Publicación:
Efecto del plasma seminal sobre el estado redox del semen equino criopreservado

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dc.contributor.authorPizarro L, Edisonspa
dc.contributor.authorRestrepo B, Giovannispa
dc.contributor.authorEcheverry Z, Joséspa
dc.contributor.authorRojano, Benjamínspa
dc.date.accessioned2013-10-05 00:00:00
dc.date.accessioned2022-07-01T14:35:56Z
dc.date.available2013-10-05 00:00:00
dc.date.available2022-07-01T14:35:56Z
dc.date.issued2013-10-05
dc.format.mimetypeapplication/pdfspa
dc.identifier.doi10.21897/rmvz.134
dc.identifier.eissn1909-0544
dc.identifier.issn0122-0268
dc.identifier.urihttps://repositorio.unicordoba.edu.co/handle/ucordoba/5353
dc.identifier.urlhttps://doi.org/10.21897/rmvz.134
dc.language.isospaspa
dc.publisherUniversidad de Córdobaspa
dc.relation.bitstreamhttps://revistamvz.unicordoba.edu.co/article/download/134/203
dc.relation.citationeditionNúm. supl , Año 2013 : Revista MVZ Córdoba Volumen 18(Supl.) Octubre 2013spa
dc.relation.citationendpage3680
dc.relation.citationissuesuplspa
dc.relation.citationstartpage3672
dc.relation.citationvolume18spa
dc.relation.ispartofjournalRevista MVZ Córdobaspa
dc.relation.referencesBall, B. Oxidative stress, osmotic stress and apoptosis: Impacts on sperm function and preservation in the horse. Anim Reprod Sci 2008; 107:257-267. http://dx.doi.org/10.1016/j.anireprosci.2008.04.014spa
dc.relation.referencesSquires E, Keith S, Graham J. Evaluation of alternative cryoprotectants for preserving stallion spermatozoa. Theriogenology 2004; 62:1056–1065. http://dx.doi.org/10.1016/j.theriogenology.2003.12.024spa
dc.relation.referencesMantovani R, Rota A, Falomo M, Bailoni L, Vincenti L. Comparison between glycerol and ethylene glycol for the cryopreservation of equine spermatozoa: semen quality assessment with standard analyses and with the hypoosmotic swelling test. Reprod Nutr Dev 2002; 42:217-226. http://dx.doi.org/10.1051/rnd:2002020spa
dc.relation.referencesPesch S, Bostedt H, Failing K, Bergmann M. Advanced fertility diagnosis in stallion semen using transmission electron microscopy. Anim Reprod Sci 2006; 91:285-298. http://dx.doi.org/10.1016/j.anireprosci.2005.04.004spa
dc.relation.referencesPommer A, Rutllant J, Meyers S. The role of osmotic resistance on equine spermatozoal function. Theriogenology 2002; 58(7):1373- 1384. http://dx.doi.org/10.1016/S0093-691X(02)01039-7spa
dc.relation.referencesDevireddy R, Swanlund D, Olin T, Vincente W, Troedsson M, Bischof J et al. Cryopreservation of equine sperm: optimal cooling rates in the presence and absence of cryoprotective agents determined using differential scanning calorimetry. Biol Reprod 2002; 66:222-231. http://dx.doi.org/10.1095/biolreprod66.1.222spa
dc.relation.referencesBurnaugh L, Sabeur K, Ball B. Generation of superoxide anion by equine spermatozoa as detected by dihydroethidium. Theriogenology 2007; 67:580-589. http://dx.doi.org/10.1016/j.theriogenology.2006.07.021spa
dc.relation.referencesKankofer M, Kolm G, Aurich J, Aurich C. Activity of glutathione peroxidase, superoxide dismutase and catalase and lipid peroxidation intensity in stallion semen during storage at 5°C. Theriogenology 2005; 63:1354-1365. http://dx.doi.org/10.1016/j.theriogenology.2004.07.005spa
dc.relation.referencesNeild D, Gadella B, Colendrander B, Agüero A, Brouwers J. lipid peroxidation in stallion spermatozoa. Theriogenology 2002; 58:295-298. http://dx.doi.org/10.1016/S0093-691X(02)00799-9spa
dc.relation.referencesIsachenko E, Isachenko V, Katkov I, Rahimi G, Schoèndorf E, Allmann P et al. DNA integrity and motility of human spermatozoa after standard slow freezing versus cryoprotectant-free vitrification. Hum Reprod 2004; 19(44):932-939. http://dx.doi.org/10.1093/humrep/deh194spa
dc.relation.referencesIsachenko V, Isachenko E, Katkov I, Montag M, Dessole S, Nawroth F. Cryoprotectant-free cryopreservation of human spermatozoa by vitrification and freezing in vapor: effect on motility, DNA integrity, and fertilization ability. Biol Reprod 2004; 71:1167-1173. http://dx.doi.org/10.1095/biolreprod.104.028811spa
