Effect of Lipopolysaccharide (LPS) on Oxidative Stress and Apoptosis in Immune Tissues from <i>Schizothorax prenanti</i>

<i>Schizothorax prenanti</i> is an economically important cold-water fish in China. Lipopolysaccharide (LPS) can induce an immune response in <i>S. prenanti</i>; however, little is known about the effects of LPS on oxidative stress (OS) and apoptosis in <i>S. prenanti&l...

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Bibliographic Details
Main Authors: Jiqin Huang, Wei Jiang, Hongying Ma, Han Zhang, Hu Zhao, Qijun Wang, Jianlu Zhang
Format: Article
Language:English
Published: MDPI AG 2025-04-01
Series:Animals
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Online Access:https://www.mdpi.com/2076-2615/15/9/1298
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Summary:<i>Schizothorax prenanti</i> is an economically important cold-water fish in China. Lipopolysaccharide (LPS) can induce an immune response in <i>S. prenanti</i>; however, little is known about the effects of LPS on oxidative stress (OS) and apoptosis in <i>S. prenanti</i>. In this study, <i>S. prenanti</i> fish were stimulated with LPS at a dose of 10 mg/kg of body weight. After 0 h, 12 h and 24 h, the tissue samples were collected. The OS- and apoptosis-related genes and enzymatic activities in the liver, head kidney (HK), and spleen of <i>S. prenanti</i> were analyzed by a two-way repeated-measures analysis of variance (ANOVA). Hematoxylin and eosin and terminal transferase uridyl nick end labeling staining were also performed. In <i>S. prenanti</i>, LPS administration downregulated the <i>catalase (CAT)</i> and <i>B-cell lymphoma/Leukemia-2</i> (<i>Bcl-2</i>) expression levels, and upregulated <i>BCL2</i>-<i>associated X</i> (<i>Bax</i>) and <i>cysteine-aspartic-specific protease-3</i> (<i>caspase-3</i>) expression levels. Meanwhile, superoxide dismutase and <i>CAT</i> enzymatic activities were inhibited and malondialdehyde (MDA) content was increased by LPS treatment. Additionally, LPS treatment induced OS damage and apoptosis in tissue sections. These results indicated that apoptosis in the liver, HK, and spleen of LPS-administered <i>S. prenanti</i> may be mediated by OS via the mitochondrial apoptotic signaling pathway. Our findings are expected to contribute to a better understanding of the responses of different tissues to bacterial challenges. In addition, we can increase the tolerance of fish to the OS through dietary manipulation in the future.
ISSN:2076-2615