Evidence map›Paper›PMID 42818933›Full record

ArticleResearch square2026

Maternal Social Support Reshapes the Offspring Brain Transcriptome to Buffer Prenatal Stress in Mice.

Monserrat Rodríguez González, Paula Thomas, Lucía Janicki, Erika Georgieff, Sergio Nemirowski, Verónica I Cantarelli, Marina F Ponzio, Mariela Chertoff, Bruno G Berardino, Eduardo T Cánepa

Abstract readPreprint
In one paragraph

Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Monserrat Rodríguez GonzálezLaboratorio de Neuroepigenética y Adversidades Tempranas, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, and Instituto de Química Biológica de Ciencias Exactas y Naturales (IQUIBICEN), CONICET, Ciudad Autónoma de Buenos Aires, Argentina.
Paula ThomasLaboratorio de Neuroepigenética y Adversidades Tempranas, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, and Instituto de Química Biológica de Ciencias Exactas y Naturales (IQUIBICEN), CONICET, Ciudad Autónoma de Buenos Aires, Argentina.
Lucía JanickiLaboratorio de Neuroepigenética y Adversidades Tempranas, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, and Instituto de Química Biológica de Ciencias Exactas y Naturales (IQUIBICEN), CONICET, Ciudad Autónoma de Buenos Aires, Argentina.
Erika GeorgieffLaboratorio de Neuroepigenética y Adversidades Tempranas, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, and Instituto de Química Biológica de Ciencias Exactas y Naturales (IQUIBICEN), CONICET, Ciudad Autónoma de Buenos Aires, Argentina.
Sergio NemirowskiDepartamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, and Instituto de Química Biológica de Ciencias Exactas y Naturales (IQUIBICEN), CONICET, Ciudad Autónoma de Buenos Aires, Argentina.
Verónica I CantarelliInstituto de Fisiología Humana "Dr. Oscar Orías", Facultad de Ciencias Médicas and Instituto de Investigaciones en Ciencias de la Salud (INICSA-CONICET), Universidad Nacional de Córdoba, Santa Rosa 1085, X5000ESU Córdoba, Argentina.
Marina F PonzioInstituto de Fisiología Humana "Dr. Oscar Orías", Facultad de Ciencias Médicas and Instituto de Investigaciones en Ciencias de la Salud (INICSA-CONICET), Universidad Nacional de Córdoba, Santa Rosa 1085, X5000ESU Córdoba, Argentina.
Mariela ChertoffLaboratorio de Neuroepigenética y Adversidades Tempranas, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, and Instituto de Química Biológica de Ciencias Exactas y Naturales (IQUIBICEN), CONICET, Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0001-5600-7445
Bruno G BerardinoLaboratorio de Neuroepigenética y Adversidades Tempranas, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, and Instituto de Química Biológica de Ciencias Exactas y Naturales (IQUIBICEN), CONICET, Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0002-8954-5546
Eduardo T CánepaLaboratorio de Neuroepigenética y Adversidades Tempranas, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, and Instituto de Química Biológica de Ciencias Exactas y Naturales (IQUIBICEN), CONICET, Ciudad Autónoma de Buenos Aires, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early-life adversity, including prenatal stress, has lasting consequences for maternal and offspring mental health. However, the mechanisms through which social support buffers these effects remain poorly understood. Using a mouse model, we examined whether gestational social support from a familiar female protects against prenatal stress and whether this protection restores a stress-free molecular phenotype or engages a distinct compensatory program. Pregnant females exposed to unpredictable prenatal stress displayed impaired maternal care, elevated peripartum corticosterone levels, and reduced prefrontal and amygdala expression of oxytocinergic and dopaminergic genes. Their offspring showed impaired maternal-odor preference and long-term spatial memory. Strikingly, socially supported mothers and their offspring were virtually indistinguishable from unstressed controls across these behavioral and candidate-gene measures. Female companions increased affiliative interactions specifically in response to the pregnant female's distress, consistent with a targeted prosocial response. However, whole-transcriptome analysis of offspring prefrontal cortex revealed a more complex picture: differentially expressed genes associated with stress and social support converged on synaptic transmission and neuronal connectivity, yet the transcriptome of socially supported offspring did not return to the control state. Instead, it diverged further along the same trajectory as prenatal stress, indicating an amplified rather than reversed molecular shift. These findings support a two-level model in which social support normalizes stress-reactive proximal signaling while activating a distinct adaptive transcriptional program in the developing brain. Maternal social support may therefore represent a modifiable factor that mitigates the intergenerational consequences of early-life adversity and reshape resilience as an active adaptation rather than restoration of baseline state.

Indexed as

Affiliative and prosocial behaviorsAmygdalaDopaminergic signalingLong term spatial memorymaternal bedding preferenceMaternal careOxytocin systemPrefrontal cortexPrenatal stressSocial support during pregnancy

Identifiers

PMID42818933
PMCPMC13622831

What OpenQuestion holds

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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.