dc.relation.referencesCocchia N, Pasolinia M, Mancini R, Petrazzuolo O, Cristofaro I, Rosapane I et al. Effect of sod (superoxide dismutase) protein supplementation in semen extenders on motility, viability, acrosome status and ERK (extracellular signal-regulated kinase) protein phosphorylation of chilled stallion spermatozoa. Theriogenology 2011; 75: 1201–1210. http://dx.doi.org/10.1016/j.theriogenology.2010.11.031spa
dc.relation.referencesBaumber J, Ball B, Linfor J. Assessment of the cryopreservation of equine spermatozoa in the presence of enzyme scavengers and antioxidants. Am J Vet Res 2005; 66(5):772–779. http://dx.doi.org/10.2460/ajvr.2005.66.772spa
dc.relation.referencesBaumber J, Ball B. Determination of glutathione peroxidase and superoxide dismutase-like activities in equine spermatozoa, seminal plasma, and reproductive tissues. Am J Vet Res 2005; 66:1415-1419. http://dx.doi.org/10.2460/ajvr.2005.66.1415spa
dc.relation.referencesBall B, Gravance C, Medina V, Baumber J. Liu I. Catalase activity in equine semen. Am J Vet Res 2000; 61(9):1026–1030. http://dx.doi.org/10.2460/ajvr.2000.61.1026spa
dc.relation.referencesBaumber J, Ball B, Gravance C, Medina V, Davies-Morel M. The effect of reactive oxygen species on equine sperm motility, viability, acrosomal integrity, mitochondrial membrane potential and membrane lipid peroxidation. J Androl 2000; 21(6):895-902.spa
dc.relation.referencesBrito L, Greene L, Kelleman A, Knobbe M, Turner R. Effect of method and clinician on stallion sperm morphology evaluation. Theriogenology 2011; 76:745–750. http://dx.doi.org/10.1016/j.theriogenology.2011.04.007spa
dc.relation.referencesGraham J, Mocé E. Fertility evaluation of frozen/thawed semen. Theriogenology 2005; 64:492-504. http://dx.doi.org/10.1016/j.theriogenology.2005.05.006spa
dc.relation.referencesNeild D, Chaves G, Flores M, Mora N, Beconi M, Agüero A. Hypoosmotic test in equine spermatozoa. Theriogenology 1999; 51:721-727. http://dx.doi.org/10.1016/S0093-691X(99)00021-7spa
dc.relation.referencesHenry M, Snoeck P, Cottorello A. Postthaw spermatozoa plasma integrity and motility of stallion semen frozen with different cryoprotectants. Theriogenology 2002; 58:245:248.spa
dc.relation.referencesPerez-Osorio J, Mello F, Juliani G, Lagares M, Lago L, Henry, M. Effect on post-thaw viability of equine sperm using stepwise addition of dimethyl formamide and varying cooling and freezing procedures. Anim Reprod 2008; 5(3/4):103-109.spa
dc.relation.referencesBustamante I, Pederzolli C, Sgaravatti A, Gregory R, Dutra C, Jobim M etal. Skim milkegg yolk based semen extender compensates for non-enzymatic antioxidant activity loss during equine semen cryopreservation. Anim Reprod 2009; 6(2):392-399.spa
dc.relation.referencesMedeiros A, Gomes G, Carmo M, Papa F, Alvarenga M. Cryopreservation of stallion sperm using different amides. Theriogenology 2002; 58:273-276. http://dx.doi.org/10.1016/S0093-691X(02)00898-1spa
dc.relation.referencesGuthrie H, Welch G. Determination of intracellular reactive oxygen species and high mitochondrial membrane potential in Percolltreated viable boar sperm using fluorescenceactivated flow cytometry. J Anim Sci 2006; 84:2089-2100. http://dx.doi.org/10.2527/jas.2005-766spa
dc.relation.referencesMorte M, Rodríguez A, Soares D, Rodrigues A, Gamboa S, Ramalho-Santos J. The quantification of lipid and protein oxidation in stallion spermatozoa and seminal plasma: Seasonal distinctions and correlations with DNA strand breaks, classical seminal parameters and stallion fertility. Anim Reprod Sci 2008; 106(1-2):36-47.spa
dc.relation.referencesSalazar J, Teague S, Love C, Brinsko S, Blanchard T, Varner D. Effect of crypreservation protocol on postthaw characteristics of stallion sperm. Theriogenology 2011; 76:409-418. http://dx.doi.org/10.1016/j.theriogenology.2011.02.016spa
