Evidence map›Paper›PMID 29115599›Full record

ArticleMolecular medicine reports2018

Aconitine induces apoptosis in H9c2 cardiac cells via mitochondria‑mediated pathway.

Xiangting Gao, Xincai Zhang, Jun Hu, Xuehua Xu, Yuanyi Zuo, Yun Wang, Jingfeng Ding, Hongfei Xu, Shaohua Zhu

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Review
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  18. Anticancer Activity ofIranian journal of pharmaceutical research : IJPR · 2021
    Article
  19. Aconitine Induces TRPV2-Mediated CaEvidence-based complementary and alternative medicine : eCAM · 2021
    Article
  20. Article
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

9 authors at 2 institutions in 1 country.

Xiangting GaoDepartment of Forensic Medicine, Medical College of Soochow University, Suzhou, Jiangsu 215123, P.R. China.
Xincai ZhangDepartment of Forensic Medicine, Medical College of Soochow University, Suzhou, Jiangsu 215123, P.R. China.
Jun HuDepartment of Forensic Medicine, Medical College of Soochow University, Suzhou, Jiangsu 215123, P.R. China.
Xuehua XuDepartment of Forensic Medicine, Medical College of Soochow University, Suzhou, Jiangsu 215123, P.R. China.
Yuanyi ZuoDepartment of Forensic Medicine, Medical College of Soochow University, Suzhou, Jiangsu 215123, P.R. China.
Yun WangDepartment of Forensic Medicine, Medical College of Soochow University, Suzhou, Jiangsu 215123, P.R. China.
Jingfeng DingDepartment of Forensic Medicine, Jiangsu Vocational College of Medicine, Yancheng, Jiangsu 224005, P.R. China.
Hongfei XuDepartment of Forensic Medicine, Medical College of Soochow University, Suzhou, Jiangsu 215123, P.R. China.
Shaohua ZhuDepartment of Forensic Medicine, Medical College of Soochow University, Suzhou, Jiangsu 215123, P.R. China.
Soochow University · CNJiangsu Vocational College of Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aconitine, a diterpenoid alkaloids derived from Aconitum plants, is widely employed to treat various diseases. The aim of the present study was to investigate the apoptotic effect of aconitine in H9c2 cardiac cells. H9c2 cell apoptosis induced by aconitine was detected by a Cell Counting kit‑8 assay, DAPI staining, Annexin V‑FITC/propidium iodide double staining and western blotting. The effects of aconitine on reactive oxygen species levels and mitochondrial membrane potential were confirmed by fluorescence microscopy and flow cytometry. In addition, ATP contents were determined using a ATP‑dependent bioluminescence assay kit. The levels of peroxisome proliferator activated receptor γ co‑activator 1α (PGC‑1α) expression and apoptosis‑associated proteins including Caspase‑3, B‑cell lymphoma 2 (Bcl‑2), Bcl‑2‑associated X protein (Bax) and Cytochrome c were also assessed. Taken together, the results indicated that aconitine may inhibit cell viability, decrease PGC‑1α expression, induce mitochondrial dysfunctions, upregulate Cytochrome c, Bax and Caspase‑3, and downregulate Bcl‑2, suggesting that aconitine may induce apoptosis through mitochondria‑mediated signaling pathways in H9c2 cells.

Indexed as

AconitineAdenosine TriphosphateAnimalsApoptosisCell SurvivalFlow CytometryMembrane Potential, MitochondrialMitochondriaMyocytes, CardiacRatsReactive Oxygen SpeciesSignal TransductionAconitineAdenosine TriphosphateReactive Oxygen Species

Identifiers

PMID29115599
PMCPMC5780139
OpenAlexW2767171292

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.