Evidence map›Paper›PMID 24551180›Full record

ArticlePloS one2014

Similar to spironolactone, oxymatrine is protective in aldosterone-induced cardiomyocyte injury via inhibition of calpain and apoptosis-inducing factor signaling.

Ting-Ting Xiao, Yuan-Yuan Wang, Yan Zhang, Cong-Hui Bai, Xiang-Chun Shen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

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  15. Cold Spring Harbor molecular case studies · 2017
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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

5 authors at 2 institutions in 2 countries.

Ting-Ting XiaoResearch Division of Pharmacology, Guiyang Medical University, Guiyang, China ; School of Chinese Medicine, Hong Kong Baptist University, Kowloon Tang, Kowloon, Hong Kong, China.
Yuan-Yuan WangResearch Division of Pathophysiology, Guiyang Medical University, Guiyang, China.
Yan ZhangResearch Division of Pharmacology, Guiyang Medical University, Guiyang, China.
Cong-Hui BaiResearch Division of Pharmacology, Guiyang Medical University, Guiyang, China.
Xiang-Chun ShenResearch Division of Pharmacology, Guiyang Medical University, Guiyang, China ; School of Life Science,Zhejiang Sci-Tech University, Hangzhou, China.
Guiyang Medical University · CNHong Kong Baptist University · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence indicates that oxymatrine (OMT) possesses variously pharmacological properties, especially on the cardiovascular system. We previously demonstrated that activated calpain/apoptosis-inducing factor (AIF)-mediated pathway was the key molecular mechanism in aldosterone (ALD) induces cardiomyocytes apoptosis. In the present study, we extended the experimentation by investigating the effect of OMT on cardiomyocytes exposed to ALD, as compared to spironolactone (Spiro), a classical ALD receptor antagonist. Cardiomyocytes were pre-incubated with OMT, Spiro or vehicle for 1 h, and then, cardiomyocytes were exposed to ALD 24 h. The cell injury was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and lactate dehydrogenase (LDH) leakage ratio. Apoptosis was determined by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) assay, annexin V/PI staining, and relative caspase-3 activity assay. Furthermore, expression of pro-apoptotic proteins including truncated Bid (tBid), calpain and AIF were evaluated by western blot analysis. ALD stimulation increased cardiomyocytes apoptosis, caspase-3 activity and protein expression of calpain, tBid and AIF in the cytosol (p<0.05). Pre-incubated with cardiomyocytes injury and increased caspase-3 activity were significantly attenuated (p<0.05). Furthermore, OMT suppressed ALD-induced high expression of calpain and AIF. And these effects of OMT could be comparable to Spiro. These findings indicated that OMT might be a potential cardioprotective-agent against excessive ALD-induced cardiotoxicity, at least in part, mediated through inhibition of calpain/AIF signaling.

Indexed as

Signal TransductionAldosteroneAlkaloidsAnimalsAnimals, NewbornApoptosisApoptosis Inducing FactorBH3 Interacting Domain Death Agonist ProteinCalpainCaspase 3Gene Expression RegulationIn Situ Nick-End LabelingL-Lactate DehydrogenaseMatrinesMyocytes, CardiacPrimary Cell CultureAifm1 protein, ratAldosteroneAlkaloidsApoptosis Inducing FactorBH3 Interacting Domain Death Agonist ProteinBid protein, ratCalpainCaspase 3L-Lactate DehydrogenaseMatrinesoxymatrineQuinolizinesSpironolactone

Identifiers

PMID24551180
PMCPMC3923837
OpenAlexW2149502393

What OpenQuestion holds

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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.