Evidence map›Paper›PMID 19560480›Full record

ArticlePhysiology & behavior2009

Social stress enhances IL-1beta and TNF-alpha production by Porphyromonas gingivalis lipopolysaccharide-stimulated CD11b+ cells.

Michael T Bailey, Steven G Kinsey, David A Padgett, John F Sheridan, Binnaz Leblebicioglu

Abstract read
In one paragraph

Article in Physiology & behavior, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
6.9field-weighted citation impact, top 2% of its field
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

43 citing papers in PubMed, 81 citations in OpenAlex.

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  8. Immune-Endocrine Links to Gregariousness in Wild House Mice.Frontiers in behavioral neuroscience · 2020
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  13. TheFrontiers in aging neuroscience · 2017
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  15. Pathogen-Host Defense in the Evolution of Depression: Insights into Epidemiology, Genetics, Bioregional Differences and Female Preponderance.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Review
  16. Article
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  20. 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

5 authors at 2 institutions in 1 country.

Michael T BaileySection of Oral Biology, College of Dentistry, The Ohio State University, Columbus, OH 43210, United States. Bailey.494@osu.edu
Steven G Kinsey
David A Padgett
John F Sheridan
Binnaz Leblebicioglu
The Ohio State University · USInstitute for Behavioral Medicine · US

Funding

Comprehensive Training in Oral &Craniofacial SciencesT32DE014320 · NIDCR · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 2001 to 2022
$10.2M
STRESS-INDUCED IMMUNOSUPPRESSION OF ANTIVIRAL IMMUNITYR01MH046801 · NIMH · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 1991 to 2008
$2.7M
Impact of Social Stress on TLR4-Induced Microbicidal Activity of CD11b+ CellsR03AI069097 · NIAID · OHIO STATE UNIVERSITY · PI BAILEY, MICHAEL T · 2007 to 2008
$149k
NIAID NIH HHS 1R03AI069097NIAID NIH HHS R03 AI069097NIDCR NIH HHS T32 DE014320NIMH NIH HHS 5R01MH046801-16NIMH NIH HHS R01 MH046801PHS HHS T32DEO14320-6
6 · The paper itself

Abstract

Psychological stress is associated with an increased expression of markers of peripheral inflammation, and there is a growing literature describing a link between periodontal pathogens and systemic inflammation. The hypothesis of the present work is that exposing mice to the social stressor, called social disruption (SDR), would enhance the inflammatory response to lipopolysaccharide (LPS) derived from the oral pathogen, Porphyromonas gingivalis. Mice were exposed to SDR for 2h per day on 6 consecutive days. On the morning following the last cycle of SDR, mice were tested for anxiety-like behavior in the open field test and novel object test. The mice were sacrificed the following day and their spleens harvested. Spleen cells were stimulated with LPS derived from P. gingivalis in the absence or presence of increasing doses of corticosterone. Social disruption resulted in anxiety-like behavior, and the production of IL-1beta and TNF-alpha was significantly higher in spleen cells from mice exposed to SDR in comparison to levels from non-stressed control mice. In addition, the viability of spleen cells from mice exposed to SDR was significantly greater than the viability of cells from non-stressed control mice, even in the presence of high doses of corticosterone. The use of cultures enriched for CD11b+ cells indicated that the stressor was affecting the activity of splenic myeloid cells. This study demonstrates that social stress enhances the inflammatory response to an oral pathogen and could provide a critical clue in the reported associations between stress, inflammation, and oral pathogens.

Indexed as

AnomieAnimalsCD11b AntigenCells, CulturedCell SurvivalExploratory BehaviorInterleukin-1betaLipopolysaccharidesMacrophagesMaleMiceMice, Inbred StrainsPorphyromonas gingivalisSpleenStress, PsychologicalTumor Necrosis Factor-alphaCD11b AntigenInterleukin-1betaLipopolysaccharidesTumor Necrosis Factor-alpha

Identifiers

PMID19560480
PMCPMC2748391
OpenAlexW2041511592

What OpenQuestion 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 OpenQuestion graph.