Evidence map›Paper›PMID 34225578›Full record

ArticlePharmaceutical biology2021

Taxifolin, a novel food, attenuates acute alcohol-induced liver injury in mice through regulating the NF-κB-mediated inflammation and PI3K/Akt signalling pathways.

Chuanbo Ding, Yingchun Zhao, Xueyan Chen, Yinan Zheng, Wencong Liu, Xinglong Liu

Abstract read
In one paragraph

Article in Pharmaceutical biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

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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

6 authors.

Chuanbo DingCollege of Chinese Medicinal Materials, Jilin Agricultural University, Changchun, Jilin, China.
Yingchun ZhaoCollege of Chinese Medicinal Materials, Jilin Agricultural University, Changchun, Jilin, China.
Xueyan ChenCollege of Chinese Medicinal Materials, Jilin Agricultural University, Changchun, Jilin, China.
Yinan ZhengCollege of Chinese Medicinal Materials, Jilin Agricultural University, Changchun, Jilin, China.
Wencong LiuCollege of Chinese Medicinal Materials, Jilin Agricultural University, Changchun, Jilin, China.
Xinglong LiuCollege of Chinese Medicinal Materials, Jilin Agricultural University, Changchun, Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextTaxifolin (TAX) has effective anti-inflammatory, antioxidant and hepatoprotective activities, but its potential mechanism has not been revealed.

objectiveTo evaluate the potential protective effect of TAX on acute alcohol-induced liver injury in mice. MATERIALS AND

methodsAlcoholic liver injury model was established by oral alcohol in mice, and randomly distributed in five groups (

resultsTAX treatment illustrated that the level of alanine aminotransferase (ALT) was reduced to 65.90 ± 2.26 U/L and aspartate aminotransferase (AST) to 33.28 ± 5.62 U/L compared with alcohol group (ALT 124.51 ± 4.40 U/L, AST 61.70 ± 4.09 U/L), while superoxide dismutase (SOD) was increased to 49.81 ± 2.39 U/mg and glutathione (GSH) to 8.16 ± 0.44 μmol/g, but MDA was reversed to 2.53 ± 0.24 nmol/mg. Histopathological examination showed TAX treatment alleviated alcohol-induced hepatocyte necrosis and inflammatory infiltration. Meanwhile, Western blot and rt-PCR indicated TAX reduced IL-6 to 2.49 ± 0.25 pg/mL and TNF-α to 1.79 ± 0.20 pg/mL, and inhibiting NF-κB activation in liver. Moreover, TAX reversed alcohol-induced apoptosis by regulating the expression of PI3K/Akt and its downstream apoptotic factors.

conclusionsThe research provides novel evidence of the hepatoprotective effect of TAX on alcohol-induced liver injury, while also providing the possibility for future treatment of alcoholic liver disease.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalAntioxidantsApoptosisDose-Response Relationship, DrugInflammationLiver Diseases, AlcoholicMaleMiceMice, Inbred ICRNF-kappa BPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktQuercetinSignal TransductionAnti-Inflammatory Agents, Non-SteroidalAntioxidantsNF-kappa BPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktQuercetintaxifolinAlcoholic liver diseaseanti-apoptosisantioxidantNF-κB-mediated inflammatory factors

Identifiers

PMID34225578
PMCPMC8259856

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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.