# Impact of Goji Berry Juice on Redox Status in Wistar Rats: A Subchronic Toxicity Assessment

**Authors:** Cristiane de Freitas Rodrigues, Jean Ramos Boldori, Félix Roman Munieweg, Marcell Valandro Soares, Bibiana Pistoia Rabuske, Thais Ribeiro Pinheiro, Cristiane Casagrande Denardin

PMC · DOI: 10.3390/ijms27020631 · 2026-01-08

## TL;DR

This study assesses the subchronic toxicity of goji berry juice in rats, finding potential redox imbalances and organ damage.

## Contribution

The study provides new insights into the potential pro-oxidant effects of goji berry juice in a rodent model.

## Key findings

- Goji berry juice caused elevated hepatic transaminase levels and reactive species in liver and kidney.
- Antioxidant defenses were imbalanced, leading to lipid and protein damage.
- Kidney damage was observed with increased Bowman space.

## Abstract

Goji berry consumption provides various beneficial health effects, although little is known about the possible toxicological and pro-oxidant effects. Therefore, this study aimed to evaluate the subchronic oral toxicity of goji berry juice (GBJ) for 28 days in Wistar rats (OECD 407). The GBJ was prepared in a blender with water and then filtered. The total phenolic compounds were evaluated using the Folin method (μg equivalent of gallic acid/mL juice). Forty 90-day-old female Wistar rats were divided into four groups of 10 animals each. The control group received an oral saline solution of 1 mL/100 g, and the treatments received daily doses of 1.85, 5.68, and 11.36 μg GAE/100 g for 28 days. Our findings revealed that GBJ does not alter animal body weight or food intake, although we observed higher hepatic transaminase levels and reactive species generation in the liver and kidney, which may have led to imbalanced antioxidant defenses and damaged lipids and proteins. Additionally, we observed kidney damage with increased Bowman space. Our 28-day findings indicate that goji berry juice at doses equivalent to typical human consumption can induce early redox imbalances and hepatic and renal biochemical alterations in female Wistar rats, warranting caution and further long-term, sex-inclusive studies.

## Linked entities

- **Chemicals:** gallic acid (PubChem CID 370)

## Full-text entities

- **Diseases:** kidney damage (MESH:D007674), Toxicity (MESH:D064420)
- **Chemicals:** water (MESH:D014867), gallic acid (MESH:D005707), lipids (MESH:D008055), GAE (-)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Lycium barbarum (Duke of Argyll's teatree, species) [taxon 112863]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12841297/full.md

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Source: https://tomesphere.com/paper/PMC12841297