Evidence map›Paper›PMID 36465659›Full record

ArticleFrontiers in endocrinology2022

Protective effects of safranal on diabetic retinopathy in human microvascular endothelial cells and related pathways analyzed with transcriptome sequencing.

Qin Xiao, Yao-Yao Sun, Zhan-Jun Lu, Shan-Shan Li, Riguga Su, Wen-Lin Chen, Lin-Lin Ran, Surina Zhang, Kaixin Deng, Wen-Zhen Yu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

11 authors at 4 institutions in 1 country.

Qin XiaoDepartment of Ophthalmology, Affiliated Hospital of Inner Mongolia University for Nationalities, Tongliao, China.
Yao-Yao SunDepartment of Ophthalmology, Peking University People's Hospital, Beijing, China.
Zhan-Jun LuDepartment of Ophthalmology, Affiliated Hospital of Inner Mongolia University for Nationalities, Tongliao, China.
Shan-Shan LiDepartment of Ophthalmology, Affiliated Hospital of Inner Mongolia University for Nationalities, Tongliao, China.
Riguga SuCollege of Clinical (Mongolian) Medicine, Inner Mongolia University for Nationalities, Tongliao, China.
Wen-Lin ChenCollege of Clinical (Mongolian) Medicine, Inner Mongolia University for Nationalities, Tongliao, China.
Lin-Lin RanCollege of Clinical (Mongolian) Medicine, Inner Mongolia University for Nationalities, Tongliao, China.
Surina ZhangDepartment of Hematology, Affiliated Hospital of Inner Mongolia University for Nationalities, Tongliao, China.
Kaixin DengDepartment of Ophthalmology, Beijing Jishuitan Hospital, Beijing, China.
Wen-Zhen YuDepartment of Ophthalmology, Peking University People's Hospital, Beijing, China.
Wenqian ChenDepartment of Ophthalmology, Peking University People's Hospital, Beijing, China.
Inner Mongolia University for Nationalities · CNPeking University · CNPeking University People's Hospital · CNBeijing Jishuitan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: To determine the effect of safranal on diabetic retinopathy Methods: We used human retinal microvascular endothelial cells (HRMECs) to test the influence of safranal Results: Cell proliferation was inhibited under a high glucose condition but could be protected by safranal at different concentrations (P<0.001). Flow cytometry results suggested safranal also protected cells from apoptosis (P=0.006). A transwell test demonstrated reduced invasiveness of safranal-treated cells in a high glucose condition (P<0.001). In a tube formation investigation, there were noticeably more new branches in the high gloucose group compared to a high glucose treated with safranal group (P<0.001). In mRNA expression patterns on transcriptome sequencing, the MAPK signaling pathway showed an expression ratio. With western blotting, the phosphorylation level of p38-AKT was elevated under a high glucose condition but could be inhibited by safranal. The expression of molecules associated with cell adhesion, including E-cadherin, N-cadherin, Snail, Twist, and fibronectin also changed significantly after safranal treatment under a high glucose condition. Conclusion: Safranal can protect diabetic retinopathy

Indexed as

Diabetes MellitusDiabetic RetinopathyCyclohexenesEndothelial CellsGlucoseHumansProto-Oncogene Proteins c-aktTerpenesTranscriptomeCyclohexenesGlucoseProto-Oncogene Proteins c-aktsafranalTerpenesdiabetic retinopathyhigh glucosehuman retinal microvascular endothelial cellssafranaltranscriptomics

Identifiers

PMID36465659
PMCPMC9708741
OpenAlexW4309153823

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.