Evidence map›Paper›PMID 39753162›Full record

ArticleNeuroImage2025

Functional connectivity within sensorimotor cortical and striatal regions is regulated by sepsis in a sex-dependent manner.

Quan Vo, Zachary D Simon, Gwoncheol Park, Dina C Nacionales, Carmelina Gorski, Evan L Barrios, Gemma Casadesus, Philip A Efron, Lyle L Moldawer, Ravinder Nagpal and 2 more

Erratum issuedAbstract read
In one paragraph

Article in NeuroImage, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Quan VoDepartment of Neuroscience, University of Florida, Gainesville, FL 32610, USA. Electronic address: vo.quan@ufl.edu.
Zachary D SimonDepartment of Neuroscience, University of Florida, Gainesville, FL 32610, USA; Department of Psychiatry, University of Florida, Gainesville, FL 32610, USA. Electronic address: zsimon@ufl.edu.
Gwoncheol ParkDepartment of Health, Nutrition, and Food Sciences, Florida State University, Tallahassee, FL 32304, USA. Electronic address: gp21p@fsu.edu.
Dina C NacionalesDepartment of Surgery, University of Florida, Gainesville, FL 32610, USA; Sepsis & Critical Illness Research Center, University of Florida, Gainesville, FL 32610, USA. Electronic address: Dina.Nacionales@surgery.ufl.edu.
Carmelina GorskiSepsis & Critical Illness Research Center, University of Florida, Gainesville, FL 32610, USA. Electronic address: carmelina.gorski@ufl.edu.
Evan L BarriosDepartment of Surgery, University of Florida, Gainesville, FL 32610, USA; Sepsis & Critical Illness Research Center, University of Florida, Gainesville, FL 32610, USA. Electronic address: Evan.Barrios@surgery.ufl.edu.
Gemma CasadesusDepartment of Neuroscience, University of Florida, Gainesville, FL 32610, USA; Center for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL 32610, USA; Department of Pharmacology & Therapeutics, University of Florida, Gainesville, FL 32610, USA; McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA. Electronic address: gcasadesus@ufl.edu.
Philip A EfronDepartment of Surgery, University of Florida, Gainesville, FL 32610, USA; Sepsis & Critical Illness Research Center, University of Florida, Gainesville, FL 32610, USA; McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA. Electronic address: Philip.Efron@surgery.ufl.edu.
Lyle L MoldawerDepartment of Surgery, University of Florida, Gainesville, FL 32610, USA; Sepsis & Critical Illness Research Center, University of Florida, Gainesville, FL 32610, USA; McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA. Electronic address: lyle.moldawer@surgery.ufl.edu.
Ravinder NagpalDepartment of Health, Nutrition, and Food Sciences, Florida State University, Tallahassee, FL 32304, USA. Electronic address: rnagpal@fsu.edu.
Paramita ChakrabartyDepartment of Neuroscience, University of Florida, Gainesville, FL 32610, USA; Sepsis & Critical Illness Research Center, University of Florida, Gainesville, FL 32610, USA; Center for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL 32610, USA; McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA. Electronic address: pchakrabarty@ufl.edu.
Marcelo FeboDepartment of Psychiatry, University of Florida, Gainesville, FL 32610, USA; McKnight Brain Institute, University of Florida, Gainesville, FL 32610, USA. Electronic address: febo@ufl.edu.

Funding

Sepsis and the Systemic Cytokine Storm in Aging and Alzheimer Disease ModelsRF1NS128626 · NINDS · UNIVERSITY OF FLORIDA · PI CHAKRABARTY, PARAMITA, EFRON, PHILIP A · 2022 to 2022
$2.2M
Seven tesla preclinical MRI/S scanner for structural, functional and molecular imagingS10OD030293 · OD · UNIVERSITY OF FLORIDA · PI LONG, JOANNA R · 2021 to 2021
$2.0M
Imaging Networks of Affective Behaviors and Dopamine in Alzheimer's DiseaseR21AG065819 · NIA · UNIVERSITY OF FLORIDA · PI FEBO, MARCELO · 2020 to 2020
$406k
NIA NIH HHS R21 AG065819NIH HHS S10 OD030293NINDS NIH HHS RF1 NS128626
6 · The paper itself

Abstract

Sepsis is a state of systemic immune dysregulation and organ failure that is frequently associated with severe brain disability. Epidemiological studies have indicated that younger females have better prognosis and clinical outcomes relative to males, though the sex-dependent response of the brain to sepsis during post-sepsis recovery remains largely uncharacterized. Using a modified polymicrobial intra-abdominal murine model of surgical sepsis, we characterized the acute effects of intra-abdominal sepsis on peripheral inflammation, brain inflammation and brain functional connectivity in young adult mice of both sexes. Following sepsis, both male and female mice survived the procedure, regained body weight within 7 days post-sepsis and showed reduced diversity in their gut microbiome. Interestingly, compared to the sepsis-induced changes observed in female mice, the post-septic male mice exhibited a comparatively robust profile of splenic cell expansion and intracerebral glial proliferation relative to their healthy counterparts. Analysis of resting-state functional Magnetic Resonance Imaging (fMRI) data collected from the post-septic mice revealed that while connectivity to the somatosensory cortex were affected equally in both sexes, intra-network connectivity strength in the striatum preferentially increased in post-septic males but remained near baseline in post-septic female mice. Additionally, the female mice showed reduced network connectivity alterations in the projections from periaqueductal gray to the superior colliculus as also between the anterior cingulate cortex and the striatum. Coupled with the sustained intracerebral gliosis response, the intra-striatal fMRI response patterns in males could signify a delayed recovery from sepsis. Together, our study provides evidence that peripheral sepsis influences peripheral immunity, brain immunity and brain connectivity in a sex-dependent manner, with the fMRI response strongly indicating cognitive benefits in young females recovering from sepsis relative to their male counterparts.

Indexed as

Corpus StriatumNerve NetSensorimotor CortexSepsisSex CharacteristicsAnimalsDisease Models, AnimalFemaleGastrointestinal MicrobiomeMagnetic Resonance ImagingMaleMiceMice, Inbred C57BLSex FactorsAstrocyteBarrel field cortexfMRIGut microbiomeICA-based fMRI analysisIntra-striatal connectivityMicrogliaSepsisSpleen

Identifiers

PMID39753162
PMCPMC12128930

What Socratic holds

Textmetadata
LicenceTDM
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.