Evidence map›Paper›PMID 38705984›Full record

ArticleBiological research2024

High-fat diet, microbiome-gut-brain axis signaling, and anxiety-like behavior in male rats.

Sylvana I S Rendeiro de Noronha, Lauro Angelo Gonçalves de Moraes, James E Hassell, Christopher E Stamper, Mathew R Arnold, Jared D Heinze, Christine L Foxx, Margaret M Lieb, Kristin E Cler, Bree L Karns and 6 more

Abstract read
In one paragraph

Article in Biological research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Sylvana I S Rendeiro de NoronhaDepartment of Biological Sciences, Laboratory of Cardiovascular Physiology, Federal University of Ouro Preto, Ouro Preto, MG, 35400-000, Brazil.
Lauro Angelo Gonçalves de MoraesDepartment of Biological Sciences, Laboratory of Cardiovascular Physiology, Federal University of Ouro Preto, Ouro Preto, MG, 35400-000, Brazil.
James E HassellDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, 80309, USA.
Christopher E StamperDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, 80309, USA.
Mathew R ArnoldDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, 80309, USA.
Jared D HeinzeDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, 80309, USA.
Christine L FoxxDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, 80309, USA.
Margaret M LiebDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, 80309, USA.
Kristin E ClerDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, 80309, USA.
Bree L KarnsDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, 80309, USA.
Sophia JaekelDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, 80309, USA.
Kelsey M LoupyDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, CO, 80309, USA.
Fernanda C S SilvaDepartment of Biological Sciences, Laboratory of Cardiovascular Physiology, Federal University of Ouro Preto, Ouro Preto, MG, 35400-000, Brazil.
Deoclécio Alves Chianca-JrDepartment of Biological Sciences, Laboratory of Cardiovascular Physiology, Federal University of Ouro Preto, Ouro Preto, MG, 35400-000, Brazil.
Christopher A Lowry *Department of Integrative Physiology, University of Colorado Boulder, Boulder, CO, 80309, USA.
Rodrigo Cunha de Menezes *Department of Biological Science Laboratory of Cardiovascular Physiology, Campus Morro do Cruzeiro s/n, Ouro Preto, 35400-000, MG, Brazil. rodrigo.menezes@ufop.edu.br.ORCID http://orcid.org/0000-0003-0286-0621

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico Conselho Nacional de Desenvolvimento Científico e TecnológicoCoordenação de Aperfeiçoamento de Pessoal de Nível Superior Financial Code 001 and the Programa de Doutorado Sanduíche no Exterior [PDSE], process #88881.132957/2016-01Financiadora de Estudos e Projetos Financiadora de Estudos e ProjetosFoundation for the National Institutes of Health Foundation for the National Institutes of HealthFundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-00359-21Fundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-00823-21Fundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-02182-17Fundação de Amparo à Pesquisa do Estado de Minas Gerais Center of Animal Science (APQ-02511-22)Institute for Cannabis Research Institute for Cannabis ResearchNational Science Foundation National Science FoundationUniversidade Federal de Ouro Preto Universidade Federal de Ouro Preto
6 · The paper itself

Abstract

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.

Indexed as

AnxietyBrain-Gut AxisDiet, High-FatGastrointestinal MicrobiomeAnimalsBehavior, AnimalMaleObesityRatsRats, Sprague-DawleySignal TransductionAnxietyDorsal raphe nucleusHigh-fat dietMicrobiomeMicrobiome-gut-brain axisObesityRaphe nucleiSerotonergic systemSerotonintph2

Identifiers

PMID38705984
PMCPMC11071217

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.