Evidence map›Paper›PMID 26612496›Full record

ArticleJournal of cellular and molecular medicine2016

P2Y12 antagonist attenuates eosinophilic inflammation and airway hyperresponsiveness in a mouse model of asthma.

Dong-Hyeon Suh, Hoang Kim Tu Trinh, Jing-Nan Liu, Le Duy Pham, Sang Myun Park, Hae-Sim Park, Yoo Seob Shin

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Cysteinyl Leukotrienes in Allergic Inflammation.Annual review of pathology · 2025
    Review
  3. The Signaling Pathway of the ADP Receptor P2YInternational journal of molecular sciences · 2023
    Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. P2YInternational journal of molecular sciences · 2020
    Review
  13. Review
  14. P2YFrontiers in pharmacology · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Leukotriene receptors as potential therapeutic targets.The Journal of clinical investigation · 2018
    Review
  19. Article
  20. Targeting cell signaling in allergic asthma.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

7 authors at 1 institution in 1 country.

Dong-Hyeon SuhDepartment of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Hoang Kim Tu TrinhDepartment of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Jing-Nan LiuDepartment of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Le Duy PhamDepartment of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Sang Myun ParkDepartment of Pharmacology, Ajou University School of Medicine, Suwon, Korea.
Hae-Sim ParkDepartment of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Yoo Seob ShinDepartment of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Ajou University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leukotriene E4 (LTE4) that plays a key role in airway inflammation is expressed on platelets and eosinophils. We investigated whether blocking of the P2Y12 receptor can suppress eosinophilic inflammation in a mouse model of asthma because platelets and eosinophils share this receptor to be activated. BALB/c mice were sensitized by intraperitoneal injection of ovalbumin (OVA), followed by OVA nebulization. On each challenge day, clopidogrel, a P2Y12 antagonist was administered 30 min. before each challenge. Forty-eight hours after the last OVA challenge, mice were assessed for airway hyperresponsiveness (AHR), cell composition and cytokine levels, including chemokine ligand 5 (CCL5), in bronchoalveolar lavage (BAL) fluid. EOL cells were treated with LTE4, with or without clopidogrel treatment, and intracellular and extracellular eosinophil cationic protein (ECP) expressions were measured to find the inhibiting function of P2Y12 antagonist on eosinophilic activation. The levels of P2Y12 expression were increased markedly in the lung homogenates of OVA-sensitized and -challenged mice after platelet depletion. Administration of clopidogrel decreased AHR and the number of airway inflammatory cells, including eosinophils, in BAL fluid following OVA challenge. These results were associated with decreased levels of Th2 cytokines and CCL5. Histological examination showed that inflammatory cells as well as mucus-containing goblet cells were reduced in clopidogrel-administered mice compared to vehicle-treated mice. Clopidogrel inhibited extracellular ECP secretion after LTE4 stimulation in EOL-1 cells. Clopidogrel could prevent development of AHR and airway inflammation in a mouse model of asthma. P2Y12 can be a novel therapeutic target to the suppression of eosinophils in asthma.

Indexed as

AnimalsAsthmaBronchial HyperreactivityBronchoalveolar Lavage FluidCytokinesDisease Models, AnimalEosinophilsFemaleInflammationMiceMice, Inbred BALB COvalbuminReceptors, Purinergic P2Y12CytokinesOvalbuminP2ry12 protein, mouseReceptors, Purinergic P2Y12asthmaclopidogreleosinophilleukotriene E4P2Y12 receptor

Identifiers

PMID26612496
PMCPMC4727565
OpenAlexW2174693377

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.