Efecto citotóxico de Deoxinivalenol sobre la proliferación de la línea celular HepG2

Autores:
Garzón-González, Harold Duván
Jaimes-Mendez, Nancy
Rojas-Contreras, Liliana
Salmen-Halabi, Siham
Gil-Durán, Manuel Alejandro
Tipo de recurso:
Article of journal
Fecha de publicación:
2021
Institución:
Universidad de Córdoba
Repositorio:
Repositorio Institucional Unicórdoba
Idioma:
spa
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oai:repositorio.unicordoba.edu.co:ucordoba/6091
Acceso en línea:
https://repositorio.unicordoba.edu.co/handle/ucordoba/6091
https://doi.org/10.21897/rmvz.2080
Palabra clave:
Fusarium spp
proliferation
toxicity
Fusarium spp
proliferación
toxicidad
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-sa/4.0/
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dc.title.spa.fl_str_mv Efecto citotóxico de Deoxinivalenol sobre la proliferación de la línea celular HepG2
dc.title.translated.eng.fl_str_mv Cytotoxic effect of Deoxynivalenol on the proliferation of the HepG2 cell line
title Efecto citotóxico de Deoxinivalenol sobre la proliferación de la línea celular HepG2
spellingShingle Efecto citotóxico de Deoxinivalenol sobre la proliferación de la línea celular HepG2
Fusarium spp
proliferation
toxicity
Fusarium spp
proliferación
toxicidad
title_short Efecto citotóxico de Deoxinivalenol sobre la proliferación de la línea celular HepG2
title_full Efecto citotóxico de Deoxinivalenol sobre la proliferación de la línea celular HepG2
title_fullStr Efecto citotóxico de Deoxinivalenol sobre la proliferación de la línea celular HepG2
title_full_unstemmed Efecto citotóxico de Deoxinivalenol sobre la proliferación de la línea celular HepG2
title_sort Efecto citotóxico de Deoxinivalenol sobre la proliferación de la línea celular HepG2
dc.creator.fl_str_mv Garzón-González, Harold Duván
Jaimes-Mendez, Nancy
Rojas-Contreras, Liliana
Salmen-Halabi, Siham
Gil-Durán, Manuel Alejandro
dc.contributor.author.spa.fl_str_mv Garzón-González, Harold Duván
Jaimes-Mendez, Nancy
Rojas-Contreras, Liliana
Salmen-Halabi, Siham
Gil-Durán, Manuel Alejandro
dc.subject.eng.fl_str_mv Fusarium spp
proliferation
toxicity
topic Fusarium spp
proliferation
toxicity
Fusarium spp
proliferación
toxicidad
dc.subject.spa.fl_str_mv Fusarium spp
proliferación
toxicidad
publishDate 2021
dc.date.accessioned.none.fl_str_mv 2021-05-02 00:00:00
2022-07-01T21:01:39Z
dc.date.available.none.fl_str_mv 2021-05-02 00:00:00
2022-07-01T21:01:39Z
dc.date.issued.none.fl_str_mv 2021-05-02
dc.type.spa.fl_str_mv Artículo de revista
dc.type.eng.fl_str_mv Journal article
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https://doi.org/10.21897/rmvz.2080
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dc.relation.references.spa.fl_str_mv Mayer E, Novak B, Springler A, Schwartz-Zimmermann H, Nagl V, Reisinger N, et al. Effects of deoxynivalenol (DON) and its microbial biotransformation product deepoxy-deoxynivalenol (DOM-1) on a trout, pig, mouse, and human cell line. Mycotoxin Res. 2017; 33(4):297–308. https://link.springer.com/article/10.1007/s12550-017-0289-7
Pestka J. Toxicological mechanisms and potential health effects of deoxynivalenol and nivalenol. World Mycotoxin J. 2010; 3(4):323–347. https://doi.org/10.3920/WMJ2010.1247
Pinton P, Tsybulskyy D, Lucioli J, Laffitte J, Callu P, Lyazhri F, et al. Toxicity of deoxynivalenol and its acetylated derivatives on the intestine: Differential effects on morphology, barrier function, tight junctions proteins and MAPKinases. Toxicol Sci. 2012; 130(1):180–190. https://www.ncbi.nlm.nih.gov/pubmed/22859312
Ren Z, Wang Y, Deng H, Deng Y, Deng J, Zuo Z, et al. Deoxynivalenol induces apoptosis in chicken splenic lymphocytes via the reactive oxygen species-mediated mitochondrial pathway. Environ Toxicol Pharmacol. 2015; 39(1):339–346. https://www.ncbi.nlm.nih.gov/pubmed/25553575
