N-acetylcysteine reduces markers of differentiation in 3T3-L1 adipocytes
- Autores
- Calzadilla, P.; Sapochnik, D.; Cosentino, S.; Diz, V.; Dicelio, L.; Calvo, J.C.; Guerra, L.N.
- Año de publicación
- 2011
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Oxidative stress plays a critical role in the pathogenesis of diabetes, hypertension and atherosclerosis. Some authors reported that fat accumulation correlates to systemic oxidative stress in humans and mice, but the relationship of lipid production and oxidative metabolism is still unclear. In our laboratory we used 3T3-L1 preadipocytes, which are able to differentiate into mature adipocytes and accumulate lipids, as obesity model. We showed that intracellular reactive oxygen species (ROS) and antioxidant enzymes superoxide dismutase (SOD) and glutathione peroxidase (GPx) activities increased in parallel with fat accumulation. Meanwhile N-acetylcysteine (NAC), a well known antioxidant and Glutathione (GSH) precursor, inhibited ROS levels as well as fat accumulation in a concentration-dependent manner. NAC also inhibited both adipogenic transcription factors CCAAT/enhancer binding protein beta (C/EBP) and peroxisomal proliferator activated receptor gamma (PPAR β) expression; we suggested that intracellular GSH content could be responsible for these effects. © 2011 by the authors; licensee MDPI, Basel, Switzerland.
Fil:Calzadilla, P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Sapochnik, D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Cosentino, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Diz, V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Dicelio, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Calvo, J.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Guerra, L.N. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. - Fuente
- Int. J. Mol. Sci. 2011;12(10):6936-6951
- Materia
-
Adipocyte differentiation
NAC
Triglyceride
acetylcysteine
beta actin
CCAAT enhancer binding protein
copper zinc superoxide dismutase
glutathione peroxidase
glutathione peroxidase 1
insulin receptor
manganese superoxide dismutase
metallothionein
peroxisome proliferator activated receptor gamma
protein kinase B
reactive oxygen metabolite
somatomedin C
superoxide dismutase
triacylglycerol
acetylcysteine
biological marker
CCAAT enhancer binding protein beta
glutathione
glutathione peroxidase
peroxisome proliferator activated receptor gamma
reactive oxygen metabolite
superoxide dismutase
triacylglycerol
adipocyte
aerobic metabolism
article
cell culture
cell differentiation
concentration response
controlled study
culture medium
DNA content
down regulation
enzyme activity
enzyme assay
human
human cell
lipid peroxidation
lipid storage
low drug dose
obesity
oxidative stress
protein content
protein expression
protein phosphorylation
Western blotting
3T3 cell line
adipocyte
animal
cell differentiation
cytology
metabolism
mouse
Mus
3T3-L1 Cells
Acetylcysteine
Adipocytes
Animals
Biological Markers
CCAAT-Enhancer-Binding Protein-beta
Cell Differentiation
Glutathione
Glutathione Peroxidase
Mice
PPAR gamma
Reactive Oxygen Species
Superoxide Dismutase
Triglycerides - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/2.5/ar
- Repositorio
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_14220067_v12_n10_p6936_Calzadilla
Ver los metadatos del registro completo
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N-acetylcysteine reduces markers of differentiation in 3T3-L1 adipocytesCalzadilla, P.Sapochnik, D.Cosentino, S.Diz, V.Dicelio, L.Calvo, J.C.Guerra, L.N.Adipocyte differentiationNACTriglycerideacetylcysteinebeta actinCCAAT enhancer binding proteincopper zinc superoxide dismutaseglutathione peroxidaseglutathione peroxidase 1insulin receptormanganese superoxide dismutasemetallothioneinperoxisome proliferator activated receptor gammaprotein kinase Breactive oxygen metabolitesomatomedin Csuperoxide dismutasetriacylglycerolacetylcysteinebiological markerCCAAT enhancer binding protein betaglutathioneglutathione peroxidaseperoxisome proliferator activated receptor gammareactive oxygen metabolitesuperoxide dismutasetriacylglyceroladipocyteaerobic metabolismarticlecell culturecell differentiationconcentration responsecontrolled studyculture mediumDNA contentdown regulationenzyme activityenzyme assayhumanhuman celllipid peroxidationlipid storagelow drug doseobesityoxidative stressprotein contentprotein expressionprotein phosphorylationWestern blotting3T3 cell lineadipocyteanimalcell differentiationcytologymetabolismmouseMus3T3-L1 CellsAcetylcysteineAdipocytesAnimalsBiological MarkersCCAAT-Enhancer-Binding Protein-betaCell DifferentiationGlutathioneGlutathione PeroxidaseMicePPAR gammaReactive Oxygen SpeciesSuperoxide DismutaseTriglyceridesOxidative stress plays a critical role in the pathogenesis of diabetes, hypertension and atherosclerosis. Some authors reported that fat accumulation correlates to systemic oxidative stress in humans and mice, but the relationship of lipid production and oxidative metabolism