Evidence map›Paper›PMID 25542778›Full record

ArticlePhysiology & behavior2015

Diet-induced obesity attenuates endotoxin-induced cognitive deficits.

Sharay E Setti, Alyssa M Littlefield, Samantha W Johnson, Rachel A Kohman

Open access · greenAbstract read
In one paragraph

Article in Physiology & behavior, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Sharay E SettiUniversity of North Carolina Wilmington, Department of Psychology, Wilmington, NC, USA. Electronic address: ses8535@uncw.edu.
Alyssa M LittlefieldUniversity of North Carolina Wilmington, Department of Psychology, Wilmington, NC, USA. Electronic address: aml8440@uncw.edu.
Samantha W JohnsonUniversity of North Carolina Wilmington, Department of Psychology, Wilmington, NC, USA. Electronic address: swj4531@uncw.edu.
Rachel A KohmanUniversity of North Carolina Wilmington, Department of Psychology, Wilmington, NC, USA. Electronic address: kohmanr@uncw.edu.
University of North Carolina Wilmington · US

Funding

Therapeutic interventions for brain-immune interactions during cognitive agingR00AG040194 · NIA · UNIVERSITY OF NORTH CAROLINA WILMINGTON · PI KOHMAN, RACHEL A. · 2012 to 2014
$717k
NIA NIH HHS R00 AG040194NIA NIH HHS R00AG040194
6 · The paper itself

Abstract

Activation of the immune system can impair cognitive function, particularly on hippocampus dependent tasks. Several factors such as normal aging and prenatal experiences can modify the severity of these cognitive deficits. One additional factor that may modulate the behavioral response to immune activation is obesity. Prior work has shown that obesity alters the activity of the immune system. Whether diet-induced obesity (DIO) influences the cognitive deficits associated with inflammation is currently unknown. The present study explored whether DIO alters the behavioral response to the bacterial endotoxin, lipopolysaccharide (LPS). Female C57BL/6J mice were fed a high-fat (60% fat) or control diet (10% fat) for a total of five months. After consuming their respective diets for four months, mice received an LPS or saline injection and were assessed for alterations in spatial learning. One month later, mice received a second injection of LPS or saline and tissue samples were collected to assess the inflammatory response within the periphery and central nervous system. Results showed that LPS administration impaired spatial learning in the control diet mice, but had no effect in DIO mice. This lack of a cognitive deficit in the DIO female mice is likely due to a blunted inflammatory response within the brain. While cytokine production within the periphery (i.e., plasma, adipose, and spleen) was similar between the DIO and control mice, the DIO mice failed to show an increase in IL-6 and CD74 in the brain following LPS administration. Collectively, these data indicate that DIO can reduce aspects of the neuroinflammatory response as well as blunt the behavioral reaction to an immune challenge.

Indexed as

AnimalsCognitionCognition DisordersDiet, High-FatEndotoxinsFemaleHippocampusInflammationInterleukin-1betaInterleukin-6Maze LearningMiceObesityEndotoxinsInterleukin-1betaInterleukin-6CD74CD86CytokinesHigh-fat dietIL-6LPSSpatial learningWater maze

Identifiers

PMID25542778
PMCPMC4475351
OpenAlexW2061979141

What OpenQuestion holds

Textmetadata
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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.