Evidence map›Paper›PMID 21830860›Full record

ArticleNanotoxicology2012

Nanoparticle inhalation alters systemic arteriolar vasoreactivity through sympathetic and cyclooxygenase-mediated pathways.

Travis L Knuckles, Jinghai Yi, David G Frazer, Howard D Leonard, Bean T Chen, Vince Castranova, Timothy R Nurkiewicz

Open access · greenAbstract read
In one paragraph

Article in Nanotoxicology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.5field-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

41 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Review
  3. NNanotoxicology · 2023
    Article
  4. Article
  5. Multi-instrument assessment of fine and ultrafine titanium dioxide aerosols.Journal of toxicology and environmental health. Part A · 2023
    Article
  6. Article
  7. Nanomaterial Inhalation During Pregnancy Alters Systemic Vascular Function in a Cyclooxygenase-Dependent Manner.Toxicological sciences : an official journal of the Society of Toxicology · 2022
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Progress ofToxicology research · 2017
    Review
  20. Maternal-engineered nanomaterial exposure disrupts progeny cardiac function and bioenergetics.American journal of physiology. Heart and circulatory physiology · 2017
    Article
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 at 2 institutions in 1 country.

Travis L KnucklesCenter for Cardiovascular and Respiratory Sciences, West Virginia University School of Medicine, Morgantown, WV, USA.
Jinghai Yi
David G Frazer
Howard D Leonard
Bean T Chen
Vince Castranova
Timothy R Nurkiewicz
West Virginia University · USNational Institute for Occupational Safety and Health · US

Funding

Remote Microvascular Dysfunction After Particulate Matter ExposureR01ES015022 · NIEHS · WEST VIRGINIA UNIVERSITY · PI NURKIEWICZ, TIMOTHY R · 2007 to 2021
$4.9M
Microvascular Health and Nanoparticle ExposureRC1ES018274 · NIEHS · WEST VIRGINIA UNIVERSITY · PI NURKIEWICZ, TIMOTHY R · 2009 to 2010
$1000k
NIEHS NIH HHS R0-1 ES015022NIEHS NIH HHS R01 ES015022NIEHS NIH HHS RC-1 ES018274NIEHS NIH HHS RC1 ES018274
6 · The paper itself

Abstract

The widespread increase in the production and use of nanomaterials has increased the potential for nanoparticle exposure; however, the biological effects of nanoparticle inhalation are poorly understood. Rats were exposed to nanosized titanium dioxide aerosols (10 μg lung burden); at 24 h post-exposure, the spinotrapezius muscle was prepared for intravital microscopy. Nanoparticle exposure did not alter perivascular nerve stimulation (PVNS)-induced arteriolar constriction under normal conditions; however, adrenergic receptor inhibition revealed a more robust effect. Nanoparticle inhalation reduced arteriolar dilation in response to active hyperaemia (AH). In both PVNS and AH experiments, nitric oxide synthase (NOS) inhibition affected only controls. Whereas cyclooxygenase (COX) inhibition only attenuated AH-induced arteriolar dilation in nanoparticle-exposed animals. This group displayed an enhanced U46619 constriction and attenuated iloprost-induced dilation. Collectively, these studies indicate that nanoparticle exposure reduces microvascular NO bioavailability and alters COX-mediated vasoreactivity. Furthermore, the enhanced adrenergic receptor sensitivity suggests an augmented sympathetic responsiveness.

Indexed as

15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic AcidAdministration, InhalationAnimalsArteriolesCyclooxygenase InhibitorsHyperemiaMaleNanoparticlesNitric OxideParticle SizeProstaglandin-Endoperoxide SynthasesRatsRats, Sprague-DawleyReceptors, Adrenergic, alphaSensitivity and SpecificitySignal Transduction15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic AcidCyclooxygenase InhibitorsNitric OxideProstaglandin-Endoperoxide SynthasesReceptors, Adrenergic, alphaTitaniumtitanium dioxide

Identifiers

PMID21830860
PMCPMC4850922
OpenAlexW2167013866

What OpenQuestion holds

Textmetadata
LicenceTDM
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.