Efectos de la concentración de glucosa sobre la activación de la movilidad espermática en bocachico Prochilodus magdalenae (Pisces, Characiformes)

Autores:: Martínez, Gregorio
Atencio G, Víctor
Pardo C, Sandra

Tipo de recurso:: Article of journal

Fecha de publicación:: 2011

Institución:: Universidad de Córdoba

Repositorio:: Repositorio Institucional Unicórdoba

Idioma:: spa

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dc.title.spa.fl_str_mv	Efectos de la concentración de glucosa sobre la activación de la movilidad espermática en bocachico Prochilodus magdalenae (Pisces, Characiformes)
dc.title.translated.eng.fl_str_mv	Effect of glucose concentration on sperm motility activation in bocachico Prochilodus magdalenae (Pisces, Characiformes)
title	Efectos de la concentración de glucosa sobre la activación de la movilidad espermática en bocachico Prochilodus magdalenae (Pisces, Characiformes)
spellingShingle	Efectos de la concentración de glucosa sobre la activación de la movilidad espermática en bocachico Prochilodus magdalenae (Pisces, Characiformes) Concentration fishes glucose glucose tolerance sperm motility semen preservation Concentración conservación del semen glucosa motilidad espermática peces tolerancia a la glucosa.
title_short	Efectos de la concentración de glucosa sobre la activación de la movilidad espermática en bocachico Prochilodus magdalenae (Pisces, Characiformes)
title_full	Efectos de la concentración de glucosa sobre la activación de la movilidad espermática en bocachico Prochilodus magdalenae (Pisces, Characiformes)
title_fullStr	Efectos de la concentración de glucosa sobre la activación de la movilidad espermática en bocachico Prochilodus magdalenae (Pisces, Characiformes)
title_full_unstemmed	Efectos de la concentración de glucosa sobre la activación de la movilidad espermática en bocachico Prochilodus magdalenae (Pisces, Characiformes)
title_sort	Efectos de la concentración de glucosa sobre la activación de la movilidad espermática en bocachico Prochilodus magdalenae (Pisces, Characiformes)
dc.creator.fl_str_mv	Martínez, Gregorio Atencio G, Víctor Pardo C, Sandra
dc.contributor.author.spa.fl_str_mv	Martínez, Gregorio Atencio G, Víctor Pardo C, Sandra
dc.subject.eng.fl_str_mv	Concentration fishes glucose glucose tolerance sperm motility semen preservation
topic	Concentration fishes glucose glucose tolerance sperm motility semen preservation Concentración conservación del semen glucosa motilidad espermática peces tolerancia a la glucosa.
dc.subject.spa.fl_str_mv	Concentración conservación del semen glucosa motilidad espermática peces tolerancia a la glucosa.
publishDate	2011
dc.date.accessioned.none.fl_str_mv	2011-05-10 00:00:00 2022-07-01T21:00:22Z
dc.date.available.none.fl_str_mv	2011-05-10 00:00:00 2022-07-01T21:00:22Z
dc.date.issued.none.fl_str_mv	2011-05-10
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dc.type.eng.fl_str_mv	Journal article
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dc.relation.references.spa.fl_str_mv	Mojica I. Lista preliminar de las especies de peces dulceacuícolas de Colombia. Rev Acad Col Cienc Exac Fís y Nat 1999; 23:547-566. INPA: Instituto Nacional de Pesca y Acuicultura. Boletín estadístico pesquero colombiano de 1995 (ed. by INPA). Publicaciones INPA-MADR, Santa fe de Bogotá. 1995. Horváth A, Miskolczi E, Urbány B. Cryopreservation of common carp sperm. Aquat Living Resour 2003; 16(5):457-460. https://doi.org/10.1016/S0990-7440(03)00084-6 Yang H, Hazlewood L, Walter RB, Tiersch TR. Effect of osmotic inmobilization on refrigerated storage and cryopreservation of sperm from a viviparous fish, the green swordtail Xiphosphorus helleri. Cryobiology 2006; 52(2):209-218. https://doi.org/10.1016/j.cryobiol.2005.11.002 Bolsover RS, Hyams JS, Shephard EA, White HA, Wiedemann CG. Cell Biology. 