Evidence map›Paper›PMID 29247241›Full record

ArticleScientific reports2017

Beneficial effects of melittin on ovalbumin-induced atopic dermatitis in mouse.

Woon-Hae Kim, Hyun-Jin An, Jung-Yeon Kim, Mi-Gyeong Gwon, Hyemin Gu, Minji Jeon, Woo Jung Sung, Sang Mi Han, Sok Cheon Pak, Min-Kyung Kim and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  5. Therapeutic Bioactivity Exerted by theMolecules (Basel, Switzerland) · 2025
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  9. Journal of experimental pharmacology · 2025
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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

11 authors at 4 institutions in 2 countries.

Woon-Hae KimDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu, Korea.ORCID 0000-0002-1536-5374
Hyun-Jin AnDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu, Korea.
Jung-Yeon KimDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu, Korea.
Mi-Gyeong GwonDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu, Korea.
Hyemin GuDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu, Korea.
Minji JeonDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu, Korea.
Woo Jung SungDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu, Korea.
Sang Mi HanDepartment of Agricultural Biology, National Academy of Agricultural Science, Jeonju-si, Korea.
Sok Cheon PakSchool of Biomedical Sciences, Charles Sturt University, Bathurst, Australia.
Min-Kyung KimDepartment of Pathology, College of Medicine, Dongguk University, Gyeongju-si, Korea.
Kwan-Kyu ParkDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu, Korea. kkpark@cu.ac.kr.ORCID 0000-0002-5317-750X
Daegu Catholic University · KRCharles Sturt University · AUDongguk University · KRNational Academy of Agricultural Science · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atopic dermatitis (AD) is an inflammatory skin disease characterized by intense pruritus and relapsable eczematous lesions. The hallmarks of AD are defects in the epidermal barrier and immunoglobulin E (IgE)-mediated sensitization to several environmental allergens, as well as an immune disorder mediated by an imbalance toward T-helper-2 response. Melittin, a major component of bee venom, has been studied in various inflammatory diseases. However, the beneficial effects of melittin on mouse with AD-like symptoms have not been explored. Therefore, we investigated the anti-allergic effects of melittin. AD was induced by ovalbumin (OVA) patch. After agent treatment, skin tissues and sera were extracted from the sacrificed mice were used to demonstrate the effects of melittin through various molecular biological methods. The results showed that OVA-induced skin thickening and inflammatory infiltration were decreased in the melittin-treated group. Melittin prevented OVA-induced filaggrin deficiency and imbalanced inflammatory mediators. Furthermore, melittin inhibited IL-4/IL-13-induced filaggrin downregulation through the blockade of STAT3 activation in human keratinocytes. In summary, this study has shown that melittin ameliorated OVA-induced AD-like symptoms from various perspectives. The findings of this study may be the first evidence of the anti-inflammatory effects of melittin on OVA-induced AD.

Indexed as

AllergensAnimalsCells, CulturedDermatitis, AtopicDisease Models, AnimalFemaleFilaggrin ProteinsImmunoglobulin EInterleukin-13KeratinocytesMelittenMiceMice, Inbred BALB COvalbuminSkinSTAT3 Transcription FactorAllergensFilaggrin ProteinsFLG protein, humanImmunoglobulin EInterleukin-13MelittenOvalbuminSTAT3 Transcription Factor

Identifiers

PMID29247241
PMCPMC5732199
OpenAlexW2774700885

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.