# Antagonistic effects of nano-copper on lead toxicity in Nile and blue Tilapia: Evidence from growth, immunity, and gene expression

**Authors:** Mohammed F. El Basuini, Rawheya Shaaban Ramadan, Medhat E. Eldenary, Islam I. Teiba, Ali A. Soliman, Mahmoud S. Gewaily, Issam Khelfaoui, Mayada Alhoshy, Akram Ismael Shehata

PMC · DOI: 10.1016/j.cirep.2025.200258 · 2025-10-25

## TL;DR

Nano-copper in fish diets reduces lead toxicity by improving growth, immunity, and tissue health in Nile and blue tilapia.

## Contribution

Nano-copper mitigates lead toxicity in fish by improving physiological and immune responses and reducing tissue damage.

## Key findings

- Nano-copper reduced lead accumulation and preserved intestinal and hepatic structure in fish.
- Nano-copper reversed lead-induced changes in gene expression related to immunity and antioxidants.
- No significant differences in treatment effects were observed between the two tilapia species.

## Abstract

•Dietary nano-copper mitigated lead (Pb) toxicity in Oreochromis niloticus and O. aureus.•Nano-copper (2 mg/kg diet) improved growth, immunity, and antioxidant status in Pb-exposed fish.•Pb increased hepatic MDA, inflammatory markers, and histopathological alterations.•Nano-copper reduced tissue Pb accumulation and preserved intestinal and hepatic structure.•Pb altered IGF-1, CAT, IL-1β, and hepcidin expression; Nano-Cu reversed these effects.•No significant treatment × species interactions were observed across most parameters.

Dietary nano-copper mitigated lead (Pb) toxicity in Oreochromis niloticus and O. aureus.

Nano-copper (2 mg/kg diet) improved growth, immunity, and antioxidant status in Pb-exposed fish.

Pb increased hepatic MDA, inflammatory markers, and histopathological alterations.

Nano-copper reduced tissue Pb accumulation and preserved intestinal and hepatic structure.

Pb altered IGF-1, CAT, IL-1β, and hepcidin expression; Nano-Cu reversed these effects.

No significant treatment × species interactions were observed across most parameters.

This study investigated the antagonistic effects of dietary nano-copper (Nano-Cu) against lead (Pb) toxicity in two tilapia species, Oreochromis niloticus (n = 360; 55.33 ± 0.54 g) and Oreochromis aureus (n = 360; 55.54 ± 0.61 g), over a 60-day feeding trial. The two tilapia species were divided into four dietary groups: control, Pb (100 µg/kg diet), Nano-Cu (2 mg/kg diet), and Pb+Nano-Cu. Growth performance, digestive enzyme activity, muscle Pb accumulation, serum biochemistry, immune responses, hepatic antioxidant status, and gene expression were assessed, along with histopathological examinations of the intestine and liver. Pb exposure significantly reduced growth indicators, digestive enzyme activities, antioxidant capacity, and immune function, while increasing hepatic malondialdehyde (MDA), serum glucose, liver enzymes, and pro-inflammatory gene expression. Histologically, Pb exposure caused evident structural damage, including villus atrophy in the intestine and hepatic vacuolation with sinusoidal dilatation. In contrast, Nano-Cu supplementation markedly improved growth, protein metabolism, enzymatic activities, and antioxidant status, and mitigated Pb accumulation and toxicity. Nano-Cu preserved normal intestinal and hepatic histoarchitecture and partially alleviated the Pb-induced tissue damage when co-administered. No significant species-specific differences or treatment × species interactions were observed for most variables. These findings demonstrate that Nano-Cu supplementation effectively counteracts Pb-induced toxicity in tilapia and enhances fish health by improving physiological function and maintaining tissue integrity. Future research should expand immunological profiling to include specific immune proteins (e.g., complement C3, IgM) and cytokines (e.g., TNF-α, IL-10), providing deeper mechanistic insight into Nano-Cu-mediated immune modulation under toxic stress, and further investigate its long-term effects under various environmental conditions.

## Linked entities

- **Genes:** IGF1 (insulin like growth factor 1) [NCBI Gene 3479], CAT (catalase) [NCBI Gene 847], IL1B (interleukin 1 beta) [NCBI Gene 3553], HAMP (hepcidin antimicrobial peptide) [NCBI Gene 512301]
- **Chemicals:** lead (PubChem CID 5352425), malondialdehyde (PubChem CID 10964), glucose (PubChem CID 5793), IgM (PubChem CID 71581418), IL-10 (PubChem CID 146070)
- **Species:** Oreochromis niloticus (taxon 8128), Oreochromis aureus (taxon 47969)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12615765/full.md

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Source: https://tomesphere.com/paper/PMC12615765