Evidence map›Paper›PMID 30177658›Full record

ArticleMolecules (Basel, Switzerland)2018

Silicon Dioxide Nanoparticles Enhance Endotoxin-Induced Lung Injury in Mice.

Je-Won Ko, Hae-Jun Lee, Na-Rae Shin, Yun-Soo Seo, Sung-Ho Kim, In-Sik Shin, Joong-Sun Kim

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
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  3. 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

7 authors.

Je-Won KoCollege of Veterinary Medicine (BK21 Plus Project Team), Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju 61186, Korea. rheoda@gmail.com.
Hae-Jun LeeDivision of Radiation Biomedical Research, Korea Institute of Radiological & Medical Sciences, Seoul 01812, Korea. hjlee@kirams.re.kr.ORCID 0000-0002-7743-0151
Na-Rae ShinCollege of Veterinary Medicine (BK21 Plus Project Team), Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju 61186, Korea. tlsskfo870220@gmail.com.
Yun-Soo SeoHerbal Medicinal Research Center, Korea Institute of Oriental Medicine, 1672 Yuseong-daero, Yuseong-gu, Daejeon 34054, Korea. sys0109@kiom.re.kr.
Sung-Ho KimCollege of Veterinary Medicine (BK21 Plus Project Team), Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju 61186, Korea. shokim@chonnam.ac.kr.
In-Sik ShinCollege of Veterinary Medicine (BK21 Plus Project Team), Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju 61186, Korea. dvmmk79@gmail.com.
Joong-Sun KimHerbal Medicinal Research Center, Korea Institute of Oriental Medicine, 1672 Yuseong-daero, Yuseong-gu, Daejeon 34054, Korea. centraline@kiom.re.kr.

Funding

Basic Science Research Program funded by the Korean government (MIST) NRF-2015R1C1A1A01053531Nuclear Research and Development Program funded by the Korean government (MIST) NRF-2015M2B2B1068627
6 · The paper itself

Abstract

Silicon dioxide nanoparticles (SiONPs), which are metal oxide nanoparticles, have been used in a wide variety of applications. In this study, acute pulmonary responses were examined after the intranasal instillation of SiONPs in mice primed with or without lipopolysaccharide (LPS, intranasal, 5 µg/mouse). The exposure to SiONPs increased the inflammatory cell counts and proinflammatory cytokines in the bronchoalveolar lavage fluid. SiONPs induced airway inflammation with increases in the phosphorylation of mitogen-activated protein kinases (MAPKs). The ratios of the inflammatory responses induced by the SiONPs were increased in the acute pulmonary disease model primed by LPS. Taken together, SiONPs exhibited toxicity to the respiratory system, which was associated with MAPK phosphorylation. In addition, the exposure to SiONPs exacerbated any existing inflammatory pulmonary diseases. These data showed the additive, as well as synergistic, interaction effects of SiONPs and LPS. We conclude that the exposure to SiONPs causes potential toxicity in humans, especially those with respiratory diseases.

Indexed as

Acute Lung InjuryAdministration, IntranasalAnimalsBronchoalveolar Lavage FluidCytokinesDisease Models, AnimalEndotoxinsHumansInstillation, DrugMaleMiceMitogen-Activated Protein KinasesNanoparticlesPhosphorylationSilicon DioxideCytokinesEndotoxinsMitogen-Activated Protein KinasesSilicon Dioxideinflammationmitogen-activated protein kinaserespiratory tractsilicon dioxide nanoparticles

Identifiers

PMID30177658
PMCPMC6225156

What OpenQuestion holds

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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.