Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitro

Autores:: Arias L, Catalina
Ruiz C, Tatiana
Olivera A, Martha
Tarazona M, Ariel

Tipo de recurso:: Article of journal

Fecha de publicación:: 2007

Institución:: Universidad de Córdoba

Repositorio:: Repositorio Institucional Unicórdoba

Idioma:: spa

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dc.title.spa.fl_str_mv	Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitro
dc.title.translated.eng.fl_str_mv	Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitro
title	Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitro
spellingShingle	Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitro Cleavage bovines embryos amino acids.
title_short	Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitro
title_full	Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitro
title_fullStr	Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitro
title_full_unstemmed	Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitro
title_sort	Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitro
dc.creator.fl_str_mv	Arias L, Catalina Ruiz C, Tatiana Olivera A, Martha Tarazona M, Ariel
dc.contributor.author.spa.fl_str_mv	Arias L, Catalina Ruiz C, Tatiana Olivera A, Martha Tarazona M, Ariel
dc.subject.spa.fl_str_mv	Cleavage bovines embryos amino acids.
topic	Cleavage bovines embryos amino acids.
publishDate	2007
dc.date.accessioned.none.fl_str_mv	2007-07-01 00:00:00 2022-07-01T20:59:32Z
dc.date.available.none.fl_str_mv	2007-07-01 00:00:00 2022-07-01T20:59:32Z
dc.date.issued.none.fl_str_mv	2007-07-01
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dc.type.eng.fl_str_mv	Journal article
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dc.identifier.doi.none.fl_str_mv	10.21897/rmvz.422
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dc.relation.references.spa.fl_str_mv	Serrano C, Olivera-Angel M. Detenimiento en el ciclo celular de embriones bovinos producidos in vitro. Taurus 2003; 5 (20): 20-35. Thompson JG, McNaughton C, Gasparini B, McGowan LT, Tervit HR. Effect of inhibitors and uncouplers of oxidative phosphorylation during compaction and blastulation of bovine embryos cultured in vitro. J Reprod Fertil 2000; 118: 47-55. http://dx.doi.org/10.1530/reprod/118.1.47 http://dx.doi.org/10.1530/jrf.0.1180047 Takahashi M, Nagai T, Okamura N, Takahashi H, Okano A. Promoting Effect of ß-Mercaptoethanol on In Vitro Development under Oxidative Stress and Cystine Uptake of Bovine Embryos. Biol Reprod 2002; 6: 562– 567. http://dx.doi.org/10.1095/biolreprod66.3.562 Edwards JL, King WA, Kawarsky SJ, Ealy PD. Responsiveness of early embryos to environmental insults. Teriogenology 2001; 55: 209-223. http://dx.doi.org/10.1016/S0093-691X(00)00455-6 Brookes P. Mitochondrial H leak and ROS Generation: an odd couple. Free Radic Biol Med 2005; 38 (1): 12-23. http://dx.doi.org/10.1016/j.freeradbiomed.2004.10.016 Fernández V Daniel, citado por Laguna P. José y Pi-a G. Enrique. Bioquímica de Laguna. 5 ed. México DF. Editorial El Manual Moderno. 2002. Cáp 9. Velez-Pardo C, Tarazona Morales A, Jimenez Del Rio M, Olivera-Angel M. Endogenously generated hydrogen peroxide induces apoptosis via mitochondrial damage independent of NF-kB and p53 activation in bovine embryos. Theriogenology 2007; 67: 1285–1296. http://dx.doi.org/10.1016/j.theriogenology.2007.01.018 Miller JGO, Schultz GA. Amino acid content of preimplantation rabbit embryos and fluids of the reproductive tract. Biol Reprod 1987; 36: 125-129. http://dx.doi.org/10.1095/biolreprod36.1.125 Boland M, Lonergan P, O' Callaghan D. Effect of nutrition on endocrine parameters, ovarian physiology, and oocyte and embryo development. Theriogenology 2001; 55: 1323-1340. http://dx.doi.org/10.1016/S0093-691X(01)00485-X Eun- Song L, Yutaka F. Synergistic Effec of Alanine and Glycine on Bovine Embryos Cultured in Chemically Defined Medium and amino Acid Uptake by in vitroproduced Bovine Morulae and Blastocysts. Biol Reprod 1996; 55: 1383-1389. http://dx.doi.org/10.1095/biolreprod55.6.1383 Duranthon V, Renard JP. The developmental competence of mammalian oocytes: a convenient but biologically fuzzy concept. Theriogenology 2001; 55 (6): 1277- 1289. http://dx.doi.org/10.1016/S0093-691X(01)00482-4 Tarazona AM, Rodriguez JI, Restrepo LF, Olivera-Angel M. Mitochondrial activity, distribution and segregation in bovine oocytes and in embryos produced in vitro. Reprod Domest Anim 2005; 40: 1-7. Leung KC, Adashi E. The ovary. Second edition. San Diego, California, Elsevier Academic Press. 