Arunachalam C, Doohan F. Trichothecene toxicity in eukaryotes: Cellular and molecular mechanisms in plants and animals. Toxicol Lett. 2013; 217(2):149– 158. https://www.ncbi.nlm.nih.gov/pubmed/23274714
Wu F, Groopman F, Pestka J. Public Health Impacts of Foodborne Mycotoxins. Annu Rev Food Sci Technol. 2014; 5:351–372. https://www.ncbi.nlm.nih.gov/pubmed/24422587
Liao Y, Peng Z, Chen L, Nüssler A, Liu L, Yang W. Deoxynivalenol, gut microbiota and immunotoxicity: A potential approach? Food Chem Toxicol. 2018; 112:342–354. https://www.ncbi.nlm.nih.gov/pubmed/29331731
Pistritto G, Trisciuoglio D, Ceci C, Garufi A, D’Orazi G. Apoptosis as anticancer mechanism: function and dysfunction of its modulators and targeted therapeutic strategies. Aging. 2016; 8(4):603–619. https://dx.doi.org/10.18632%2Faging.100934
Gordeziani M, Adamia G, Khatisashvili G, Gigolashvili G. Programmed cell self-liquidation (apoptosis). Annals of Agrarian Science. 2017;15(1):148–154. https://www.sciencedirect.com/science/article/pii/S151218871630029X
Redza M, Averill D. Activation of apoptosis signalling pathways by reactive oxygen species. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 2016; 1863(12):2977–2992. https://doi.org/10.1016/j.bbamcr.2016.09.012
Pestka J. Toxicological mechanisms and potential health effects of deoxynivalenol and nivalenol. World Mycotoxin J. 2010; 3(4):323–347. https://doi.org/10.3920/WMJ2010.1247
Oshikata A, Takezawa, T. Development of an oxygenation culture method for activating the liver-specific functions of HepG2 cells utilizing a collagen vitrigel membrane chamber. Cytotechnology. 2015; 68(5):1801–1811. https://doi.org/10.1007/s10616-015-9934-1
Pinton P, Oswald I. Effect of Deoxynivalenol and Other Type B Trichothecenes on the Intestine: A Review. Toxins. 2014; 6(5):1615-1643. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052256/
Juan A, Berrada H, Font G, Ruiz M. Evaluation of acute toxicity and genotoxicity of DON, 3-ADON and 15-ADON in HepG2 cells. Toxicology Letters. 2017; 280S: S254-S266.
Kupcsik L. Estimation of Cell Number Based on Metabolic Activity: The MTT Reduction Assay. Mammalian Cell Viability. Methods Mol Biol. 2011; 740:13–19. https://doi.org/10.1007/978-1-61779-108-6_3
Jaimes N, Salmen S, Colmenares M, Burgos A, Tamayo L, Mendoza V, et al. Efecto citotóxico de los compuestos de inclusión de paladio (II) en la beta-ciclodextrina. Biomédica. 2016; 36(4):603-611. https://doi.org/10.7705/biomedica.v36i4.2880
Dinu D, Bodea G, Ceapa C, Munteanu M, Roming F, Serban A, et al. Adapted response of the antioxidant defense system to oxidative stress induced by deoxynivalenol in Hek-293 cells. Toxicon. 2011; 57(7-8):1023–1032. https://doi.org/10.1016/j.toxicon.2011.04.006
Alassane I, Kolf M, Gauthier T, Abrami R, Abiola F, Oswald I. New insights into mycotoxin mixtures: the toxicity of low doses of Type B trichothecenes on intestinal epithelial cells is synergistic. Toxicol Appl Pharmacol. 2013; 272(1):191–198. https://doi.org/10.1016/j.taap.2013.05.023
Fernández C, Elmo L, Waldner T, Ruiz M. Cytotoxic effects induced by patulin, deoxynivalenol and toxin T2 individually and in combination in hepatic cells (HepG2). Food Chem Toxicol. 2018; 120:12–23. https://doi.org/10.1016/j.fct.2018.06.019
Lei Y, Guanghui Z, Xi W, Yingting W, Xialu L, Fangfang Y, et al. Cellular responses to T-2 toxin and/or deoxynivalenol that induce cartilage damage are not specific to chondrocytes. Sci Rep. 2017; 7(2231):1-14. https://www.nature.com/articles/s41598-017-02568-5
Mikami O, Yamaguchi H, Murata H, Nakajima Y, Miyazaki S. Induction of apoptotic lesions in liver and lymphoid tissues and modulation of cytokine mRNA expression by acute exposure to deoxynivalenol in piglets. J Vet Sci. 2010; 11(2):107-113. https://dx.doi.org/10.4142%2Fjvs.2010.11.2.107
Ma Y, Zhang A, Shi Z, He C, Ding J, Wang X, et al. A mitochondria-mediated apoptotic pathway induced by deoxynivalenol in human colon cancer cells. Toxicol in Vitro. 2012; 26(3):414–420. https://doi.org/10.1016/j.tiv.2012.01.010
