# Dietary Rutin Ameliorates Nanoparticle Zinc Oxide-Induced Toxicity in Mice by Potentiating Antioxidant Defense Mechanisms

**Authors:** Xiaofang He, Longfei Ma, Jiaqi Zhang, Binbin Zhou, Shun Chen, Minhang Tu, Gentan Cai, Tian Wang, Chao Wang

PMC · DOI: 10.3390/nu17091495 · Nutrients · 2025-04-29

## TL;DR

Dietary rutin helps reduce nanoparticle zinc oxide toxicity in mice by boosting antioxidant defenses, though it doesn't fully reverse all harmful effects.

## Contribution

This study demonstrates rutin's protective role against zinc oxide nanoparticle-induced toxicity via antioxidant mechanisms in mice.

## Key findings

- Rutin improved relative organ indexes in the liver and kidney despite not reversing body weight decline.
- Rutin enhanced antioxidant capacity in the jejunum and serum through Nrf2 activation.
- Rutin partially restored hepatic function and mitigated HZn-induced injuries at 600 mg/kg.

## Abstract

In animal production, nanoparticulate zinc oxide exhibits synergistic antibacterial efficacy coupled with growth-promoting effects, positioning itself as a novel antibiotic alternative with enhanced biosafety profiles. However, its dose-dependent toxicity poses challenges. Objective: The experimental design sought to quantify the protective effects of dietary rutin against zinc-overload-induced damage. Methods: A zinc-overload murine model was established by giving high-dose ZnO nanoparticles (HZn, 5000 mg/kg/day) for 21 days. Mice were then fed rutin at doses of 300, 600, or 1200 mg/kg. Body weight, relative organ indexes, zinc concentrations, serum enzyme activities, and tissue-level indicators of apoptosis, autophagy, mitochondrial function, and antioxidant capacity were measured. Results: The results showed that rutin could not reverse HZn-induced body weight decline but improved relative organ indexes in liver and kidney. It alleviated HZn-induced cell damage and enhanced antioxidant capacity in jejunum and serum through Nrf2 activation, without inhibiting HZn-induced zinc elevation. Conclusions: Rutin, especially at 600 mg/kg, can partially restore hepatic function and organ index and mitigate HZn-induced hepatic and jejunal injuries.

## Linked entities

- **Proteins:** GABPA (GA binding protein transcription factor subunit alpha)
- **Chemicals:** Rutin (PubChem CID 5280805), zinc oxide (PubChem CID 3007857), ZnO (PubChem CID 14806)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}
- **Diseases:** hepatic and jejunal injuries (MESH:D007579), weight decline (MESH:D015431), Toxicity (MESH:D064420)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12073253/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12073253/full.md

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Source: https://tomesphere.com/paper/PMC12073253