Evidence map›Paper›PMID 30641903›Full record

ArticleMolecules (Basel, Switzerland)2019

A Novel Synthetic Steroid of 2β,3α,5α-Trihydroxy-androst-6-one Alleviates the Loss of Rat Retinal Ganglion Cells Caused by Acute Intraocular Hypertension via Inhibiting the Inflammatory Activation of Microglia.

Hong-Jia-Qi Sun, Dong-Dong Xue, Bing-Zheng Lu, Yuan Li, Long-Xiang Sheng, Zhu Zhu, Yu-Wei Zhou, Jing-Xia Zhang, Gan-Jian Lin, Sui-Zhen Lin and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

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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

13 authors at 1 institution in 1 country.

Hong-Jia-Qi SunDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China. Elinor_Sun@outlook.com.
Dong-Dong XueDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China. xuedd@mail2.sysu.edu.cn.
Bing-Zheng LuDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China. lubzh3@mail2.sysu.edu.cn.
Yuan LiDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China. zmd2012spring@126.com.
Long-Xiang ShengDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China. shenglx@mail2.sysu.edu.cn.
Zhu ZhuDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China. zhuzhucute@163.com.
Yu-Wei ZhouDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China. zhouyw7@mail2.sysu.edu.cn.
Jing-Xia ZhangSchool of Pharmaceutical Sciences, Sun Yat-sen University, 132 East Circle at University City, Guangzhou 510006, China. zhjingx@mail.sysu.edu.cn.
Gan-Jian LinGuangzhou Cellprotek Pharmaceutical Co. Ltd., G Building F/4, 3 Lanyue Road, Science City, Guangzhou 510663, China. linganjian@cellprotek.com.
Sui-Zhen LinGuangzhou Cellprotek Pharmaceutical Co. Ltd., G Building F/4, 3 Lanyue Road, Science City, Guangzhou 510663, China. linsuizhen@cellprotek.com.
Guang-Mei YanDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China. ygm@mail.sysu.edu.cn.
Yu-Pin ChenDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China. chenyp39@mail.sysu.edu.cn.
Wei YinDepartment of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China. yinwei@mail.sysu.edu.cn.ORCID 0000-0001-8862-3197
Sun Yat-sen University · CN

Funding

China Postdoctoral Science Foundation No. 2017M612828Guangzhou Cellprotek Pharmaceutical Co. Ltd. No. 50000-71020079Guangzhou Science and Technology Program key projects No. 201704020103National Major Scientific and Technological Special Project for "Significant New Drugs Development" No. 20155ZX09J15106-001National Major Scientific and Technological Special Project for "Significant New Drugs Development" No. 2016ZX09101026National Natural Science Foundation of China No. 81773711the Introduction of Innovative R&D Team Program of Guangdong Province No. 2013Y104
6 · The paper itself

Abstract

Neuroinflammation has been well recognized as a key pathological event in acute glaucoma. The medical therapy of acute glaucoma mainly focuses on lowering intraocular pressure (IOP), while there are still scarce anti-inflammatory agents in the clinical treatment of acute glaucoma. Here we reported that β,3α,5α-trihydroxy-androst-6-one (sterone), a novel synthetic polyhydric steroid, blocked neuroinflammation mediated by microglia/macrophages and alleviated the loss of retinal ganglion cells (RGCs) caused by acute intraocular hypertension (AIH). The results showed that sterone significantly inhibited the morphological changes, the up-regulation of inflammatory biomarker ionized calcium-binding adapter molecule 1 (Iba-1), and the mRNA increase of proinflammatory tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6) induced by lipopolysaccharide (LPS) in BV2 microglia and RAW264.7 macrophages. Moreover, immunofluorescence and western blotting analysis revealed that sterone markedly abrogated the nuclear translocation and phosphorylation of nuclear factor-κB (NF-κB) p65 subunit. Furthermore, sterone significantly suppressed the inflammatory microglial activation and RGCs' reduction caused by retinal ischemia/reperfusion (I/R) injury in a rat AIH model. These results suggest sterone may be a potential candidate in the treatment of acute glaucoma caused by microglial activation-mediated neuroinflammatory injury.

Indexed as

Acute DiseaseAnimalsAnti-Inflammatory AgentsCell CountCell SurvivalDisease Models, AnimalGlaucomaLipopolysaccharidesMiceMicrogliaMolecular StructureNeuroprotective AgentsNF-kappa BOcular HypertensionRatsRAW 264.7 CellsAnti-Inflammatory AgentsLipopolysaccharidesNeuroprotective AgentsNF-kappa BSteroids2β,3α,5α-trihydroxy-androst-6-oneacute glaucomaischemia/reperfusion injurylipopolysaccharidemicroglial activationnuclear factor-κ B

Identifiers

PMID30641903
PMCPMC6358879
OpenAlexW2909797819

What OpenQuestion holds

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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.