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dc.relation.citationedition.spa.fl_str_mv Núm. 3 , Año 2021 : Revista MVZ Córdoba Volumen 26(3) Septiembre-Diciembre 2021
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spelling Garzón-González, Harold Duván7d25a761-26a0-480c-a6a2-2dcd316b3d35-1Jaimes-Mendez, Nancy0c9e74fc-5f68-4865-95a3-e33b23a8963b-1Rojas-Contreras, Liliana5f57482a-e419-4698-a549-6480795a2c75-1Salmen-Halabi, Siham51356075-0005-4b8b-a56e-9a562f1bd0ff-1Gil-Durán, Manuel Alejandro040d2424-c8ae-4d5b-bb45-501cfd024b30-12021-05-02 00:00:002022-07-01T21:01:39Z2021-05-02 00:00:002022-07-01T21:01:39Z2021-05-020122-0268https://repositorio.unicordoba.edu.co/handle/ucordoba/609110.21897/rmvz.2080https://doi.org/10.21897/rmvz.20801909-0544application/pdfapplication/pdfapplication/zipapplication/zipapplication/xmlapplication/xmlaudio/mpegaudio/mpegspaUniversidad de CórdobaHarold Duván Garzón-González, Nancy Jaimes-Mendez, Liliana Rojas-Contreras, Siham Salmen-Halabi, Manuel Alejandro Gil-Durán - 2021https://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/e2080Fusarium sppproliferationtoxicityFusarium sppproliferacióntoxicidadEfecto citotóxico de Deoxinivalenol sobre la proliferación de la línea celular HepG2Cytotoxic effect of Deoxynivalenol on the proliferation of the HepG2 cell lineArtículo 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_970fb48d4fbd8a85Mayer E, Novak B, Springler A, Schwartz-Zimmermann H, Nagl V, Reisinger N, et al. Effects of deoxynivalenol (DON) and its microbial biotransformation product deepoxy-deoxynivalenol (DOM-1) on a trout, pig, mouse, and human cell line. Mycotoxin Res. 2017; 33(4):297–308. https://link.springer.com/article/10.1007/s12550-017-0289-7Pestka J. Toxicological mechanisms and potential health effects of deoxynivalenol and nivalenol. World Mycotoxin J. 2010; 3(4):323–347. https://doi.org/10.3920/WMJ2010.1247Pinton P, Tsybulskyy D, Lucioli J, Laffitte J, Callu P, Lyazhri F, et al. Toxicity of deoxynivalenol and its acetylated derivatives on the intestine: Differential effects on morphology, barrier function, tight junctions proteins and MAPKinases. Toxicol Sci. 2012; 130(1):180–190. https://www.ncbi.nlm.nih.gov/pubmed/22859312Ren Z, Wang Y, Deng H, Deng Y, Deng J, Zuo Z, et al. Deoxynivalenol induces apoptosis in chicken splenic lymphocytes via the reactive oxygen species-mediated mitochondrial pathway. Environ Toxicol Pharmacol. 2015; 39(1):339–346. https://www.ncbi.nlm.nih.gov/pubmed/25553575Arunachalam C, Doohan F. Trichothecene toxicity in eukaryotes: Cellular and molecular mechanisms in plants and animals. Toxicol Lett. 2013; 217(2):149– 158. https://www.ncbi.nlm.nih.gov/pubmed/23274714Wu F, Groopman F, Pestka J. Public Health Impacts of Foodborne Mycotoxins. Annu Rev Food Sci Technol. 2014; 5:351–372. https://www.ncbi.nlm.nih.gov/pubmed/24422587Liao Y, Peng Z, Chen L, Nüssler A, Liu L, Yang W. Deoxynivalenol, gut microbiota and immunotoxicity: A potential approach? Food Chem Toxicol. 2018; 112:342–354. https://www.ncbi.nlm.nih.gov/pubmed/29331731Pistritto G, Trisciuoglio D, Ceci C, Garufi A, D’Orazi G. Apoptosis as anticancer mechanism: function and dysfunction of its modulators and targeted therapeutic strategies. Aging. 2016; 8(4):603–619. https://dx.doi.org/10.18632%2Faging.100934Gordeziani M, Adamia G, Khatisashvili G, Gigolashvili G. Programmed cell self-liquidation (apoptosis). Annals of Agrarian Science. 2017;15(1):148–154. https://www.sciencedirect.com/science/article/pii/S151218871630029XRedza M, Averill D. Activation of apoptosis signalling pathways by reactive oxygen species. