Evidence map›Paper›PMID 41061380›Full record

ArticlePsychoneuroendocrinology2025

Social isolation, but not partner separation, lowers hippocampal synaptosome mitochondrial respiration in female California mice (Peromyscus californicus).

Amy J Wegener, Hannah D Fulenwider, Hannah Stadtler, Paul A Howell, Nour Abosamak, Susie Turkson, Charlotte A Ream, Niyomi H Shah, Erica R Glasper, Gretchen N Neigh

Abstract read
In one paragraph

Article in Psychoneuroendocrinology, 2025. 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.

Amy J WegenerDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, United States.
Hannah D FulenwiderDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, United States.
Hannah StadtlerDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, United States.
Paul A HowellDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, United States.
Nour AbosamakWright Center for Clinical and Translational Research, Virginia Commonwealth University, Richmond, VA, United States.
Susie TurksonDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, United States.
Charlotte A ReamDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, United States.
Niyomi H ShahDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, United States.
Erica R GlasperDepartment of Neuroscience, The Ohio State University, Columbus, OH, United States; Institute for Behavioral Medicine Research, The Ohio State University, Columbus, OH, United States.
Gretchen N NeighDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, United States. Electronic address: gretchen.mccandless@vcuhealth.org.

Funding

Virginia Commonwealth University IRADCAK12GM093857 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI DANIEL C BULLARD, John J Ryan · 2010 to 2026
$7.0M
From Social Discruption to Neural Compromise: Establishing Markers and MediatorsR01NS125589 · NINDS · OHIO STATE UNIVERSITY · PI Erica R Glasper, Gretchen N Neigh · 2022 to 2026
$3.2M
CTSA Predoctoral T32 at Virginia Commonwealth UniversityT32TR004362 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI MAGHBOEBA MOSAVEL, Gretchen N Neigh · 2024 to 2026
$526k
NCATS NIH HHS T32 TR004362NIGMS NIH HHS K12 GM093857NINDS NIH HHS R01 NS125589
6 · The paper itself

Abstract

Social isolation, loneliness, and loss profoundly impact health and quality of life, but the complex nature of these constructs can prohibit mechanistic examination in rodent models. Assessment of the peripheral and neural effects of environment manipulations in a social rodent species, such as California mice (Peromyscus californicus), can facilitate inquiry into the biological repercussions of experiencing different types of loss. Stressors can compromise neural function in the hippocampus and a portion of this effect is due to deficits in mitochondrial function at the synapse. Mitochondria at the synapse are essential to facilitate neural transmission and compromise can impair neurotransmission and thereby behavior. In the current study, we used genetically monogamous male and female California mice to evaluate synaptic mitochondrial respiration following removal of a same-sex cage mate for 10- or 30-days (i.e., social isolation; Experiment 1) OR a 10-day separation from an opposite-sex partner following 10-days of cohabitation (i.e., partner separation; Experiment 2). In the social isolation cohort, males, but not females, exhibited physical changes consistent with a prolonged stress response, including reduction in body mass and hypertrophy of the adrenal glands following isolation. In contrast, isolated female mice demonstrated a reduction in hippocampal synaptic mitochondrial respiration at both 10- and 30-days following social isolation, compared to females that remained pair-housed. No effects were observed in males. Social isolation did not alter open field outcomes for either sex. We then investigated the impact of separation from an opposite sex partner on the same metrics. Separation from an opposite sex partner was qualitatively less impactful, such that there were no statistically significant changes observed in body mass, adrenal weight, open field behavior, or mitochondrial respiration following separation from an opposite sex mate. Collectively, these data suggest that males and females differentially manifest the impact of social stress on synaptic mitochondria respiration.

Indexed as

HippocampusMitochondriaSocial IsolationAnimalsFemaleMaleMicePeromyscusSex FactorsStress, PsychologicalSynapsesCalifornia miceHippocampusIsolationMitochondriaSocial loss

Identifiers

PMID41061380
PMCPMC13182572

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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.