Evidence map›Paper›PMID 28507320›Full record

ArticleMolecular psychiatry2018

The microbiome regulates amygdala-dependent fear recall.

A E Hoban, R M Stilling, G Moloney, F Shanahan, T G Dinan, G Clarke, J F Cryan

Abstract read
In one paragraph

Article in Molecular psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing 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

99 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. A defined community of core gut microbiota members promotes cognitive performance in honey bees.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Article
  6. Gut-brain axis in health and brain disease.Chinese medical journal · 2026
    Review
  7. The Microbiota Shapes Central Nervous System Myelination in Early Life.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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  18. Article
  19. Article
  20. Review

39 more citing papers are in PubMed but not listed here.

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

7 authors.

A E HobanAPC Microbiome Institute, University College Cork, Cork, Ireland.
R M StillingAPC Microbiome Institute, University College Cork, Cork, Ireland.ORCID 0000-0001-7637-5851
G MoloneyDepartment of Anatomy and Neuroscience, University College Cork, Cork, Ireland.
F ShanahanAPC Microbiome Institute, University College Cork, Cork, Ireland.
T G DinanAPC Microbiome Institute, University College Cork, Cork, Ireland.
G ClarkeAPC Microbiome Institute, University College Cork, Cork, Ireland.
J F CryanAPC Microbiome Institute, University College Cork, Cork, Ireland.ORCID 0000-0001-5887-2723

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The amygdala is a key brain region that is critically involved in the processing and expression of anxiety and fear-related signals. In parallel, a growing number of preclinical and human studies have implicated the microbiome-gut-brain in regulating anxiety and stress-related responses. However, the role of the microbiome in fear-related behaviours is unclear. To this end we investigated the importance of the host microbiome on amygdala-dependent behavioural readouts using the cued fear conditioning paradigm. We also assessed changes in neuronal transcription and post-transcriptional regulation in the amygdala of naive and stimulated germ-free (GF) mice, using a genome-wide transcriptome profiling approach. Our results reveal that GF mice display reduced freezing during the cued memory retention test. Moreover, we demonstrate that under baseline conditions, GF mice display altered transcriptional profile with a marked increase in immediate-early genes (for example, Fos, Egr2, Fosb, Arc) as well as genes implicated in neural activity, synaptic transmission and nervous system development. We also found a predicted interaction between mRNA and specific microRNAs that are differentially regulated in GF mice. Interestingly, colonized GF mice (ex-GF) were behaviourally comparable to conventionally raised (CON) mice. Together, our data demonstrates a unique transcriptional response in GF animals, likely because of already elevated levels of immediate-early gene expression and the potentially underlying neuronal hyperactivity that in turn primes the amygdala for a different transcriptional response. Thus, we demonstrate for what is to our knowledge the first time that the presence of the host microbiome is crucial for the appropriate behavioural response during amygdala-dependent memory retention.

Indexed as

AmygdalaAnimalsAnxietyBrainCuesFearGastrointestinal MicrobiomeGene Expression RegulationGene OntologyMaleMemoryMental RecallMiceMice, Inbred C57BLNeuronsRNA, MessengerRNA, Messenger

Identifiers

PMID28507320
PMCPMC5984090

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LicenceCC BY-NC-ND
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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.