Evidence map›Paper›PMID 26251593›Full record

ArticleInternational journal of nanomedicine2015

Characterization of pulmonary protein profiles in response to zinc oxide nanoparticles in mice: a 24-hour and 28-day follow-up study.

Chih-Hong Pan, Kai-Jen Chuang, Jen-Kun Chen, Ta-Chih Hsiao, Ching-Huang Lai, Tim P Jones, Kelly A BéruBé, Gui-Bing Hong, Kin-Fai Ho, Hsiao-Chi Chuang

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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.

Chih-Hong PanInstitute of Occupational Safety and Health, Council of Labor Affairs, Executive Yuan, Taiwan ; School of Public Health, National Defense Medical Center, Taipei Medical University, Taipei, Taiwan.
Kai-Jen ChuangSchool of Public Health, College of Public Health and Nutrition, Taipei Medical University, Taipei, Taiwan ; Department of Public Health, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Jen-Kun ChenInstitute of Biomedical Engineering and Nanomedicine, National Health Research Institutes, Miaoli, Taiwan.
Ta-Chih HsiaoGraduate Institute of Environmental Engineering, National Central University, Taoyuan, Taiwan.
Ching-Huang LaiSchool of Public Health, National Defense Medical Center, Taipei Medical University, Taipei, Taiwan.
Tim P JonesSchool of Earth and Ocean Sciences, Cardiff University, Cardiff, Wales, UK.
Kelly A BéruBéSchool of Biosciences, Cardiff University, Cardiff, Wales, UK.
Gui-Bing HongDepartment of Chemical Engineering and Biotechnology, National Taipei University of Technology, Taipei, Taiwan.
Kin-Fai HoJockey Club School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong, People's Republic of China ; Shenzhen Municipal Key Laboratory for Health Risk Analysis, Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, People's Republic of China.
Hsiao-Chi ChuangSchool of Respiratory Therapy, College of Medicine, Taipei Medical University, Taipei, Taiwan ; Division of Pulmonary Medicine, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, Taipei, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although zinc oxide nanoparticles (ZnONPs) are recognized to cause systemic disorders, little is known about the mechanisms that underlie the time-dependent differences that occur after exposure. The objective of this study was to investigate the mechanistic differences at 24 hours and 28 days after the exposure of BALB/c mice to ZnONPs via intratracheal instillation. An isobaric tag for the relative and absolute quantitation coupled with liquid chromatography/tandem mass spectrometry was used to identify the differential protein expression, biological processes, molecular functions, and pathways. A total of 18 and 14 proteins displayed significant changes in the lung tissues at 24 hours and 28 days after exposure, respectively, with the most striking changes being observed for S100-A9 protein. Metabolic processes and catalytic activity were the main biological processes and molecular functions, respectively, in the responses at the 24-hour and 28-day follow-up times. The glycolysis/gluconeogenesis pathway was continuously downregulated from 24 hours to 28 days, whereas detoxification pathways were activated at the 28-day time-point after exposure. A comprehensive understanding of the potential time-dependent effects of exposure to ZnONPs was provided, which highlights the metabolic mechanisms that may be important in the responses to ZnONP.

Indexed as

LungMetal NanoparticlesZinc OxideAnimalsFollow-Up StudiesMiceToxicity TestsZinc OxideglycolysisiTRAQmetabolismnanoparticlesS100-A9

Identifiers

PMID26251593
PMCPMC4524458

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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.