Evidence map›Paper›PMID 35262582›Full record

ArticleArquivos brasileiros de cardiologia2022

The Dysfunctional Scenario of the Major Components Responsible for Myocardial Calcium Balance in Heart Failure Induced by Aortic Stenosis.

Vitor Loureiro da Silva, Sérgio Luiz Borges de Souza, Gustavo Augusto Ferreira Mota, Dijon H S Campos, Alexandre Barroso Melo, Danielle Fernandes Vileigas, Paula Grippa Sant'Ana, Priscila Murucci Coelho, Silméia Garcia Zanati Bazan, André Soares Leopoldo and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Arquivos brasileiros de cardiologia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-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

3 citing papers in PubMed, 3 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Vitor Loureiro da SilvaUniversidade de São Paulo - Departamento de Medicina Interna, Botucatu, SP - Brasil.ORCID 0000-0001-7796-6215
Sérgio Luiz Borges de SouzaUniversidade de São Paulo - Departamento de Medicina Interna, Botucatu, SP - Brasil.
Gustavo Augusto Ferreira MotaUniversidade de São Paulo - Departamento de Medicina Interna, Botucatu, SP - Brasil.ORCID 0000-0001-8103-3338
Dijon H S CamposUniversidade de São Paulo - Departamento de Medicina Interna, Botucatu, SP - Brasil.ORCID 0000-0002-4933-0604
Alexandre Barroso MeloUniversidade Federal do Espírito Santo - Departamento de Desportos, Vitória, ES - Brasil.
Danielle Fernandes VileigasUniversidade de São Paulo - Departamento de Medicina Interna, Botucatu, SP - Brasil.
Paula Grippa Sant'AnaUniversidade de São Paulo - Departamento de Medicina Interna, Botucatu, SP - Brasil.
Priscila Murucci CoelhoUniversidade Federal do Espírito Santo - Departamento de Desportos, Vitória, ES - Brasil.
Silméia Garcia Zanati BazanUniversidade de São Paulo - Departamento de Medicina Interna, Botucatu, SP - Brasil.ORCID 0000-0002-0607-8189
André Soares LeopoldoUniversidade Federal do Espírito Santo - Departamento de Desportos, Vitória, ES - Brasil.ORCID 0000-0001-5999-2671
Antônio Carlos CicognaUniversidade de São Paulo - Departamento de Medicina Interna, Botucatu, SP - Brasil.
Inclusione Andicap Ticino · CHUniversidade Federal do Espírito Santo · BRUniversidade Paulista · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMaladaptive cardiac remodelling is characterized by diastolic and systolic dysfunction, culminating in heart failure. In this context, the dysfunctional scenario of cardiac calcium (Ca2+) handling has been poorly studied. An experimental model of aortic stenosis has been extensively used to improve knowledge about the key mechanisms of cardiac pathologic remodelling.

objectiveTo understand the dysfunctional process of the major components responsible for Ca2+ balance and its influence on cardiac function in heart failure induced by aortic stenosis.

methodsMale 21-day-old Wistar rats were distributed into two groups: control (sham; n= 28) and aortic stenosis (AoS; n= 18). Cardiac function was analysed by echocardiogram, isolated papillary muscle, and isolated cardiomyocytes. In the papillary muscle assay, SERCA2a and L-type Ca2+ channel activity was evaluated. The isolated cardiomyocyte assay evaluated Ca2+ handling. Ca2+ handling protein expression was analysed by western blot. Statistical significance was set at p <0.05.

resultsPapillary muscles and cardiomyocytes from AoS hearts displayed mechanical malfunction. AoS rats presented a slower time to the Ca2+ peak, reduced Ca2+ myofilament sensitivity, impaired sarcoplasmic reticulum Ca2+ influx and reuptake ability, and SERCA2a and L-type calcium channel (LTCC) dysfunction. Moreover, AoS animals presented increased expression of SERCA2a, LTCCs, and the Na+/Ca2+ exchanger.

conclusionSystolic and diastolic heart failure due to supravalvular aortic stenosis was paralleled by impairment of cellular Ca2+ influx and inhibition of sarcoplasmic reticulum Ca2+ reuptake due to LTCC and SERCA2a dysfunction, as well as changes in Ca2+ handling and expression of the major proteins responsible for cellular Ca2+ homeostasis.

Indexed as

Aortic Valve StenosisHeart FailureAnimalsCalciumMaleMyocardial ContractionMyocytes, CardiacPapillary MusclesRatsRats, WistarSarcoplasmic Reticulum Calcium-Transporting ATPasesCalciumSarcoplasmic Reticulum Calcium-Transporting ATPases

Identifiers

PMID35262582
PMCPMC8856692
OpenAlexW4200107026

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.