is still unclear. In our laboratory we used 3T3-L1 preadipocytes, which are able to differentiate into mature adipocytes and accumulate lipids, as obesity model. We showed that intracellular reactive oxygen species (ROS) and antioxidant enzymes superoxide dismutase (SOD) and glutathione peroxidase (GPx) activities increased in parallel with fat accumulation. Meanwhile N-acetylcysteine (NAC), a well known antioxidant and Glutathione (GSH) precursor, inhibited ROS levels as well as fat accumulation in a concentration-dependent manner. NAC also inhibited both adipogenic transcription factors CCAAT/enhancer binding protein beta (C/EBP) and peroxisomal proliferator activated receptor gamma (PPAR β) expression; we suggested that intracellular GSH content could be responsible for these effects. © 2011 by the authors; licensee MDPI, Basel, Switzerland.Fil:Calzadilla, P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Sapochnik, D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Cosentino, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Diz, V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Dicelio, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Calvo, J.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Guerra, L.N. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.2011info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_14220067_v12_n10_p6936_CalzadillaInt. J. Mol. Sci. 2011;12(10):6936-6951reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-09-18T10:09:08Zpaperaa:paper_14220067_v12_n10_p6936_CalzadillaInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-09-18 10:09:09.15Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse |
dc.title.none.fl_str_mv |
N-acetylcysteine reduces markers of differentiation in 3T3-L1 adipocytes |
title |
N-acetylcysteine reduces markers of differentiation in 3T3-L1 adipocytes |
spellingShingle |
N-acetylcysteine reduces markers of differentiation in 3T3-L1 adipocytes Calzadilla, P. Adipocyte differentiation NAC Triglyceride acetylcysteine beta actin CCAAT enhancer binding protein copper zinc superoxide dismutase glutathione peroxidase glutathione peroxidase 1 insulin receptor manganese superoxide dismutase metallothionein peroxisome proliferator activated receptor gamma protein kinase B reactive oxygen metabolite somatomedin C superoxide dismutase triacylglycerol acetylcysteine biological marker CCAAT enhancer binding protein beta glutathione glutathione peroxidase peroxisome proliferator activated receptor gamma reactive oxygen metabolite superoxide dismutase triacylglycerol adipocyte aerobic metabolism article cell culture cell differentiation concentration response controlled study culture medium DNA content down regulation enzyme activity enzyme assay human human cell lipid peroxidation lipid storage low drug dose obesity oxidative stress protein content protein expression protein phosphorylation Western blotting 3T3 cell line adipocyte animal cell differentiation cytology metabolism mouse Mus 3T3-L1 Cells Acetylcysteine Adipocytes Animals Biological Markers CCAAT-Enhancer-Binding Protein-beta Cell Differentiation Glutathione Glutathione Peroxidase Mice PPAR gamma Reactive Oxygen Species Superoxide Dismutase Triglycerides |
title_short |
N-acetylcysteine reduces markers of differentiation in 3T3-L1 adipocytes |
title_full |
N-acetylcysteine reduces markers of differentiation in 3T3-L1 adipocytes |
title_fullStr |
N-acetylcysteine reduces markers of differentiation in 3T3-L1 adipocytes |
title_full_unstemmed |
N-acetylcysteine reduces markers of differentiation in 3T3-L1 adipocytes |
title_sort |
N-acetylcysteine reduces markers of differentiation in 3T3-L1 adipocytes |
dc.creator.none.fl_str_mv |
Calzadilla, P. Sapochnik, D. Cosentino, S. Diz, V. Dicelio, L. Calvo, J.C. Guerra, L.N. |
author |
Calzadilla, P. |
author_facet |
Calzadilla, P. Sapochnik, D. Cosentino, S. Diz, V. Dicelio, L. Calvo, J.C. Guerra, L.N. |
author_role |
author |
author2 |
Sapochnik, D. Cosentino, S. Diz, V. Dicelio, L. Calvo, J.C. Guerra, L.N. |
author2_role |
author author author author author author |
dc.subject.none.fl_str_mv |
Adipocyte differentiation NAC Triglyceride acetylcysteine beta actin CCAAT enhancer binding protein copper zinc superoxide dismutase glutathione peroxidase glutathione peroxidase 1 insulin receptor manganese superoxide dismutase metallothionein peroxisome proliferator activated receptor gamma protein kinase B reactive oxygen metabolite somatomedin C superoxide dismutase triacylglycerol acetylcysteine biological marker CCAAT enhancer binding protein beta glutathione glutathione peroxidase peroxisome proliferator activated receptor gamma reactive oxygen metabolite superoxide dismutase triacylglycerol adipocyte aerobic metabolism article cell culture cell differentiation concentration response controlled study culture medium DNA content down regulation enzyme activity enzyme assay human human cell lipid peroxidation lipid storage low drug dose obesity oxidative stress protein content protein expression protein phosphorylation Western blotting 3T3 cell line adipocyte animal cell differentiation cytology metabolism mouse Mus 3T3-L1 Cells Acetylcysteine Adipocytes Animals Biological Markers CCAAT-Enhancer-Binding Protein-beta Cell Differentiation Glutathione Glutathione Peroxidase Mice PPAR gamma Reactive Oxygen Species Superoxide Dismutase Triglycerides |
