# Effects of Dietary Supplementation with Chitosan on the Muscle Composition, Digestion, Lipid Metabolism, and Stress Resistance of Juvenile Tilapia (Oreochromis niloticus) Exposed to Cadmium-Induced Stress

**Authors:** Qin Zhang, Yi Xie, Yuanhui Zhang, Enhao Huang, Liuqing Meng, Yongqiang Liu, Tong Tong

PMC · DOI: 10.3390/ani14040541 · Animals : an Open Access Journal from MDPI · 2024-02-06

## TL;DR

This study shows that adding chitosan to tilapia diets helps reduce the harmful effects of cadmium exposure by improving muscle composition, digestion, lipid metabolism, and stress resistance.

## Contribution

The study demonstrates that dietary chitosan mitigates cadmium-induced stress in tilapia by enhancing physiological and gene expression responses.

## Key findings

- Chitosan supplementation increased crude fat and protein in tilapia muscle and digestive enzyme activities.
- Gene expression related to lipid metabolism and stress resistance was significantly upregulated with chitosan.
- Chitosan reduced the toxic effects of cadmium on juvenile tilapia's health and metabolism.

## Abstract

Long-term exposure to cadmium can cause liver toxicity, kidney toxicity, bone toxicity, and cancer in aquatic animals, which seriously endangers the health of aquatic animals and the quality of aquatic products. Chitosan can be combined with cadmium in aquaculture water through adsorption, thus alleviating the toxic effects of cadmium on aquatic animals. In this study, juvenile tilapia was fed with a formulated feed containing five different levels (0%, 0.5%, 1.0%, 1.5%, and 2.0%) of chitosan for 60 days, while the water in all experimental groups contained a Cd2+ concentration of 0.2 mg/L. The results indicated that dietary chitosan supplementation could alleviate the effects of Cd2+ stress on the muscle composition, digestive enzymes, lipid metabolism, and stress resistance, and their related gene expression, of juvenile tilapia.

The aim of this study was to investigate the effects of dietary chitosan supplementation on the muscle composition, digestion, lipid metabolism, and stress resistance, and their related gene expression, of juvenile tilapia (Oreochromis niloticus) subjected to cadmium (Cd2+) stress. Juvenile tilapia with an initial body weight of 21.21 ± 0.24 g were fed with a formulated feed containing five different levels (0%, 0.5%, 1.0%, 1.5%, and 2.0%) of chitosan for 60 days, while the water in all experimental groups contained a Cd2+ concentration of 0.2 mg/L. The results showed that, compared with the control group (0% chitosan), the contents of crude fat and crude protein in the muscle, the activities of lipase, trypsin, and amylase in the intestine, as well as the relative expression levels of metallothionein (mt), cytochrome P450 1A (cyp1a), carnitine palmitoyltransferase-1 (cpt-1), peroxisome proliferator-activated receptor alpha (pparα), peroxisome proliferator-activated receptor gamma (pparγ), hormone-sensitive lipase (hsl), lipoprotein lipase (lpl), malate dehydrogenase (mdh), leptin (lep), fatty acid synthase (fas), sterol regulatory element-binding protein 1 (srebp1), and stearoyl-CoA desaturase (scd) genes in the liver of juveniles were significantly increased (p < 0.05). In conclusion, dietary chitosan supplementation could alleviate the effects of Cd2+ stress on the muscle composition, digestive enzymes, lipid metabolism, and stress resistance, and their related gene expression, of juvenile tilapia, and to some extent reduce the toxic effect of Cd2+ stress on tilapia.

## Linked entities

- **Genes:** MCAT (malonyl-CoA-acyl carrier protein transacylase) [NCBI Gene 27349], cyp1a (cytochrome P450, family 1, subfamily A) [NCBI Gene 140634], CPT1A (carnitine palmitoyltransferase 1A) [NCBI Gene 1374], PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465], PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468], LIPE (lipase E, hormone sensitive type) [NCBI Gene 3991], LPL (lipoprotein lipase) [NCBI Gene 4023], MDH2 (malate dehydrogenase 2) [NCBI Gene 4191], LEP (leptin) [NCBI Gene 3952], FAS (Fas cell surface death receptor) [NCBI Gene 355], SREBF1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 6720], SCD (stearoyl-CoA desaturase) [NCBI Gene 6319]
- **Chemicals:** chitosan (PubChem CID 129662530), Cd2+ (PubChem CID 31193)
- **Species:** Oreochromis niloticus (taxon 8128)

## Full-text entities

- **Genes:** cyp1a [NCBI Gene 100706338], lipoprotein lipase [NCBI Gene 100534504], metallothionein [NCBI Gene 100696451], fas [NCBI Gene 100534502], peroxisome proliferator-activated receptor alpha [NCBI Gene 100709869], pparalpha [NCBI Gene 100697805], trypsin [NCBI Gene 100534516], scd [NCBI Gene 100695729], hormone-sensitive lipase [NCBI Gene 100534456], lep [NCBI Gene 100704227], amylase [NCBI Gene 100534494], peroxisome proliferator-activated receptor gamma [NCBI Gene 100711231]
- **Diseases:** toxic (MESH:D064420)
- **Chemicals:** Chitosan (MESH:D048271), Cadmium (MESH:D002104), Lipid (MESH:D008055)
- **Species:** Oreochromis niloticus (Nile tilapia, species) [taxon 8128], Tilapia (genus) [taxon 8126]

## Full text

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## Figures

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## References

66 references — full list in the complete paper: https://tomesphere.com/paper/PMC10886040/full.md

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Source: https://tomesphere.com/paper/PMC10886040