2004. Chapter 7: 113-129. Stojkovic M, Machado SA, Stojkovic P, Zakhartchenko V, Hutzler P, Goncalves PB, Wolf E. Mitochondrial distribution and adenosine triphosphate content of bovine oocytes before and after in vitro maturation: correlation with morphological criteria and developmental capacity after in vitro fertilization and culture. Biol Reprod 2001; 64(3): 904-909. http://dx.doi.org/10.1095/biolreprod64.3.904 Fukui Y. Effect of follicle cells on the acrosome reaction, fertilization, and developmental competence of bovine oocytes matured in vitro. Mol Reprod Dev 1990; 26(1) 40-46. Parrish JJ, Krogenaes IA, SuskoParrish JL. Effect of bovine sperm separation by either swim-up or percoll method on success of in vitro fertilization and early embryonic development. Theriogenology 1995; 44: 859-869. http://dx.doi.org/10.1016/0093-691X(95)00271-9 Rosenkrans Jr CF, Zeng GQ, MCNamara GT, Schoff PK, First NL. Development of bovine embryos in vitro as affected by energy substrates. Biol Reprod 1993; 49:459–62. http://dx.doi.org/10.1095/biolreprod49.3.459 Gardner DK. Development of serumfree culture systems for the ruminant embryo and subsequent assessment of embryo viability. J Reprod Fertil 1999; suppl 54: 461-475. Kerri MD, Baltz JM. Organic Osmolytes and Embryos: Substrates of the Gly and ß Transport Systems Protect Mouse Zigotes against the effects of raised Osmolarity. Biol Reprod 1997; 56: 1550-1558. http://dx.doi.org/10.1095/biolreprod56.6.1550 Legge M, Sellens MH. Free radical scavengers ameliorate the 2 cell Block in mouse embryo culture. Human Reprod 1991; 6: 867- 87. Cummins J. The role of mitochondria in the establishment of oocyte functional competence. Eur J Obstet Gynecol Reprod Biol 2004; 115: (Suppl 1) 23-29. Halliwell B. Superoxide-dependet formation of hydroxy radicals in presence of iron chelaters. FEBS Lett 1987; 92: 321-326. http://dx.doi.org/10.1016/0014-5793(78)80779-0 Moore K, Bondioli K. Glycine and Alanine Supplementation of Culture Medium Enhances Development of in vitro Matured and Fertilized Cattle Embryos. Biol Reprod 1993; 48: 833- 840. http://dx.doi.org/10.1095/biolreprod48.4.833
dc.relation.bitstream.none.fl_str_mv	https://revistamvz.unicordoba.edu.co/article/download/422/490
dc.relation.citationedition.spa.fl_str_mv	Núm. 2 , Año 2007 : Revista MVZ Córdoba Volumen 12(2) Julio-Diciembre 2007
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spelling	Arias L, Catalina67f385ec-e2a8-4dae-91f7-65e8bc773449-1Ruiz C, Tatiana9c8e0b9f-24b4-4ad0-a752-5357ea2a9b3e-1Olivera A, Martha67a8023c-3cea-4f8a-aefe-dc80f5193535-1Tarazona M, Ariel4be4c23d-80e0-4733-aa78-4d1c8af2e18e-12007-07-01 00:00:002022-07-01T20:59:32Z2007-07-01 00:00:002022-07-01T20:59:32Z2007-07-010122-0268https://repositorio.unicordoba.edu.co/handle/ucordoba/564310.21897/rmvz.422https://doi.org/10.21897/rmvz.4221909-0544application/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/422Cleavagebovinesembryosamino acids.Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitroEfecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitroArtículo 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_970fb48d4fbd8a85Serrano C, Olivera-Angel M. Detenimiento en el ciclo celular de embriones bovinos producidos in vitro. Taurus 2003; 5 (20): 20-35.Thompson JG, McNaughton C, Gasparini B, McGowan LT, Tervit HR. Effect of inhibitors and uncouplers of oxidative phosphorylation during compaction and blastulation of bovine embryos cultured in vitro. J Reprod Fertil 2000; 118: 47-55. http://dx.doi.org/10.1530/reprod/118.1.47 http://dx.doi.org/10.1530/jrf.0.1180047Takahashi M, Nagai T, Okamura N, Takahashi H, Okano A. Promoting Effect of ß-Mercaptoethanol on In Vitro Development under Oxidative Stress and Cystine Uptake of Bovine Embryos. Biol Reprod 2002; 6: 562– 567. http://dx.doi.org/10.1095/biolreprod66.3.562Edwards JL, King WA, Kawarsky SJ, Ealy PD. Responsiveness of early embryos to environmental insults. Teriogenology 2001; 55: 209-223. http://dx.doi.org/10.1016/S0093-691X(00)00455-6Brookes P. Mitochondrial H leak and ROS Generation: an odd couple. Free Radic Biol Med 2005; 38 (1): 12-23. http://dx.doi.org/10.1016/j.freeradbiomed.2004.10.016Fernández V Daniel, citado por Laguna P. José y Pi-a G. Enrique. Bioquímica de Laguna. 