Lesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coli
- Autores:
-
Gutiérrez V, Cristian
López H, Albeiro
Parra S, Jaime
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2013
- Institución:
- Universidad de Córdoba
- Repositorio:
- Repositorio Institucional Unicórdoba
- Idioma:
- spa
- OAI Identifier:
- oai:repositorio.unicordoba.edu.co:ucordoba/5399
- Acceso en línea:
- https://repositorio.unicordoba.edu.co/handle/ucordoba/5399
https://doi.org/10.21897/rmvz.178
- Palabra clave:
- Diarrheas
fever
piglet
weaning
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by-nc-sa/4.0/
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Lesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coli |
| dc.title.translated.eng.fl_str_mv |
Lesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coli |
| title |
Lesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coli |
| spellingShingle |
Lesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coli Diarrheas fever piglet weaning |
| title_short |
Lesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coli |
| title_full |
Lesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coli |
| title_fullStr |
Lesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coli |
| title_full_unstemmed |
Lesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coli |
| title_sort |
Lesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coli |
| dc.creator.fl_str_mv |
Gutiérrez V, Cristian López H, Albeiro Parra S, Jaime |
| dc.contributor.author.spa.fl_str_mv |
Gutiérrez V, Cristian López H, Albeiro Parra S, Jaime |
| dc.subject.spa.fl_str_mv |
Diarrheas fever piglet weaning |
| topic |
Diarrheas fever piglet weaning |
| publishDate |
2013 |
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2013-05-06 00:00:00 2022-07-01T20:58:10Z |
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2013-05-06 00:00:00 2022-07-01T20:58:10Z |
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2013-05-06 |
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Pitman RS, Blumberg RS. First line of defense: the role of the intestinal epithelium as an active component of the mucosal immune system. J Gastroenterol 2000; 35:805-814. http://dx.doi.org/10.1007/s005350070017 Eckmann L, Kagnoff MF, Fierer J. Intestinal epithelial cells as watchdogs for the natural immune system. Trends Microbiol 1995; 3:118-120. http://dx.doi.org/10.1016/S0966-842X(00)88894-0 Pié S, Lallès SP, Blazy F, Laffitte J, Sève B, Oswald IP. Weaning is associated with an upregulation of expression of inflammatory cytokines in the intestine of piglets. J Nutr 2004; 134:641-647. Stadnyk AW. Intestinal epithelial cells as a source of inflammatory cytokines and chemokines. Can J Gastroenterol 2002; 16:241-246. http://dx.doi.org/10.1155/2002/941087 Gopal R, Birdsell D, Monroy FP. Regulation of toll-like receptors in intestinal epithelial cells by stress and Toxoplasma gondii infection. Parasite Immunol 2008; 30:563-576. http://dx.doi.org/10.1111/j.1365-3024.2008.01055.x García-Herrera J, Navarro MA, Marca MC, Osada J, Rodríguez-Yoldi MJ. The effect of tumor necrosis factor-α on D-fructose intestinal transport in rabbits. Cytokine 2004; 25:21-30. http://dx.doi.org/10.1016/j.cyto.2003.09.005 Amador P, Garcia-Herrera J, Marca MC, de la Osada J, Acin S, Navarro MA, Salvador MT, Lostao MP, Rodriguez-Yoldi MJ. Intestinal D-galactose transport in an endotoxemia model in the rabbit. J Membr Biol 2007; 215:125-133. http://dx.doi.org/10.1007/s00232-007-9012-5 Garcia-Herrera J, Marca MC, Brot-Laroche E, Guillen N, Acin S, Navarro MA et al. Protein kinases, TNF-α and proteasome contribute in the inhibition of fructose intestinal transport by sepsis in vivo. Am J Physiol Gastrointest Liver Physiol 2008, 294:G155-G164. NRC (National Research Council). Nutrient Requirements of Swine (10th Ed), Washington DC: National Academy Press: 1998. Segalés J, Domingo