Abstract
Background: Repeated apnoea events cause intermittent hypoxia (IH), which alters the function of various systems and produces free radicals and oxidative stress.Methods: We investigated hepatic oxidative stress in adult mice subjected to intermittent hypoxia, simulating sleep apnoea. Three groups were submitted to 21 days of IH (IH-21), 35 days of IH (IH-35), or 35 days of sham IH. We assessed the oxidative damage to lipids by TBARS and to DNA by comet assay; hepatic tissue inflammation was assessed in HE-stained slides. Antioxidants were gauged by catalase, superoxide dismutase, glutathione peroxidase activity and by total glutathione.Results: After IH-21, no significant change was observed in hepatic oxidative stress. After IH-35, significant oxidative stress, lipid peroxidation, DNA damage and reduction of endogenous antioxidants were detected.Conclusions: In an animal model of sleep apnoea, intermittent hypoxia causes liver damage due to oxidative stress after 35 days, but not after 21 days. © 2011 Rosa et al; licensee BioMed Central Ltd.
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CITATION STYLE
Rosa, D. P., Martinez, D., Picada, J. N., Semedo, J. G., & Marroni, N. P. (2011). Hepatic oxidative stress in an animal model of sleep apnoea: Effects of different duration of exposure. Comparative Hepatology, 10. https://doi.org/10.1186/1476-5926-10-1
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