Evidence map›Paper›PMID 32848773›Full record

ArticleFrontiers in pharmacology2020

Intranasal Delivery of Targeted Nanoparticles Loaded With miR-132 to Brain for the Treatment of Neurodegenerative Diseases.

Yu Su, Bixi Sun, Xiaoshu Gao, Xinyue Dong, Lanbo Fu, Yingxin Zhang, Zhulin Li, Yue Wang, Hongyu Jiang, Bing Han

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.3field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
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  4. Intranasal Dimethyl Trisulfide: Long-Term Efficacy in an Acutely Lethal Large Swine Model of Cyanide Exposure.Journal of medical toxicology : official journal of the American College of Medical Toxicology · 2025
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  14. Silicosis: from pathogenesis to therapeutics.Frontiers in pharmacology · 2025
    Review
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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

10 authors at 1 institution in 1 country.

Yu SuDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Bixi SunDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Xiaoshu GaoDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Xinyue DongDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Lanbo FuDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Yingxin ZhangDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Zhulin LiDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Yue WangDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Hongyu JiangDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Bing HanDepartment of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective treatments for neurodegenerative diseases need to be developed. MiR132 is abundantly expressed in the brain, and it modulates neuron morphology and plays a key role in maintaining neuron survival. Regulating miR132 can effectively improve the symptoms of Alzheimer's disease. It can also reduce cell death after cerebral hemorrhage, improve the microenvironment of hematoma lesions and provide a certain protective effect from brain damage after cerebral ischemia. MiR132 has great potential in the treatment of cerebral ischemia and Alzheimer's disease. To prevent the decline of miR132 of miR132 levels in the blood, we used mouse and rat models of Alzheimer's disease with ischemic brain injury, and then delivered Wheat germ agglutinin (WGA)-NPs-miR132 intranasally to treat neurological damage after cerebral ischemia. Synaptic protein expression levels in Alzheimer's mouse models increased significantly after administration. We propose that, nasal delivery of WGA-NPs-miR132 is an interesting novel therapeutic approach for the treatment of neurodegenerative diseases.

Indexed as

MiR132nanoparticlesneurodegenerative diseasesnose to brain deliverywheat germ agglutinin

Identifiers

PMID32848773
PMCPMC7424054
OpenAlexW3049634014

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.