M. 2003. La necropsia en el ganado porcino, diagnóstico anatomopatológico y toma de muestras, Madrid (Espa-a): Boehringer Ingelheim; 2003. Reis de Souza TC, Guerrero CMJ, Aguilera BA, Mariscal LG. Efecto de diferentes cereales sobre la morfología intestinal de lechones recién destetados. Téc Pecu Mex 2005; 43:309-321. Nabuurs MJ, Hoogendoorn A, Van der Molen EJ, Van Osta LM. Villus height and crypt depth in weanead and unweanead pigs, reared under various circumstances in the Netherlands. Res Vet Sci 1993; 55:78-84. http://dx.doi.org/10.1016/0034-5288(93)90038-H Steel RG, Torrie JH. Principles and Procedures of Statistics: a biometrical approach (2a Ed), New York (USA): McGraw-Hill Book Co; 1985. SAS®. SAS/STAT User's Guide. Institute Inc. Statistical Analysis Systems Institute. Version 9.1th Ed. Cary, NC: SAS Institute Inc. 2006. CIOMS (Council for International Organizations of Medical Sciences). Geneva: International Guiding Principles for Biomedical Research Involving Animals; 1985. Wang J, Chen L, Li P, Li X, Zhou H, Wang F et al. Gene expression is altered in piglet small intestine by weaning and dietary glutamine supplementation. J Nutr 2008; 138:1025-1032. Jiang Y, Sun LH, Lin YC, Ma XY, Zheng CT, Zhou GL et al. Effects of dietary glycyl-glutamine on growth performance, small intestinal integrity, and immune responses of weaning piglets challenged with lipopolysaccharide. J Anim Sci 2009; 87:4050-4056. http://dx.doi.org/10.2527/jas.2008-1120 Bertelsen LS, Eckmann L, Barrett KE. Prolonged interferon-g exposure decreases ion transport, NKCC1, and Na+-K+-ATPase expression in human intestinal xenografts in vivo. Am J Physiol Gastrointest Liver Physiol 2004; 286:G157-G165. Yu LC, Perdue MH. Immunologically mediated transport of ions and macromolecules. Ann NY Acad Sci 2000; 915:247-259. Liu Y, Huang J, Hou Y, Zhu H, Zhao S, Ding B et al. Dietary arginine supplementation alleviates intestinal mucosal disruption induced by Escherichia coli lipopolysaccharide in weaned pigs. Br J Nutr 2008; 100:552-560. http://dx.doi.org/10.1017/S0007114508911612 González RND, Alvarez MA, Juaristi JA, Cardoso L, Brandan N. Lipopolisacáridos (LPS) inducen apoptosis y necrosis en macrófagos murinos. Universidad Nacional del Nordeste. Comunicaciones Científicas y Tecnológicas. 2005. http://www.unne.edu.ar/Web/cyt/ com2005/3-Medicina/M-060.pdf H ew e t t JA , Ro th RA . H ep a ti c and extrahepatic pathobiology of bacterial lipopolysaccharides. Pharmacol Rev 1993; 45:382-411. Ulevitch RJ, Mathison JC, Schumann RR, Tobias PS. A new model of macrophage stimulation by bacterial lipopolysaccharide. J Trauma 1990; 30:189s-192s. Amador P, Garcia-Herrera J, Marca MC, de la Osada J, Acin S, Navarro MA et al. Inhibitory effect of TNF-α on the intestinal absorption of galactose. J Cell Biochem 2007; 101:99-111. http://dx.doi.org/10.1002/jcb.21168 Berkes J, Viswanathan VK, Savkovic SD, Hecht G. Intestinal epithelial responses to enteric pathogens: effects on tight junction barrier, ion transport, and inflammation. Gut 2003; 52:439-451. http://dx.doi.org/10.1136/gut.52.3.439 Liu YL, Li DF, Gong LM, Yi GF, Gaines AM, Carroll JA. Effects of fish oil supplementation on the performance and the immunological, adrenal, and somatotropic responses of weaned pigs after an Escherichia coli lipopolysaccharide challenge. J Anim Sci 2003; 81:2758-2765. http://dx.doi.org/10.2527/2003.81112758x Johnson IR, Ball RO, Baracos VE, Catherine JF. Glutamine supplementation influences immune development in the newly weaned piglet. Dev Comp Immunol 2006; 30:1191-1202. http://dx.doi.org/10.1016/j.dci.2006.03.003 Abad B, Mesoreno JE, Salvador MT, GarcíaHerrera J, Rodríguez-Yoldi MJ. Tumor necrosis factor-α mediates inhibitory effect of lipopolysaccharide on L-leucine intestinal uptake. Dig Dis Sci 2002; 47:1316 1322. http://dx.doi.org/10.1023/A:1015374631385 Wang F, Graham WV, Wang Y, Witkowski ED, Schwarz BT, Turner J. Interferon-γ and tumor necrosis factor-α synergize to induce intestinal epithelial barrier dysfunction by up-regulating myosin light chain kinase expression. Am J Pathol 2005; 166(2):409-419. http://dx.doi.org/10.1016/S0002-9440(10)62264-X Rugeles MT, Pati-o PJ. Inmunología: Una Ciencia activa, Tomo I (1era Ed), Medellín, Colombia: Biogénesis; 2004. |
