Evidence map›Paper›PMID 21849270›Full record

ArticleEnvironmental health perspectives2011

Aryl hydrocarbon receptor deficiency enhances insulin sensitivity and reduces PPAR-α pathway activity in mice.

Chun Wang, Can-Xin Xu, Stacey L Krager, Kathleen M Bottum, Duan-Fang Liao, Shelley A Tischkau

Open access · diamondAbstract read
In one paragraph

Article in Environmental health perspectives, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

80 citing papers in PubMed, 131 citations in OpenAlex.

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  20. The Role of the Kynurenine/AhR Pathway in Diseases Related to Metabolism and Cancer.International journal of tryptophan research : IJTR · 2023
    Review

20 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 3 countries.

Chun WangDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, Illinois 62974-9629, USA.
Can-Xin Xu
Stacey L Krager
Kathleen M Bottum
Duan-Fang Liao
Shelley A Tischkau
Southern Illinois University School of Medicine · USHunan University of Traditional Chinese Medicine · CN

Funding

Circadian Clock Disruption: A Mechanism for Dioxin-induced Metabolic SyndromeR01ES017774 · NIEHS · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI TISCHKAU, SHELLEY A · 2010 to 2013
$1.3M
NIEHS NIH HHS ES017774NIEHS NIH HHS R01 ES017774
6 · The paper itself

Abstract

backgroundNumerous man-made pollutants activate the aryl hydrocarbon receptor (AhR) and are risk factors for type 2 diabetes. AhR signaling also affects molecular clock genes to influence glucose metabolism.

objectiveWe investigated mechanisms by which AhR activation affects glucose metabolism.

methodsGlucose tolerance, insulin resistance, and expression of peroxisome proliferator-activated receptor-α (PPAR-α) and genes affecting glucose metabolism or fatty acid oxidation and clock gene rhythms were investigated in wild-type (WT) and AhR-deficient [knockout (KO)] mice. AhR agonists and small interfering RNA (siRNA) were used to examine the effect of AhR on PPAR-α expression and glycolysis in the liver cell line Hepa-1c1c7 (c7) and its c12 and c4 derivatives. Brain, muscle ARNT-like protein 1 (Bmal1) siRNA and Ahr or Bmal1 expression plasmids were used to analyze the effect of BMAL1 on PPAR-α expression in c7 cells.

resultsKO mice displayed enhanced insulin sensitivity and improved glucose tolerance, accompanied by decreased PPAR-α and key gluconeogenic and fatty acid oxidation enzymes. AhR agonists increased PPAR-α expression in c7 cells. Both Ahr and Bmal1 siRNA reduced PPAR-α and metabolism genes. Moreover, rhythms of BMAL1 and blood glucose were altered in KO mice.

conclusionsThese results indicate a link between AhR signaling, circadian rhythms, and glucose metabolism. Furthermore, hepatic activation of the PPAR-α pathway provides a mechanism underlying AhR-mediated insulin resistance.

Indexed as

Analysis of VarianceAnimalsARNTL Transcription FactorsCell LineCircadian RhythmGene Expression RegulationGlucoseGlucose Tolerance TestGlycolysisInsulin ResistanceLiverMiceMice, KnockoutPPAR alphaReceptors, Aryl HydrocarbonRNA, Small InterferingARNTL Transcription FactorsBmal1 protein, mouseGlucosePPAR alphaReceptors, Aryl HydrocarbonRNA, Small Interfering

Identifiers

PMID21849270
PMCPMC3261983
OpenAlexW2078044412

What OpenQuestion holds

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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.