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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Main Authors: 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
Format: Article
Language:English
Published: Universidade Estadual de Londrina 2015-08-01
Series:Semina: Ciências Agrárias
Subjects:
Online Access:http://www.uel.br/revistas/uel/index.php/semagrarias/editor/submission/18174
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spelling 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.
topic Cryopreservation; Semen; Enzymatic antioxidants; Santa Inês
url http://www.uel.br/revistas/uel/index.php/semagrarias/editor/submission/18174
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