Evidence map›Paper›PMID 32178728›Full record

ArticleBMC pharmacology & toxicology2020

Isoniazid causes heart looping disorder in zebrafish embryos by the induction of oxidative stress.

Jie Ni, Hongye Wang, Xiyi Wei, Kangjie Shen, Yeqin Sha, Yuxiang Dong, Yimei Shu, Xiaojie Wan, Jingwen Cheng, Fang Wang and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 18 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Jie NiDepartment of Emergency, Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing, 210008, Jiangsu Province, China.
Hongye WangThe First Clinical Medical School, Nanjing Medical University, Nanjing, China.ORCID 0000-0002-6467-0316
Xiyi WeiThe First Clinical Medical School, Nanjing Medical University, Nanjing, China.
Kangjie ShenThe First Clinical Medical School, Nanjing Medical University, Nanjing, China.
Yeqin ShaThe First Clinical Medical School, Nanjing Medical University, Nanjing, China.
Yuxiang DongThe First Clinical Medical School, Nanjing Medical University, Nanjing, China.
Yimei ShuThe First Clinical Medical School, Nanjing Medical University, Nanjing, China.
Xiaojie WanClinical School of Imaging, Nanjing Medical University, Nanjing, China.
Jingwen ChengThe Medical School of Pediatrics, Nanjing Medical University, Nanjing, China.
Fang WangDepartment of Emergency, Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing, 210008, Jiangsu Province, China. 771647652@qq.com.
Yihai LiuDepartment of Cardiology, Nanjing Drum Tower Hospital, Clinical College of Nanjing Medical University, Nanjing, China. drhai@njmu.edu.cn.
Nanjing Medical University · CNNanjing Drum Tower Hospital · CNJiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe cardiotoxicity of isoniazid on zebrafish embryos and its underlying mechanism is unclear.

methodsHere, we exposed zebrafish embryos at 4 h post-fertilization to different levels of isoniazid and recorded the morphology and number of malformed and dead embryos under the microscope.

resultsThe high concentration of isoniazid group showed more malformed and dead embryos than the low concentration of isoniazid group and control group. The morphology of the heart and its alteration were visualized using transgenic zebrafish (cmlc2: GFP) and confirmed by in situ hybridization. The negative effects of isoniazid on the developing heart were characterized by lower heart rate and more heart looping disorders. Mechanistically, PCR showed decreased expression of heart-specific transcription factors when exposed to isoniazid. Oxidative stress was induced by isoniazid in cardiomyocytes, mediated by decreased activities of catalase and superoxide dismutase, which were rescued by scavengers of reactive oxygen species.

conclusionIn conclusion, this study demonstrated that isoniazid led to heart looping disturbance by the downregulation of cardiac-specific transcription factors and induction of cardiomyocyte apoptosis.

Indexed as

AnimalsAnimals, Genetically ModifiedAntitubercular AgentsApoptosisDown-RegulationEmbryonic DevelopmentEmbryo, NonmammalianHeart Defects, CongenitalHeart RateIsoniazidMyocytes, CardiacOxidative StressReactive Oxygen SpeciesTranscription FactorsZebrafishAntitubercular AgentsIsoniazidReactive Oxygen SpeciesTranscription FactorsHeart looping disorderIsoniazidOxidative stress

Identifiers

PMID32178728
PMCPMC7076990
OpenAlexW3011259437

What OpenQuestion holds

Textmetadata
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.