Evidence map›Paper›PMID 35837687›Full record

ArticleAsian cardiovascular & thoracic annals2022

The combination approach with Rhokinase inhibition and mechanical circulatory support in myocardial ischemia-reperfusion injury: Rho-kinase inhibition and ventricular unloading.

Shunsuke Miyahara, Alexander Jenke, Mariam Yazdanyar, Julia Kistner, Moritz Benjamin Immohr, Yukiharu Sugimura, Hug Aubin, Hiroyuki Kamiya, Yutaka Okita, Artur Lichtenberg and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Asian cardiovascular & thoracic annals, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
–field-weighted citation impact, top 87% 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

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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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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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 3 institutions in 2 countries.

Shunsuke MiyaharaDepartment of Cardiac Surgery, 9170Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Alexander JenkeDepartment of Cardiac Surgery, 9170Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Mariam YazdanyarDepartment of Cardiac Surgery, 9170Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Julia KistnerDepartment of Cardiac Surgery, 9170Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Moritz Benjamin ImmohrDepartment of Cardiac Surgery, 9170Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.ORCID 0000-0003-1051-8105
Yukiharu SugimuraDepartment of Cardiac Surgery, 9170Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.ORCID 0000-0001-8408-8457
Hug AubinDepartment of Cardiac Surgery, 9170Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Hiroyuki KamiyaDepartment of Cardiac Surgery, 38051Asahikawa Medical University, Asahikawa, Japan.
Yutaka OkitaDepartment of Surgery, Division of Cardiovascular Surgery, 38303Kobe University Graduate School of Medicine, Kobe, Japan.ORCID 0000-0003-0217-7363
Artur LichtenbergDepartment of Cardiac Surgery, 9170Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Payam AkhyariDepartment of Cardiac Surgery, 9170Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.ORCID 0000-0002-6452-8678
Heinrich Heine University Düsseldorf · DEAsahikawa Medical University · JPKobe University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt remains unclear whether the Rho-kinase (ROCK) inhibition in combination with mechanical circulatory support (MCS) had a synergic protective effect on myocardial ischemia (MI)/reperfusion injury in therapeutic strategies for acute myocardial infarction (AMI). We report the results of an approach using a rat model consisting of a miniaturized cardiopulmonary bypass (CPB) and AMI.

methodsA total of 25 male Wistar rats were randomized into 5 groups: (1) Sham: a suture was passed under the left anterior descending artery (LAD) creating no MI. A vehicle solution (0.9% saline) was injected intraperitoneally. (2) Myocardial ischemia (MI) + vehicle (MI + V): LAD was ligated for 30 min and reperfused for 120 min, followed by administration of vehicle solution. (3) MI + fasudil (MI + F): the work sequence of group 2, but the selective ROCK inhibitor fasudil (10 mg/kg) was administered instead. (4) MI + V + CPB: CPB was initiated 15 min after the ligation of the LAD to the end of the reperfusion, in addition to the work sequence in group 2. (5) In the MI + F + CPB group, the work sequence of group 4, but with fasudil administration (10 mg/kg).

resultsMeasurements of cardiac function through conductance catheter indicated that the drop of + dP/dt after reperfusion was moderately limited in MI + F + CPB (vs. MI + V, dP/dt

conclusionTherefore, fasudil administration with MCS resulted in a moderately better left ventricular performance.

Indexed as

Coronary Artery DiseaseMyocardial InfarctionMyocardial IschemiaMyocardial Reperfusion Injury1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineAnimalsHumansMaleProto-Oncogene Proteins c-aktRatsRats, Wistarrho-Associated KinasesSaline SolutionTreatment Outcome1-(5-Isoquinolinesulfonyl)-2-MethylpiperazinefasudilProto-Oncogene Proteins c-aktrho-Associated KinasesSaline Solutionischemia/reperfusion injurymechanical circulatory supportmyocardial infractionPI3K/Akt pathwayRho-kinase

Identifiers

PMID35837687
PMCPMC9513506
OpenAlexW4285592336

What OpenQuestion holds

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LicenceCC BY-NC
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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.