Evidence map›Paper›PMID 41991521›Full record

ArticleTranslational psychiatry2026

Sex-dependent modulation of social distance by lipopolysaccharide-induced inflammation in mice.

Mizuki Yamamoto, Kazuko Hayashi, Masashi Kanayama, Hiroto Inoue, Shuntaro Matsushima, Koji Toda

Abstract read
In one paragraph

Article in Translational psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

6 authors.

Mizuki YamamotoDepartment of Psychology, Keio University, Tokyo, Japan.
Kazuko Hayashi *Department of Psychology, Keio University, Tokyo, Japan.
Masashi Kanayama *Medical Research Laboratory, Institute of Integrated Research, Institute of Science Tokyo, Tokyo, Japan.
Hiroto InoueDepartment of Psychology, Keio University, Tokyo, Japan.
Shuntaro MatsushimaDepartment of Psychology, Keio University, Tokyo, Japan.
Koji TodaDepartment of Psychology, Keio University, Tokyo, Japan. koji@keio.jp.ORCID http://orcid.org/0000-0002-2194-8998

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depression is a major psychiatric disorder, and accumulating evidence indicates that inflammatory processes contribute to its pathophysiology. Peripheral administration of lipopolysaccharide (LPS) reliably induces systemic inflammation and is widely used to model inflammation-related depression and sickness behavior. However, despite the strong association between social behavior and depressive states, the impact of LPS-induced inflammation on social interactions remains insufficiently understood. Here, we investigated how acute inflammatory responses influence social and non-social behaviors in C57BL/6 J mice following intraperitoneal LPS administration. Immunological analyses using ELISA and flow cytometry revealed marked increases in circulating IL-1β, IL-6, and TNF-α, accompanied by reductions in T cells, B cells, neutrophils, and monocytes. Baseline levels of B cells, neutrophils, and monocytes differed between sexes. Behavioral assessments demonstrated that LPS-treated male mice exhibited increased social contact and reduced social distance in both familiar and unfamiliar dyads, whereas these effects were absent in female pairs. In contrast, LPS induced comparable reductions in body weight, locomotor activity, and fecal output in the open-field test, as well as decreased sucrose preference and overall licking counts in the sucrose preference task, in both sexes. These findings indicate that LPS-induced inflammation modulates social behavior in a sex-dependent manner. Notably, the enhanced social contact observed in male dyads cannot be attributed to weight loss, hypoactivity, altered orofacial movements, or reduced reward sensitivity, as these physiological and motivational impairments were similarly present in both sexes. This study highlights distinct social behavioral consequences of inflammatory activation and advances our understanding of immune-behavior interactions.

Indexed as

Behavior, AnimalInflammationLipopolysaccharidesSocial BehaviorAnimalsDisease Models, AnimalFemaleMaleMiceMice, Inbred C57BLSex FactorsTumor Necrosis Factor-alphaLipopolysaccharidesTumor Necrosis Factor-alpha

Identifiers

PMID41991521
PMCPMC13201586

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.