Hypoxia is one of the most significant abiotic stresses affecting organisms in aquatic environments. However, dissolved oxygen in water is not always at the low concentrations that cause hypoxia, but their levels often fluctuate. Here, golden pompano (Trachinotus blochii) was subjected to low oxygen concentrations for 28 days (intermittent hypoxia, 2 h per day), and their metabolic indexes were systematically evaluated. RNA-seq was used to construct a regulatory network to elucidate the transcriptional regulation of golden pompano metabolism under intermittent hypoxia. We found that the liver lactic acid content, as well as hexokinase and phosphofructokinase activities, were elevated during the first 7 days, suggesting that anaerobic glycolysis was enhanced during the preceding period. In addition, triglyceride, lipoprotein lipase, and carnitine palmitoyltransferase-1 levels were elevated in the liver after 14 days, suggesting that lipid utilization was activated after 14 days. Intermittent hypoxia increased the activity of aspartate aminotransferase and alanine aminotransferase in the liver, decreased total plasma protein and amino acid levels, and enhanced the metabolism of proteins and amino acids. Decreased levels of oxidative stress and LOEcrit (the O tension for loss of equilibrium) were observed in golden pompano after 28 days of intermittent hypoxia. Transcriptome analysis showed that the fatty acid metabolism, PPAR signaling pathway, fatty acid degradation, D-amino acid metabolism, and cholesterol metabolism pathway were activated. These results suggest that intermittent hypoxia improves the metabolic activities of golden pompano, increases its hypoxia tolerance, and promotes its adaptation to hypoxic environments.
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http://dx.doi.org/10.1016/j.scitotenv.2025.178921 | DOI Listing |
Physiol Rep
March 2025
Centre for Biological Timing and Cognition, Department of Cell & Systems Biology, University of Toronto, Toronto, Ontario, Canada.
The respiratory control system can exhibit neuronal plasticity following exposures to repetitive respiratory challenges. For example, repeated obstructive apneas can trigger a form of respiratory plasticity that results in the enhancement of inspiratory hypoglossal (XII) motoneuron activity. This increase in respiratory motor output is known as hypoglossal long-term facilitation (hLTF).
View Article and Find Full Text PDFAm J Physiol Lung Cell Mol Physiol
March 2025
Molecular Biomedicine Program, Children's Hospital of Eastern Ontario Research Institute.
Deficient nitric oxide (NO) signaling plays a critical role in the pathogenesis of bronchopulmonary dysplasia (BPD); however, clinical trials of inhaled NO (iNO) as preventive therapy for BPD have shown little to no benefit. A biochemical obstacle to effective NO-based therapy relates to the high reactivity of NO, potentially leading to harmful oxidation and nitration. Hypothesizing that nitrite-based therapy has less potential to produce adverse reactions, we compared the preventive effects of sodium nitrite (NaNO) and iNO on lung morphology, NO content and signaling, S-nitrosothiols (SNOs) and tyrosine nitration in a novel rat model of experimental BPD.
View Article and Find Full Text PDFEur J Pharmacol
March 2025
The First School of Clinical Medicine, Lanzhou University, Lanzhou 730000, China; Department of Pulmonary and Critical Care Medicine, The First Hospital of Lanzhou University, Lanzhou 730000, China. Electronic address:
Obstructive sleep apnoea hypopnea syndrome (OSAHS) is a sleep disorder associated with significant cardiovascular complications, characterized by intermittent hypoxia (IH). IH causes endothelial dysfunction, an early event in cardiovascular disease. We investigated the role of dual-specificity phosphatase 8 (DUSP8), a key negative regulator of the mitogen-activated protein kinase (MAPK) signalling pathway, in IH-induced endothelial cell damage, and the therapeutic effects of N-acetylcysteine (NAC) by establishing IH models in human umbilical vein endothelial cells and C57BL/6 mice.
View Article and Find Full Text PDFBiochim Biophys Acta Mol Basis Dis
March 2025
Laboratório de Proteómica, Departamento de Genética Humana, Instituto Nacional de Saúde Dr. Ricardo Jorge - INSA, 1649-016 Lisboa, Portugal; Centro de Toxicogenómica e Saúde Humana (ToxOmics), Comprehensive Health Research Center (CHRC), Universidade Nova de Lisboa, 1150-082 Lisboa, Portugal. Electronic address:
Obstructive Sleep Apnea (OSA) is characterized by recurrent-episodes of apneas/hypopneas during sleep, leading to recurrent intermittent-hypoxia and sleep fragmentation. Non-treated OSA can result in cardiometabolic diseases. In this study, we applied a shotgun-proteomics strategy to deeper investigate the red blood cell-(RBC) homeostasis regulation in the context of OSA-severity and their response to six months of positive airway pressure (PAP)-treatment.
View Article and Find Full Text PDFFunction (Oxf)
March 2025
Department of Physiology & Biomedical Engineering, Mayo Clinic, Rochester, MN 55906.
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