Evidence map›Paper›PMID 37880377›Full record

ArticleScientific reports2023

Effect of AT1 receptor blockade on cardiovascular outcome after cardiac arrest: an experimental study in rats.

E A F Araújo Filho, M J C Carmona, D A Otsuki, D R R Maia, L G C A Lima, M F Vane

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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 1 country.

E A F Araújo FilhoDepartamento de Cirurgia (LIM 08), Faculdade de Medicina da USP (FMUSP), EAF: Av. Dr. Arnaldo, 455, sala 2120 (LIM-08), São Paulo, SP, 01246-903, Brazil. elsonfilho2@hotmail.com.ORCID http://orcid.org/0000-0002-9255-3950
M J C CarmonaDepartamento de Cirurgia, Disciplina de Anestesiologia, Universidade de São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-3031-2924
D A OtsukiDepartamento de Cirurgia (LIM 08), Faculdade de Medicina da USP (FMUSP), EAF: Av. Dr. Arnaldo, 455, sala 2120 (LIM-08), São Paulo, SP, 01246-903, Brazil.ORCID http://orcid.org/0000-0002-7411-3898
D R R MaiaDepartamento de Cirurgia (LIM 08), Faculdade de Medicina da USP (FMUSP), EAF: Av. Dr. Arnaldo, 455, sala 2120 (LIM-08), São Paulo, SP, 01246-903, Brazil.ORCID http://orcid.org/0000-0002-5098-6627
L G C A LimaDepartamento de Patologia, Faculdade de Medicina da USP (FMUSP), São Paulo, Brazil.ORCID http://orcid.org/0000-0002-3718-358X
M F VaneDepartamento de Cirurgia (LIM 08), Faculdade de Medicina da USP (FMUSP), EAF: Av. Dr. Arnaldo, 455, sala 2120 (LIM-08), São Paulo, SP, 01246-903, Brazil.ORCID http://orcid.org/0000-0003-3062-1484
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiotensin II receptor 1(AT1) antagonists are beneficial in focal ischemia/reperfusion (I/R). However, in cases of global I/R, such as cardiac arrest (CA), AT1 blocker's potential benefits are still unknown. Wistar male rats were allocated into four groups: Control group (CG)-animals submitted to CA by ventricular fibrillation induced by direct electrical stimulation for 3 min, and anoxia for 5 min; Group AT1 (GAT1)-animals subjected to CA and treated with 0.2 mg/kg of candesartan diluted in dimethylsulfoxide (DMSO) (0.1%); Vehicle Group (VG): animals subjected to CA and treated with 0.2 ml/kg of DMSO and Sham group (SG)-animals submitted to surgical interventions, without CA. Cardiopulmonary resuscitation consisted of group medications, chest compressions, ventilation, epinephrine (20 mcg/kg) and defibrillation. The animals were observed up to 4 h after spontaneous circulation (ROSC) return, and survival rates, hemodynamic variables, histopathology, and markers of tissue injury were analyzed. GAT1 group had a higher rate of ROSC (62.5% vs. 42.1%, p < 0.0001), survival (100% vs. 62.5%, p = 0.027), lower incidence of arrhythmia after 10 min of ROSC (10% vs. 62.5%, p = 0.000), and lower neuronal and cardiac injury scores on histology evaluation (p = 0.025 and p = 0.0052, respectively) than GC group. The groups did not differ regarding CA duration, number of adrenaline doses, or number of defibrillations. AT1 receptor blockade with candesartan yielded higher rates of ROSC and survival, in addition to neuronal and myocardial protection.

Indexed as

Cardiopulmonary ResuscitationHeart ArrestAnimalsBenzimidazolesBiphenyl CompoundsDimethyl SulfoxideDisease Models, AnimalEpinephrineMaleRatsRats, WistarReceptor, Angiotensin, Type 1TetrazolesBenzimidazolesBiphenyl CompoundscandesartanDimethyl SulfoxideEpinephrineReceptor, Angiotensin, Type 1Tetrazoles

Identifiers

PMID37880377
PMCPMC10600238
OpenAlexW4387937575

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.