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High-fat diet, microbiome-gut-brain axis signaling, and anxiety-like behavior in male rats
Obesity, associated with the intake of a high-fat diet (HFD), and anxiety are common among those living in modern urban societies. Recent studies suggest a role of microbiome-gut-brain axis signaling, including a role for brain serotonergic systems in the relationship between HFD and anxiety. Eviden...
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Published in: | Biological research 2024-05, Vol.57 (1), p.23-23, Article 23 |
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creator | de Noronha, Sylvana I S Rendeiro de Moraes, Lauro Angelo Gonçalves Hassell, Jr, James E Stamper, Christopher E Arnold, Mathew R Heinze, Jared D Foxx, Christine L Lieb, Margaret M Cler, Kristin E Karns, Bree L Jaekel, Sophia Loupy, Kelsey M Silva, Fernanda C S Chianca-Jr, Deoclécio Alves Lowry, Christopher A de Menezes, Rodrigo Cunha |
description | Obesity, associated with the intake of a high-fat diet (HFD), and anxiety are common among those living in modern urban societies. Recent studies suggest a role of microbiome-gut-brain axis signaling, including a role for brain serotonergic systems in the relationship between HFD and anxiety. Evidence suggests the gut microbiome and the serotonergic brain system together may play an important role in this response. Here we conducted a nine-week HFD protocol in male rats, followed by an analysis of the gut microbiome diversity and community composition, brainstem serotonergic gene expression (tph2, htr1a, and slc6a4), and anxiety-related defensive behavioral responses. We show that HFD intake decreased alpha diversity and altered the community composition of the gut microbiome in association with obesity, increased brainstem tph2, htr1a and slc6a4 mRNA expression, including in the caudal part of the dorsomedial dorsal raphe nucleus (cDRD), a subregion previously associated with stress- and anxiety-related behavioral responses, and, finally, increased anxiety-related defensive behavioral responses. The HFD increased the Firmicutes/Bacteroidetes ratio relative to control diet, as well as higher relative abundances of Blautia, and decreases in Prevotella. We found that tph2, htr1a and slc6a4 mRNA expression were increased in subregions of the dorsal raphe nucleus in the HFD, relative to control diet. Specific bacterial taxa were associated with increased serotonergic gene expression in the cDRD. Thus, we propose that HFD-induced obesity is associated with altered microbiome-gut-serotonergic brain axis signaling, leading to increased anxiety-related defensive behavioral responses in rats. |
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Recent studies suggest a role of microbiome-gut-brain axis signaling, including a role for brain serotonergic systems in the relationship between HFD and anxiety. Evidence suggests the gut microbiome and the serotonergic brain system together may play an important role in this response. Here we conducted a nine-week HFD protocol in male rats, followed by an analysis of the gut microbiome diversity and community composition, brainstem serotonergic gene expression (tph2, htr1a, and slc6a4), and anxiety-related defensive behavioral responses. We show that HFD intake decreased alpha diversity and altered the community composition of the gut microbiome in association with obesity, increased brainstem tph2, htr1a and slc6a4 mRNA expression, including in the caudal part of the dorsomedial dorsal raphe nucleus (cDRD), a subregion previously associated with stress- and anxiety-related behavioral responses, and, finally, increased anxiety-related defensive behavioral responses. The HFD increased the Firmicutes/Bacteroidetes ratio relative to control diet, as well as higher relative abundances of Blautia, and decreases in Prevotella. We found that tph2, htr1a and slc6a4 mRNA expression were increased in subregions of the dorsal raphe nucleus in the HFD, relative to control diet. Specific bacterial taxa were associated with increased serotonergic gene expression in the cDRD. Thus, we propose that HFD-induced obesity is associated with altered microbiome-gut-serotonergic brain axis signaling, leading to increased anxiety-related defensive behavioral responses in rats.</description><identifier>ISSN: 0717-6287</identifier><identifier>ISSN: 0716-9760</identifier><identifier>EISSN: 0717-6287</identifier><identifier>DOI: 10.1186/s40659-024-00505-1</identifier><identifier>PMID: 38705984</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Animals ; Anxiety ; Anxiety - microbiology ; Behavior ; Behavior, Animal - physiology ; Biological diversity ; BIOLOGY ; Body fat ; Brain ; Brain stem ; Brain-Gut Axis - physiology ; Child development ; Community composition ; Comorbidity ; Diet ; Diet, High-Fat - adverse effects ; Dorsal raphe nucleus ; Gastrointestinal Microbiome - physiology ; Gene expression ; Genes ; High fat diet ; Intestinal microflora ; Laboratory animals ; Male ; Microbiome ; Microbiome-gut-brain axis ; Microbiomes ; Obesity ; Obesity - metabolism ; Obesity - microbiology ; Obesity - psychology ; Physiology ; Raphe nuclei ; Rats ; Rats, Sprague-Dawley ; RNA ; Serotonin ; Signal Transduction - physiology</subject><ispartof>Biological research, 2024-05, Vol.57 (1), p.23-23, Article 23</ispartof><rights>2024. The Author(s).