Evidence map›Paper›PMID 31298558›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2019

Reversal of heart failure in a chemogenetic model of persistent cardiac redox stress.

Andrea Sorrentino, Benjamin Steinhorn, Luca Troncone, Seyed Soheil Saeedi Saravi, Sachin Badole, Emrah Eroglu, Marie Foley Kijewski, Sanjay Divakaran, Marcelo Di Carli, Thomas Michel

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

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  12. Metabolomic and transcriptomic signatures of chemogenetic heart failure.American journal of physiology. Heart and circulatory physiology · 2022
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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

10 authors at 1 institution in 1 country.

Andrea SorrentinoDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Benjamin SteinhornDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Luca TronconeDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Seyed Soheil Saeedi SaraviDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Sachin BadoleDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Emrah ErogluDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Marie Foley KijewskiDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Sanjay DivakaranDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Marcelo Di CarliDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Thomas MichelDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0003-1193-9841
Brigham and Women's Hospital · US

Funding

Medical Scientist Training ProgramT32GM007753 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WALENSKY, LOREN DAVID · 1985 to 2021
$50.0M
Transgenic CoreP30DK057521 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BROWN, DENNIS · 2000 to 2019
$31.4M
Tissue AnalysesP01HL048743 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI MICHEL, THOMAS · 1992 to 2014
$26.3M
TRAINING PROGRAM IN CARDIOVASCULAR RESEARCHT32HL007604 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI MARK W FEINBERG · 1985 to 2026
$19.0M
Noninvasive Cardiovascular Imaging Research Training ProgramT32HL094301 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Marcelo F DI CARLI · 2010 to 2026
$7.8M
Hydrogen peroxide in endothelial function and dysfunctionR01HL152173 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI MICHEL, THOMAS · 2021 to 2024
$2.2M
Chemogenetic approaches to define the roles of redox dysfunction in the cardiomyopathy of agingR21AG063073 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI MICHEL, THOMAS · 2019 to 2020
$480k
Austrian Science Fund FWF J 4113NHLBI NIH HHS P01 HL048743NHLBI NIH HHS R01 HL152173NHLBI NIH HHS T32 HL007604NHLBI NIH HHS T32 HL094301NIA NIH HHS R21 AG063073NIDDK NIH HHS P30 DK057521NIGMS NIH HHS T32 GM007753
6 · The paper itself

Abstract

We previously described a novel "chemogenetic" animal model of heart failure that recapitulates a characteristic feature commonly found in human heart failure: chronic oxidative stress. This heart failure model uses a chemogenetic approach to activate a recombinant yeast d-amino acid oxidase in rat hearts in vivo to generate oxidative stress, which then rapidly leads to the development of a dilated cardiomyopathy. Here we apply this new model to drug testing by studying its response to treatment with the angiotensin II (ANG II) receptor blocker valsartan, administered either alone or with the neprilysin inhibitor sacubitril. Echocardiographic and [

Indexed as

AminobutyratesAngiotensin II Type 1 Receptor BlockersAnimalsApoptosisBiphenyl CompoundsCardiomyopathy, DilatedD-Amino-Acid OxidaseDependovirusDisease Models, AnimalDrug CombinationsEnergy MetabolismFungal ProteinsGenetic VectorsHydrogen PeroxideInjections, IntravenousMaleAminobutyratesAngiotensin II Type 1 Receptor BlockersBiphenyl CompoundsD-Amino-Acid OxidaseDrug CombinationsFungal ProteinsHydrogen PeroxideNeprilysinProtease Inhibitorssacubitril and valsartan sodium hydrate drug combinationTetrazolesTroponin TValsartanangiotensin receptorchemogeneticsheart failureoxidative stress

Identifiers

PMID31298558
PMCPMC6766720
OpenAlexW2959531793

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.