Evidence map›Paper›PMID 26938530›Full record

ArticleInternational journal of molecular sciences2016

Dietary Apigenin Exerts Immune-Regulatory Activity in Vivo by Reducing NF-κB Activity, Halting Leukocyte Infiltration and Restoring Normal Metabolic Function.

Horacio Cardenas, Daniel Arango, Courtney Nicholas, Silvia Duarte, Gerard J Nuovo, Wei He, Oliver H Voss, M Elba Gonzalez-Mejia, Denis C Guttridge, Erich Grotewold and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
8.9field-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

42 citing papers in PubMed, 87 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

11 authors at 1 institution in 1 country.

Horacio CardenasDepartment of Physiology and Cell Biology, the Heart and Lung Research Institute, the Ohio State University, Columbus, OH 43210, USA. horacio.cardenas@northwestern.edu.
Daniel ArangoDepartment of Physiology and Cell Biology, the Heart and Lung Research Institute, the Ohio State University, Columbus, OH 43210, USA. dany33co@gmail.com.
Courtney NicholasDepartment of Physiology and Cell Biology, the Heart and Lung Research Institute, the Ohio State University, Columbus, OH 43210, USA. nicholas.40@buckeyemail.osu.edu.
Silvia DuarteDepartment of Physiology and Cell Biology, the Heart and Lung Research Institute, the Ohio State University, Columbus, OH 43210, USA. duartesanmiguel.1@osu.edu.
Gerard J NuovoComprehensive Cancer Center, the Ohio State University, Columbus, OH 43210, USA. gerard.nuovo@osumc.edu.
Wei HeMolecular Cellular and Developmental Biology Graduate Program, the Ohio State University, Columbus, OH 43210, USA. he.115@osu.edu.
Oliver H VossDepartment of Molecular Genetics, the Ohio State University, Columbus, OH 43210, USA. ollivoss39@gmail.com.
M Elba Gonzalez-MejiaDepartment of Physiology and Cell Biology, the Heart and Lung Research Institute, the Ohio State University, Columbus, OH 43210, USA. elba.gonzalezmejia@gmail.com.
Denis C GuttridgeComprehensive Cancer Center, the Ohio State University, Columbus, OH 43210, USA. denis.guttridge@osumc.edu.
Erich GrotewoldDepartment of Molecular Genetics, the Ohio State University, Columbus, OH 43210, USA. Grotewold.1@osu.edu.
Andrea I DoseffDepartment of Physiology and Cell Biology, the Heart and Lung Research Institute, the Ohio State University, Columbus, OH 43210, USA. doseff.1@osu.edu.
The Ohio State University · US

Funding

Molecular Mechanisms of Apoptosis in MonocytesR01HL075040 · NHLBI · OHIO STATE UNIVERSITY · PI DOSEFF, ANDREA · 2006 to 2010
$1.9M
NHLBI NIH HHS R01 HL075040NHLBI NIH HHS R01 HL075040-01
6 · The paper itself

Abstract

The increasing prevalence of inflammatory diseases and the adverse effects associated with the long-term use of current anti-inflammatory therapies prompt the identification of alternative approaches to reestablish immune balance. Apigenin, an abundant dietary flavonoid, is emerging as a potential regulator of inflammation. Here, we show that apigenin has immune-regulatory activity in vivo. Apigenin conferred survival to mice treated with a lethal dose of Lipopolysaccharide (LPS) restoring normal cardiac function and heart mitochondrial Complex I activity. Despite the adverse effects associated with high levels of splenocyte apoptosis in septic models, apigenin had no effect on reducing cell death. However, we found that apigenin decreased LPS-induced apoptosis in lungs, infiltration of inflammatory cells and chemotactic factors' accumulation, re-establishing normal lung architecture. Using NF-κB luciferase transgenic mice, we found that apigenin effectively modulated NF-κB activity in the lungs, suggesting the ability of dietary compounds to exert immune-regulatory activity in an organ-specific manner. Collectively, these findings provide novel insights into the underlying immune-regulatory mechanisms of dietary nutraceuticals in vivo.

Indexed as

AnimalsAnti-Inflammatory AgentsApigeninApoptosisDietary SupplementsLeukemic InfiltrationLipopolysaccharidesLungMaleMiceMice, Inbred BALB CMice, Inbred C57BLNF-kappa BSepsisSpleenAnti-Inflammatory AgentsApigeninLipopolysaccharidesNF-kappa Bapigeninapoptosiscardiac dysfunctionflavonoidsinflammationleukocytesmitochondriaNF-κBsepsis

Identifiers

PMID26938530
PMCPMC4813185
OpenAlexW2288921983

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.