Cargando…

Dietary fat and gut microbiota interactions determine diet-induced obesity in mice

OBJECTIVE: Gut microbiota may promote positive energy balance; however, germfree mice can be either resistant or susceptible to diet-induced obesity (DIO) depending on the type of dietary intervention. We here sought to identify the dietary constituents that determine the susceptibility to body fat...

Descripción completa

Detalles Bibliográficos
Autores principales: Kübeck, Raphaela, Bonet-Ripoll, Catalina, Hoffmann, Christina, Walker, Alesia, Müller, Veronika Maria, Schüppel, Valentina Luise, Lagkouvardos, Ilias, Scholz, Birgit, Engel, Karl-Heinz, Daniel, Hannelore, Schmitt-Kopplin, Philippe, Haller, Dirk, Clavel, Thomas, Klingenspor, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123202/
https://www.ncbi.nlm.nih.gov/pubmed/27900259
http://dx.doi.org/10.1016/j.molmet.2016.10.001
_version_ 1782469684334952448
author Kübeck, Raphaela
Bonet-Ripoll, Catalina
Hoffmann, Christina
Walker, Alesia
Müller, Veronika Maria
Schüppel, Valentina Luise
Lagkouvardos, Ilias
Scholz, Birgit
Engel, Karl-Heinz
Daniel, Hannelore
Schmitt-Kopplin, Philippe
Haller, Dirk
Clavel, Thomas
Klingenspor, Martin
author_facet Kübeck, Raphaela
Bonet-Ripoll, Catalina
Hoffmann, Christina
Walker, Alesia
Müller, Veronika Maria
Schüppel, Valentina Luise
Lagkouvardos, Ilias
Scholz, Birgit
Engel, Karl-Heinz
Daniel, Hannelore
Schmitt-Kopplin, Philippe
Haller, Dirk
Clavel, Thomas
Klingenspor, Martin
author_sort Kübeck, Raphaela
collection PubMed
description OBJECTIVE: Gut microbiota may promote positive energy balance; however, germfree mice can be either resistant or susceptible to diet-induced obesity (DIO) depending on the type of dietary intervention. We here sought to identify the dietary constituents that determine the susceptibility to body fat accretion in germfree (GF) mice. METHODS: GF and specific pathogen free (SPF) male C57BL/6N mice were fed high-fat diets either based on lard or palm oil for 4 wks. Mice were metabolically characterized at the end of the feeding trial. FT-ICR-MS and UPLC-TOF-MS were used for cecal as well as hepatic metabolite profiling and cecal bile acids quantification, respectively. Hepatic gene expression was examined by qRT-PCR and cecal gut microbiota of SPF mice was analyzed by high-throughput 16S rRNA gene sequencing. RESULTS: GF mice, but not SPF mice, were completely DIO resistant when fed a cholesterol-rich lard-based high-fat diet, whereas on a cholesterol-free palm oil-based high-fat diet, DIO was independent of gut microbiota. In GF lard-fed mice, DIO resistance was conveyed by increased energy expenditure, preferential carbohydrate oxidation, and increased fecal fat and energy excretion. Cecal metabolite profiling revealed a shift in bile acid and steroid metabolites in these lean mice, with a significant rise in 17β-estradiol, which is known to stimulate energy expenditure and interfere with bile acid metabolism. Decreased cecal bile acid levels were associated with decreased hepatic expression of genes involved in bile acid synthesis. These metabolic adaptations were largely attenuated in GF mice fed the palm-oil based high-fat diet. We propose that an interaction of gut microbiota and cholesterol metabolism is essential for fat accretion in normal SPF mice fed cholesterol-rich lard as the main dietary fat source. This is supported by a positive correlation between bile acid levels and specific bacteria of the order Clostridiales (phylum Firmicutes) as a characteristic feature of normal SPF mice fed lard. CONCLUSIONS: In conclusion, our study identified dietary cholesterol as a candidate ingredient affecting the crosstalk between gut microbiota and host metabolism.
format Online
Article
Text
id pubmed-5123202