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Gutiérrez V, Cristian9a9b36e3-cb2d-44df-a420-021907303d79-1López H, Albeiro9614724d-9baa-425d-84ca-83b134e6643c-1Parra S, Jaimea61a0454-21dd-4974-8b21-08276394febd-12013-05-06 00:00:002022-07-01T20:58:10Z2013-05-06 00:00:002022-07-01T20:58:10Z2013-05-060122-0268https://repositorio.unicordoba.edu.co/handle/ucordoba/539910.21897/rmvz.178https://doi.org/10.21897/rmvz.1781909-0544application/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/178DiarrheasfeverpigletweaningLesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coliLesiones en órganos de cerdos posdestete, inducidas por el lipopolisacárido de E. coliArtículo 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_970fb48d4fbd8a85Pitman RS, Blumberg RS. First line of defense: the role of the intestinal epithelium as an active component of the mucosal immune system. J Gastroenterol 2000; 35:805-814. http://dx.doi.org/10.1007/s005350070017Eckmann L, Kagnoff MF, Fierer J. Intestinal epithelial cells as watchdogs for the natural immune system. Trends Microbiol 1995; 3:118-120. http://dx.doi.org/10.1016/S0966-842X(00)88894-0Pié S, Lallès SP, Blazy F, Laffitte J, Sève B, Oswald IP. Weaning is associated with an upregulation of expression of inflammatory cytokines in the intestine of piglets. J Nutr 2004; 134:641-647.Stadnyk AW. Intestinal epithelial cells as a source of inflammatory cytokines and chemokines. Can J Gastroenterol 2002; 16:241-246. http://dx.doi.org/10.1155/2002/941087Gopal R, Birdsell D, Monroy FP. Regulation of toll-like receptors in intestinal epithelial cells by stress and Toxoplasma gondii infection. Parasite Immunol 2008; 30:563-576. http://dx.doi.org/10.1111/j.1365-3024.2008.01055.xGarcía-Herrera J, Navarro MA, Marca MC, Osada J, Rodríguez-Yoldi MJ. The effect of tumor necrosis factor-α on D-fructose intestinal transport in rabbits. Cytokine 2004; 25:21-30. http://dx.doi.org/10.1016/j.cyto.2003.09.005Amador P, Garcia-Herrera J, Marca MC, de la Osada J, Acin S, Navarro MA, Salvador MT, Lostao MP, Rodriguez-Yoldi MJ. Intestinal D-galactose transport in an endotoxemia model in the rabbit. J Membr Biol 2007; 215:125-133. http://dx.doi.org/10.1007/s00232-007-9012-5Garcia-Herrera J, Marca MC, Brot-Laroche E, Guillen N, Acin S, Navarro MA et al. Protein kinases, TNF-α and proteasome contribute in the inhibition of fructose intestinal transport by sepsis in vivo. Am J Physiol Gastrointest Liver Physiol 2008, 294:G155-G164.NRC (National Research Council). Nutrient Requirements of Swine (10th Ed), Washington DC: National Academy Press: 1998.Segalés J, Domingo M. 2003. La necropsia en el ganado porcino, diagnóstico anatomopatológico y toma de muestras, Madrid (Espa-a): Boehringer Ingelheim; 2003.Reis de Souza TC, Guerrero CMJ, Aguilera BA, Mariscal LG. Efecto de diferentes cereales sobre la morfología intestinal de lechones recién destetados. Téc Pecu Mex 2005; 43:309-321.Nabuurs MJ, Hoogendoorn A, Van der Molen EJ, Van Osta LM. Villus height and crypt depth in weanead and unweanead pigs, reared under various circumstances in the Netherlands. Res Vet Sci 1993; 55:78-84. http://dx.doi.org/10.1016/0034-5288(93)90038-HSteel RG, Torrie JH. Principles and Procedures of Statistics: a biometrical approach (2a Ed), New York (USA): McGraw-Hill Book Co; 1985.SAS®. SAS/STAT User's Guide. Institute Inc. Statistical Analysis Systems Institute. Version 9.1th Ed. Cary, NC: SAS Institute Inc. 2006.CIOMS (Council for International Organizations