topic |
Adipocyte differentiation NAC Triglyceride acetylcysteine beta actin CCAAT enhancer binding protein copper zinc superoxide dismutase glutathione peroxidase glutathione peroxidase 1 insulin receptor manganese superoxide dismutase metallothionein peroxisome proliferator activated receptor gamma protein kinase B reactive oxygen metabolite somatomedin C superoxide dismutase triacylglycerol acetylcysteine biological marker CCAAT enhancer binding protein beta glutathione glutathione peroxidase peroxisome proliferator activated receptor gamma reactive oxygen metabolite superoxide dismutase triacylglycerol adipocyte aerobic metabolism article cell culture cell differentiation concentration response controlled study culture medium DNA content down regulation enzyme activity enzyme assay human human cell lipid peroxidation lipid storage low drug dose obesity oxidative stress protein content protein expression protein phosphorylation Western blotting 3T3 cell line adipocyte animal cell differentiation cytology metabolism mouse Mus 3T3-L1 Cells Acetylcysteine Adipocytes Animals Biological Markers CCAAT-Enhancer-Binding Protein-beta Cell Differentiation Glutathione Glutathione Peroxidase Mice PPAR gamma Reactive Oxygen Species Superoxide Dismutase Triglycerides |
dc.description.none.fl_txt_mv |
Oxidative stress plays a critical role in the pathogenesis of diabetes, hypertension and atherosclerosis. Some authors reported that fat accumulation correlates to systemic oxidative stress in humans and mice, but the relationship of lipid production and oxidative metabolism is still unclear. In our laboratory we used 3T3-L1 preadipocytes, which are able to differentiate into mature adipocytes and accumulate lipids, as obesity model. We showed that intracellular reactive oxygen species (ROS) and antioxidant enzymes superoxide dismutase (SOD) and glutathione peroxidase (GPx) activities increased in parallel with fat accumulation. Meanwhile N-acetylcysteine (NAC), a well known antioxidant and Glutathione (GSH) precursor, inhibited ROS levels as well as fat accumulation in a concentration-dependent manner. NAC also inhibited both adipogenic transcription factors CCAAT/enhancer binding protein beta (C/EBP) and peroxisomal proliferator activated receptor gamma (PPAR β) expression; we suggested that intracellular GSH content could be responsible for these effects. © 2011 by the authors; licensee MDPI, Basel, Switzerland. Fil:Calzadilla, P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Sapochnik, D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Cosentino, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Diz, V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Dicelio, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Calvo, J.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Guerra, L.N. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. |
description |
Oxidative stress plays a critical role in the pathogenesis of diabetes, hypertension and atherosclerosis. Some authors reported that fat accumulation correlates to systemic oxidative stress in humans and mice, but the relationship of lipid production and oxidative metabolism is still unclear. In our laboratory we used 3T3-L1 preadipocytes, which are able to differentiate into mature adipocytes and accumulate lipids, as obesity model. We showed that intracellular reactive oxygen species (ROS) and antioxidant enzymes superoxide dismutase (SOD) and glutathione peroxidase (GPx) activities increased in parallel with fat accumulation. Meanwhile N-acetylcysteine (NAC), a well known antioxidant and Glutathione (GSH) precursor, inhibited ROS levels as well as fat accumulation in a concentration-dependent manner. NAC also inhibited both adipogenic transcription factors CCAAT/enhancer binding protein beta (C/EBP) and peroxisomal proliferator activated receptor gamma (PPAR β) expression; we suggested that intracellular GSH content could be responsible for these effects. © 2011 by the authors; licensee MDPI, Basel, Switzerland. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/20.500.12110/paper_14220067_v12_n10_p6936_Calzadilla |
url |
http://hdl.handle.net/20.500.12110/paper_14220067_v12_n10_p6936_Calzadilla |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by/2.5/ar |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
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Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales |
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UBA-FCEN |
institution |
UBA-FCEN |
repository.name.fl_str_mv |
Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales |
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