dc.relation.referencesMoore A, Squires E, Graham J. Effect of seminal plasma on the cryopreservation of equine. Theriogenologyy 2005; 63:2372-2381. http://dx.doi.org/10.1016/j.theriogenology.2004.05.032spa
dc.relation.referencesLozano Benito D, Gil Huerta L, Álvarez San Martín C. Efecto de la adición de plasma seminal en el semen equino descongelado. Sanid mil 2011; 67(3):284-290. http://dx.doi.org/10.4321/S1887-85712011000400005spa
dc.relation.referencesKatila T, Anderson M, Reilas T, Koskinen E. Post-thaw motility and viability of fractionated and frozen stallion ejaculates. Theriogenology 2002; 58:241-244. http://dx.doi.org/10.1016/S0093-691X(02)00783-5spa
dc.relation.referencesAlghamdi A, Foster D, Troedsson M. Equine seminal plasma reduces sperm binding to polymorphonuclear neutrophils (PMNs) and improves the fertility of fresh semen inseminated into inflamed uteri. Reproduc 2004; 127(5):593-600. http://dx.doi.org/10.1530/rep.1.00096spa
dc.relation.referencesNovak S , Smith T, Paradis F, Burwash L, Dyck M, Foxcroft G. Biomarkers of in vivo fertility in sperm and seminal plasma of fertile stallions. Theriogenology 2010; 74:956–967. http://dx.doi.org/10.1016/j.theriogenology.2010.04.025spa
dc.relation.referencesPessanha M, Straggiotti J, Fagundes B, Costa J, De Souza G, Shimoya A. Efeito de proteínas do plasma seminal eqüino com massa superior a 10 kDa concentradas 10 vezes sobre a congelabilidade do sêmen. R Bras Zootec 2008; 37(12):2115-2119. http://dx.doi.org/10.1590/S1516-35982008001200006spa
dc.relation.referencesVasconcelos A, Santana M, Santos A, Santero M, Lagares M. Metabolic evaluation of cooled equine spermatozoa. Androl 2010; 42:106–111. http://dx.doi.org/10.1111/j.1439-0272.2009.00963.xspa
dc.relation.referencesWeir C, Robaire B. Spermatozoa have decreased antioxidant enzymatic capacity and increased reactive oxygen species production during aging in the Brown Norway rat. J Androl 2007; 28:229-240. http://dx.doi.org/10.2164/jandrol.106.001362spa
dc.relation.referencesBrum A, Sabeur K, Ball B. Apoptotic-like changes in equine spermatozoa separated by density-gradient centrifugation or after cryopreservation. Theriogenology 2008; 69:1041-1055. http://dx.doi.org/10.1016/j.theriogenology.2008.01.014spa
dc.relation.referencesAitken RJ, Paterson M, Fisher H, Buckingham DW, Van Duin M. Redox regulation of tyrosine phosphorylation in human spermatozoa and its role in the control of human sperm function. J Cell Sci 1995; 108:2017–2025.spa
dc.relation.referencesVilla N, Casta-o D, Duque P, Ceballos A. Actividad de la glutatión peroxidasa y la superóxido dismutasa en sangre y plasma seminal en caballos colombianos. Rev Colomb Cienc Pecu 2012; 25:64-70.spa
dc.relation.referencesKoskinen E, Karlsson M, Reilas T, Sankari S, Esala A, Katila T. Catalase activity and total protein in fractionated stallion seminal plasma. Theriogenology 2002; 58:337-340. http://dx.doi.org/10.1016/S0093-691X(02)00767-7spa
dc.relation.referencesBaumber J, Ball B, Linfor J, Meyers S. Reactive oxygen species and cryopreservation promote DNA fragmentation in equine Spermatozoa. J Androl 2003; 24(4):621-628. http://dx.doi.org/10.1002/j.1939-4640.2003.tb02714.xspa
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessspa
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dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/spa
dc.sourcehttps://revistamvz.unicordoba.edu.co/article/view/134spa
dc.subjectAntioxidantsspa
dc.subjectcryopreservationspa
dc.subjectreactive oxygen speciesspa
dc.titleEfecto del plasma seminal sobre el estado redox del semen equino criopreservadospa
dc.title.translatedEfecto del plasma seminal sobre el estado redox del semen equino criopreservadoeng
dc.typeArtículo de revistaspa
dc.typeJournal articleeng
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dc.type.coarhttp://purl.org/coar/resource_type/c_6501spa
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