Evidence map›Paper›PMID 42671997›Full record

ArticleMolecular nutrition & food research2026

Theabrownin Alleviates Alcoholic Liver Disease in Mice by Improving Gut Microbiota and Tryptophan Metabolism.

Lingxiao Ye, Zizhen Wang, Sihao Zhu, Xiaoyan Ding, Jianrong Han, Yuanwei Hao, Chengyong He, Yu Jiang, Zonghong Liu, Zhenghong Zuo

Abstract read
In one paragraph

Article in Molecular nutrition & food research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Lingxiao YeState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Cardiovascular Surgery, Xiang'an Hospital of Xiamen University, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Zizhen WangState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Cardiovascular Surgery, Xiang'an Hospital of Xiamen University, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Sihao ZhuState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Cardiovascular Surgery, Xiang'an Hospital of Xiamen University, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Xiaoyan DingState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Cardiovascular Surgery, Xiang'an Hospital of Xiamen University, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Jianrong HanState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Cardiovascular Surgery, Xiang'an Hospital of Xiamen University, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Yuanwei HaoState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Cardiovascular Surgery, Xiang'an Hospital of Xiamen University, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Chengyong HeState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Cardiovascular Surgery, Xiang'an Hospital of Xiamen University, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.ORCID 0000-0002-9614-103X
Yu JiangMolecular Diagnostic Laboratory For Precision Medicine, Xiang'an Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, Fujian, China.
Zonghong LiuState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Cardiovascular Surgery, Xiang'an Hospital of Xiamen University, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Zhenghong ZuoState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Cardiovascular Surgery, Xiang'an Hospital of Xiamen University, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.

Funding

Natural Science Foundation of Fujian Province, China 2021Y4006
6 · The paper itself

Abstract

Theabrownin (TB) is a bioactive compound derived from tea. Alcoholic liver disease (ALD), caused by chronic alcohol consumption, leads to progressive liver damage associated with inflammation and steatosis. This study aimed to investigate TB's protective effects against ALD and elucidate its mechanisms. A chronic-binge ethanol feeding model was used to induce ALD in mice. Mice were administered TB alongside ethanol exposure. Liver function markers, oxidative stress parameters, inflammatory cytokines, and apoptosis indicators were evaluated. Intestinal barrier integrity and gut inflammation were assessed, along with the expression of tight junction proteins. 16S rRNA sequencing was performed to analyze gut microbiota composition. TB supplementation significantly alleviated hepatic oxidative stress and inflammation and decreased hepatocellular apoptosis. In the gut, TB mitigated ethanol-induced inflammation and restored barrier function by enhancing tight junction protein expression. Microbiota analysis revealed that TB notably increased the abundance of Akkermansia muciniphila, which was associated with altered tryptophan metabolism and activation of the aryl hydrocarbon receptor (AhR) signaling pathway. These changes contributed to the overall protective effect of TB against alcohol-induced toxicity. TB exhibits nutritionally relevant hepatoprotective effects through its antioxidant properties, enhancement of gut barrier integrity, and modulation of the gut microbiota and metabolite-mediated signaling pathways. These findings support the potential of TB as a dietary intervention for preventing or managing ALD.

Indexed as

Gastrointestinal MicrobiomeLiver Diseases, AlcoholicTryptophanAkkermansiaAnimalsApoptosisEthanolLiverMaleMiceMice, Inbred C57BLOxidative StressReceptors, Aryl HydrocarbonEthanolReceptors, Aryl HydrocarbonTryptophanalcoholic liver diseasegut‐liver axistheabrownintryptophan metabolism

Identifiers

PMID42671997
PMCPMC13528973

What Socratic holds

Textmetadata
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.