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-51232022016-11-29 Dietary fat and gut microbiota interactions determine diet-induced obesity in mice Kübeck, Raphaela Bonet-Ripoll, Catalina Hoffmann, Christina Walker, Alesia Müller, Veronika Maria Schüppel, Valentina Luise Lagkouvardos, Ilias Scholz, Birgit Engel, Karl-Heinz Daniel, Hannelore Schmitt-Kopplin, Philippe Haller, Dirk Clavel, Thomas Klingenspor, Martin Mol Metab Original Article OBJECTIVE: Gut microbiota may promote positive energy balance; however, germfree mice can be either resistant or susceptible to diet-induced obesity (DIO) depending on the type of dietary intervention. We here sought to identify the dietary constituents that determine the susceptibility to body fat accretion in germfree (GF) mice. METHODS: GF and specific pathogen free (SPF) male C57BL/6N mice were fed high-fat diets either based on lard or palm oil for 4 wks. Mice were metabolically characterized at the end of the feeding trial. FT-ICR-MS and UPLC-TOF-MS were used for cecal as well as hepatic metabolite profiling and cecal bile acids quantification, respectively. Hepatic gene expression was examined by qRT-PCR and cecal gut microbiota of SPF mice was analyzed by high-throughput 16S rRNA gene sequencing. RESULTS: GF mice, but not SPF mice, were completely DIO resistant when fed a cholesterol-rich lard-based high-fat diet, whereas on a cholesterol-free palm oil-based high-fat diet, DIO was independent of gut microbiota. In GF lard-fed mice, DIO resistance was conveyed by increased energy expenditure, preferential carbohydrate oxidation, and increased fecal fat and energy excretion. Cecal metabolite profiling revealed a shift in bile acid and steroid metabolites in these lean mice, with a significant rise in 17β-estradiol, which is known to stimulate energy expenditure and interfere with bile acid metabolism. Decreased cecal bile acid levels were associated with decreased hepatic expression of genes involved in bile acid synthesis. These metabolic adaptations were largely attenuated in GF mice fed the palm-oil based high-fat diet. We propose that an interaction of gut microbiota and cholesterol metabolism is essential for fat accretion in normal SPF mice fed cholesterol-rich lard as the main dietary fat source. This is supported by a positive correlation between bile acid levels and specific bacteria of the order Clostridiales (phylum Firmicutes) as a characteristic feature of normal SPF mice fed lard. CONCLUSIONS: In conclusion, our study identified dietary cholesterol as a candidate ingredient affecting the crosstalk between gut microbiota and host metabolism. Elsevier 2016-10-13 /pmc/articles/PMC5123202/ /pubmed/27900259 http://dx.doi.org/10.1016/j.molmet.2016.10.001 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Kübeck, Raphaela
Bonet-Ripoll, Catalina
Hoffmann, Christina
Walker, Alesia
Müller, Veronika Maria
Schüppel, Valentina Luise
Lagkouvardos, Ilias
Scholz, Birgit
Engel, Karl-Heinz
Daniel, Hannelore
Schmitt-Kopplin, Philippe
Haller, Dirk
Clavel, Thomas
Klingenspor, Martin
Dietary fat and gut microbiota interactions determine diet-induced obesity in mice
title Dietary fat and gut microbiota interactions determine diet-induced obesity in mice
title_full Dietary fat and gut microbiota interactions determine diet-induced obesity in mice
title_fullStr Dietary fat and gut microbiota interactions determine diet-induced obesity in mice
title_full_unstemmed Dietary fat and gut microbiota interactions determine diet-induced obesity in mice
title_short Dietary fat and gut microbiota interactions determine diet-induced obesity in mice
title_sort dietary fat and gut microbiota interactions determine diet-induced obesity in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123202/
https://www.ncbi.nlm.nih.gov/pubmed/27900259
http://dx.doi.org/10.1016/j.molmet.2016.10.001
work_keys_str_mv AT kubeckraphaela dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT bonetripollcatalina dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT hoffmannchristina dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT walkeralesia dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT mullerveronikamaria dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT schuppelvalentinaluise dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT lagkouvardosilias dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT scholzbirgit dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT engelkarlheinz dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT danielhannelore dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT schmittkopplinphilippe dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT hallerdirk dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT clavelthomas dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice
AT klingenspormartin dietaryfatandgutmicrobiotainteractionsdeterminedietinducedobesityinmice