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ORIGINAL RESEARCH article

Front. Nutr.

Sec. Nutrition and Metabolism

Volume 12 - 2025 | doi: 10.3389/fnut.2025.1682308

This article is part of the Research TopicTherapeutic Potential of Food-Derived Bioactive Compounds and Endogenous Metabolites for Diabetes, Cardiovascular, and Cerebrovascular DiseasesView all 8 articles

.Dihydromyricetin Preserves β-Cell Function in Type 1 Diabetes via PI3K/AKT-Mediated Metabolic Reprogramming

Provisionally accepted
Jia  LiJia Li1Lijia  LiLijia Li1Tahui  LinTahui Lin2Houtan  HuangHoutan Huang2Jie  RenJie Ren1Jengyuan  YaoJengyuan Yao1,2*
  • 1School of Public Health, Fujian Medical University, Fuzhou, Fujian, China, Fuzhou, China
  • 2Key laboratory of functional and clinical translational medicine, Fujian province university, Xiamen Medical College, Fujian Province, China, Xiamen, China

The final, formatted version of the article will be published soon.

Background: Food-derived flavonoids are emerging as nutraceutical agents for glycemic control. Dihydromyricetin (DMY), the signature flavanonol of vine tea (Ampelopsis grossedentata), has long been consumed in South China, yet its antidiabetic potential remains underexplored. Methods: We administered DMY (50 and 100 mg/kg/day, 12 days) to streptozotocin-induced type 1 diabetic mice. Fasting glycemia, lipid panels, and HOMA-β were evaluated 4 weeks after DMY administration. Untargeted UPLC-QTOF metabolomics combined with network pharmacology pinpointed pathway hubs, while experiments in INS-1 β-cells using the PI3K inhibitor LY294002 verified the pathway's involvement. Results: DMY reduced hyperglycemia, corrected dyslipidemia, and preserved islet architecture. Metabolomics indicated a shift toward a normal5 plasma profile, with the arachidonic acid, linoleic acid, and steroid hormone pathways being the most responsive. Six hub targets (PTGS2, IL6, AKT1, IL1B, BCL2, CASP3) mapped to eicosanoid signaling, apoptosis, and PI3K/AKT axis. Docking and cell assays confirmed direct binding and PI3K/AKT-dependent cytoprotection, evidenced by restored p-AKT, lowered ROS, and reduced caspase-3 cleavage. Conclusion: DMY, a readily accessible food-derived bioactive compound, reprograms lipid-inflammatory metabolism and activates PI3K/AKT to safeguard β-cell viability, highlighting its nutraceutical promise for dietary management of autoimmune diabetes.

Keywords: Dihydromyricetin1, vine tea2, nutraceutica3, metabolomics4, Ttype 1 diabetes5

Received: 08 Aug 2025; Accepted: 19 Sep 2025.

Copyright: © 2025 Li, Li, Lin, Huang, Ren and Yao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Jengyuan Yao, 201500080004@xmmc.edu.cn

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