Evidence map›Paper›PMID 32606599›Full record

ArticleDrug design, development and therapy2020

Nimodipine Improves Cognitive Impairment After Subarachnoid Hemorrhage in Rats Through IncRNA NEAT1/miR-27a/MAPT Axis.

Jun-Wei Li, Shao-Hua Ren, Jin-Rui Ren, Zi-Gang Zhen, Li-Rong Li, Xu-Dong Hao, Hong-Ming Ji

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 20 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

7 authors.

Jun-Wei LiDepartment of Neurosurgery, The People's Hospital of Shanxi Province, Taiyuan, Shanxi Province, People's Republic of China.
Shao-Hua RenDepartment of Neurosurgery, The People's Hospital of Shanxi Province, Taiyuan, Shanxi Province, People's Republic of China.
Jin-Rui RenDepartment of Neurosurgery, The People's Hospital of Shanxi Province, Taiyuan, Shanxi Province, People's Republic of China.
Zi-Gang ZhenDepartment of Neurosurgery, The People's Hospital of Shanxi Province, Taiyuan, Shanxi Province, People's Republic of China.
Li-Rong LiDepartment of Neurosurgery, The People's Hospital of Shanxi Province, Taiyuan, Shanxi Province, People's Republic of China.
Xu-Dong HaoDepartment of Neurosurgery, The People's Hospital of Shanxi Province, Taiyuan, Shanxi Province, People's Republic of China.
Hong-Ming JiDepartment of Neurosurgery, The People's Hospital of Shanxi Province, Taiyuan, Shanxi Province, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSubarachnoid hemorrhage (SAH) is a cerebral hemorrhage disease that severely damages the brain and causes cognitive impairment (CI). Therefore, accurate and appropriate treatment strategies are urgently needed. The application of nimodipine can not only improve blood circulation in patients with SAH but also repair ischemic neuron injury. PURPOSE: To investigate the effects of nimodipine and lncRNA nuclear paraspeckle assembly transcript 1 (NEAT1)/miR-27a/microtubule-associated protein tau (MAPT) axis on CI after SAH.

methodsOne hundred and twenty healthy male rats were selected and equally divided into control group, sham operation group, model group, PBS group, nimodipine group (drug group), NC siRNA group, NC mimics group, NEAT1 siRNA, miR-27a mimics, MAPT siRNA, drug + NEAT1-ad, and drug + NC-ad groups by random number table. Rats in the model group were constructed by double-hemorrhage model, and expression vectors were injected into the tail to regulate the expression of lncRNA NEAT1, miR-27a and MAPT. In addition, Western blot was employed to detect brain tissue protein, flow cytometry was applied to measure brain tissue apoptosis, and MTT was utilized to determine cell activity, so as to evaluate brain damage and cognitive function in each group.

resultsNimodipine, down-regulated lncRNA NEAT1, up-regulated miR-27a and down-regulated MAPT all improved brain damage and CI, inhibited brain tissue cell apoptosis, and enhanced brain cell activity. The common binding sites of lncRNA NEAT1 and MAPT were found on the miR-27a sequence fragment, and miR-27a could be paired with the former two. Nimodipine was found to cause the down-regulation of lncRNA NEAT1 and MAPT, as well as the up-regulation of miR-27a.

conclusionNimodipine can improve CI after SAH in rats through the lncRNA NEAT1/miR-27a/MAPT axis.

Indexed as

AnimalsAntihypertensive AgentsCognitive DysfunctionDisease Models, AnimalDown-RegulationMaleMicroRNAsNimodipineRatsRats, Sprague-DawleyRNA, Long NoncodingSubarachnoid Hemorrhagetau ProteinsUp-RegulationAntihypertensive AgentsMapt protein, ratMicroRNAsMIRN27 microRNA, ratNimodipineRNA, Long Noncodingtau Proteinscognitive impairmentlncRNA NEAT1/miR-27a/MAPT axisnimodipinesubarachnoid hemorrhage

Identifiers

PMID32606599
PMCPMC7293909
OpenAlexW3035103747

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LicenceCC BY-NC
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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.