5 ed. México DF. Editorial El Manual Moderno. 2002. Cáp 9.Velez-Pardo C, Tarazona Morales A, Jimenez Del Rio M, Olivera-Angel M. Endogenously generated hydrogen peroxide induces apoptosis via mitochondrial damage independent of NF-kB and p53 activation in bovine embryos. Theriogenology 2007; 67: 1285–1296. http://dx.doi.org/10.1016/j.theriogenology.2007.01.018Miller JGO, Schultz GA. Amino acid content of preimplantation rabbit embryos and fluids of the reproductive tract. Biol Reprod 1987; 36: 125-129. http://dx.doi.org/10.1095/biolreprod36.1.125Boland M, Lonergan P, O' Callaghan D. Effect of nutrition on endocrine parameters, ovarian physiology, and oocyte and embryo development. Theriogenology 2001; 55: 1323-1340. http://dx.doi.org/10.1016/S0093-691X(01)00485-XEun- Song L, Yutaka F. Synergistic Effec of Alanine and Glycine on Bovine Embryos Cultured in Chemically Defined Medium and amino Acid Uptake by in vitroproduced Bovine Morulae and Blastocysts. Biol Reprod 1996; 55: 1383-1389. http://dx.doi.org/10.1095/biolreprod55.6.1383Duranthon V, Renard JP. The developmental competence of mammalian oocytes: a convenient but biologically fuzzy concept. Theriogenology 2001; 55 (6): 1277- 1289. http://dx.doi.org/10.1016/S0093-691X(01)00482-4Tarazona AM, Rodriguez JI, Restrepo LF, Olivera-Angel M. Mitochondrial activity, distribution and segregation in bovine oocytes and in embryos produced in vitro. Reprod Domest Anim 2005; 40: 1-7.Leung KC, Adashi E. The ovary. Second edition. San Diego, California, Elsevier Academic Press. 2004. Chapter 7: 113-129.Stojkovic M, Machado SA, Stojkovic P, Zakhartchenko V, Hutzler P, Goncalves PB, Wolf E. Mitochondrial distribution and adenosine triphosphate content of bovine oocytes before and after in vitro maturation: correlation with morphological criteria and developmental capacity after in vitro fertilization and culture. Biol Reprod 2001; 64(3): 904-909. http://dx.doi.org/10.1095/biolreprod64.3.904Fukui Y. Effect of follicle cells on the acrosome reaction, fertilization, and developmental competence of bovine oocytes matured in vitro. Mol Reprod Dev 1990; 26(1) 40-46.Parrish JJ, Krogenaes IA, SuskoParrish JL. Effect of bovine sperm separation by either swim-up or percoll method on success of in vitro fertilization and early embryonic development. Theriogenology 1995; 44: 859-869. http://dx.doi.org/10.1016/0093-691X(95)00271-9Rosenkrans Jr CF, Zeng GQ, MCNamara GT, Schoff PK, First NL. Development of bovine embryos in vitro as affected by energy substrates. Biol Reprod 1993; 49:459–62. http://dx.doi.org/10.1095/biolreprod49.3.459Gardner DK. Development of serumfree culture systems for the ruminant embryo and subsequent assessment of embryo viability. J Reprod Fertil 1999; suppl 54: 461-475.Kerri MD, Baltz JM. Organic Osmolytes and Embryos: Substrates of the Gly and ß Transport Systems Protect Mouse Zigotes against the effects of raised Osmolarity. Biol Reprod 1997; 56: 1550-1558. http://dx.doi.org/10.1095/biolreprod56.6.1550Legge M, Sellens MH. Free radical scavengers ameliorate the 2 cell Block in mouse embryo culture. Human Reprod 1991; 6: 867- 87.Cummins J. The role of mitochondria in the establishment of oocyte functional competence. Eur J Obstet Gynecol Reprod Biol 2004; 115: (Suppl 1) 23-29.Halliwell B. Superoxide-dependet formation of hydroxy radicals in presence of iron chelaters. FEBS Lett 1987; 92: 321-326. http://dx.doi.org/10.1016/0014-5793(78)80779-0Moore K, Bondioli K. Glycine and Alanine Supplementation of Culture Medium Enhances Development of in vitro Matured and Fertilized Cattle Embryos. Biol Reprod 1993; 48: 833- 840. http://dx.doi.org/10.1095/biolreprod48.4.833https://revistamvz.unicordoba.edu.co/article/download/422/490Núm. 2 , Año 2007 : Revista MVZ Córdoba Volumen 12(2) Julio-Diciembre 2007212Revista MVZ CórdobaPublicationOREORE.xmltext/xml2704http://172.16.14.198/bitstreams/4a7006a6-a1f2-44a4-9375-55f32dc8ac31/downloadeed0ea0584f900187bec5bd431843bf2MD51ucordoba/5643oai:172.16.14.198:ucordoba/56432023-10-06 00:45:30.486https://creativecommons.org/licenses/by-nc-sa/4.0/metadata.onlyhttp://172.16.14.198Repositorio Universidad de Córdobabdigital@metabiblioteca.com

Efecto de la suplementación con alanina y glicina sobre los clivajes iniciales de embiones bovinos producidos in vitro

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