Evidence map›Paper›PMID 29593572›Full record

ArticleFrontiers in physiology2018

Identification of Exosomal miRNAs in Rats With Pulmonary Neutrophilic Inflammation Induced by Zinc Oxide Nanoparticles.

Yamei Qiao, Xiao Liang, Yingjie Yan, Yake Lu, Di Zhang, Wu Yao, Weidong Wu, Zhen Yan

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2018. 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
1.2field-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, 30 citations in OpenAlex.

  1. Review
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  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Crucial Role of Extracellular Vesicles in Bronchial Asthma.International journal of molecular sciences · 2019
    Review
  15. Exosomes in Allergic Airway Diseases.Current allergy and asthma reports · 2019
    Review
  16. Article
  17. The roles of exosomal miRNAs and lncRNAs in lung diseases.Signal transduction and targeted therapy
    Review
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

8 authors at 3 institutions in 1 country.

Yamei QiaoDepartment of Occupational and Environmental Health Sciences, College of Public Health, Zhengzhou University, Zhengzhou, China.
Xiao LiangDepartment of Occupational and Environmental Health Sciences, College of Public Health, Zhengzhou University, Zhengzhou, China.
Yingjie YanDepartment of Occupational and Environmental Health Sciences, College of Public Health, Zhengzhou University, Zhengzhou, China.
Yake LuDepartment of Occupational and Environmental Health Sciences, College of Public Health, Zhengzhou University, Zhengzhou, China.
Di ZhangDepartment of Occupational and Environmental Health Sciences, College of Public Health, Zhengzhou University, Zhengzhou, China.
Wu YaoDepartment of Occupational and Environmental Health Sciences, College of Public Health, Zhengzhou University, Zhengzhou, China.
Weidong WuDepartment of Occupational and Environmental Health Sciences, School of Public Health, Xinxiang Medical University, Xinxiang, China.
Zhen YanDepartment of Occupational and Environmental Health Sciences, School of Public Health, Hainan Medical University, Haikou, China.
Zhengzhou University · CNHainan Medical University · CNXinxiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been previously shown that inhaled zinc oxide nanoparticles (ZnO-NPs) can modulate inflammation. MicroRNAs (miRNAs) enclosed in exosomes have been identified as an important signature for inflammatory responses. However, the role of exosomal miRNAs during pathogenic inflammation has not been investigated. Healthy rats were exposed to ZnO-NPs (41.7 nm; 2, 4, and 8 mg/kg) or saline (control) via oropharyngeal aspiration. ZnO-NPs induced significant increases in the serum levels of interleukin 8 (IL-8), interleukin-1 beta (IL-1β), and tumor necrosis factor α (TNF-α), and elevated the number of cells and the percentage of neutrophils in the blood. Moreover, exposure to ZnO-NPs increased the levels of lactate dehydrogenase (LDH) activity and total protein in bronchoalveolar lavage fluid (BALF). Differential profiling of miRNAs in isolated serum exosomes revealed that 16 miRNAs were up-regulated and 7 down-regulated in ZnO-NP-treated rats compared with the controls. Functional and pathway analysis indicated that miRNAs may participate in inflammation directly and indirectly through protein and vesicle-mediated transport or regulation of IL-1, oxidative stress, apoptosis, and autophagy. These results suggest that miRNAs in serum exosomes are involved in pulmonary neutrophilic inflammation induced by ZnO-NPs.

Indexed as

bioinformatics analysisexosomesmiRNAspulmonary inflammationzinc oxide nanoparticles

Identifiers

PMID29593572
PMCPMC5859358
OpenAlexW2791925838

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.