LDL on frozen ovine sperm.
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topic |
Cryopreservation; Semen; Enzymatic antioxidants; Santa Inês |
url |
http://www.uel.br/revistas/uel/index.php/semagrarias/editor/submission/18174 |
work_keys_str_mv |
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