Evidence map›Paper›PMID 40684874›Full record

ArticleProgress in neuro-psychopharmacology & biological psychiatry2025

Role of gut microbiota and its functional products in prenatal alcohol-induced anxiety-like behavior.

Kingston E Wong, Carolina Luft, Victoria R Vella, Garrett R J Ainsworth-Cruickshank, Kanishka K Wijesundara, Parker J Holman, Tamara S Bodnar, Charlis Raineki

Abstract read
In one paragraph

Article in Progress in neuro-psychopharmacology & biological psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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

8 authors.

Kingston E WongDepartment of Psychology, Brock University, St. Catharines, Ontario, Canada.
Carolina LuftDepartment of Psychology, Brock University, St. Catharines, Ontario, Canada.
Victoria R VellaDepartment of Psychology, Brock University, St. Catharines, Ontario, Canada.
Garrett R J Ainsworth-CruickshankDepartment of Biological Sciences, University of Calgary, Calgary, Alberta, Canada.
Kanishka K WijesundaraDepartment of Psychology, Brock University, St. Catharines, Ontario, Canada.
Parker J HolmanDepartment of Psychology, Brock University, St. Catharines, Ontario, Canada.
Tamara S BodnarDepartment of Biological Sciences, University of Calgary, Calgary, Alberta, Canada; Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada; Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Charlis RainekiDepartment of Psychology, Brock University, St. Catharines, Ontario, Canada; Centre for Neuroscience, Brock University, St. Catharines, Ontario, Canada. Electronic address: craineki@brocku.ca.

Funding

Prenatal Alcohol and NeuroimmunityR01AA022460 · NIAAA · UNIVERSITY OF BRITISH COLUMBIA · PI BODNAR, TAMARA SONIA, RAINEKI, CHARLIS · 2013 to 2024
$2.3M
NIAAA NIH HHS R01 AA022460
6 · The paper itself

Abstract

Prenatal alcohol exposure (PAE) has been shown to increase vulnerability to anxiety. Alterations in the gut microbiota and its functional products (i.e., short-chain fatty acids, SCFAs) are a potential mechanism underlying anxiety behaviors induced by PAE. Here, we used a rat model of PAE to examine the impact of alcohol consumption during gestation on anxiety-like behaviors, gut microbiota, and SCFA levels in adult male and female offspring. PAE male and female rats exhibited increased anxiety-like behavior on the open field test; moreover, control animals displayed striking sex differences in the light-dark test, but sex differences were attenuated among PAE males and females. Furthermore, using an anxiety index composed of open field and light-dark behaviors, we showed that PAE animals had higher anxiety scores compared to controls. PAE did not affect bacterial diversity and community structure; however, in males, PAE reduced the abundance of the Firmicutes phylum, increased the abundance of the Bacteroidota phylum, and decreased the abundance of the Lachnospiraceae NK4A136 group genus compared to controls. In females, PAE increased abundance of Turicibacter genus compared to controls. PAE did not affect fecal SCFA levels; however, lower levels of butyric and valeric acid were associated with higher anxiety among PAE females. This study identified several bacterial taxa and SCFAs potentially involved in the mechanisms through which PAE induces anxiety-like behaviors. These findings also underscore the importance of considering sex differences when assessing anxiety-like behavior and gut microbiota to identify potential biomarkers for interventions targeting mental health issues in individuals with PAE.

Indexed as

AnxietyEthanolFatty Acids, VolatileGastrointestinal MicrobiomePrenatal Exposure Delayed EffectsAnimalsFemaleMalePregnancyRatsRats, Sprague-DawleySex CharacteristicsEthanolFatty Acids, VolatileAnxiety-like behaviorGut microbiomePrenatal alcohol exposureShort-chain fatty acids

Identifiers

PMID40684874
PMCPMC13135774

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.