Correlation of tryptophan metabolites with connectivity of extended central reward network in healthy subjects.

OBJECTIVE:A growing body of preclinical and clinical literature suggests that brain-gut-microbiota interactions play an important role in human health and disease, including hedonic food intake and obesity. We performed a tripartite network analysis based on graph theory to test the hypothesis that...

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Main Authors: Vadim Osadchiy, Jennifer S Labus, Arpana Gupta, Jonathan Jacobs, Cody Ashe-McNalley, Elaine Y Hsiao, Emeran A Mayer
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC6078307?pdf=render
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spelling doaj-a18b15ec3f804ad193d994ed84928ca72020-11-25T02:31:05ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01138e020177210.1371/journal.pone.0201772Correlation of tryptophan metabolites with connectivity of extended central reward network in healthy subjects.Vadim OsadchiyJennifer S LabusArpana GuptaJonathan JacobsCody Ashe-McNalleyElaine Y HsiaoEmeran A MayerOBJECTIVE:A growing body of preclinical and clinical literature suggests that brain-gut-microbiota interactions play an important role in human health and disease, including hedonic food intake and obesity. We performed a tripartite network analysis based on graph theory to test the hypothesis that microbiota-derived fecal metabolites are associated with connectivity of key regions of the brain's extended reward network and clinical measures related to obesity. METHODS:DTI and resting state fMRI imaging was obtained from 63 healthy subjects with and without elevated body mass index (BMI) (29 males and 34 females). Subjects submitted fecal samples, completed questionnaires to assess anxiety and food addiction, and BMI was recorded. RESULTS:The study results demonstrate associations between fecal microbiota-derived indole metabolites (indole, indoleacetic acid, and skatole) with measures of functional and anatomical connectivity of the amygdala, nucleus accumbens, and anterior insula, in addition to BMI, food addiction scores (YFAS) and anxiety symptom scores (HAD Anxiety). CONCLUSIONS:The findings support the hypothesis that gut microbiota-derived indole metabolites may influence hedonic food intake and obesity by acting on the extended reward network, specifically the amygdala-nucleus accumbens circuit and the amygdala-anterior insula circuit. These cross sectional, data-driven results provide valuable information for future mechanistic studies.http://europepmc.org/articles/PMC6078307?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Vadim Osadchiy
Jennifer S Labus
Arpana Gupta
Jonathan Jacobs
Cody Ashe-McNalley
Elaine Y Hsiao
Emeran A Mayer
spellingShingle Vadim Osadchiy
Jennifer S Labus
Arpana Gupta
Jonathan Jacobs
Cody Ashe-McNalley
Elaine Y Hsiao
Emeran A Mayer
Correlation of tryptophan metabolites with connectivity of extended central reward network in healthy subjects.
PLoS ONE
author_facet Vadim Osadchiy
Jennifer S Labus
Arpana Gupta
Jonathan Jacobs
Cody Ashe-McNalley
Elaine Y Hsiao
Emeran A Mayer
author_sort Vadim Osadchiy
title Correlation of tryptophan metabolites with connectivity of extended central reward network in healthy subjects.
title_short Correlation of tryptophan metabolites with connectivity of extended central reward network in healthy subjects.
title_full Correlation of tryptophan metabolites with connectivity of extended central reward network in healthy subjects.
title_fullStr Correlation of tryptophan metabolites with connectivity of extended central reward network in healthy subjects.
title_full_unstemmed Correlation of tryptophan metabolites with connectivity of extended central reward network in healthy subjects.
title_sort correlation of tryptophan metabolites with connectivity of extended central reward network in healthy subjects.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description OBJECTIVE:A growing body of preclinical and clinical literature suggests that brain-gut-microbiota interactions play an important role in human health and disease, including hedonic food intake and obesity. We performed a tripartite network analysis based on graph theory to test the hypothesis that microbiota-derived fecal metabolites are associated with connectivity of key regions of the brain's extended reward network and clinical measures related to obesity. METHODS:DTI and resting state fMRI imaging was obtained from 63 healthy subjects with and without elevated body mass index (BMI) (29 males and 34 females). Subjects submitted fecal samples, completed questionnaires to assess anxiety and food addiction, and BMI was recorded. RESULTS:The study results demonstrate associations between fecal microbiota-derived indole metabolites (indole, indoleacetic acid, and skatole) with measures of functional and anatomical connectivity of the amygdala, nucleus accumbens, and anterior insula, in addition to BMI, food addiction scores (YFAS) and anxiety symptom scores (HAD Anxiety). CONCLUSIONS:The findings support the hypothesis that gut microbiota-derived indole metabolites may influence hedonic food intake and obesity by acting on the extended reward network, specifically the amygdala-nucleus accumbens circuit and the amygdala-anterior insula circuit. These cross sectional, data-driven results provide valuable information for future mechanistic studies.
url http://europepmc.org/articles/PMC6078307?pdf=render
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