# Unraveling the mechanism of mulberry leaf in alleviating hyperuricemia: key role of kaempferol by modulating AKT pathway and gut-kidney axis

**Authors:** Jiawei Huang, Qianqian Wang, Xiaowen Guo, Yuanyuan Niu, Junhong Huang, Boyi Zhang, Zixuan Guo, Zilong Wang, Shuying Feng

PMC · DOI: 10.3389/fmicb.2026.1752775 · 2026-01-22

## TL;DR

Mulberry leaf helps reduce high uric acid levels mainly through kaempferol, which affects kidney inflammation and gut health.

## Contribution

Kaempferol's role in modulating the AKT pathway and gut-kidney axis in hyperuricemia is newly identified.

## Key findings

- Kaempferol binds strongly to AKT1 and TNF, as shown by molecular simulations.
- Kaempferol reduces AKT expression and kidney inflammation in hyperuricemia.
- Kaempferol helps restore gut microbiota disrupted by hyperuricemia.

## Abstract

Mulberry leaf (Morus alba L.) is an edible plant that has been found to have medicinal effects in the treatment of hyperuricemia (HUA). The bioactive compounds of mulberry leaf and their mechanisms of action have not been determined yet.

In-silico methodologies were used to identify bioactive compounds and to determine the underlying mechanisms of mulberry leaf. In order to verify the biochemical mechanism and intestinal microbiota, in vivo experiments were conducted.

Kaempferol was identified as the principal bioactive compound, while the key targets were AKT1 and TNF. Molecular docking and dynamics simulations revealed that AKT1-kaempferol and TNF-kaempferol complexes showed strong and stable binding pattern after a 100 ns simulation. In vivo studies demonstrated that kaempferol exerted significant anti-HUA effects. Specifically, kaempferol reduces AKT expression and phosphorylation, which may in turn reduces the oxidative stress and inflammatory pathways and signal transmission of the kidneys. Meanwhile, the application of kaempferol attenuated gut microbiota dysbiosis caused by HUA.

Kaempferol may regulate UA metabolism and inflammatory injury by modulating the AKT signaling pathway, and exert its effects on the gut-kidney axis and restoring gut microbiota composition.

## Linked entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], TNF (tumor necrosis factor) [NCBI Gene 7124]
- **Chemicals:** kaempferol (PubChem CID 5280863)
- **Diseases:** hyperuricemia (MONDO:0002144)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}
- **Diseases:** microbiota dysbiosis (MESH:D064806), inflammatory (MESH:D007249), HUA (MESH:D033461)
- **Chemicals:** Kaempferol (MESH:C006552)
- **Species:** Morus alba (white mulberry, species) [taxon 3498]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12872837/full.md

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Source: https://tomesphere.com/paper/PMC12872837