Evidence map›Paper›PMID 27456026›Full record

ArticleCellular and molecular neurobiology2017

Neuroprotection of Ro25-6981 Against Ischemia/Reperfusion-Induced Brain Injury via Inhibition of Autophagy.

Fuxing Dong, Ruiqin Yao, Hongli Yu, Yaping Liu

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular neurobiology, 2017. 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
3.6field-weighted citation impact, top 7% 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, 31 citations in OpenAlex.

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  3. Long Non-coding RNAs (lncRNAs), A New Target in Stroke.Cellular and molecular neurobiology · 2022
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  17. Environmental Enrichment Improves Spatial Learning and Memory in Vascular Dementia Rats with Activation of Wnt/β-Catenin Signal Pathway.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
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

4 authors at 1 institution in 1 country.

Fuxing DongResearch Center for Neurobiology, Xuzhou Medical University, No. 209, Tongshan Road, Yunlong District, Xuzhou, 221004, Jiangsu, People's Republic of China.
Ruiqin YaoResearch Center for Neurobiology, Xuzhou Medical University, No. 209, Tongshan Road, Yunlong District, Xuzhou, 221004, Jiangsu, People's Republic of China.
Hongli YuResearch Center for Neurobiology, Xuzhou Medical University, No. 209, Tongshan Road, Yunlong District, Xuzhou, 221004, Jiangsu, People's Republic of China.
Yaping LiuLaboratory of National Experimental Teaching and Demonstration Center of Basic Medicine, Xuzhou Medical University, No. 209, Tongshan Road, Yunlong District, Xuzhou, 221004, Jiangsu, People's Republic of China. ya-ping-liu@163.com.
Xuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we investigated the neuroprotective effect of Ro25-6981 against cerebral ischemia/reperfusion injury. Ro25-6981 alone or in combination with rapamycin was intracerebroventricularly administered to rats which suffered transient forebrain ischemia inducing by 4-vessel occlusion and reperfusion. Nissl staining was used to determine the survival of CA1 pyramidal cells of the hippocampus, while immunohistochemistry was performed to measure neuron-specific enolase (NSE) expression. The expression of autophagy-related proteins, such as microtubule-associated protein l light chain 3 (LC3), Beclin 1, and sequestosome 1 (p62), was assessed by immunoblotting. Nissl staining showed that neuronal damage was reduced in the hippocampal CA1 pyramidal layer in rats that received Ro25-6981. The protective effect of Ro25-6981 was dose-dependent, with a significant effect in the middle-dose range. The expression of NSE increased after Ro25-6981 treatment. Ro25-6981 significantly decreased LC3II (which is membrane bound) and Beclin 1, and increased p62. In addition, Ro25-6981 decreased rapamycin-induced neuronal damage and excessive activation of autophagy after I/R. Taken together, the results suggest that Ro25-6981 could suppress ischemic brain injury by regulating autophagy-related proteins during ischemia/reperfusion.

Indexed as

AnimalsApoptosis Regulatory ProteinsAutophagyBrainBrain InjuriesBrain IschemiaDisease Models, AnimalMaleMicrotubule-Associated ProteinsNeuroprotectionNeuroprotective AgentsPhenolsPiperidinesRats, Sprague-DawleyReperfusion InjuryApoptosis Regulatory ProteinsMicrotubule-Associated ProteinsNeuroprotective AgentsPhenolsPiperidinesRo 25-6981AutophagyIschemia/reperfusionN-methyl-D-aspartate receptorRo25-6981

Identifiers

PMID27456026
PMCPMC11482226
OpenAlexW2494396943

What OpenQuestion holds

Textmetadata
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.