# Dandelion Leaf Aqueous Extract Relieves Hyperuricemia and Its Complications via Modulating Uric Acid Metabolism, Renal Inflammation, and Gut Microbes

**Authors:** Xiaofei Zhou, Tianxu Liu, Bingye Xu, Weiqian Zhang, Xiang Li, Fan Wei, Huan Lv, Xuemeng Ji, Bowei Zhang, Shuo Wang

PMC · DOI: 10.3390/foods14223843 · 2025-11-10

## TL;DR

Dandelion leaf extract reduces high uric acid levels and kidney inflammation in mice by regulating metabolism, inflammation, and gut microbes.

## Contribution

This study identifies dandelion leaf extract as a natural remedy for hyperuricemia and kidney complications through multiple mechanisms.

## Key findings

- Dandelion leaf extract lowered serum uric acid and protected liver and kidney function in hyperuricemic mice.
- The extract inhibited inflammatory pathways and reduced pro-inflammatory cytokine expression in the kidneys.
- Dandelion leaf extract modulated gut microbiota and increased short-chain fatty acid-producing bacteria.

## Abstract

Dandelion is an edible and medicinal plant that has beneficial effects in various complex disorders. In this study, we investigated the regulatory effects of dandelion leaf aqueous extract (DAE) on mice with hyperuricemia (HUA) and explored its underlying mechanisms. DAE exhibited a high total phenolic content (363.31 ± 0.61 mg GAC/g) and contained 20 identified polyphenolic compounds. The administration of DAE significantly reduced serum uric acid levels and exerted protective effects on both liver and kidney function in mice with HUA. Mechanistically, DAE inhibited the NLRP3/Caspase-1 and TLR4/MyD88/NF-κB signaling pathways, leading to the downregulated mRNA expression of pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α), thereby alleviating renal inflammation. Additionally, DAE modulated the gut microbiota composition and increased SCFA-producing bacteria, along with increases in fecal SCFA contents. These findings suggest that DAE effectively mitigates HUA and its associated renal complications by regulating uric acid metabolism, suppressing renal inflammation, and restoring gut microbial homeostasis. Thus, DAE holds promise as a natural adjuvant therapy for HUA and related kidney inflammation.

## Linked entities

- **Proteins:** NLRP3 (NLR family pyrin domain containing 3), Caspase1 (caspase-1), TLR4 (toll like receptor 4), MYD88 (MYD88 innate immune signal transduction adaptor), NFKB1 (nuclear factor kappa B subunit 1), IL1B (interleukin 1 beta), IL6 (interleukin 6), TNF (tumor necrosis factor)
- **Chemicals:** uric acid (PubChem CID 1175)
- **Diseases:** hyperuricemia (MONDO:0002144)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** kidney inflammation (MESH:D007674), Renal Inflammation (MESH:D007249), HUA (MESH:D033461)
- **Chemicals:** Uric Acid (MESH:D014527), DAE (-), SCFA (MESH:D005232)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12651310/full.md

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Source: https://tomesphere.com/paper/PMC12651310