Evidence map›Paper›PMID 29483387›Full record

ArticleChinese medical journal2018

Sigma-1 Receptor Stimulation with PRE-084 Ameliorates Myocardial Ischemia-Reperfusion Injury in Rats.

Qi-Jun Gao, Bo Yang, Jing Chen, Shao-Bo Shi, Hong-Jie Yang, Xin Liu

Open access · goldAbstract read
In one paragraph

Article in Chinese medical journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

  1. The Role of Sigmar1 in Autophagy Regulation and Disease Therapy.International journal of molecular sciences · 2026
    Review
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  6. Unfolding the cardioprotective potential of sigma-1 receptor-directed molecular imaging.Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology · 2023
    Article
  7. Review
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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

6 authors at 1 institution in 1 country.

Qi-Jun GaoDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430000; Department of Cardiology, First Hospital of Jingmen, Jingmen, Hubei 448000, China.
Bo YangDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430000, China.
Jing ChenDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430000, China.
Shao-Bo ShiDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430000, China.
Hong-Jie YangDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430000, China.
Xin LiuDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430000, China.
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe sigma receptors are a relatively novel receptor group with respect to knowledge of their effect on health. Although the sigma-1 receptor agonist PRE-084 exhibits a cardioprotective effect in some studies, the benefits in cases of myocardial ischemia/reperfusion (I/R) are not clear. The aim of this study was to explore the mechanism of action and assess the effect of PRE-084 on myocardial I/R injury in rats.

methodsIn this study, rats were assigned randomly to three groups with computer (n = 14 for each group): a sham group, an I/R group, and a PRE-084 group. In the PRE-084 group, rats were administered PRE-084 1 h before operation. In the myocardial I/R model, the left anterior descending branch of rats was ligated and opened half an hour later. Cardiac function was assessed, and the apoptosis index was evaluated. The mechanisms of the cardioprotective effects of PRE-084 were explored.

resultsPRE-084 pretreatment preserved cardiac function and reduced myocardial apoptosis (F = 86.0, P < 0.01) with Western blotting analysis, showing significantly reduced expression of Bax (F = 75.7, P < 0.01) and cleaved-caspase 3 (F = 44.7, P < 0.01), along with increased expression of the Bcl-2 protein (P < 0.01) and phosphorylated protein kinase B (p-Akt) (P < 0.01) and phosphorylated-endothelial nitric oxide synthase (p-eNOS; P < 0.01).

conclusionPRE-084 preserved cardiac function and reduced myocardial apoptosis through the activation of Akt and eNOS.

Indexed as

AnimalsBlotting, WesternCaspase 3MaleMorpholinesMyocardial IschemiaMyocardial Reperfusion InjuryNitric Oxide SynthaseNitric Oxide Synthase Type IIIProto-Oncogene Proteins c-bcl-2RatsRats, Sprague-DawleyReceptors, sigmaSigma-1 ReceptorSignal Transduction2-(4-morpholino)ethyl-1-phenylcyclohexane-1-carboxylateCaspase 3MorpholinesNitric Oxide SynthaseNitric Oxide Synthase Type IIIProto-Oncogene Proteins c-bcl-2Receptors, sigmaSigma-1 ReceptorMyocardial Ischemia/ReperfusionPRE-084Sigma-1 Receptor

Identifiers

PMID29483387
PMCPMC5850669
OpenAlexW2792269528

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.