Evidence map›Paper›PMID 33167932›Full record

ArticleBMC complementary medicine and therapies2020

Emodin protected against retinal ischemia insulted neurons through the downregulation of protein overexpression of β-catenin and vascular endothelium factor.

Howard Wen-Haur Chao, Yu-Kuang Chen, Jorn-Hon Liu, Hwai-Tzong Pan, Hsin-May Lin, Hsiao-Ming Chao

Open access · goldAbstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Retinal Ischemia: Therapeutic Effects and Mechanisms of Paeoniflorin.International journal of molecular sciences · 2025
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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

6 authors at 2 institutions in 1 country.

Howard Wen-Haur ChaoDepartment of Ophthalmology, Cheng Hsin General Hospital, Taipei, Taiwan.
Yu-Kuang ChenDepartment of Ophthalmology, Cheng Hsin General Hospital, Taipei, Taiwan.
Jorn-Hon LiuDepartment of Ophthalmology, Cheng Hsin General Hospital, Taipei, Taiwan.
Hwai-Tzong PanInstitute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei, Taiwan.
Hsin-May LinDepartment of Ophthalmology, Cheng Hsin General Hospital, Taipei, Taiwan.
Hsiao-Ming ChaoDepartment of Ophthalmology, Cheng Hsin General Hospital, Taipei, Taiwan. hsiaoming.chao@gmail.com.ORCID http://orcid.org/0000-0002-1545-9936
Cheng Hsin General Hospital · TWNational Yang Ming Chiao Tung University · TW

Funding

Cheng Hsin General Hospital Foundation CHGH107-17
6 · The paper itself

Abstract

backgroundEmodin has been proved to have an anti-ischemic effect on the brain, however little research has been done on its effect on vision-threatening retinal ischemia. Thus, an investigation was carried out into the hypothetical efficacy of emodin against retinal ischemia and the role of β-catenin/VEGF in its therapeutic mechanism.

methodsRetinal ischemia, followed by reperfusion (IR), was inducted by raising the intraocular pressure of a Wistar rat's eye to 120 mmHg for 60 min. Additionally, pre-ischemic/post-ischemic intravitreous injections of emodin (4, 10 and 20 μM) or vehicle were carried out on the eye with retinal ischemia. MTT assay, electroretinograms, cresyl violet staining retinal thickness measurements, and fluorogold retrograde labelling of retinal ganglion cells (RGCs) as well as Western blotting were carried out.

resultsCultured RGC-5 cells subjected to oxygen glucose deprivation (OGD) were used to confirm the effective concentrations of emodin (administered 1 h pre-OGD, pre-OGD emodin). The most effective and significant (P = 0.04) dose of pre-OGD emodin was observed at 0.5 μM (cell viability: 47.52 ± 3.99%) as compared to pre-OGD vehicle treatment group (38.30 ± 2.51%). Furthermore, pre-ischemic intravitreous injection of 20 μM emodin (Emo20 + IR = 0.99 ± 0.18, P < 0.001) significantly attenuated the ischemia induced reduction in ERG b-wave amplitude, as compared to pre-ischemic intravitreous vehicle (Vehicle+IR = 0.04 ± 0.02). Post-ischemic intravitreous 20 μM emodin also significantly (P < 0.001) attenuated the ischemia associated b-wave reduction (IR + Em20 = 0.24 ± 0.09). Compared with pre-ischemic intravitreous vehicle (Vehicle+IR; whole retina thickness = 71.80 ± 1.08 μm; inner retina thickness = 20.97 ± 0.85 μm; RGC =2069.12 ± 212.82/0.17mm

conclusionsThe present results suggest that emodin might protect against retinal ischemia insulted neurons such as RGCs by significantly downregulating the upregulation of β-catenin/VEGF protein that occurs during ischemia.

Indexed as

Animalsbeta CateninDisease Models, AnimalDown-RegulationEmodinRatsRats, WistarRetinal DiseasesRetinal Ganglion CellsVascular Endothelial Growth Factorsbeta CateninEmodinVascular Endothelial Growth FactorsEmodinRetinal ischemiaVascular endothelium factorβ-Catenin

Identifiers

PMID33167932
PMCPMC7654144
OpenAlexW3101239555

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LicenceCC BY
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Registered trials

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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.