</rights><rights>COPYRIGHT 2024 BioMed Central Ltd.</rights><rights>2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2024</rights><rights>This work is licensed under a Creative Commons Attribution 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c588t-34fad47c77acb090fb6739bfd6aa0e3a7ed345e64cc3529047c7bcf530fce76d3</cites><orcidid>0000-0003-0286-0621</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/3054192567?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,24151,25753,27924,27925,37012,37013,38516,43895,44590</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38705984$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Noronha, Sylvana I S Rendeiro</creatorcontrib><creatorcontrib>de Moraes, Lauro Angelo Gonçalves</creatorcontrib><creatorcontrib>Hassell, Jr, James E</creatorcontrib><creatorcontrib>Stamper, Christopher E</creatorcontrib><creatorcontrib>Arnold, Mathew R</creatorcontrib><creatorcontrib>Heinze, Jared D</creatorcontrib><creatorcontrib>Foxx, Christine L</creatorcontrib><creatorcontrib>Lieb, Margaret M</creatorcontrib><creatorcontrib>Cler, Kristin E</creatorcontrib><creatorcontrib>Karns, Bree L</creatorcontrib><creatorcontrib>Jaekel, Sophia</creatorcontrib><creatorcontrib>Loupy, Kelsey M</creatorcontrib><creatorcontrib>Silva, Fernanda C S</creatorcontrib><creatorcontrib>Chianca-Jr, Deoclécio Alves</creatorcontrib><creatorcontrib>Lowry, Christopher A</creatorcontrib><creatorcontrib>de Menezes, Rodrigo Cunha</creatorcontrib><title>High-fat diet, microbiome-gut-brain axis signaling, and anxiety-like behavior in male rats</title><title>Biological research</title><addtitle>Biol Res</addtitle><description>Obesity, associated with the intake of a high-fat diet (HFD), and anxiety are common among those living in modern urban societies. Recent studies suggest a role of microbiome-gut-brain axis signaling, including a role for brain serotonergic systems in the relationship between HFD and anxiety. Evidence suggests the gut microbiome and the serotonergic brain system together may play an important role in this response. Here we conducted a nine-week HFD protocol in male rats, followed by an analysis of the gut microbiome diversity and community composition, brainstem serotonergic gene expression (tph2, htr1a, and slc6a4), and anxiety-related defensive behavioral responses. We show that HFD intake decreased alpha diversity and altered the community composition of the gut microbiome in association with obesity, increased brainstem tph2, htr1a and slc6a4 mRNA expression, including in the caudal part of the dorsomedial dorsal raphe nucleus (cDRD), a subregion previously associated with stress- and anxiety-related behavioral responses, and, finally, increased anxiety-related defensive behavioral responses. The HFD increased the Firmicutes/Bacteroidetes ratio relative to control diet, as well as higher relative abundances of Blautia, and decreases in Prevotella. We found that tph2, htr1a and slc6a4 mRNA expression were increased in subregions of the dorsal raphe nucleus in the HFD, relative to control diet. Specific bacterial taxa were associated with increased serotonergic gene expression in the cDRD. Thus, we propose that HFD-induced obesity is associated with altered microbiome-gut-serotonergic brain axis signaling, leading to increased anxiety-related defensive behavioral responses in rats.</description><subject>Animals</subject><subject>Anxiety</subject><subject>Anxiety - microbiology</subject><subject>Behavior</subject><subject>Behavior, Animal - physiology</subject><subject>Biological diversity</subject><subject>BIOLOGY</subject><subject>Body fat</subject><subject>Brain</subject><subject>Brain stem</subject><subject>Brain-Gut Axis - physiology</subject><subject>Child development</subject><subject>Community composition</subject><subject>Comorbidity</subject><subject>Diet</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Dorsal raphe nucleus</subject><subject>Gastrointestinal Microbiome - physiology</subject><subject>Gene expression</subject><subject>Genes</subject><subject>High fat diet</subject><subject>Intestinal microflora</subject><subject>Laboratory animals</subject><subject>Male</subject><subject>Microbiome</subject><subject>Microbiome-gut-brain axis</subject><subject>Microbiomes</subject><subject>Obesity</subject><subject>Obesity - metabolism</subject><subject>Obesity - microbiology</subject><subject>Obesity - psychology</subject><subject>Physiology</subject><subject>Raphe nuclei</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA</subject><subject>Serotonin</subject><subject>Signal Transduction - physiology</subject><issn>0717-6287</issn><issn>0716-9760</issn><issn>0717-6287</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkl1r1TAcxosobk6_gBdS8EZhnf-8t1cyhroDA8HpjTchzUtPjm2zJe3Yvr05O_NslVJakt_zJHnyFMVbBCcI1fxTosBZUwGmFQADVqFnxSEIJCqOa_H8yf9B8SqlDQBmgPnL4oDUAlhT08Pi97nv1pVTU2m8nY7LwesYWh8GW3XzVLVR-bFUtz6VyXej6v3YHZdqNPm9zYK7qvd_bNnatbrxIZYZHlRvy6im9Lp44VSf7JuH71Hx6-uXn2fn1cX3b6uz04tKs7qeKkKdMlRoIZRuoQHXckGa1hmuFFiihDWEMsup1oThBrZoqx0j4LQV3JCjYrXzNUFt5FX0g4p3Migv7wdC7KSKk9e9lVup5YTmBTWlTV3XjTHaCdNihzmj2etk55W0t32QmzDHfOokL3OWXDaCA855AwDKaWKSBZ93gqu5HazRdpyi6he7WM6Mfi27cCMRyo4Yiezw4cEhhuvZpkkOPmnb92q0YU6SAEMUMwZNRt__h-73lymKGsy4eKS6fBPSjy7khfXWVJ6KhiBEsOCPJ11Q-TE2dyCM1vk8vhB8XAgyM9nbqVNzSnJ1-WPJ4h2by5RStG4fCAK57a7cdVfmLOV9dyXKondPo9xL_pWV_AX6nOVc</recordid><startdate>20240506</startdate><enddate>20240506</enddate><creator>de Noronha, Sylvana I S Rendeiro</creator><creator>de Moraes, Lauro Angelo Gonçalves</creator><creator>Hassell, Jr, James E</creator><creator>Stamper, Christopher E</creator><creator>Arnold, Mathew R</creator><creator>Heinze, Jared D</creator><creator>Foxx, Christine L</creator><creator>Lieb, Margaret M</creator><creator>Cler, Kristin E</creator><creator>Karns, Bree L</creator><creator>Jaekel, Sophia</creator><creator>Loupy, Kelsey M</creator><creator>Silva, Fernanda C S</creator><creator>Chianca-Jr, Deoclécio Alves</creator><creator>Lowry, Christopher A</creator><creator>de Menezes, Rodrigo Cunha</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>Sociedad de Biología de Chile</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>INF</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>GPN</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0286-0621</orcidid></search><sort><creationdate>20240506</creationdate><title>High-fat diet, microbiome-gut-brain axis signaling, and anxiety-like behavior in male rats</title><author>de Noronha, Sylvana I S Rendeiro ; de Moraes, Lauro Angelo Gonçalves ; Hassell, Jr, James E ; Stamper, Christopher E ; Arnold, Mathew R ; Heinze, Jared D ; Foxx, Christine L ; Lieb, Margaret M ; Cler, Kristin E ; Karns, Bree L ; Jaekel, Sophia ; Loupy, Kelsey M ; Silva, Fernanda C S ; Chianca-Jr, Deoclécio Alves ; Lowry, Christopher A ; de Menezes, Rodrigo Cunha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c588t-34fad47c77acb090fb6739bfd6aa0e3a7ed345e64cc3529047c7bcf530fce76d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Anxiety</topic><topic>Anxiety - 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Recent studies suggest a role of microbiome-gut-brain axis signaling, including a role for brain serotonergic systems in the relationship between HFD and anxiety. Evidence suggests the gut microbiome and the serotonergic brain system together may play an important role in this response. Here we conducted a nine-week HFD protocol in male rats, followed by an analysis of the gut microbiome diversity and community composition, brainstem serotonergic gene expression (tph2, htr1a, and slc6a4), and anxiety-related defensive behavioral responses. We show that HFD intake decreased alpha diversity and altered the community composition of the gut microbiome in association with obesity, increased brainstem tph2, htr1a and slc6a4 mRNA expression, including in the caudal part of the dorsomedial dorsal raphe nucleus (cDRD), a subregion previously associated with stress- and anxiety-related behavioral responses, and, finally, increased anxiety-related defensive behavioral responses. The HFD increased the Firmicutes/Bacteroidetes ratio relative to control diet, as well as higher relative abundances of Blautia, and decreases in Prevotella. We found that tph2, htr1a and slc6a4 mRNA expression were increased in subregions of the dorsal raphe nucleus in the HFD, relative to control diet. Specific bacterial taxa were associated with increased serotonergic gene expression in the cDRD. Thus, we propose that HFD-induced obesity is associated with altered microbiome-gut-serotonergic brain axis signaling, leading to increased anxiety-related defensive behavioral responses in rats.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>38705984</pmid><doi>10.1186/s40659-024-00505-1</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-0286-0621</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Anxiety Anxiety - microbiology Behavior Behavior, Animal - physiology Biological diversity BIOLOGY Body fat Brain Brain stem Brain-Gut Axis - physiology Child development Community composition Comorbidity Diet Diet, High-Fat - adverse effects Dorsal raphe nucleus Gastrointestinal Microbiome - physiology Gene expression Genes High fat diet Intestinal microflora Laboratory animals Male Microbiome Microbiome-gut-brain axis Microbiomes Obesity Obesity - metabolism Obesity - microbiology Obesity - psychology Physiology Raphe nuclei Rats Rats, Sprague-Dawley RNA Serotonin Signal Transduction - physiology |
title | High-fat diet, microbiome-gut-brain axis signaling, and anxiety-like behavior in male rats |
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