Evidence map›Paper›PMID 30212490›Full record

ArticlePloS one2018

Treatment with placental growth factor attenuates myocardial ischemia/reperfusion injury.

Yabing Zhang, Chang Cao, Juan Xin, Peilin Lv, Dongxu Chen, Shiyue Li, Hui Yang, Chan Chen, Bin Liu, Qian Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. VEGFR1 as a Target for Cardiovascular Gene Therapy.Journal of cardiovascular translational research · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
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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.

Yabing ZhangDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Chang CaoDepartment of Burn and Plastic Surgery, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Juan XinDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Peilin LvDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Dongxu ChenDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Shiyue LiDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Hui YangDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Chan ChenDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Bin LiuDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Qian LiDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.ORCID 0000-0002-6802-3343
Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies have established that oxidative stress plays an important role in the pathology of myocardial ischemia/reperfusion injury (MIRI). Vascular endothelial growth factor receptor 1 (VEGFR1) activation was reported to reduce oxidative stress and apoptosis. In the present study, we tested the hypothesis that the activation of VEGFR1 by placental growth factor (PlGF) could reduce MIRI by regulating oxidative stress. Mouse hearts and neonatal mouse cardiomyocytes were subjected to ischemia/reperfusion (I/R) and oxygen glucose deprivation (OGD), respectively. PlGF pretreatment markedly ameliorated I/R injury, as demonstrated by reduced infarct size and improved cardiac function. The protection was associated with a reduction of cardiomyocyte apoptosis. Similarly, our in vitro study showed that PlGF treatment improved cell viability and reduced cardiomyocyte apoptosis. Also, activation of VEGFR1 by PlGF suppressed intracellular and mitochondrial reactive oxygen species (ROS) generation. However, VEGFR1 neutralizing monoclonal antibody, which preventing PlGF binding, totally blocked this protective effect. In conclusion, activation of VEGFR1 could protect heart from I/R injury by suppression of oxidative stress and apoptosis.

Indexed as

AnimalsApoptosisCells, CulturedDisease Models, AnimalFemaleGene Expression RegulationHeart Function TestsMiceMyocardial Reperfusion InjuryMyocytes, CardiacOxidative StressPlacenta Growth FactorReactive Oxygen SpeciesTreatment OutcomeVascular Endothelial Growth Factor Receptor-1Flt1 protein, mousePlacenta Growth FactorReactive Oxygen SpeciesVascular Endothelial Growth Factor Receptor-1

Identifiers

PMID30212490
PMCPMC6136704
OpenAlexW2891803879

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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.