Evidence map›Paper›PMID 26657007›Full record

ArticleHypertension research : official journal of the Japanese Society of Hypertension2016

Cacao polyphenols ameliorate autoimmune myocarditis in mice.

Hirofumi Zempo, Jun-ichi Suzuki, Ryo Watanabe, Kouji Wakayama, Hidetoshi Kumagai, Yuichi Ikeda, Hiroshi Akazawa, Issei Komuro, Mitsuaki Isobe

Erratum issuedAbstract read
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In one paragraph

Article in Hypertension research : official journal of the Japanese Society of Hypertension, 2016. 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Hirofumi ZempoDepartment of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.
Jun-ichi SuzukiDepartment of Advanced Clinical Science and Therapeutics, University of Tokyo, Tokyo, Japan.
Ryo WatanabeDepartment of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.
Kouji WakayamaDepartment of Advanced Clinical Science and Therapeutics, University of Tokyo, Tokyo, Japan.
Hidetoshi KumagaiDepartment of Advanced Clinical Science and Therapeutics, University of Tokyo, Tokyo, Japan.
Yuichi IkedaDepartment of Cardiovascular Medicine, University of Tokyo, Tokyo, Japan.
Hiroshi AkazawaDepartment of Advanced Clinical Science and Therapeutics, University of Tokyo, Tokyo, Japan.
Issei KomuroDepartment of Cardiovascular Medicine, University of Tokyo, Tokyo, Japan.
Mitsuaki IsobeDepartment of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.
The University of Tokyo · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myocarditis is a clinically severe disease; however, no effective treatment has been established. The aim of this study was to determine whether cacao bean (Theobroma cacao) polyphenols ameliorate autoimmune myocarditis. We used an experimental autoimmune myocarditis (EAM) model in Balb/c mice. Mice with induced EAM were treated with a cacao polyphenol extract (CPE, n=12) or vehicle (n=12). On day 21, hearts were harvested and analyzed. Elevated heart weight to body weight and fibrotic area ratios as well as high cardiac cell infiltration were observed in the vehicle-treated EAM mice. However, these increases were significantly suppressed in the CPE-treated mice. Reverse transcriptase-PCR revealed that mRNA expressions of interleukin (Il)-1β, Il-6, E-selectin, vascular cell adhesion molecule-1 and collagen type 1 were lower in the CPE group compared with the vehicle group. The mRNA expressions of nicotinamide adenine dinucleotide phosphate-oxidase (Nox)2 and Nox4 were increased in the vehicle-treated EAM hearts, although CPE treatment did not significantly suppress the transcription levels. However, compared with vehicle treatment of EAM hearts, CPE treatment significantly suppressed hydrogen peroxide concentrations. Cardiac myeloperoxidase activity, the intensity of dihydroethidium staining and the phosphorylation of nuclear factor-κB p65 were also lower in the CPE group compared with the vehicle group. Our data suggest that CPE ameliorates EAM in mice. CPE is a promising dietary supplement to suppress cardiovascular inflammation and oxidative stress.

Indexed as

AnimalsAutoimmune DiseasesCacaoDisease Models, AnimalE-SelectinHeartInterleukin-1betaInterleukin-6Membrane GlycoproteinsMiceMyocarditisMyocardiumNADPH Oxidase 2NADPH Oxidase 4NADPH OxidasesOxidative StressCybb protein, mouseE-SelectinInterleukin-1betaInterleukin-6Membrane GlycoproteinsNADPH Oxidase 2NADPH Oxidase 4NADPH OxidasesNox4 protein, mousePlant ExtractsPolyphenolsVascular Cell Adhesion Molecule-1

Identifiers

PMID26657007
OpenAlexW2264262914

What OpenQuestion holds

Textmetadata
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.