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A High Fat/High Sugar Diet Alters the Gastrointestinal Metabolome in a Sex Dependent Manner
The gut metabolome offers insight for identifying the source of diet related pathology. As such, the purpose of this study was to characterize alterations of the gut metabolome in female and male C57BL/6J mice randomly assigned to a standard “chow” diet (CHOW) or a high fat/high sugar diet (HFHS; 45...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589395/ https://www.ncbi.nlm.nih.gov/pubmed/33092034 http://dx.doi.org/10.3390/metabo10100421 |
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author | Letsinger, Ayland C. Menon, Rani Iyer, Anjushree R. Vellers, Heather L. Granados, Jorge Z. Jayaraman, Arul Lightfoot, J. Timothy |
author_facet | Letsinger, Ayland C. Menon, Rani Iyer, Anjushree R. Vellers, Heather L. Granados, Jorge Z. Jayaraman, Arul Lightfoot, J. Timothy |
author_sort | Letsinger, Ayland C. |
collection | PubMed |
description | The gut metabolome offers insight for identifying the source of diet related pathology. As such, the purpose of this study was to characterize alterations of the gut metabolome in female and male C57BL/6J mice randomly assigned to a standard “chow” diet (CHOW) or a high fat/high sugar diet (HFHS; 45% fat and 20% fructose drinking solution) for nine weeks. Cecal metabolites were extracted and an untargeted analysis via LC-MS/MS was performed. Partial Least Sums Discriminate Analysis (PLS-DA) presented significant differences between the two diet groups in a sex-dependent manner. Mann–Whitney U-tests revealed 2443 and 1669 features to be significantly different between diet groups in the females and males, respectively. The majority of altered metabolites were depleted within the cecum of the HFHS fed mice. Metabolic pathways associated with galactose metabolism, leukotriene metabolism, and androgen and estrogen biosynthesis and metabolism were differentially altered with an HFHS diet between sexes. We concluded the immense metabolite depletion and elevation of adverse metabolites associated with the HFHS diet is suggestive of poor gut health. Further, the differential alterations between female and male mice suggests that sex plays an important role in determining the effect of diet on the metabolome and host health. |
format | Online Article Text |
id | pubmed-7589395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75893952020-10-29 A High Fat/High Sugar Diet Alters the Gastrointestinal Metabolome in a Sex Dependent Manner Letsinger, Ayland C. Menon, Rani Iyer, Anjushree R. Vellers, Heather L. Granados, Jorge Z. Jayaraman, Arul Lightfoot, J. Timothy Metabolites Article The gut metabolome offers insight for identifying the source of diet related pathology. As such, the purpose of this study was to characterize alterations of the gut metabolome in female and male C57BL/6J mice randomly assigned to a standard “chow” diet (CHOW) or a high fat/high sugar diet (HFHS; 45% fat and 20% fructose drinking solution) for nine weeks. Cecal metabolites were extracted and an untargeted analysis via LC-MS/MS was performed. Partial Least Sums Discriminate Analysis (PLS-DA) presented significant differences between the two diet groups in a sex-dependent manner. Mann–Whitney U-tests revealed 2443 and 1669 features to be significantly different between diet groups in the females and males, respectively. The majority of altered metabolites were depleted within the cecum of the HFHS fed mice. Metabolic pathways associated with galactose metabolism, leukotriene metabolism, and androgen and estrogen biosynthesis and metabolism were differentially altered with an HFHS diet between sexes. We concluded the immense metabolite depletion and elevation of adverse metabolites associated with the HFHS diet is suggestive of poor gut health. Further, the differential alterations between female and male mice suggests that sex plays an important role in determining the effect of diet on the metabolome and host health. MDPI 2020-10-20 /pmc/articles/PMC7589395/ /pubmed/33092034 http://dx.doi.org/10.3390/metabo10100421 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Letsinger, Ayland C. Menon, Rani Iyer, Anjushree R. Vellers, Heather L. Granados, Jorge Z. Jayaraman, Arul Lightfoot, J. Timothy A High Fat/High Sugar Diet Alters the Gastrointestinal Metabolome in a Sex Dependent Manner |
title | A High Fat/High Sugar Diet Alters the Gastrointestinal Metabolome in a Sex Dependent Manner |
title_full | A High Fat/High Sugar Diet Alters the Gastrointestinal Metabolome in a Sex Dependent Manner |
title_fullStr | A High Fat/High Sugar Diet Alters the Gastrointestinal Metabolome in a Sex Dependent Manner |
title_full_unstemmed | A High Fat/High Sugar Diet Alters the Gastrointestinal Metabolome in a Sex Dependent Manner |
title_short | A High Fat/High Sugar Diet Alters the Gastrointestinal Metabolome in a Sex Dependent Manner |
title_sort | high fat/high sugar diet alters the gastrointestinal metabolome in a sex dependent manner |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589395/ https://www.ncbi.nlm.nih.gov/pubmed/33092034 http://dx.doi.org/10.3390/metabo10100421 |
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