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Reprogramming the Human Gut Microbiome Reduces Dietary Energy Harvest
The gut microbiome is emerging as a key modulator of host energy balance(1). We conducted a quantitative bioenergetics study aimed at understanding microbial and host factors contributing to energy balance. We used a Microbiome Enhancer Diet (MBD) to reprogram the gut microbiome by delivering more d...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9901041/ https://www.ncbi.nlm.nih.gov/pubmed/36747835 http://dx.doi.org/10.21203/rs.3.rs-2382790/v1 |
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author | Corbin, Karen D. Carnero, Elvis A. Dirks, Blake Igudesman, Daria Yi, Fanchao Marcus, Andrew Davis, Taylor L. Pratley, Richard E. Rittmann, Bruce E. Krajmalnik-Brown, Rosa Smith, Steven R. |
author_facet | Corbin, Karen D. Carnero, Elvis A. Dirks, Blake Igudesman, Daria Yi, Fanchao Marcus, Andrew Davis, Taylor L. Pratley, Richard E. Rittmann, Bruce E. Krajmalnik-Brown, Rosa Smith, Steven R. |
author_sort | Corbin, Karen D. |
collection | PubMed |
description | The gut microbiome is emerging as a key modulator of host energy balance(1). We conducted a quantitative bioenergetics study aimed at understanding microbial and host factors contributing to energy balance. We used a Microbiome Enhancer Diet (MBD) to reprogram the gut microbiome by delivering more dietary substrates to the colon and randomized healthy participants into a within-subject crossover study with a Western Diet (WD) as a comparator. In a metabolic ward where the environment was strictly controlled, we measured energy intake, energy expenditure, and energy output (fecal, urinary, and methane)(2). The primary endpoint was the within-participant difference in host metabolizable energy between experimental conditions. The MBD led to an additional 116 ± 56 kcals lost in feces daily and thus, lower metabolizable energy for the host by channeling more energy to the colon and microbes. The MBD drove significant shifts in microbial biomass, community structure, and fermentation, with parallel alterations to the host enteroendocrine system and without altering appetite or energy expenditure. Host metabolizable energy on the MBD had quantitatively significant interindividual variability, which was associated with differences in the composition of the gut microbiota experimentally and colonic transit time and short-chain fatty acid absorption in silico. Our results provide key insights into how a diet designed to optimize the gut microbiome lowers host metabolizable energy in healthy humans. |
format | Online Article Text |
id | pubmed-9901041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
spelling | pubmed-99010412023-02-07 Reprogramming the Human Gut Microbiome Reduces Dietary Energy Harvest Corbin, Karen D. Carnero, Elvis A. Dirks, Blake Igudesman, Daria Yi, Fanchao Marcus, Andrew Davis, Taylor L. Pratley, Richard E. Rittmann, Bruce E. Krajmalnik-Brown, Rosa Smith, Steven R. Res Sq Article The gut microbiome is emerging as a key modulator of host energy balance(1). We conducted a quantitative bioenergetics study aimed at understanding microbial and host factors contributing to energy balance. We used a Microbiome Enhancer Diet (MBD) to reprogram the gut microbiome by delivering more dietary substrates to the colon and randomized healthy participants into a within-subject crossover study with a Western Diet (WD) as a comparator. In a metabolic ward where the environment was strictly controlled, we measured energy intake, energy expenditure, and energy output (fecal, urinary, and methane)(2). The primary endpoint was the within-participant difference in host metabolizable energy between experimental conditions. The MBD led to an additional 116 ± 56 kcals lost in feces daily and thus, lower metabolizable energy for the host by channeling more energy to the colon and microbes. The MBD drove significant shifts in microbial biomass, community structure, and fermentation, with parallel alterations to the host enteroendocrine system and without altering appetite or energy expenditure. Host metabolizable energy on the MBD had quantitatively significant interindividual variability, which was associated with differences in the composition of the gut microbiota experimentally and colonic transit time and short-chain fatty acid absorption in silico. Our results provide key insights into how a diet designed to optimize the gut microbiome lowers host metabolizable energy in healthy humans. American Journal Experts 2023-01-25 /pmc/articles/PMC9901041/ /pubmed/36747835 http://dx.doi.org/10.21203/rs.3.rs-2382790/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Corbin, Karen D. Carnero, Elvis A. Dirks, Blake Igudesman, Daria Yi, Fanchao Marcus, Andrew Davis, Taylor L. Pratley, Richard E. Rittmann, Bruce E. Krajmalnik-Brown, Rosa Smith, Steven R. Reprogramming the Human Gut Microbiome Reduces Dietary Energy Harvest |
title | Reprogramming the Human Gut Microbiome Reduces Dietary Energy Harvest |
title_full | Reprogramming the Human Gut Microbiome Reduces Dietary Energy Harvest |
title_fullStr | Reprogramming the Human Gut Microbiome Reduces Dietary Energy Harvest |
title_full_unstemmed | Reprogramming the Human Gut Microbiome Reduces Dietary Energy Harvest |
title_short | Reprogramming the Human Gut Microbiome Reduces Dietary Energy Harvest |
title_sort | reprogramming the human gut microbiome reduces dietary energy harvest |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9901041/ https://www.ncbi.nlm.nih.gov/pubmed/36747835 http://dx.doi.org/10.21203/rs.3.rs-2382790/v1 |
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