2a ed. USA: John Wiley & Sons, Inc. 2004. Krasznai Z, Marian T, Izumi H, Damjanovich S, Balkay L, Tron L, Morisawa M. Membrane hyperpolarization removes inactivation of Ca2+ channels, leading to Ca2+ influx and subsequent initialization of sperm motility in the common carp. Proc Natl Acad Sci USA 2000; 97:2052-2057. https://doi.org/10.1073/pnas.040558097 Viveiros ATM, Lock EJ, Woelders H, Komen J. Influence of cooling rates and plunging temperatures in an interrupted slow-freezing procedure for semen of the African catfish, Clarias gariepinus. Cryobiology 2001; 43:276-287. https://doi.org/10.1006/cryo.2001.2362 Pegg D. Principles of cryopreservation. En: Day JG, Stacy GN, editors. Cryopreservation and Freeze-Drying Protocols. Totowa NJ: Human Press Inc; 2007. https://doi.org/10.1007/978-1-59745-362-2_3 Jiang Z, Li Q, Li W, Hu J, Zhao H, Zhang S. Effect of low density lipoprotein on DNA integrity of freezing–thawing boar sperm by neutral comet assay. Anim Reprod Sci 2007; 99:401-407. https://doi.org/10.1016/j.anireprosci.2006.08.022 Tabares CJ, Tarazona A, Olivera A. Fisiología de la activación del espermatozoide en peces de agua dulce. Rev Col Cienc Pec 2005; 18: 149-161. Linhart O, Cosson J, Mims SD, Shelton WI, Rodina M. Effects of ions on the motility of fresh and demembranated paddlefish (Polyodon spathula) spermatozoa. Reproduction 2002; 124:713-719. https://doi.org/10.1530/rep.0.1240713 Alavi SMH, Cosson J. Sperm motility in fishes: (II) Effects of ions and osmotic pressure. Cell Biol Int 2006; 30:1–14. https://doi.org/10.1016/j.cellbi.2005.06.004 Ciereszko A, Glogowski J, Dabrowski K. Biochemical characteristics of seminal plasma and spermatozoa of freshwater fishes. En: Tiersch TR and Mazik PM, editores. Cryopreservation in Aquaculture Species. Baton Roue, Louisiana: World Aquaculture Society; 2000. Inaba K. Molecular architecture of sperm flagella: molecules for motility and signaling. Zool Sci 2003; 20:1043-1056. https://doi.org/10.2108/zsj.20.1043 Ingermann RL. Energy metabolism and respiration in fish spermatozoa. En: Alavi SMH, Cosson JJ, Coward K y Raffie C, editors. Fish spermatology. Oxford, UK: Alpha Science International Ltda.; 2008. Shimoda E, de Andrade DR, Vásquez- Vidal M, Shigueky-Yasui G, Straggiotti- Sliva JF, Pereira-Godinho H, Souza G. Efeitos da osmolaridade sobre a motilidade espermática na Piabanha Brycon insignis. Revista Ceres 2007; 54 (315):430-433. Ortiz-Mu-oz V, Álvarez-León R. Caracterización de la tolerancia ambiental de las comunidades ícticas en subsidiarios de los ríos Cauca y Magdalena, Colombia. Memoria de la Fundación La Salle de Ciencias Naturales. 2008; 68:7-20. Cosson J. The ionic and osmotic factors controlling motility of fish spermatozoa. Aquaculture 2004; 12:69–85. https://doi.org/10.1023/B:AQUI.0000017189.44263.bc Martins GB, Piedras SRN, Pouey JLOF, Robaldo RB. Qualidade espermática de jundiá sob salinidades reduzidas. XVIII Congreso de iniciación científica, XI Encuentro de pos-graduacao y I Mostra científica. Brazil: Universidade Federal de Pelotas; 2009. URL Disponible en: http://www.ufpel. tche.br/cic/2009/cd/biologicas.html . 2563 Alavi SMH, Rodina H, Policar T, Linhart O. Relationship between semen characteristics and body size in Barbus barbus L. (Teleostei: Cyprinidae) and effects of ions and osmolality on sperm motility. Comp Biochem Physiol A Mol Integr Physiol 2009a; 153:430–437. https://doi.org/10.1016/j.cbpa.2009.04.001 Alavi SMH, Rodina M, Policar T, Kozak P, Psenicka M, Linhart O. Semen of Perca fluviatilis L: sperm volume and density, seminal plasma indices and effects of dilution ratio, ions and osmolality on sperm motility. Theriogenology 2007; 68:276–283. https://doi.org/10.1016/j.theriogenology.2007.05.045 Alavi SMH, Rodina M, Viveiros ATM, Cosson J, Gela D, Boryshpolets S, Linhart O. Effects of osmolality on sperm morphology, motility and flagellar wave parameters in Northern pike (Esox lucius L.). Theriogenology 2009b; 72:32–43. https://doi.org/10.1016/j.theriogenology.2009.01.015 Legendre M, Cosson J, Alavi SMH, Linhart O. Sperm motility activation in the euryhaline tilapia Sarotherodon melanotheron heudelotii (Dumeril, 1859) acclimatized to fresh, sea or hypersaline waters. Cybium 2008; 32(2):181–182. Hu J, Zhang Y, Zhou R, Zhang Y. Changes in extracellular osmolality initiate sperm motility in freshwater teleost rosy barb Puntius conchonius. Theriogenology 1995; 72:704–710. https://doi.org/10.1016/j.theriogenology.2009.05.009 Thorogood J, Blackshaw A. Factors affecting the activation, motility and cryopreservation of the spermatozoa of the yellowfin bream, Acanthopagrus australis (Günter). Aquacult Res 2008; 23:377–344.
