Evidence map›Paper›PMID 25349218›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2015

SG-HQ2 inhibits mast cell-mediated allergic inflammation through suppression of histamine release and pro-inflammatory cytokines.

In-Gyu Je, Hui-Hun Kim, Pil-Hoon Park, Taeg Kyu Kwon, Seung-Yong Seo, Tae-Yong Shin, Sang-Hyun Kim

Open access · greenAbstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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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

7 authors at 5 institutions in 1 country.

In-Gyu JeCMRI, BK21 Plus KNU Biomedical Convergence Program, Department of Pharmacology, School of Medicine, Kyungpook National University, Daegu 700-422, Republic of Korea.
Hui-Hun KimCMRI, BK21 Plus KNU Biomedical Convergence Program, Department of Pharmacology, School of Medicine, Kyungpook National University, Daegu 700-422, Republic of Korea.
Pil-Hoon ParkCollege of Pharmacy, Yeungnam University, Gyeongbuk 712-749, Republic of Korea.
Taeg Kyu KwonDepartment of Immunology, Keimyung University, Daegu 704-701, Republic of Korea.
Seung-Yong SeoCollege of Pharmacy, Gachon University, Incheon 406-840, Republic of Korea shkim72@knu.ac.kr syseo@gachon.ac.kr tyshin@woosuk.ac.kr.
Tae-Yong ShinCollege of Pharmacy, Woosuk University, Jeonju 565-701, Republic of Korea shkim72@knu.ac.kr syseo@gachon.ac.kr tyshin@woosuk.ac.kr.
Sang-Hyun KimCMRI, BK21 Plus KNU Biomedical Convergence Program, Department of Pharmacology, School of Medicine, Kyungpook National University, Daegu 700-422, Republic of Korea shkim72@knu.ac.kr syseo@gachon.ac.kr tyshin@woosuk.ac.kr.
Kyungpook National University · KRGachon University · KRKeimyung University · KRWoosuk University · KRYeungnam University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we investigated the effect of 3,4,5-trihydroxy-N-(8-hydroxyquinolin-2-yl)benzamide) (SG-HQ2), a synthetic analogue of gallic acid (3,4,5-trihydroxybenzoic acid), on the mast cell-mediated allergic inflammation and the possible mechanism of action. Mast cells play major roles in immunoglobulin E-mediated allergic responses by the release of histamine, lipid-derived mediators, and pro-inflammatory cytokines. We previously reported the potential effects of gallic acid using allergic inflammation models. For incremental research, we synthesized the SG-HQ2 by the modification of functional groups from gallic acid. SG-HQ2 attenuated histamine release by the reduction of intracellular calcium in human mast cells and primary peritoneal mast cells. The inhibitory efficacy of SG-HQ2 was similar with gallic acid. Enhanced expression of pro-inflammatory cytokines such as tumor necrosis factor-α, interleukin-1β, interleukin-4, and interleukin-6 in activated mast cells was significantly diminished by SG-HQ2 100 times lower concentration of gallic acid. This inhibitory effect was mediated by the reduction of nuclear factor-κB. In animal models, SG-HQ2 inhibited compound 48/80-induced serum histamine release and immunoglobulin E-mediated local allergic reaction, passive cutaneous anaphylaxis. Our results indicate that SG-HQ2, an analogue of gallic acid, might be a possible therapeutic candidate for mast cell-mediated allergic inflammatory diseases through suppression of histamine release and pro-inflammatory cytokines.

Indexed as

AnimalsCalciumCytokinesGallic AcidHistamine ReleaseHydroxyquinolinesHypersensitivityImmunoglobulin EInflammationInflammation MediatorsMaleMast CellsMiceNF-kappa BPassive Cutaneous AnaphylaxisRatsCalciumCytokinesGallic AcidHydroxyquinolinesImmunoglobulin EInflammation MediatorsNF-kappa BSG-HQ2Allergic inflammationhistaminemast cellspro-inflammatory cytokine

Identifiers

PMID25349218
PMCPMC4935276
OpenAlexW2330381740

What OpenQuestion holds

Textmetadata
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.