Evidence map›Paper›PMID 36573084›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2022

Morroniside Regulates Endothelial Cell Function via the EphrinB Signaling Pathway after Oxygen-Glucose Deprivation

Tingting Liu, Songyang Zheng, Fangling Sun, Xin Tian, Zixin Zhu, Wenrong Zheng, Yufeng Wang, Jianguo Xing, Wen Wang

Open access · hybridAbstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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

9 authors at 2 institutions in 1 country.

Tingting LiuDepartment of Experimental Animal Laboratory, Xuanwu Hospital of Capital Medical University, Beijing 100053, China.
Songyang ZhengDepartment of Experimental Animal Laboratory, Xuanwu Hospital of Capital Medical University, Beijing 100053, China.
Fangling SunDepartment of Experimental Animal Laboratory, Xuanwu Hospital of Capital Medical University, Beijing 100053, China.
Xin TianDepartment of Experimental Animal Laboratory, Xuanwu Hospital of Capital Medical University, Beijing 100053, China.
Zixin ZhuDepartment of Experimental Animal Laboratory, Xuanwu Hospital of Capital Medical University, Beijing 100053, China.
Wenrong ZhengDepartment of Experimental Animal Laboratory, Xuanwu Hospital of Capital Medical University, Beijing 100053, China.
Yufeng WangDepartment of Experimental Animal Laboratory, Xuanwu Hospital of Capital Medical University, Beijing 100053, China.
Jianguo XingCollege of Pharmacy, Xinjiang Medical University, Xinjiang, Urumqi 830054, China.ORCID https://orcid.org/0000-0002-0411-254X
Wen WangDepartment of Experimental Animal Laboratory, Xuanwu Hospital of Capital Medical University, Beijing 100053, China.ORCID https://orcid.org/0000-0001-7596-9930
Capital Medical University · CNXinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proangiogenic treatment is a potential treatment for acute myocardial infarction (AMI). Morroniside was previously discovered to increase post-AMI angiogenesis in rats as well as the proliferation of rat coronary artery endothelial cells (RCAECs). However, the effects of morroniside on other endothelial cell (EC) functions and underlying mechanisms are unknown. To further clarify the vascular biological activity of morroniside, this work focused on investigating how morroniside influenced endothelial cell functions, such as cell viability, tube formation capacity, migration, and adhesion, and to explore the signaling pathway. Oxygen-glucose deprivation causes ischemic damage in RCAECs (OGD). In vitro investigations were carried out to explore the involvement of morroniside in EC function and pathways mediated by ephrinB. The results revealed that the number of BrdU

Identifiers

PMID36573084
PMCPMC9789905
OpenAlexW4313279426

What OpenQuestion holds

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LicenceCC BY
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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.