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spelling	Martínez, Gregorio4b07fb49-b710-4526-9cad-a2c9e09e43f4-1Atencio G, Víctorce57d528-afa7-43e4-bd45-8c8be44840aa-1Pardo C, Sandra60afd694-707c-4860-8ba2-b8ebeec04fa3-12011-05-10 00:00:002022-07-01T21:00:22Z2011-05-10 00:00:002022-07-01T21:00:22Z2011-05-100122-0268https://repositorio.unicordoba.edu.co/handle/ucordoba/583510.21897/rmvz.1020https://doi.org/10.21897/rmvz.10201909-0544application/pdfspaUniversidad de Córdobahttps://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2https://revistamvz.unicordoba.edu.co/article/view/1020Concentrationfishesglucoseglucose tolerancesperm motilitysemen preservationConcentraciónconservación del semenglucosamotilidad espermáticapecestolerancia a la glucosa.Efectos de la concentración de glucosa sobre la activación de la movilidad espermática en bocachico Prochilodus magdalenae (Pisces, Characiformes)Effect of glucose concentration on sperm motility activation in bocachico Prochilodus magdalenae (Pisces, Characiformes)Artículo de revistaJournal articleinfo:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/publishedVersionTexthttp://purl.org/redcol/resource_type/ARTREFhttp://purl.org/coar/version/c_970fb48d4fbd8a85Mojica I. Lista preliminar de las especies de peces dulceacuícolas de Colombia. Rev Acad Col Cienc Exac Fís y Nat 1999; 23:547-566.INPA: Instituto Nacional de Pesca y Acuicultura. Boletín estadístico pesquero colombiano de 1995 (ed. by INPA). Publicaciones INPA-MADR, Santa fe de Bogotá. 1995.Horváth A, Miskolczi E, Urbány B. Cryopreservation of common carp sperm. Aquat Living Resour 2003; 16(5):457-460. https://doi.org/10.1016/S0990-7440(03)00084-6Yang H, Hazlewood L, Walter RB, Tiersch TR. Effect of osmotic inmobilization on refrigerated storage and cryopreservation of sperm from a viviparous fish, the green swordtail Xiphosphorus helleri. Cryobiology 2006; 52(2):209-218. https://doi.org/10.1016/j.cryobiol.2005.11.002Bolsover RS, Hyams JS, Shephard EA, White HA, Wiedemann CG. Cell Biology. 2a ed. USA: John Wiley & Sons, Inc. 2004.Krasznai Z, Marian T, Izumi H, Damjanovich S, Balkay L, Tron L, Morisawa M. Membrane hyperpolarization removes inactivation of Ca2+ channels, leading to Ca2+ influx and subsequent initialization of sperm motility in the common carp. Proc Natl Acad Sci USA 2000; 97:2052-2057. https://doi.org/10.1073/pnas.040558097Viveiros ATM, Lock EJ, Woelders H, Komen J. Influence of cooling rates and plunging temperatures in an interrupted slow-freezing procedure for semen of the African catfish, Clarias gariepinus. Cryobiology 2001; 43:276-287. https://doi.org/10.1006/cryo.2001.2362Pegg D. Principles of cryopreservation. En: Day JG, Stacy GN, editors. Cryopreservation and Freeze-Drying Protocols. Totowa NJ: Human Press Inc; 2007. https://doi.org/10.1007/978-1-59745-362-2_3Jiang Z, Li Q, Li W, Hu J, Zhao H, Zhang S. Effect of low density lipoprotein on DNA integrity of freezing–thawing boar sperm by neutral comet assay. Anim Reprod Sci 2007; 99:401-407. https://doi.org/10.1016/j.anireprosci.2006.08.022Tabares CJ, Tarazona A, Olivera A. Fisiología de la activación del espermatozoide en peces de agua dulce. Rev Col Cienc Pec 2005; 18: 149-161.Linhart O, Cosson J, Mims SD, Shelton WI, Rodina M. Effects of ions on the motility of fresh and demembranated paddlefish (Polyodon spathula) spermatozoa. Reproduction 2002; 124:713-719. https://doi.org/10.1530/rep.0.1240713Alavi SMH, Cosson J. Sperm