Evidence map›Paper›PMID 32252692›Full record

ArticleBMC ophthalmology2020

Ripasudil alleviated the inflammation of RPE cells by targeting the miR-136-5p/ROCK/NLRP3 pathway.

Zhao Gao, Qiang Li, Yunda Zhang, Xiaohong Gao, Haiyan Li, Zhigang Yuan

Open access · goldAbstract read
In one paragraph

Article in BMC ophthalmology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-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

17 citing papers in PubMed, 26 citations in OpenAlex.

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  8. Differential Spleen miRNA Expression Profile of Beagle Dogs Infected withAnimals : an open access journal from MDPI · 2022
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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.

Zhao GaoDepartment of Vitreoretinopathy, Shanxi Eye Hospital, No.100 Fudong Street, Xinghualing district, Taiyuan city, 030001, Shanxi province, China.
Qiang LiDepartment of Orthopedics, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Taiyuan city, 030032, Shanxi province, China.
Yunda ZhangDepartment of Vitreoretinopathy, Shanxi Eye Hospital, No.100 Fudong Street, Xinghualing district, Taiyuan city, 030001, Shanxi province, China.
Xiaohong GaoDepartment of Vitreoretinopathy, Shanxi Eye Hospital, No.100 Fudong Street, Xinghualing district, Taiyuan city, 030001, Shanxi province, China.
Haiyan LiDepartment of Pathology, Shanxi Eye Hospital, Taiyuan city, 030001, Shanxi province, China.
Zhigang YuanDepartment of Vitreoretinopathy, Shanxi Eye Hospital, No.100 Fudong Street, Xinghualing district, Taiyuan city, 030001, Shanxi province, China. yzgsxeye@sina.com.
Shanxi Eye Hospital · CNShanxi Academy of Medical Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInflammation of RPE cells led to different kinds of eye diseases and affected the normal function of the retina. Furthermore, higher levels of ROCK1 and ROCK2 induced injury of endothelial cells and many inflammatory diseases of the eyes. Ripasudil, which was used for the treatment of glaucoma, was one kind of the inhibitor of ROCK1 and ROCK2, but whether ripasudil could relieve the LPS-induced inflammation and damage of RPE cells was not clear.

methodsWe used LPS to stimulate ARPE-19 cells, the RPE cell line. After that, we detected the levels of ROCK1 and ROCK2 by western-blotting after the stimulation of LPS and treatment of ripasudil. Then luciferase reporter assays were used to confirm the targeting effect of miR-136-5p on ROCK1 and ROCK2. At last, the levels of NLRP3, ASC, caspase1, IL-1β and IL-18 were detected with the western-blotting after the knockdown of miR-136-5p.

resultsThe levels of ROCK1, ROCK2 and miR-136-5p in ARPE-19 cells were promoted after the stimulation of LPS. After the treatment of ripasudil, the expression levels of ROCK1, ROCK2 and miR-136-5p were suppressed. The expression of ROCK1 and ROCK2 was targeted and inhibited by the miR-136-5p. The levels of inflammation related proteins NLRP3, ASC, caspase1, IL-1β and IL-18 was also inhibited after the treatment of ripasudil. However, the expression of these proteins was rescued after the knockdown of miR-136-5p.

conclusionRipasudil relieved the inflammatory injury of RPE cells by upregulating miR-136-5p, therefore inhibiting the expression of ROCK1, ROCK2, NLRP3, ASC, caspase1, IL-1β and IL-18.

Indexed as

ApoptosisBlotting, WesternCell LineDrug Delivery SystemsEnzyme-Linked Immunosorbent AssayGene Expression RegulationHumansInflammationIsoquinolinesMicroRNAsNLR Family, Pyrin Domain-Containing 3 ProteinReal-Time Polymerase Chain ReactionRetinal Pigment Epitheliumrho-Associated KinasesSincalideSulfonamidesIsoquinolinesK-115MicroRNAsMIRN136 microRNA, humanNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanrho-Associated KinasesSincalideSulfonamidesmiR-136-5pNLRP3RipasudilROCK1ROCK2RPE cells

Identifiers

PMID32252692
PMCPMC7137504
OpenAlexW3014182756

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.