Effects of ammonia nitrogen stress on liver tissue structure and physiological indicators, and metabolomic analysis of juvenile four-finger threadfin (Eleutheronema tetradactylum)

In intensive aquaculture, ammonia nitrogen (NH₃-N) is a major pollutant, causing oxidative stress and immune damage to aquatic organisms. The liver is crucial in protecting against biotic and abiotic stresses, but the response mechanisms to ammonia stress in juvenile four-finger threadfin ( Eleutheronema tetradactylum ) are not well understood. This study investigated these mechanisms by examining liver tissue structure, enzyme activities, and metabolomic changes in response to ammonia stress. Juvenile four-finger threadfin (7.4 ± 0.6 g) were divided into control, NH₃-N stress (50% LC 50 96 h , 10 ± 0.4 mg/L), and postexposure recovery groups. Stress durations of 12, 24, 48, and 96 h were evaluated, followed by 48 h recovery. Prolonged ammonia stress led to increased liver tissue damage, including disordered hepatocyte arrangement, swelling, necrosis, and the disappearance of nucleoli. After 48 h recovery, liver damage was alleviated but did not fully return to control levels, suggesting that the toxic effects of ammonia are recoverable yet persistent. Antioxidant enzyme activities (superoxide dismutase, catalase, and glutathione peroxidase) initially showed significant increases peaking at 24 h after stress, before declining by 96 h. Malondialdehyde levels rose initially and remained elevated compared with controls. After 48 h of recovery, antioxidant enzyme activity had not returned to control levels, indicating inadequate recovery from ROS-induced stress. Metabolomic analysis revealed 1219 significantly different metabolites in the 96 h stress group, with increases in L -histidine, L -threonine, and cholesterol. In the recovery group, 904 metabolites differed from controls, with notable reductions in urea and choline. The key affected pathways included amino acid, lipid, and nucleotide metabolism. This study elucidates the toxic effects of ammonia nitrogen on juvenile four-finger threadfin and their adaptive responses through physiological and metabolomic changes, providing insights for aquaculture practices and breeding ammonia-tolerant strains.

Authors

Institutions

Publication Details

Journal
Frontiers in Marine Science
Published
2025-02-26
DOI
https://doi.org/10.3389/fmars.2025.1549668
Citations
1
Primary Topic
Aquaculture Nutrition and Growth
Type
article
Field-Weighted Citation Impact
2.27
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Effects of ammonia nitrogen stress on liver tissue structure and physiological indicators, and metabolomic analysis of juvenile four-finger threadfin (Eleutheronema tetradactylum)

Rui-Tao Xie, Jing-hui Jin, Eric Amenyogbe, Yi Lu et al.
1 citations
Frontiers in Marine Science
Aquaculture Nutrition and Growth
2.27
article

Effects of ammonia nitrogen stress on liver tissue structure and physiological indicators, and metabolomic analysis of juvenile four-finger threadfin (Eleutheronema tetradactylum)

Rui-Tao Xie, Jing-hui Jin, Eric Amenyogbe, Yi Lu, Zhongliang Wang, Haojie Wang, Jiansheng Huang
article en
1 citations

Abstract

In intensive aquaculture, ammonia nitrogen (NH₃-N) is a major pollutant, causing oxidative stress and immune damage to aquatic organisms. The liver is crucial in protecting against biotic and abiotic stresses, but the response mechanisms to ammonia stress in juvenile four-finger threadfin ( Eleutheronema tetradactylum ) are not well understood. This study investigated these mechanisms by examining liver tissue structure, enzyme activities, and metabolomic changes in response to ammonia stress. Juvenile four-finger threadfin (7.4 ± 0.6 g) were divided into control, NH₃-N stress (50% LC 50 96 h , 10 ± 0.4 mg/L), and postexposure recovery groups. Stress durations of 12, 24, 48, and 96 h were evaluated, followed by 48 h recovery. Prolonged ammonia stress led to increased liver tissue damage, including disordered hepatocyte arrangement, swelling, necrosis, and the disappearance of nucleoli. After 48 h recovery, liver damage was alleviated but did not fully return to control levels, suggesting that the toxic effects of ammonia are recoverable yet persistent. Antioxidant enzyme activities (superoxide dismutase, catalase, and glutathione peroxidase) initially showed significant increases peaking at 24 h after stress, before declining by 96 h. Malondialdehyde levels rose initially and remained elevated compared with controls. After 48 h of recovery, antioxidant enzyme activity had not returned to control levels, indicating inadequate recovery from ROS-induced stress. Metabolomic analysis revealed 1219 significantly different metabolites in the 96 h stress group, with increases in L -histidine, L -threonine, and cholesterol. In the recovery group, 904 metabolites differed from controls, with notable reductions in urea and choline. The key affected pathways included amino acid, lipid, and nucleotide metabolism. This study elucidates the toxic effects of ammonia nitrogen on juvenile four-finger threadfin and their adaptive responses through physiological and metabolomic changes, providing insights for aquaculture practices and breeding ammonia-tolerant strains.

Frontiers in Marine ScienceVol. 12
ID-FISH Technology (United States) (US), University of Environment and Sustainable Development, Guangdong Ocean University (CN)
Openalex Percentile: Top 15%
Aquaculture Nutrition and Growth
2.27
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.