of Medical Sciences). Geneva: International Guiding Principles for Biomedical Research Involving Animals; 1985.Wang J, Chen L, Li P, Li X, Zhou H, Wang F et al. Gene expression is altered in piglet small intestine by weaning and dietary glutamine supplementation. J Nutr 2008; 138:1025-1032.Jiang Y, Sun LH, Lin YC, Ma XY, Zheng CT, Zhou GL et al. Effects of dietary glycyl-glutamine on growth performance, small intestinal integrity, and immune responses of weaning piglets challenged with lipopolysaccharide. J Anim Sci 2009; 87:4050-4056. http://dx.doi.org/10.2527/jas.2008-1120Bertelsen LS, Eckmann L, Barrett KE. Prolonged interferon-g exposure decreases ion transport, NKCC1, and Na+-K+-ATPase expression in human intestinal xenografts in vivo. Am J Physiol Gastrointest Liver Physiol 2004; 286:G157-G165.Yu LC, Perdue MH. Immunologically mediated transport of ions and macromolecules. Ann NY Acad Sci 2000; 915:247-259.Liu Y, Huang J, Hou Y, Zhu H, Zhao S, Ding B et al. Dietary arginine supplementation alleviates intestinal mucosal disruption induced by Escherichia coli lipopolysaccharide in weaned pigs. Br J Nutr 2008; 100:552-560. http://dx.doi.org/10.1017/S0007114508911612González RND, Alvarez MA, Juaristi JA, Cardoso L, Brandan N. Lipopolisacáridos (LPS) inducen apoptosis y necrosis en macrófagos murinos. Universidad Nacional del Nordeste. Comunicaciones Científicas y Tecnológicas. 2005. http://www.unne.edu.ar/Web/cyt/ com2005/3-Medicina/M-060.pdfH ew e t t JA , Ro th RA . H ep a ti c and extrahepatic pathobiology of bacterial lipopolysaccharides. Pharmacol Rev 1993; 45:382-411.Ulevitch RJ, Mathison JC, Schumann RR, Tobias PS. A new model of macrophage stimulation by bacterial lipopolysaccharide. J Trauma 1990; 30:189s-192s.Amador P, Garcia-Herrera J, Marca MC, de la Osada J, Acin S, Navarro MA et al. Inhibitory effect of TNF-α on the intestinal absorption of galactose. J Cell Biochem 2007; 101:99-111. http://dx.doi.org/10.1002/jcb.21168Berkes J, Viswanathan VK, Savkovic SD, Hecht G. Intestinal epithelial responses to enteric pathogens: effects on tight junction barrier, ion transport, and inflammation. Gut 2003; 52:439-451. http://dx.doi.org/10.1136/gut.52.3.439Liu YL, Li DF, Gong LM, Yi GF, Gaines AM, Carroll JA. Effects of fish oil supplementation on the performance and the immunological, adrenal, and somatotropic responses of weaned pigs after an Escherichia coli lipopolysaccharide challenge. J Anim Sci 2003; 81:2758-2765. http://dx.doi.org/10.2527/2003.81112758xJohnson IR, Ball RO, Baracos VE, Catherine JF. Glutamine supplementation influences immune development in the newly weaned piglet. Dev Comp Immunol 2006; 30:1191-1202. http://dx.doi.org/10.1016/j.dci.2006.03.003Abad B, Mesoreno JE, Salvador MT, GarcíaHerrera J, Rodríguez-Yoldi MJ. Tumor necrosis factor-α mediates inhibitory effect of lipopolysaccharide on L-leucine intestinal uptake. Dig Dis Sci 2002; 47:1316 1322. http://dx.doi.org/10.1023/A:1015374631385Wang F, Graham WV, Wang Y, Witkowski ED, Schwarz BT, Turner J. Interferon-γ and tumor necrosis factor-α synergize to induce intestinal epithelial barrier dysfunction by up-regulating myosin light chain kinase expression. Am J Pathol 2005; 166(2):409-419. http://dx.doi.org/10.1016/S0002-9440(10)62264-XRugeles MT, Pati-o PJ. Inmunología: Una Ciencia activa, Tomo I (1era Ed), Medellín, Colombia: Biogénesis; 2004.https://revistamvz.unicordoba.edu.co/article/download/178/247Núm. 2 , Año 2013 : Revista MVZ Córdoba Volumen 18(2) Mayo-Agosto 201335422353418Revista MVZ CórdobaPublicationOREORE.xmltext/xml2598http://172.16.14.198/bitstreams/2b2fed5c-13a3-41ff-92cf-7cc2a496118b/download342a8f98cf32a2c71d15106debcebbc5MD51ucordoba/5399oai:172.16.14.198:ucordoba/53992023-10-06 00:45:26.336https://creativecommons.org/licenses/by-nc-sa/4.0/metadata.onlyhttp://172.16.14.198Repositorio Universidad de Córdobabdigital@metabiblioteca.com |