Cargando…

A Mouse Model of Diet-Induced Obesity Resembling Most Features of Human Metabolic Syndrome

Increased chicken-derived fat and fructose consumption in the human diet is paralleled by an increasing prevalence of obesity and metabolic syndrome (MS). Herein, we aimed at developing and characterizing a mouse model of diet-induced obesity (DIO) resembling most of the key features of the human MS...

Descripción completa

Detalles Bibliográficos
Autores principales: Della Vedova, Maria C., Muñoz, Marcos D., Santillan, Lucas D., Plateo-Pignatari, Maria G., Germanó, Maria J., Rinaldi Tosi, Martín E., Garcia, Silvina, Gomez, Nidia N., Fornes, Miguel W., Gomez Mejiba, Sandra E., Ramirez, Dario C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5140012/
https://www.ncbi.nlm.nih.gov/pubmed/27980421
http://dx.doi.org/10.4137/NMI.S32907
_version_ 1782472349987110912
author Della Vedova, Maria C.
Muñoz, Marcos D.
Santillan, Lucas D.
Plateo-Pignatari, Maria G.
Germanó, Maria J.
Rinaldi Tosi, Martín E.
Garcia, Silvina
Gomez, Nidia N.
Fornes, Miguel W.
Gomez Mejiba, Sandra E.
Ramirez, Dario C.
author_facet Della Vedova, Maria C.
Muñoz, Marcos D.
Santillan, Lucas D.
Plateo-Pignatari, Maria G.
Germanó, Maria J.
Rinaldi Tosi, Martín E.
Garcia, Silvina
Gomez, Nidia N.
Fornes, Miguel W.
Gomez Mejiba, Sandra E.
Ramirez, Dario C.
author_sort Della Vedova, Maria C.
collection PubMed
description Increased chicken-derived fat and fructose consumption in the human diet is paralleled by an increasing prevalence of obesity and metabolic syndrome (MS). Herein, we aimed at developing and characterizing a mouse model of diet-induced obesity (DIO) resembling most of the key features of the human MS. To accomplish this, we fed male C57BL/6J mice for 4, 8, 12, and 16 weeks with either a low-fat diet (LFD) or a high-chicken-fat diet (HFD) and tap water with or without 10% fructose (F). This experimental design resulted in the following four experimental groups: LFD, LFD + F, HFD, and HFD + F. Over the feeding period, and on a weekly basis, the HFD + F group had more caloric intake and gained more weight than the other experimental groups. Compared to the other groups, and at the end of the feeding period, the HFD + F group had a higher adipogenic index, total cholesterol, low-density lipoprotein cholesterol, fasting basal glycemia, insulin resistance, hypertension, and atherogenic index and showed steatohepatitis and systemic oxidative stress/inflammation. A mouse model of DIO that will allow us to study the effect of MS in different organs and systems has been developed and characterized.
format Online
Article
Text
id pubmed-5140012
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Libertas Academica
record_format MEDLINE/PubMed
spelling pubmed-51400122016-12-15 A Mouse Model of Diet-Induced Obesity Resembling Most Features of Human Metabolic Syndrome Della Vedova, Maria C. Muñoz, Marcos D. Santillan, Lucas D. Plateo-Pignatari, Maria G. Germanó, Maria J. Rinaldi Tosi, Martín E. Garcia, Silvina Gomez, Nidia N. Fornes, Miguel W. Gomez Mejiba, Sandra E. Ramirez, Dario C. Nutr Metab Insights Original Research Increased chicken-derived fat and fructose consumption in the human diet is paralleled by an increasing prevalence of obesity and metabolic syndrome (MS). Herein, we aimed at developing and characterizing a mouse model of diet-induced obesity (DIO) resembling most of the key features of the human MS. To accomplish this, we fed male C57BL/6J mice for 4, 8, 12, and 16 weeks with either a low-fat diet (LFD) or a high-chicken-fat diet (HFD) and tap water with or without 10% fructose (F). This experimental design resulted in the following four experimental groups: LFD, LFD + F, HFD, and HFD + F. Over the feeding period, and on a weekly basis, the HFD + F group had more caloric intake and gained more weight than the other experimental groups. Compared to the other groups, and at the end of the feeding period, the HFD + F group had a higher adipogenic index, total cholesterol, low-density lipoprotein cholesterol, fasting basal glycemia, insulin resistance, hypertension, and atherogenic index and showed steatohepatitis and systemic oxidative stress/inflammation. A mouse model of DIO that will allow us to study the effect of MS in different organs and systems has been developed and characterized. Libertas Academica 2016-12-05 /pmc/articles/PMC5140012/ /pubmed/27980421 http://dx.doi.org/10.4137/NMI.S32907 Text en © 2016 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License.
spellingShingle Original Research
Della Vedova, Maria C.
Muñoz, Marcos D.
Santillan, Lucas D.
Plateo-Pignatari, Maria G.
Germanó, Maria J.
Rinaldi Tosi, Martín E.
Garcia, Silvina
Gomez, Nidia N.
Fornes, Miguel W.
Gomez Mejiba, Sandra E.
Ramirez, Dario C.
A Mouse Model of Diet-Induced Obesity Resembling Most Features of Human Metabolic Syndrome
title A Mouse Model of Diet-Induced Obesity Resembling Most Features of Human Metabolic Syndrome
title_full A Mouse Model of Diet-Induced Obesity Resembling Most Features of Human Metabolic Syndrome
title_fullStr A Mouse Model of Diet-Induced Obesity Resembling Most Features of Human Metabolic Syndrome
title_full_unstemmed A Mouse Model of Diet-Induced Obesity Resembling Most Features of Human Metabolic Syndrome
title_short A Mouse Model of Diet-Induced Obesity Resembling Most Features of Human Metabolic Syndrome
title_sort mouse model of diet-induced obesity resembling most features of human metabolic syndrome
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5140012/
https://www.ncbi.nlm.nih.gov/pubmed/27980421
http://dx.doi.org/10.4137/NMI.S32907
work_keys_str_mv AT dellavedovamariac amousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT munozmarcosd amousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT santillanlucasd amousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT plateopignatarimariag amousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT germanomariaj amousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT rinalditosimartine amousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT garciasilvina amousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT gomeznidian amousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT fornesmiguelw amousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT gomezmejibasandrae amousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT ramirezdarioc amousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT dellavedovamariac mousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT munozmarcosd mousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT santillanlucasd mousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT plateopignatarimariag mousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT germanomariaj mousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT rinalditosimartine mousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT garciasilvina mousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT gomeznidian mousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT fornesmiguelw mousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT gomezmejibasandrae mousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome
AT ramirezdarioc mousemodelofdietinducedobesityresemblingmostfeaturesofhumanmetabolicsyndrome