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 | Acesso ao texto completo restrito à biblioteca da Embrapa Semiárido. Para informações adicionais entre em contato com cpatsa.biblioteca@embrapa.br. |
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Registro Completo |
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Biblioteca(s): |
Embrapa Semiárido. |
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Data corrente: |
06/03/2015 |
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Data da última atualização: |
06/03/2015 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
MAIA, M. da S.; SICHERLE, C. C.; RODELLO, L.; GALLEGO, I. C. S. |
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Afiliação: |
MARCIANE DA SILVA MAIA, CPATSA; CARMEN CECILIA SICHERLE, São Paulo State University, Faculty of Veterinary Medicine and Animal Science; LEANDRO RODELLO, São Paulo State University, Faculty of Veterinary Medicine and Animal Science; ISABEL CRISTINA SALTAREN GALLEGO, São Paulo State University, Faculty of Veterinary Medicine and Animal Science. |
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Título: |
Lipid peroxidation and generation of hydrogen peroxide in frozen-thawed ram semen cryopreserved in extenders with antioxidants. |
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Ano de publicação: |
2010 |
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Fonte/Imprenta: |
Animal Reproduction Science, v. 122, p. 118-123, 2010. |
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DOI: |
10.1016/j.anireprosci.2010.08.004 |
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Idioma: |
Inglês |
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Conteúdo: |
The objective of this study was to evaluate the effect of addition of the antioxidants Trolox and catalase to a ram semen cryopreservation extender on lipid peroxidation and hydrogen peroxide generation on the extender and in the thawed semen. Semen was collected from 23 Santa Inês rams (one ejaculate per ram) and diluted at 32 ?C to a concentration of 400×106 cells/ml in one of the following solution: Tris-egg yolk extender (control), or the same extender supplemented with either 50M Trolox/108 sperm (Trolox), 50g catalase/ml (Catalase) or a combination of Trolox and catalase (Tro + cat, 50M Trolox/108 sperm and 50g catalase/ml). The semen was loaded into 0.25 ml straws, cooled and frozen in a programmable freezer and subsequently stored in liquid nitrogen. Prior to evaluation, frozen straws were thawed in a water bath (42? C for 20 s). Lipid peroxidation (LPO), both spontaneous and catalyzed, on the semen and the extender were measured using the thiobarbituric acid (TBA) assay in accordance with the method described by Buege and Aust (1978). Hydrogen peroxide (H2O2) generation was measured using the horseradish peroxidase-dependent oxidation of phenol red to a derivative with absorbance at 610 nm, according to the method described by Pick and Keisari (1980). Spontaneous LPO resulted in the least production of thiobarbituric acid-reactive substances (TBARS) in the Tro + cat (1.37±0.02 nMol/108 sperm), compared to amounts in the other treatments groups. In the catalyzed LPO experiments, the least (P < 0.05) amounts of TBARS were observed in Trolox (2.52±0.02 nMol/108 sperm) and Tro + cat (2.54±0.02 nMol/108 sperm) groups, compared to the control (3.81±0.02 nMol/108 sperm) and catalase (3.83±0.02 nMol/108 sperm) groups. Hydrogen peroxide generation was less (P < 0.05) in the Trolox (6.00±0.18 nMol/40×106 sperm/±40 min) and Tro + cat (6.08±0.18 nMol/40×106 sperm/±40 min) groups than in the control (6.97±0.18 nMol/40×106 sperm/±40 min) and catalase (6.53±0.18 nMol/40×106 sperm/±40 min) groups. Compared to the control group, Trolox and catalase treatment significantly reduced TBARS in catalyzed LPO and hydrogen peroxide concentrations in the samples (P < 0.05). ROS (reactive oxygen species) generation occurred in all extenders MenosThe objective of this study was to evaluate the effect of addition of the antioxidants Trolox and catalase to a ram semen cryopreservation extender on lipid peroxidation and hydrogen peroxide generation on the extender and in the thawed semen. Semen was collected from 23 Santa Inês rams (one ejaculate per ram) and diluted at 32 ?C to a concentration of 400×106 cells/ml in one of the following solution: Tris-egg yolk extender (control), or the same extender supplemented with either 50M Trolox/108 sperm (Trolox), 50g catalase/ml (Catalase) or a combination of Trolox and catalase (Tro + cat, 50M Trolox/108 sperm and 50g catalase/ml). The semen was loaded into 0.25 ml straws, cooled and frozen in a programmable freezer and subsequently stored in liquid nitrogen. Prior to evaluation, frozen straws were thawed in a water bath (42? C for 20 s). Lipid peroxidation (LPO), both spontaneous and catalyzed, on the semen and the extender were measured using the thiobarbituric acid (TBA) assay in accordance with the method described by Buege and Aust (1978). Hydrogen peroxide (H2O2) generation was measured using the horseradish peroxidase-dependent oxidation of phenol red to a derivative with absorbance at 610 nm, according to the method described by Pick and Keisari (1980). Spontaneous LPO resulted in the least production of thiobarbituric acid-reactive substances (TBARS) in the Tro + cat (1.37±0.02 nMol/108 sperm), compared to amounts in the other treatments groups. In the catalyzed LPO ... Mostrar Tudo |
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Palavras-Chave: |
Peroxidação lipídica; Peróxido de hidrogênio; Sêmen ovino congelado; Sêmen ovino descongelado. |
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Thesagro: |
Ovino; Produção animal. |
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Thesaurus Nal: |
Animal production. |
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Categoria do assunto: |
L Ciência Animal e Produtos de Origem Animal |
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Marc: |
LEADER 03117naa a2200253 a 4500
001 2010763
005 2015-03-06
008 2010 bl uuuu u00u1 u #d
024 7 $a10.1016/j.anireprosci.2010.08.004$2DOI
100 1 $aMAIA, M. da S.
245 $aLipid peroxidation and generation of hydrogen peroxide in frozen-thawed ram semen cryopreserved in extenders with antioxidants.$h[electronic resource]
260 $c2010
520 $aThe objective of this study was to evaluate the effect of addition of the antioxidants Trolox and catalase to a ram semen cryopreservation extender on lipid peroxidation and hydrogen peroxide generation on the extender and in the thawed semen. Semen was collected from 23 Santa Inês rams (one ejaculate per ram) and diluted at 32 ?C to a concentration of 400×106 cells/ml in one of the following solution: Tris-egg yolk extender (control), or the same extender supplemented with either 50M Trolox/108 sperm (Trolox), 50g catalase/ml (Catalase) or a combination of Trolox and catalase (Tro + cat, 50M Trolox/108 sperm and 50g catalase/ml). The semen was loaded into 0.25 ml straws, cooled and frozen in a programmable freezer and subsequently stored in liquid nitrogen. Prior to evaluation, frozen straws were thawed in a water bath (42? C for 20 s). Lipid peroxidation (LPO), both spontaneous and catalyzed, on the semen and the extender were measured using the thiobarbituric acid (TBA) assay in accordance with the method described by Buege and Aust (1978). Hydrogen peroxide (H2O2) generation was measured using the horseradish peroxidase-dependent oxidation of phenol red to a derivative with absorbance at 610 nm, according to the method described by Pick and Keisari (1980). Spontaneous LPO resulted in the least production of thiobarbituric acid-reactive substances (TBARS) in the Tro + cat (1.37±0.02 nMol/108 sperm), compared to amounts in the other treatments groups. In the catalyzed LPO experiments, the least (P < 0.05) amounts of TBARS were observed in Trolox (2.52±0.02 nMol/108 sperm) and Tro + cat (2.54±0.02 nMol/108 sperm) groups, compared to the control (3.81±0.02 nMol/108 sperm) and catalase (3.83±0.02 nMol/108 sperm) groups. Hydrogen peroxide generation was less (P < 0.05) in the Trolox (6.00±0.18 nMol/40×106 sperm/±40 min) and Tro + cat (6.08±0.18 nMol/40×106 sperm/±40 min) groups than in the control (6.97±0.18 nMol/40×106 sperm/±40 min) and catalase (6.53±0.18 nMol/40×106 sperm/±40 min) groups. Compared to the control group, Trolox and catalase treatment significantly reduced TBARS in catalyzed LPO and hydrogen peroxide concentrations in the samples (P < 0.05). ROS (reactive oxygen species) generation occurred in all extenders
650 $aAnimal production
650 $aOvino
650 $aProdução animal
653 $aPeroxidação lipídica
653 $aPeróxido de hidrogênio
653 $aSêmen ovino congelado
653 $aSêmen ovino descongelado
700 1 $aSICHERLE, C. C.
700 1 $aRODELLO, L.
700 1 $aGALLEGO, I. C. S.
773 $tAnimal Reproduction Science$gv. 122, p. 118-123, 2010.
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