Evidence map›Paper›PMID 39702695›Full record

ArticleMolecular psychiatry2025

OXTR-mediated signaling in astrocytes contributes to anxiolysis.

Carl-Philipp Meinung, Laura Boi, Sareh Pandamooz, David Mazaud, Grégory Ghézali, Nathalie Rouach, Inga D Neumann

Abstract read
In one paragraph

Article in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Astrocytes mediate a positive feedback loop for oxytocin.bioRxiv : the preprint server for biology · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. The psychedelic-peptide paradox: a hormetic hypothesis.Comprehensive psychoneuroendocrinology · 2025
    Review
  9. Physical exercise activates a PVN-NAc oxytocin circuit to relieve stress-induced depressive-like behaviors.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Astrocytes in Rodent Anxiety-Related Behavior: Role of Calcium and Beyond.International journal of molecular sciences · 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

7 authors.

Carl-Philipp MeinungDepartment of Behavioral and Molecular Neurobiology, University of Regensburg, Regensburg, Germany.ORCID 0000-0002-3627-4754
Laura BoiDepartment of Behavioral and Molecular Neurobiology, University of Regensburg, Regensburg, Germany.ORCID 0000-0002-2878-0761
Sareh PandamoozDepartment of Behavioral and Molecular Neurobiology, University of Regensburg, Regensburg, Germany.ORCID 0000-0002-6877-7102
David MazaudCenter for Interdisciplinary Research in Biology, Collège de France, CNRS, INSERM, Université PSL, Labex Memolife, Paris, France.ORCID 0000-0003-3998-9330
Grégory GhézaliCenter for Interdisciplinary Research in Biology, Collège de France, CNRS, INSERM, Université PSL, Labex Memolife, Paris, France.
Nathalie RouachCenter for Interdisciplinary Research in Biology, Collège de France, CNRS, INSERM, Université PSL, Labex Memolife, Paris, France.ORCID 0000-0002-5574-888X
Inga D NeumannDepartment of Behavioral and Molecular Neurobiology, University of Regensburg, Regensburg, Germany. inga.neumann@ur.de.ORCID 0000-0002-3911-5062

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) GRK2174Deutsche Forschungsgemeinschaft (German Research Foundation) NE465/34-1Deutsche Forschungsgemeinschaft (German Research Foundation) NE465/37-1
6 · The paper itself

Abstract

Astrocytes are an indispensable part of signal processing within the mammalian brain. Thus, the mode of action of a neuropeptide such as oxytocin (OXT) can only be fully understood considering this integral part of the CNS. Here, we show that OXT regulates astrocytic gene expression, intracellular signaling and specific proteins both in vitro and in vivo. This translates into rapid regulation of astroglial structural and functional properties including cytoskeletal plasticity, coverage of synapses and gap-junction coupling. At the molecular level, we identify the previously undescribed Sp1-Gem signaling cascade as the key driver for these cell type-specific OXT effects. Finally at the behavioral level, we found in vivo that OXT requires astrocytes to exert its well described anxiolytic properties within the hypothalamic paraventricular nucleus. Thus, our study points to OXT receptor-expressing astrocytes as a critical component of the brain OXT system.

Indexed as

AnxietyAstrocytesReceptors, OxytocinAnimalsBrainCells, CulturedMaleMiceMice, Inbred C57BLOxytocinParaventricular Hypothalamic NucleusSignal TransductionOXTR protein, mouseOxytocinReceptors, Oxytocin

Identifiers

PMID39702695
PMCPMC12092269

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.