# Quercetin as an Anti-Diabetic Agent in Rodents—Is It Worth Testing in Humans?

**Authors:** Tomasz Szkudelski, Katarzyna Szkudelska, Aleksandra Łangowska

PMC · DOI: 10.3390/ijms26157391 · International Journal of Molecular Sciences · 2025-07-31

## TL;DR

Quercetin shows anti-diabetic effects in rodents by improving metabolic and hormonal functions, suggesting it may be worth testing in humans.

## Contribution

The paper reviews quercetin's pleiotropic anti-diabetic mechanisms and safety in rodents, advocating for human clinical trials.

## Key findings

- Quercetin mitigates diabetes-related hormonal and metabolic disorders in rodents.
- It reduces oxidative and inflammatory stress through multiple enzymes and signaling pathways.
- No side effects were observed in rodent studies, supporting its potential for human trials.

## Abstract

Quercetin is a biologically active flavonoid compound that exerts numerous beneficial effects in humans and animals, including anti-diabetic activity. Its action has been explored in rodent models of type 1 and type 2 diabetes. It was revealed that quercetin mitigated diabetes-related hormonal and metabolic disorders and reduced oxidative and inflammatory stress. Its anti-diabetic effects were associated with advantageous changes in the relevant enzymes and signaling molecules. Quercetin positively affected, among others, superoxide dismutase, catalase, glutathione peroxidase, glucose transporter-2, glucokinase, glucose-6-phosphatase, glycogen phosphorylase, glycogen synthase, glycogen synthase kinase-3β, phosphoenolpyruvate carboxykinase, silent information regulator-1, sterol regulatory element-binding protein-1, insulin receptor substrate 1, phosphoinositide 3-kinase, and protein kinase B. The available data support the conclusion that the action of quercetin was pleiotropic since it alleviates a wide range of diabetes-related disorders. Moreover, no side effects were observed during treatment with quercetin in rodents. Given that human diabetes affects a large part of the population worldwide, the results of animal studies encourage clinical trials to evaluate the potential of quercetin as an adjunct to pharmacological therapies.

## Linked entities

- **Genes:** gck (glucokinase (hexokinase 4)) [NCBI Gene 100124905], PCK1 (phosphoenolpyruvate carboxykinase 1) [NCBI Gene 829943]
- **Proteins:** Cat (Catalase), GPX2 (glutathione peroxidase 2)
- **Chemicals:** quercetin (PubChem CID 5280343)
- **Diseases:** type 1 diabetes (MONDO:0005147), type 2 diabetes (MONDO:0005148)

## Full-text entities

- **Genes:** SREBF1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 6720] {aka HMD, IFAP2, SREBP1, bHLHd1}, GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], GCK (glucokinase) [NCBI Gene 2645] {aka FGQTL3, GK, GLK, HHF3, HK4, HKIV}, IRS1 (insulin receptor substrate 1) [NCBI Gene 3667] {aka HIRS-1}, G6PC1 (glucose-6-phosphatase catalytic subunit 1) [NCBI Gene 2538] {aka G6PC, G6PT, G6Pase, GSD1, GSD1a}, PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}, CAT (catalase) [NCBI Gene 847]
- **Diseases:** metabolic disorders (MESH:D008659), diabetes-related disorders (MESH:D048909), inflammatory (MESH:D007249), type 1 and type 2 diabetes (MESH:D003924), Diabetic (MESH:D003920)
- **Chemicals:** Quercetin (MESH:D011794), flavonoid (MESH:D005419)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12347388/full.md

## References

129 references — full list in the complete paper: https://tomesphere.com/paper/PMC12347388/full.md

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Source: https://tomesphere.com/paper/PMC12347388