# Microplastics and Nitrite Stress Affect Physiological and Metabolic Functions of the Hepatopancreas in Marine Shrimp

**Authors:** Yi-Fu Xing, Xuan-Yi Zhu, Hong-Biao Dong, Jian-Hua Huang, Ya-Fei Duan, Jia-Song Zhang

PMC · DOI: 10.3390/jox16010022 · Journal of Xenobiotics · 2026-01-27

## TL;DR

This study shows that nitrite and microplastics harm the hepatopancreas of marine shrimp, causing tissue damage and metabolic issues.

## Contribution

The study identifies specific metabolic biomarkers and gene responses to combined nitrite and microplastic stress in shrimp.

## Key findings

- Combined nitrite and microplastic stress worsens hepatopancreatic tissue damage in shrimp.
- Oxidative stress and immune-related genes are upregulated under both individual and combined stress.
- 17 metabolic biomarkers, including lipids, amino acids, and carbohydrates, are altered by the stressors.

## Abstract

Nitrite is a common toxic substance in aquaculture, and microplastics are environmental pollutants capable of adsorbing small molecules/particles. Shrimp rely mainly on the hepatopancreas to accomplish detoxification metabolism. In this study, we investigated the individual and combined effects of nitrite and microplastics on the physiological function of the P. vannamei hepatopancreas. The results demonstrated that both nitrite and microplastics induced morphological damage, with the combined stress exacerbating tissue damage. Oxidative stress biochemical indicators were disrupted, and most enzyme activities and gene expression levels were upregulated to varying degrees in each experimental group. The expression levels of immune genes (cytC, CASP-3, Crus, ALF, and proPO), detoxification metabolism genes (CYP450, EH1, SULT, and UGT), and oxidative-stress-related genes (ROMO1, SOD, GPx, and Trx) exhibited different fluctuations. Nitrite and microplastic stress resulted in altered hepatopancreatic function, mainly involving amino acid biosynthesis and metabolism, ABC transporters, oxidative phosphorylation, and the mTOR pathway. We identified 17 metabolic biomarkers, including 6 lipids (Oleic acid, Prostaglandin G2, Linoleic acid, Palmitic acid, Docosahexaenoic acid, Docosapentaenoic acid), 6 amino acids (L-Leucine, Agmatine, L-Arginine, L-Tyrosine, Ornithine, N-Acetylornithine), and 5 carbohydrates (Glyceric acid, Citric acid, D-Mannose, Sorbitol, Fumaric acid). These findings suggest that nitrite and microplastic stresses cause hepatopancreatic tissue damage and induce oxidative stress, physiological and metabolic dysfunction in the shrimp P. vannamei, thereby impacting its normal physiological functions.

## Linked entities

- **Genes:** CytC (mitochondrial cytochrome C) [NCBI Gene 408270], CASP3 (caspase 3) [NCBI Gene 836], AFM (afamin) [NCBI Gene 173], PPO1 (Prophenoloxidase 1) [NCBI Gene 37044], LOC107927610 (alkane hydroxylase MAH1-like) [NCBI Gene 107927610], Eh1 (epoxide hydrolase 1) [NCBI Gene 100119118], SULT (sulfotransferase) [NCBI Gene 395933], SLC35A2 (solute carrier family 35 member A2) [NCBI Gene 7355], ROMO1 (reactive oxygen species modulator 1) [NCBI Gene 140823], SOD1 (superoxide dismutase 1) [NCBI Gene 6647], GPX (probable phospholipid hydroperoxide glutathione peroxidase) [NCBI Gene 103970350], TXN (thioredoxin) [NCBI Gene 7295]
- **Chemicals:** Oleic acid (PubChem CID 445639), Prostaglandin G2 (PubChem CID 5280883), Linoleic acid (PubChem CID 5280450), Palmitic acid (PubChem CID 985), Docosahexaenoic acid (PubChem CID 445580), Docosapentaenoic acid (PubChem CID 5497182), L-Leucine (PubChem CID 857), Agmatine (PubChem CID 199), L-Arginine (PubChem CID 232), L-Tyrosine (PubChem CID 6057), Ornithine (PubChem CID 389), N-Acetylornithine (PubChem CID 907), Glyceric acid (PubChem CID 752), Citric acid (PubChem CID 311), D-Mannose (PubChem CID 206), Sorbitol (PubChem CID 5780), Fumaric acid (PubChem CID 444972)

## Full-text entities

- **Genes:** LOC113801825 (glycine-rich protein) [NCBI Gene 113801825] {aka CruIIa-2, crustin}
- **Diseases:** metabolic disorders (MESH:D008659), necrosis (MESH:D009336), MP (MESH:D003057), hepatopancreatic dysfunction (MESH:D006331), toxicity (MESH:D064420), atrophy (MESH:D001284), inflammation (MESH:D007249), injury to (MESH:D014947)
- **Chemicals:** Oleic acid (MESH:D019301), eosin (MESH:D004801), glutamate (MESH:D018698), NO (MESH:D009569), glucose (MESH:D005947), N-Acetylornithine (MESH:C021951), ethanol (MESH:D000431), formalin (MESH:D005557), pyrimidine (MESH:C030986), arsenite (MESH:C015001), ROS (MESH:D017382), MP (MESH:D000080545), 2-heptanone (MESH:C011917), ATP (MESH:D000255), water (MESH:D014867), L-Tyrosine (MESH:D014443), NM (MESH:D008466), L-Leucine (MESH:D007930), Sorbitol (MESH:D013012), mannitol (MESH:D008353), polystyrene (MESH:D011137), Citric acid (MESH:D019343), nicotinamide (MESH:D009536), acetyl-CoA (MESH:D000105), lipid (MESH:D008055), glycogen (MESH:D006003), chloroform (MESH:D002725), Palmitic acid (MESH:D019308), Docosahexaenoic acid (MESH:D004281), lipopolysaccharide (MESH:D008070), spermine (MESH:D013096), Trizol (MESH:C411644), n-3 polyunsaturated fatty acids (MESH:D015525), nicotinate (MESH:D009525), NO2- (MESH:D009585), aspartate (MESH:D001224), Nitrite (MESH:D009573), amino acid (MESH:D000596), N (MESH:D009584), 4-methylbenzaldehyde (MESH:C020627), Fumaric acid (MESH:C032005), prostaglandins (MESH:D011453), phenylalanine (MESH:D010649), Agmatine (MESH:D000376), Prostaglandin G2 (MESH:C038291), L-Alanine (MESH:D000409), Fatty acids (MESH:D005227), Arginine (MESH:D001120), MDA (MESH:D008315), 4-quinolinecarboxylic acid (MESH:C059924), carbohydrates (MESH:D002241), tricarboxylic acid (MESH:D014233), paraffin (MESH:D010232), Docosapentaenoic acid (MESH:C026219), superoxide anion (MESH:D013481), D-arginine (-), H2O2 (MESH:D006861), D-Mannose (MESH:D008358), Ornithine (MESH:D009952), methanol (MESH:D000432)
- **Species:** Penaeus vannamei (Pacific white shrimp, species) [taxon 6689], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** A007-1 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_C668), Y002-1-1 — Mus musculus (Mouse), Mouse adrenal cortical carcinoma, Cancer cell line (CVCL_0585), A003-1 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_B4KF), A106-1-2 — Mus musculus (Mouse), Hybridoma (CVCL_B0D4), A064-5-1 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_JT62), A001 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_B4K8)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12921717/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921717/full.md

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Source: https://tomesphere.com/paper/PMC12921717