Evidence map›Paper›PMID 26068872›Full record

ArticlePloS one2015

Tyrosol Suppresses Allergic Inflammation by Inhibiting the Activation of Phosphoinositide 3-Kinase in Mast Cells.

In-Gyu Je, Duk-Sil Kim, Sung-Wan Kim, Soyoung Lee, Hyun-Shik Lee, Eui Kyun Park, Dongwoo Khang, Sang-Hyun Kim

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Efficacy and safety of three species ofFrontiers in pharmacology · 2023
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  9. Phenotype-Specific Therapeutic Effect ofInternational journal of molecular sciences · 2019
    Article
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  14. Coumarins from the roots ofExperimental and therapeutic medicine · 2017
    Article
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  16. Review
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  18. 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 3 institutions in 1 country.

In-Gyu JeDepartment of Pharmacology, School of Medicine, Kyungpook National University, Daegu 700-422, Republic of Korea.
Duk-Sil KimDepartment of Thoracic and Cardiovascular Surgery, CHA Gumi Medical Center, CHA University, Gumi 730-040, Republic of Korea.
Sung-Wan KimDepartment of Thoracic and Cardiovascular Surgery, CHA Gumi Medical Center, CHA University, Gumi 730-040, Republic of Korea.
Soyoung LeeDepartment of Pharmacology, School of Medicine, Kyungpook National University, Daegu 700-422, Republic of Korea.
Hyun-Shik LeeSchool of Life Sciences, Kyungpook National University, Daegu 702-701, Republic of Korea.
Eui Kyun ParkDepartment of Oral Pathology and Regenerative Medicine, School of Dentistry, Kyungpook National University, Daegu 700-412, Republic of Korea.
Dongwoo KhangDepartment of Molecular Medicine, School of Medicine, Gachon University, Incheon 406-840, Republic of Korea.
Sang-Hyun KimDepartment of Pharmacology, School of Medicine, Kyungpook National University, Daegu 700-422, Republic of Korea.
Kyungpook National University · KRGachon University · KRCHA University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allergic diseases such as atopic dermatitis, rhinitis, asthma, and anaphylaxis are attractive research areas. Tyrosol (2-(4-hydroxyphenyl)ethanol) is a polyphenolic compound with diverse biological activities. In this study, we investigated whether tyrosol has anti-allergic inflammatory effects. Ovalbumin-induced active systemic anaphylaxis and immunoglobulin E-mediated passive cutaneous anaphylaxis models were used for the immediate-type allergic responses. Oral administration of tyrosol reduced the allergic symptoms of hypothermia and pigmentation in both animal models. Mast cells that secrete allergic mediators are key regulators on allergic inflammation. Tyrosol dose-dependently decreased mast cell degranulation and expression of inflammatory cytokines. Intracellular calcium levels and activation of inhibitor of κB kinase (IKK) regulate cytokine expression and degranulation. Tyrosol blocked calcium influx and phosphorylation of the IKK complex. To define the molecular target for tyrosol, various signaling proteins involved in mast cell activation such as Lyn, Syk, phosphoinositide 3-kinase (PI3K), and Akt were examined. Our results showed that PI3K could be a molecular target for tyrosol in mast cells. Taken together, these findings indicated that tyrosol has anti-allergic inflammatory effects by inhibiting the degranulation of mast cells and expression of inflammatory cytokines; these effects are mediated via PI3K. Therefore, we expect tyrosol become a potential therapeutic candidate for allergic inflammatory disorders.

Indexed as

Phosphoinositide-3 Kinase InhibitorsAnimalsAnti-Allergic AgentsAnti-Inflammatory AgentsAntioxidantsApoptosisBlotting, WesternCell DegranulationCell ProliferationCells, CulturedCytokinesEnzyme ActivationEnzyme-Linked Immunosorbent AssayHypersensitivityInflammationMale4-hydroxyphenylethanolAnti-Allergic AgentsAnti-Inflammatory AgentsAntioxidantsCytokinesPhenylethyl AlcoholPhosphoinositide-3 Kinase InhibitorsRNA, Messenger

Identifiers

PMID26068872
PMCPMC4465982
OpenAlexW1590937134

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.