Evidence map›Paper›PMID 26045738›Full record

ArticleInternational journal of clinical and experimental pathology2015

Protective effects of isorhamnetin on apoptosis and inflammation in TNF-α-induced HUVECs injury.

Tie-Long Chen, Guang-Li Zhu, Jian-An Wang, Guo-Dong Zhang, Hong-Fei Liu, Jin-Ru Chen, Yu Wang, Xiao-Long He

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
5.7field-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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Research progress of sea buckthorn (Frontiers in cardiovascular medicine · 2024
    Review
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  17. Proteomic Analysis of Anticancer TCMs Targeted at Mitochondria.Evidence-based complementary and alternative medicine : eCAM · 2015
    Review
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

8 authors at 2 institutions in 1 country.

Tie-Long ChenDepartment of Cardiology, Hangzhou Hospital of TCM 453 Ti Yu Chang Road, Hangzhou 310007, China.
Guang-Li ZhuDepartment of Cardiology, Hangzhou Hospital of TCM 453 Ti Yu Chang Road, Hangzhou 310007, China.
Jian-An WangDepartment of Cardiology, The Second Affiliated Hospital, College of Medicine, Zhejiang University 88 Fang Road, Hangzhou 310009, China.
Guo-Dong ZhangDepartment of Cardiology, Hangzhou Hospital of TCM 453 Ti Yu Chang Road, Hangzhou 310007, China.
Hong-Fei LiuDepartment of Cardiology, Hangzhou Hospital of TCM 453 Ti Yu Chang Road, Hangzhou 310007, China.
Jin-Ru ChenDepartment of Cardiology, Hangzhou Hospital of TCM 453 Ti Yu Chang Road, Hangzhou 310007, China.
Yu WangDepartment of Cardiology, Hangzhou Hospital of TCM 453 Ti Yu Chang Road, Hangzhou 310007, China ; Zhejiang University of TCM Hangzhou 310000, China.
Xiao-Long HeDepartment of Cardiology, Hangzhou Hospital of TCM 453 Ti Yu Chang Road, Hangzhou 310007, China.
Zhejiang Provincial Hospital of TCM · CNSecond Affiliated Hospital of Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Little is known about the role of isorhamnetin on endothelial cell apoptosis and inflammation when insulted by TNF-α injury. In our study, HUVECs were treated with TNF-α for 6 hours. HUVECs apoptosis were detected using flow cytometry. The expressions of ICAM-1, VCAM-1, E-selectin, NF-κB, AP-1 and eNOS were determined with western blotting or flow cytometry. The results showed TNF-α increased of apoptosis and the expression of ICAM-1, VCAM-1 and E-selectin in HUVECs, accompanied by significant augmentation of NF-κB and AP-1 expression. Pretreatment with isorhamnetin significantly reduced apoptosis in TNF-α-treated HUVECs. Moreover, isorhamnetin significantly attenuated TNF-α-induced upregulation of ICAM-1, VCAM-1, AP-1, E-selectin and NF-κB expression. Meanwhile, isorhamnetin also increased the expression of eNOS. So, isorhamnetin could suppress TNF-α-induced apoptosis and inflammation by blocking NF-κB and AP-1 signaling in HUVECs, which might be one of the underlying mechanisms for treatment of coronary heart disease.

Indexed as

Anti-Inflammatory AgentsApoptosisCells, CulturedCytoprotectionE-SelectinHumansHuman Umbilical Vein Endothelial CellsInflammationIntercellular Adhesion Molecule-1NF-kappa BNitric Oxide Synthase Type IIIQuercetinSignal TransductionTime FactorsTranscription Factor AP-1Tumor Necrosis Factor-alpha3-methylquercetinAnti-Inflammatory AgentsE-SelectinICAM1 protein, humanIntercellular Adhesion Molecule-1NF-kappa BNitric Oxide Synthase Type IIINOS3 protein, humanQuercetinSELE protein, humanTranscription Factor AP-1Tumor Necrosis Factor-alphaVascular Cell Adhesion Molecule-1AP-1apoptosiseNOSE-selectinHUVECsICAM-1IsorhamnetinNF-κBVCAM-1

Identifiers

PMID26045738
PMCPMC4440047
OpenAlexW574357133

What OpenQuestion holds

Textmetadata
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.