Evidence map›Paper›PMID 27123161›Full record

ArticleToxicological research2016

External Application of Apo-9'-fucoxanthinone, Isolated from Sargassum muticum, Suppresses Inflammatory Responses in a Mouse Model of Atopic Dermatitis.

Sang-Chul Han, Na-Jin Kang, Weon-Jong Yoon, Sejin Kim, Min-Chull Na, Young-Sang Koh, Jin-Won Hyun, Nam-Ho Lee, Mi-Hee Ko, Hee-Kyoung Kang and 1 more

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In one paragraph

Article in Toxicological research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

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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 2 institutions in 1 country.

Sang-Chul HanDepartment of Medicine, School of Medicine, Jeju National University, Jeju, Korea.
Na-Jin KangDepartment of Medicine, School of Medicine, Jeju National University, Jeju, Korea.
Weon-Jong YoonJeju Biodiversity Research Institute (JBRI), Jeju Technopark (JTP), Jeju, Korea.
Sejin KimDepartment of Medicine, School of Medicine, Jeju National University, Jeju, Korea.
Min-Chull NaDepartment of Medicine, School of Medicine, Jeju National University, Jeju, Korea.
Young-Sang KohDepartment of Medicine, School of Medicine, Jeju National University, Jeju, Korea.
Jin-Won HyunDepartment of Medicine, School of Medicine, Jeju National University, Jeju, Korea.
Nam-Ho LeeDepartment of Chemistry, College of Natural Science, Jeju National University, Jeju, Korea.
Mi-Hee KoJeju Biodiversity Research Institute (JBRI), Jeju Technopark (JTP), Jeju, Korea.
Hee-Kyoung KangDepartment of Medicine, School of Medicine, Jeju National University, Jeju, Korea.
Eun-Sook YooDepartment of Medicine, School of Medicine, Jeju National University, Jeju, Korea.
Jeju National University · KRJeju TechnoPark · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allergic skin inflammation such as atopic dermatitis is characterized by skin barrier dysfunction, edema, and infiltration with various inflammatory cells. The anti-inflammatory effects of Apo-9'-fucoxanthinone, isolated from Sargassum muticum, have been described in many diseases, but the mechanism by which it modulates the immune system is poorly understood. In this study, the ability of Apo-9'-fucoxanthinone to suppress allergic reactions was investigated using a mouse model of atopic dermatitis. The Apo-9'-fucoxanthinone-treated group showed significantly decreased immunoglobulin E in serum. Also, Apo-9'-fucoxanthinone treatment resulted in a smaller lymph node size with reduced the thickness and length compared to the induction group. In addition, Apo-9'-fucoxanthinone inhibited the expression of interleukin-4, interferon-gamma and tumor necrosis factor-alpha by phorbol 12-myristate 13-acetate and ionomycin-stimulated lymphocytes. These results suggest that Apo-9'-fucoxanthinone may be a useful therapeutic strategy for treating chronic inflammatory diseases.

Indexed as

2, 4-DinitrochlorobenzeneApo-9′-fucoxanthinoneAtopic dermatitisImmunoglobulin EIonomycinPhorbol 12-myristate 13-acetate

Identifiers

PMID27123161
PMCPMC4843979
OpenAlexW2339480624

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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.