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 2016; 1863(12):2977–2992. https://doi.org/10.1016/j.bbamcr.2016.09.012Pestka J. Toxicological mechanisms and potential health effects of deoxynivalenol and nivalenol. World Mycotoxin J. 2010; 3(4):323–347. https://doi.org/10.3920/WMJ2010.1247Oshikata A, Takezawa, T. Development of an oxygenation culture method for activating the liver-specific functions of HepG2 cells utilizing a collagen vitrigel membrane chamber. Cytotechnology. 2015; 68(5):1801–1811. https://doi.org/10.1007/s10616-015-9934-1Pinton P, Oswald I. Effect of Deoxynivalenol and Other Type B Trichothecenes on the Intestine: A Review. Toxins. 2014; 6(5):1615-1643. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052256/Juan A, Berrada H, Font G, Ruiz M. Evaluation of acute toxicity and genotoxicity of DON, 3-ADON and 15-ADON in HepG2 cells. Toxicology Letters. 2017; 280S: S254-S266.Kupcsik L. Estimation of Cell Number Based on Metabolic Activity: The MTT Reduction Assay. Mammalian Cell Viability. Methods Mol Biol. 2011; 740:13–19. https://doi.org/10.1007/978-1-61779-108-6_3Jaimes N, Salmen S, Colmenares M, Burgos A, Tamayo L, Mendoza V, et al. Efecto citotóxico de los compuestos de inclusión de paladio (II) en la beta-ciclodextrina. Biomédica. 2016; 36(4):603-611. https://doi.org/10.7705/biomedica.v36i4.2880Dinu D, Bodea G, Ceapa C, Munteanu M, Roming F, Serban A, et al. Adapted response of the antioxidant defense system to oxidative stress induced by deoxynivalenol in Hek-293 cells. Toxicon. 2011; 57(7-8):1023–1032. https://doi.org/10.1016/j.toxicon.2011.04.006Alassane I, Kolf M, Gauthier T, Abrami R, Abiola F, Oswald I. New insights into mycotoxin mixtures: the toxicity of low doses of Type B trichothecenes on intestinal epithelial cells is synergistic. Toxicol Appl Pharmacol. 2013; 272(1):191–198. https://doi.org/10.1016/j.taap.2013.05.023Fernández C, Elmo L, Waldner T, Ruiz M. Cytotoxic effects induced by patulin, deoxynivalenol and toxin T2 individually and in combination in hepatic cells (HepG2). Food Chem Toxicol. 2018; 120:12–23. https://doi.org/10.1016/j.fct.2018.06.019Lei Y, Guanghui Z, Xi W, Yingting W, Xialu L, Fangfang Y, et al. Cellular responses to T-2 toxin and/or deoxynivalenol that induce cartilage damage are not specific to chondrocytes. Sci Rep. 2017; 7(2231):1-14. https://www.nature.com/articles/s41598-017-02568-5Mikami O, Yamaguchi H, Murata H, Nakajima Y, Miyazaki S. Induction of apoptotic lesions in liver and lymphoid tissues and modulation of cytokine mRNA expression by acute exposure to deoxynivalenol in piglets. J Vet Sci. 2010; 11(2):107-113. https://dx.doi.org/10.4142%2Fjvs.2010.11.2.107Ma Y, Zhang A, Shi Z, He C, Ding J, Wang X, et al. A mitochondria-mediated apoptotic pathway induced by deoxynivalenol in human colon cancer cells. Toxicol in Vitro. 2012; 26(3):414–420. https://doi.org/10.1016/j.tiv.2012.01.010https://revistamvz.unicordoba.edu.co/article/download/e2080/3406https://revistamvz.unicordoba.edu.co/article/download/e2080/3407https://revistamvz.unicordoba.edu.co/article/download/e2080/3539https://revistamvz.unicordoba.edu.co/article/download/e2080/3541https://revistamvz.unicordoba.edu.co/article/download/e2080/3540https://revistamvz.unicordoba.edu.co/article/download/e2080/3542https://revistamvz.unicordoba.edu.co/article/download/e2080/3408https://revistamvz.unicordoba.edu.co/article/download/e2080/3409Núm. 3 , Año 2021 : Revista MVZ Córdoba Volumen 26(3) Septiembre-Diciembre 2021e20803e208026Revista MVZ CórdobaPublicationOREORE.xmltext/xml3350https://repositorio.unicordoba.edu.co/bitstreams/8faff4d9-9434-4517-b292-ebe35fcc7051/downloadf66a664e13573d9233fea00083f9622bMD51ucordoba/6091oai:repositorio.unicordoba.edu.co:ucordoba/60912023-10-06 00:46:34.288https://creativecommons.org/licenses/by-nc-sa/4.0/Harold Duván Garzón-González, Nancy Jaimes-Mendez, Liliana Rojas-Contreras, Siham Salmen-Halabi, Manuel Alejandro Gil-Durán - 2021metadata.onlyhttps://repositorio.unicordoba.edu.coRepositorio Universidad de Córdobabdigital@metabiblioteca.com