Evidence map›Paper›PMID 24381715›Full record

ArticleOxidative medicine and cellular longevity2013

Magnolia extract (BL153) ameliorates kidney damage in a high fat diet-induced obesity mouse model.

Wenpeng Cui, Yangwei Wang, Qiang Chen, Weixia Sun, Lu Cai, Yi Tan, Ki-Soo Kim, Ki Ho Kim, Young Heui Kim

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2013. 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
2.2field-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

15 citing papers in PubMed, 26 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

9 authors at 5 institutions in 3 countries.

Wenpeng CuiThe Second Hospital of Jilin University, Changchun 130041, China ; The Kosair Children's Hospital Research Institute, Department of Pediatrics of the University of Louisville, Louisville, KY 20202, USA.
Yangwei WangThe Second Hospital of Jilin University, Changchun 130041, China ; The Kosair Children's Hospital Research Institute, Department of Pediatrics of the University of Louisville, Louisville, KY 20202, USA.
Qiang ChenThe Kosair Children's Hospital Research Institute, Department of Pediatrics of the University of Louisville, Louisville, KY 20202, USA ; School of Public Health, Jilin University, Changchun 130021, China.
Weixia SunThe Kosair Children's Hospital Research Institute, Department of Pediatrics of the University of Louisville, Louisville, KY 20202, USA ; The First Hospital of Jilin University, Changchun 130021, China.
Lu CaiThe Kosair Children's Hospital Research Institute, Department of Pediatrics of the University of Louisville, Louisville, KY 20202, USA.
Yi TanThe Kosair Children's Hospital Research Institute, Department of Pediatrics of the University of Louisville, Louisville, KY 20202, USA.
Ki-Soo KimBioland Biotec Co., Ltd., Zhangjiang Modern Medical Device Park, Pudong, Shanghai 201201, China.
Ki Ho KimBioland R&D Center, 59 Songjeongni 2-gil, Byeongcheon, Dongnam, Cheonan, Chungnam 330-863, Republic of Korea.
Young Heui KimBioland R&D Center, 59 Songjeongni 2-gil, Byeongcheon, Dongnam, Cheonan, Chungnam 330-863, Republic of Korea.
Bioland (South Korea) · KRUniversity of Louisville · USJilin University · CNKosair Children's Hospital · USSecond Affiliated Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence demonstrated that obesity is a risk factor for renal structural and functional changes, leading to the end-stage renal disease which imposes a heavy economic burden on the community. However, no effective therapeutic method for obesity-associated kidney disease is available. In the present study, we explored the therapeutic potential of a magnolia extract (BL153) for treating obesity-associated kidney damage in a high fat diet- (HFD-) induced mouse model. The results showed that inflammation markers (tumor necrosis factor- α and plasminogen activator inhibitor-1) and oxidative stress markers (3-nitrotyrosine and 4-hydroxy-2-nonenal) were all significantly increased in the kidney of HFD-fed mice compared to mice fed with a low fat diet (LFD). Additionally, proteinuria and renal structure changes in HFD-fed mice were much more severe than that in LFD-fed mice. However, all these alterations were attenuated by BL153 treatment, accompanied by upregulation of peroxisome proliferator-activated receptor- γ coactivator-1 α (PGC-1 α ) and hexokinase II (HK II) expression in the kidney. The present study indicates that BL153 administration may be a novel approach for renoprotection in obese individuals by antiinflammation and anti-oxidative stress most likely via upregulation of PGC-1 α and HK II signal in the kidney.

Indexed as

AnimalsDiet, High-FatDisease Models, AnimalHexokinaseInflammationKidneyKidney Function TestsMagnoliaMaleMiceMice, Inbred C57BLModels, BiologicalNAD(P)H Dehydrogenase (Quinone)ObesityOxidative StressPlant ExtractsBL153 extractHexokinaseNAD(P)H Dehydrogenase (Quinone)Nqo1 protein, mousePlant ExtractsPPAR gammaProtective Agents

Identifiers

PMID24381715
PMCPMC3863519
OpenAlexW2041083840

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.