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
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_14220067_v12_n10_p6936_Calzadilla

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oai_identifier_str paperaa:paper_14220067_v12_n10_p6936_Calzadilla
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling 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 Int. J. Mol. Sci. 2011;12(10):6936-6951
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str 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
repository.mail.fl_str_mv ana@bl.fcen.uba.ar
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