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Research Article | Open Access

Black tea extract ameliorates fatty liver and fatty kidney in HFD-induced obese mice

Peng Maa,1Li Zhanga,b,1Zijing WangaTianshu XuaHaiguang YangaBiyu HouaYiwei LicPing HeaSin Man LamdGuanghou ShuidXiangyan LieGuanhua DuaJian Yingf ( )Guifen Qianga( )
Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College and Beijing Key Laboratory of Drug Target and Screening Research, Beijing 100050, China
Inner Mongolia Clinical College, Inner Mongolia Medical University, Hohhot 010110, China
Faculty of Environment and Life, Beijing University of Technology, Beijing 100124, China
State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China
Northeast Asia Research Institute of Traditional Chinese Medicine, Key Laboratory of Active Substances and Biological Mechanisms of Ginseng Efficacy, Ministry of Education, Jilin Provincial Key Laboratory of Bio-Macromolecules of Chinese Medicine, Changchun University of Chinese Medicine, Changchun 130117, China
Wuhan Polytechnic University, Nutrition and Health Research Institute, School of Life Science and Technology, School of Food Science and Engineering, Wuhan 430000, China

1 These authors contributed equally to this work.

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Highlights

• Up-regulated phosphatidylcholines, phosphatidylglycerols and phosphatidylethanolamines and down-regulated cardiolipin are the characteristic changes in ELD.

Black tea extract induces lipidomics remodeling in ELD.

• The improvement effect of BTE on renal sphingolipids, phospholipids and BMP is stronger than that on fatty liver.

• The downregulation of glycerides is the pharmacological fundament of BTE on alleviating ELD.

• CE18:2 and TAG56:4 (20:2) are the potential lipid biomarkers and targets of ELD.

Abstract

Black tea is a kind of full-fermented tea with therapeutic potential for metabolic diseases. Ectopic lipid deposition (ELD) is an essential risk factor for organ injury in metabolic syndrome, especially in liver and kidney, for which effective interventions are lacking. Here, we explored whether black tea extract (BTE) improves fatty liver and fatty kidney, as well as identified the potential lipid biomarkers for ELD and lipid targets of BTE on the improvement of ELD. Transcriptome data from diet-induced obese mice were analyzed to confirm high-fat-diet feeding disturbs lipid metabolism in the liver and kidney. BTE prominently inhibited body weight gain, improved glucose metabolism, as well as reduced lipid droplet accumulation in the liver and kidney. Moreover, lipidomic profiling analyses identified 28 lipid classes in the liver while 29 in the kidney with that up-regulated glycerides and phosphatidylcholines, as well as down-regulated cardiolipin were the characteristic changes in ELD. BTE prominently reduced glycerides in ELD, thereby constituting the basis of its anti-ELD effect. Specifically, BTE displayed stronger effects on lowering cholesterol ester (CE) in fatty liver, while also affecting phospholipids and sphingolipids in fatty kidney. Ultimately, integrative analysis identified CE18:2 and triglyceride (TAG)56:4 (20:2) as the potential lipid biomarkers for BTE in improvement of ELD. BTE could be an effective food supplement for the prevention and treatment of ELD. Notably, CE18:2 and TAG56:4(20:2), as the potential lipid biomarkers, may facilitate the research and development of anti-ELD drug.

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Food Science and Human Wellness
Article number: 9250391

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Cite this article:
Ma P, Zhang L, Wang Z, et al. Black tea extract ameliorates fatty liver and fatty kidney in HFD-induced obese mice. Food Science and Human Wellness, 2026, 15(3): 9250391. https://doi.org/10.26599/FSHW.2024.9250391

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Received: 01 April 2024
Revised: 21 April 2024
Accepted: 05 September 2024
Published: 10 April 2026
© 2026 Beijing Academy of Food Sciences. Publishing services by Tsinghua University Press.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).