# High Starch Induces Hematological Variations, Metabolic Changes, Oxidative Stress, Inflammatory Responses, and Histopathological Lesions in Largemouth Bass (Micropterus salmoides)

**Authors:** Yuanyuan Xie, Xianping Shao, Penghui Zhang, Hao Zhang, Jiaxing Yu, Xinfeng Yao, Yifan Fu, Jiao Wei, Chenglong Wu

PMC · DOI: 10.3390/metabo14040236 · 2024-04-19

## TL;DR

Feeding largemouth bass a high-starch diet causes metabolic issues, oxidative stress, inflammation, and liver damage.

## Contribution

This study reveals new insights into how high starch diets affect fish metabolism, inflammation, and liver health through specific molecular pathways.

## Key findings

- High starch diets increase lipid accumulation and disrupt glucose and cholesterol metabolism in largemouth bass.
- High starch activates the NLRP3 inflammasome, leading to increased inflammatory responses and oxidative stress.
- Histopathological changes like lipid droplets and vacuolization are observed in the livers of fish fed high starch.

## Abstract

This study evaluated effects of high starch (20%) on hematological variations, glucose and lipid metabolism, antioxidant ability, inflammatory responses, and histopathological lesions in largemouth bass. Results showed hepatic crude lipid and triacylglycerol (TAG) contents were notably increased in fish fed high starch. High starch could increase counts of neutrophils, lymphocytes, monocytes, eosinophils, and basophils and serum contents of TAG, TBA, BUN, and LEP (p < 0.05). There were increasing trends in levels of GLUT2, glycolysis, gluconeogenesis, and LDH in fish fed high starch through the AKT/PI3K signal pathway. Meanwhile, high starch not only triggered TAG and cholesterol synthesis, but mediated cholesterol accumulation by reducing ABCG5, ABCG8, and NPC1L1. Significant increases in lipid droplets and vacuolization were also shown in hepatocytes of D3–D7 groups fed high starch. In addition, high starch could decrease levels of mitochondrial Trx2, TrxR2, and Prx3, while increasing ROS contents. Moreover, high starch could notably increase amounts of inflammatory factors (IL-1β, TNF-α, etc.) by activating NLRP3 inflammasome key molecules (GSDME, caspase 1, etc.). In conclusion, high starch could not only induce metabolic disorders via gluconeogenesis and accumulation of glycogen, TAG, and cholesterol, but could disturb redox homeostasis and cause inflammatory responses by activating the NLRP3 inflammasome in largemouth bass.

## Linked entities

- **Genes:** ABCG5 (ATP binding cassette subfamily G member 5) [NCBI Gene 64240], ABCG8 (ATP binding cassette subfamily G member 8) [NCBI Gene 64241], NPC1L1 (NPC1 like intracellular cholesterol transporter 1) [NCBI Gene 29881], GSDME (gasdermin E) [NCBI Gene 1687], Caspase1 (caspase-1) [NCBI Gene 692604], SLC2A2 (solute carrier family 2 member 2) [NCBI Gene 6514], KMT2B (lysine methyltransferase 2B) [NCBI Gene 9757], TXNRD2 (thioredoxin reductase 2) [NCBI Gene 10587], Prx3 (Peroxiredoxin 3) [NCBI Gene 42109], IL1B (interleukin 1 beta) [NCBI Gene 3553], TNF (tumor necrosis factor) [NCBI Gene 7124]
- **Chemicals:** triacylglycerol (TAG) (PubChem CID 5460048), BUN (PubChem CID 91971254)
- **Species:** Micropterus salmoides (taxon 27706)

## Full-text entities

- **Diseases:** Inflammatory (MESH:D007249), metabolic disorders (MESH:D008659)
- **Chemicals:** lipid (MESH:D008055), glycogen (MESH:D006003), cholesterol (MESH:D002784), ROS (-), TAG (MESH:D014280), glucose (MESH:D005947), Starch (MESH:D013213)
- **Species:** Micropterus salmoides (largemouth bass, species) [taxon 27706]

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11051861/full.md

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Source: https://tomesphere.com/paper/PMC11051861