Evidence map›Paper›PMID 28598982›Full record

ArticlePloS one2017

α-Mangostin ameliorates hepatic steatosis and insulin resistance by inhibition C-C chemokine receptor 2.

Hong Min Kim, You Mi Kim, Ji Hye Huh, Eun Soo Lee, Mi Hye Kwon, Bo Ra Lee, Hyun-Jeong Ko, Choon Hee Chung

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.6field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  6. The Herbal Blend ofFoods (Basel, Switzerland) · 2024
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  13. Crude α-Mangostin Suppresses the Development of Atherosclerotic Lesions inInternational journal of molecular sciences · 2019
    Article
  14. Article
  15. 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 2 institutions in 1 country.

Hong Min KimDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
You Mi KimDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Ji Hye HuhDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Eun Soo LeeDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Mi Hye KwonDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Bo Ra LeeLaboratory of Microbiology and Immunology, College of Pharmacy, Kangwon National University, Chuncheon, Korea.
Hyun-Jeong KoLaboratory of Microbiology and Immunology, College of Pharmacy, Kangwon National University, Chuncheon, Korea.
Choon Hee ChungDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.ORCID http://orcid.org/0000-0003-1144-7206
Yonsei University · KRKangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity induces various metabolic diseases such as dyslipidemia, nonalcoholic fatty liver disease (NAFLD), and type 2 diabetes. Fat expansion in adipose tissue induces adipose tissue dysfunction and inflammation, insulin resistance, and other metabolic syndromes. α-Mangostin (α-MG) has been previously studied for its anti-cancer, anti-inflammatory, and antioxidant activities. In this study, we investigated the effects of α-MG on adipose tissue inflammation and hepatic steatosis. We categorized study animals into four groups: regular diet control mice, RD mice treated with α-MG, high fat diet-induced obese mice, and HFD mice treated with α-MG. α-MG treatment significantly reduced not only the body, liver, and fat weights, but also plasma glucose, insulin, and triglyceride levels in HFD mice. Additionally, adiponectin levels of α-MG-treated mice were significantly higher than those of control HFD mice. Immunohistochemistry of liver and adipose tissue showed that CD11c expression was reduced in α-MG fed obese mice. α-MG treatment of HFD mice down-regulated the adipose-associated inflammatory cytokines and CCR2 in both liver and adipose tissue. Moreover, glucose tolerance and insulin sensitivity were significantly improved in α-MG fed obese mice. α-Mangostin ameliorates adipose inflammation and hepatic steatosis in HFD-induced obese mice.

Indexed as

Insulin ResistanceAdipose TissueAnimalsBody WeightBone Marrow CellsCell LineCytokinesDiet, High-FatDisease Models, AnimalFatty AcidsGlucose Tolerance TestInflammation MediatorsLiverMacrophagesMiceNon-alcoholic Fatty Liver DiseaseCytokinesFatty AcidsInflammation MediatorsmangostinProtein Kinase InhibitorsReceptors, CCR2Xanthones

Identifiers

PMID28598982
PMCPMC5466328
OpenAlexW2624059108

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.