Evidence map›Paper›PMID 26810232›Full record

ArticleJournal of nanobiotechnology2016

Anti-inflammatory effect of fullerene C60 in a mice model of atopic dermatitis.

Nadezda Shershakova, Elena Baraboshkina, Sergey Andreev, Daria Purgina, Irina Struchkova, Oleg Kamyshnikov, Alexandra Nikonova, Musa Khaitov

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
7.1field-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

30 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Fullerene CToxicology research · 2023
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. CGeroScience · 2021
    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

8 authors at 1 institution in 1 country.

Nadezda ShershakovaNRC Institute of Immunology FMBA of Russia, Moscow, Russia. nn.shershakova@nrcii.ru.
Elena BaraboshkinaNRC Institute of Immunology FMBA of Russia, Moscow, Russia. en.bashkatova@nrcii.ru.
Sergey AndreevNRC Institute of Immunology FMBA of Russia, Moscow, Russia. sm.andreev@nrcii.ru.
Daria PurginaNRC Institute of Immunology FMBA of Russia, Moscow, Russia. dd.purgina@nrcii.ru.
Irina StruchkovaNRC Institute of Immunology FMBA of Russia, Moscow, Russia. ira9ctpy4@rambler.ru.
Oleg KamyshnikovNRC Institute of Immunology FMBA of Russia, Moscow, Russia. oy.kamyshnikov@nrcii.ru.
Alexandra NikonovaNRC Institute of Immunology FMBA of Russia, Moscow, Russia. aa.nikonova@nrcii.ru.
Musa KhaitovNRC Institute of Immunology FMBA of Russia, Moscow, Russia. mr.khaitov@nrcii.ru.
Institute of Immunology and Physiology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWater-soluble form of fullerene C60 is a promising tool for the control of ROS-dependent inflammation including allergic diseases. Anti-inflammatory effects of C60 (nC60) aqueous dispersion were evaluated in the mouse models of atopic dermatitis using subcutaneous (SC) and epicutaneous (EC) applications during 50 days period. A highly stable nC60 was prepared by exhaustive dialysis of water-organic C60 solution against water, where the size and ζ-potential of fullerene nanoparticles are about 100 nm and -30 mV, respectively.

resultsTo induce skin inflammation, female BALB/c mice were EC sensitized with ovalbumin three times during one-weekly exposures. The nC60 solution was administrated in mice subcutaneously (SC) (0.1 mg/kg) and epicutaneously (EC) (1 mg/kg). Significant suppression of IgE and Th2 cytokines production and a concomitant rise in concentrations of Th1 cytokines were observed in nC60-treated groups. In addition, a significant increase in the levels of Foxp3(+) and filaggrin mRNA expression was observed at EC application. Histological examination of skin samples indicated that therapeutic effect was achieved by both EC and SC treatment, but it was more effective with EC. Pronounced reduction of the eosinophil and leukocyte infiltration in treated skin samples was observed.

conclusionsWe suppose that nC60 treatment shifts immune response from Th2 to Th1 and restores to some extent the function of the skin barrier. This approach can be a good alternative to the treatment of allergic and other inflammatory diseases.

Indexed as

AnimalsAnti-Inflammatory AgentsCytokinesDermatitis, AtopicDisease Models, AnimalFemaleFilaggrin ProteinsForkhead Transcription FactorsFullerenesImmunoglobulin EInflammationIntermediate Filament ProteinsMiceMice, Inbred BALB COvalbuminRNA, MessengerAnti-Inflammatory AgentsCytokinesFilaggrin ProteinsForkhead Transcription Factorsfullerene C60FullerenesImmunoglobulin EIntermediate Filament ProteinsOvalbuminRNA, Messenger

Identifiers

PMID26810232
PMCPMC4727272
OpenAlexW2264329878

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.