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Antioxidants inhibit the inflammatory and apoptotic processes in an intermittent hypoxia model of sleep apnea

Background Sleep apnea causes intermittent hypoxia (IH). We aimed to investigate the proteins related to oxidative stress, inflammation and apoptosis in liver tissue subjected to IH as a simulation of sleep apnea in conjunction with the administration of either melatonin (MEL, 200 μL/kg) or N -acety...

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Bibliographic Details
Published in:Inflammation research 2015-01, Vol.64 (1), p.21-29
Main Authors: da Rosa, Darlan Pase, Forgiarini, Luiz Felipe, e Silva, Mariel Barbachan, Fiori, Cíntia Zappe, Andrade, Cristiano Feijó, Martinez, Dênis, Marroni, Norma Possa
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Language:English
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Summary:Background Sleep apnea causes intermittent hypoxia (IH). We aimed to investigate the proteins related to oxidative stress, inflammation and apoptosis in liver tissue subjected to IH as a simulation of sleep apnea in conjunction with the administration of either melatonin (MEL, 200 μL/kg) or N -acetylcysteine (NAC, 10 mg/kg). Methods Seventy-two adult male Balb-C mice were divided: simulation of IH (SIH), SIH + MEL, SIH + NAC, IH, IH + MEL and IH + NAC. The animals were subjected to simulations of sleep apnea for 8 h a day for 35 days. The data were analyzed with ANOVA and Tukey tests with the significance set at p  
ISSN:1023-3830
1420-908X
DOI:10.1007/s00011-014-0778-5