Evidence map›Paper›PMID 30787975›Full record

ArticleAmerican journal of translational research2019

Osthole protects against Ang II-induced endotheliocyte death by targeting NF-κB pathway and Keap-1/Nrf2 pathway.

Luyuan Tao, Xingjian Gu, Enguo Xu, Shijia Ren, Li Zhang, Wenhua Liu, Xiaofeng Lin, Jianguang Yang, Changgong Chen

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Vasorelaxant and Blood Pressure-Lowering Effects ofInternational journal of molecular sciences · 2024
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  6. Review
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  8. Article
  9. Coumarins as Modulators of the Keap1/Nrf2/ARE Signaling Pathway.Oxidative medicine and cellular longevity · 2020
    Review
  10. Article
  11. 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 1 institution in 1 country.

Luyuan TaoDepartment of Cardiology, Taizhou First People's Hospital Taizhou 318020, Zhejiang, P. R. China.
Xingjian GuDepartment of Cardiology, Taizhou First People's Hospital Taizhou 318020, Zhejiang, P. R. China.
Enguo XuDepartment of Cardiology, Taizhou First People's Hospital Taizhou 318020, Zhejiang, P. R. China.
Shijia RenDepartment of Cardiology, Taizhou First People's Hospital Taizhou 318020, Zhejiang, P. R. China.
Li ZhangDepartment of Cardiology, Taizhou First People's Hospital Taizhou 318020, Zhejiang, P. R. China.
Wenhua LiuDepartment of Cardiology, Taizhou First People's Hospital Taizhou 318020, Zhejiang, P. R. China.
Xiaofeng LinDepartment of Cardiology, Taizhou First People's Hospital Taizhou 318020, Zhejiang, P. R. China.
Jianguang YangDepartment of Cardiology, Taizhou First People's Hospital Taizhou 318020, Zhejiang, P. R. China.
Changgong ChenDepartment of Cardiology, Taizhou First People's Hospital Taizhou 318020, Zhejiang, P. R. China.
Taizhou First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osthole, the main active constituents in traditional Chinese medicine fructus cnidii, has anti-inflammatory and anti-oxidant activities. Apoptosis of vascular endothelial cells is an important cause of cardiovascular disease. Inflammation and oxidative stress are two key factors in injury of endotheliocyte. In this study, we investigated the effect of osthole on Ang II-induced apoptosis of rat aortic endothelial cells (RAECs) and explored the underlying mechanisms. In the present study, the protective effects of osthole on RAECs induced by Ang II in vitro were tested. Additionally, molecular docking and molecular dynamics (MD) simulations were utilized to investigate the potential binding mode of osthole to NF-κB and Keap1. Our results showed osthole remarkably attenuates Ang II-induced apoptosis of RAECs via alleviating inflammation and oxidative stress. Molecular docking and MD simulations revealed the potential interaction of osthole bind to the P65 subunit of NF-κB and the Keap1 protein, an adaptor for the degradation of Nrf2. We further found that osthole decreased Ang II-induced inflammation and oxidative stress through respectively modulating NF-κB and Nrf2 pathways in RAECs. These studies provide evidence that osthole may represent a potential therapeutic agent for the treatment of vascular injury.

Indexed as

Ang IIinflammationOstholeoxidative stressrat aortic endothelial cells

Identifiers

PMID30787975
PMCPMC6357313
OpenAlexW3021094601

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.