Evidence map›Paper›PMID 37096379›Full record

ArticleDiabetes & metabolism journal2023

Beneficial Effects of a Curcumin Derivative and Transforming Growth Factor-β Receptor I Inhibitor Combination on Nonalcoholic Steatohepatitis.

Kyung Bong Ha, Eun Soo Lee, Na Won Park, Su Ho Jo, Soyeon Shim, Dae-Kee Kim, Chan Mug Ahn, Choon Hee Chung

Open access · goldAbstract read
In one paragraph

Article in Diabetes & metabolism journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 10 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

8 authors at 2 institutions in 1 country.

Kyung Bong HaDepartment 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.
Na Won ParkDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Su Ho JoDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Soyeon ShimDepartment of Pharmacy, College of Pharmacy, Ewha Womans University, Seoul, Korea.
Dae-Kee KimDepartment of Pharmacy, College of Pharmacy, Ewha Womans University, Seoul, Korea.
Chan Mug AhnDepartment of Basic Science, Yonsei University Wonju College of Medicine, Wonju, Korea.
Choon Hee ChungDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Yonsei University · KREwha Womans University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgruoundCurcumin 2005-8 (Cur5-8), a derivative of curcumin, improves fatty liver disease via AMP-activated protein kinase activation and autophagy regulation. EW-7197 (vactosertib) is a small molecule inhibitor of transforming growth factor β (TGF-β) receptor I and may scavenge reactive oxygen species and ameliorate fibrosis through the SMAD2/3 canonical pathway. This study aimed to determine whether co-administering these two drugs having different mechanisms is beneficial.

methodsHepatocellular fibrosis was induced in mouse hepatocytes (alpha mouse liver 12 [AML12]) and human hepatic stellate cells (LX-2) using TGF-β (2 ng/mL). The cells were then treated with Cur5-8 (1 μM), EW-7197 (0.5 μM), or both. In animal experiments were also conducted during which, methionine-choline deficient diet, Cur5-8 (100 mg/kg), and EW-7197 (20 mg/kg) were administered orally to 8-week-old C57BL/6J mice for 6 weeks.

resultsTGF-β-induced cell morphological changes were improved by EW-7197, and lipid accumulation was restored on the administration of EW-7197 in combination with Cur5-8. In a nonalcoholic steatohepatitis (NASH)-induced mouse model, 6 weeks of EW-7197 and Cur5-8 co-administration alleviated liver fibrosis and improved the nonalcoholic fatty liver disease (NAFLD) activity score.

conclusionCo-administering Cur5-8 and EW-7197 to NASH-induced mice and fibrotic hepatocytes reduced liver fibrosis and steatohepatitis while maintaining the advantages of both drugs. This is the first study to show the effect of the drug combination against NASH and NAFLD. Similar effects in other animal models will confirm its potential as a new therapeutic agent.

Indexed as

CurcuminNon-alcoholic Fatty Liver DiseaseAniline CompoundsAnimalsFibrosisHumansLiver CirrhosisMiceMice, Inbred C57BLTransforming Growth Factor betaTransforming Growth FactorsTriazolesAniline CompoundsCurcuminTransforming Growth Factor betaTransforming Growth FactorsTriazolesvactosertibALK5 inhibitorCurcuminFibrosisNon-alcoholic fatty liver diseaseTransforming growth factor beta

Identifiers

PMID37096379
PMCPMC10404525
OpenAlexW4366990257

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.