motility in fishes: (II) Effects of ions and osmotic pressure. Cell Biol Int 2006; 30:1–14. https://doi.org/10.1016/j.cellbi.2005.06.004Ciereszko A, Glogowski J, Dabrowski K. Biochemical characteristics of seminal plasma and spermatozoa of freshwater fishes. En: Tiersch TR and Mazik PM, editores. Cryopreservation in Aquaculture Species. Baton Roue, Louisiana: World Aquaculture Society; 2000.Inaba K. Molecular architecture of sperm flagella: molecules for motility and signaling. Zool Sci 2003; 20:1043-1056. https://doi.org/10.2108/zsj.20.1043Ingermann RL. Energy metabolism and respiration in fish spermatozoa. En: Alavi SMH, Cosson JJ, Coward K y Raffie C, editors. Fish spermatology. Oxford, UK: Alpha Science International Ltda.; 2008.Shimoda E, de Andrade DR, Vásquez- Vidal M, Shigueky-Yasui G, Straggiotti- Sliva JF, Pereira-Godinho H, Souza G. Efeitos da osmolaridade sobre a motilidade espermática na Piabanha Brycon insignis. Revista Ceres 2007; 54 (315):430-433.Ortiz-Mu-oz V, Álvarez-León R. Caracterización de la tolerancia ambiental de las comunidades ícticas en subsidiarios de los ríos Cauca y Magdalena, Colombia. Memoria de la Fundación La Salle de Ciencias Naturales. 2008; 68:7-20.Cosson J. The ionic and osmotic factors controlling motility of fish spermatozoa. Aquaculture 2004; 12:69–85. https://doi.org/10.1023/B:AQUI.0000017189.44263.bcMartins GB, Piedras SRN, Pouey JLOF, Robaldo RB. Qualidade espermática de jundiá sob salinidades reduzidas. XVIII Congreso de iniciación científica, XI Encuentro de pos-graduacao y I Mostra científica. Brazil: Universidade Federal de Pelotas; 2009. URL Disponible en: http://www.ufpel. tche.br/cic/2009/cd/biologicas.html . 2563Alavi SMH, Rodina H, Policar T, Linhart O. Relationship between semen characteristics and body size in Barbus barbus L. (Teleostei: Cyprinidae) and effects of ions and osmolality on sperm motility. Comp Biochem Physiol A Mol Integr Physiol 2009a; 153:430–437. https://doi.org/10.1016/j.cbpa.2009.04.001Alavi SMH, Rodina M, Policar T, Kozak P, Psenicka M, Linhart O. Semen of Perca fluviatilis L: sperm volume and density, seminal plasma indices and effects of dilution ratio, ions and osmolality on sperm motility. Theriogenology 2007; 68:276–283. https://doi.org/10.1016/j.theriogenology.2007.05.045Alavi SMH, Rodina M, Viveiros ATM, Cosson J, Gela D, Boryshpolets S, Linhart O. Effects of osmolality on sperm morphology, motility and flagellar wave parameters in Northern pike (Esox lucius L.). Theriogenology 2009b; 72:32–43. https://doi.org/10.1016/j.theriogenology.2009.01.015Legendre M, Cosson J, Alavi SMH, Linhart O. Sperm motility activation in the euryhaline tilapia Sarotherodon melanotheron heudelotii (Dumeril, 1859) acclimatized to fresh, sea or hypersaline waters. Cybium 2008; 32(2):181–182.Hu J, Zhang Y, Zhou R, Zhang Y. Changes in extracellular osmolality initiate sperm motility in freshwater teleost rosy barb Puntius conchonius. Theriogenology 1995; 72:704–710. https://doi.org/10.1016/j.theriogenology.2009.05.009Thorogood J, Blackshaw A. Factors affecting the activation, motility and cryopreservation of the spermatozoa of the yellowfin bream, Acanthopagrus australis (Günter). Aquacult Res 2008; 23:377–344.https://revistamvz.unicordoba.edu.co/article/download/1020/1246Núm. 2 , Año 2011 : Revista MVZ Córdoba Volumen 16(2) Mayo-Agosto 201125632255416Revista MVZ CórdobaPublicationOREORE.xmltext/xml2725https://repositorio.unicordoba.edu.co/bitstreams/cd8dd5eb-3cc5-4478-8c44-57c0297e6c0a/download3852699c213c0153ec3ac5f989b51d37MD51ucordoba/5835oai:repositorio.unicordoba.edu.co:ucordoba/58352023-10-06 00:46:18.675https://creativecommons.org/licenses/by-nc-sa/4.0/metadata.onlyhttps://repositorio.unicordoba.edu.coRepositorio Universidad de Córdobabdigital@metabiblioteca.com

Efectos de la concentración de glucosa sobre la activación de la movilidad espermática en bocachico Prochilodus magdalenae (Pisces, Characiformes)

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