Evidence map›Paper›PMID 41430076›Full record

ArticleNature communications2025

Distinct mechanisms of transcriptomic habituation to repeated stress in the mouse hippocampus.

Rebecca Waag, Lukas von Ziegler, Emanuel Sonder, Oliver Sturman, Justine Leonardi, Selina Frei, Rosie Longster, Katharina Gapp, Pierre-Luc Germain, Johannes Bohacek

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. A practical guide to sequencing in neuropsychiatric research.NPP - digital psychiatry and neuroscience · 2025
    Review
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

10 authors.

Rebecca WaagLaboratory of Molecular and Behavioral Neuroscience, Department of Health Sciences and Technology, Institute for Neuroscience, Zurich, Switzerland.ORCID http://orcid.org/0000-0001-5103-2860
Lukas von ZieglerLaboratory of Molecular and Behavioral Neuroscience, Department of Health Sciences and Technology, Institute for Neuroscience, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-5942-7928
Emanuel SonderComputational Neurogenomics, Department of Health Sciences and Technology, Institute for Neuroscience, ETH Zürich, Zurich, Switzerland.ORCID http://orcid.org/0000-0003-4788-9508
Oliver SturmanLaboratory of Molecular and Behavioral Neuroscience, Department of Health Sciences and Technology, Institute for Neuroscience, Zurich, Switzerland.ORCID http://orcid.org/0000-0001-6859-4800
Justine LeonardiLaboratory of Molecular and Behavioral Neuroscience, Department of Health Sciences and Technology, Institute for Neuroscience, Zurich, Switzerland.
Selina FreiNeuroscience Center Zurich, ETH Zurich and University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0009-0003-2948-1733
Rosie LongsterNeuroscience Center Zurich, ETH Zurich and University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0009-0001-7952-8283
Katharina GappNeuroscience Center Zurich, ETH Zurich and University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-9622-1478
Pierre-Luc GermainLaboratory of Molecular and Behavioral Neuroscience, Department of Health Sciences and Technology, Institute for Neuroscience, Zurich, Switzerland. pierre-luc.germain@hest.ethz.ch.ORCID http://orcid.org/0000-0003-3418-4218
Johannes BohacekLaboratory of Molecular and Behavioral Neuroscience, Department of Health Sciences and Technology, Institute for Neuroscience, Zurich, Switzerland. johannes.bohacek@hest.ethz.ch.ORCID http://orcid.org/0000-0002-8442-653X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic stress is a risk factor for neuropsychiatric disorders, making the ability to adapt to repeated stress a crucial determinant of mental health. It remains unclear whether repeated stress exposure leads to habituation or new adaptive responses. Here, we investigated how the transcriptomic response to acute restraint stress changes - in the mouse ventral hippocampus - with repeated exposure. Using bulk RNA-seq across multiple timepoints, we observed widespread transcriptional habituation: stress-induced gene expression was blunted without the emergence of new response profiles or changes in baseline gene expression. Temporally resolved single-nucleus multi-omic profiling (RNA and chromatin accessibility) confirmed that the transcriptional habituation occurs across cell types, revealing cell type-specific patterns. We identify gene clusters whose expression habituates with repeated exposure, which appear primarily related to two distinct mechanisms: an early blunting of cAMP-associated genes chiefly linked to a reduced number of activated cells, and a shortened transcriptional response of corticosterone-associated genes, independent of the number of activated cells. Our study provides a comprehensive resource, accessible as an interactive app, that characterizes the dynamic transcriptomic response to stress in the mouse hippocampus and how it habituates with repeated exposure to stress.

Indexed as

Habituation, PsychophysiologicHippocampusStress, PsychologicalTranscriptomeAnimalsCorticosteroneGene Expression ProfilingGene Expression RegulationMaleMiceMice, Inbred C57BLRestraint, PhysicalCorticosterone

Identifiers

PMID41430076
PMCPMC12748579

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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.