Journalartikel
Autorenliste: Schulz, Richard; Murzabekova, Gulsina; Egemnazarov, Bakytbek; Kraut, Simone; Eisele, Hans-Joachim; Dumitrascu, Rio; Heitmann, Joerg; Seimetz, Michael; Witzenrath, Martin; Ghofrani, Hossein A.; Schermuly, Ralph T.; Grimminger, Friedrich; Seeger, Werner; Weissmann, Norbert
Jahr der Veröffentlichung: 2014
Seiten: 300-305
Zeitschrift: Journal of Hypertension
Bandnummer: 32
Heftnummer: 2
ISSN: 0263-6352
eISSN: 1473-5598
DOI Link: https://doi.org/10.1097/HJH.0000000000000016
Verlag: Lippincott, Williams & Wilkins
Abstract:
Objectives:To investigate whether NADPH oxidase 2 (NOX2), a major source of reactive oxygen species (ROS), contributes to the emergence of arterial hypertension in a murine model of sleep apnea.Background:Obstructive sleep apnea (OSA) is a risk factor for arterial hypertension and it is linked to oxidative stress.Methods:C57BL/6J mice were exposed to chronic intermittent hypoxia (CIH) for 6 weeks (5 days/week, 8h/day, alternating cycles of hypoxia and normoxia, each lasting 120s, nadir FiO(2): 7%). Blood pressure was monitored by telemetric catheters implanted into the abdominal aorta. Pharmacological inhibition of NOX by apocynin and NOX2-deficient mice were used to assess the role of NOX in CIH-induced arterial hypertension. NOX2 gene expression was measured by real-time PCR in different cardiovascular tissues.Results:When compared with room air conditions, wild-type mice showed significant blood pressure elevations after exposure to CIH. This response was attenuated after treating animals with apocynin and in NOX2 (=gp91(phox)) knockout mice, whereas NOX2 was not upregulated in the heart, aorta, and femoral/carotid arteries of CIH mice.Conclusion:We suggest that the CIH-induced arterial hypertension is mediated by ROS derived from an activation of NOX2 within cells located outside the cardiovascular system.
Zitierstile
Harvard-Zitierstil: Schulz, R., Murzabekova, G., Egemnazarov, B., Kraut, S., Eisele, H., Dumitrascu, R., et al. (2014) Arterial hypertension in a murine model of sleep apnea: role of NADPH oxidase 2, Journal of Hypertension, 32(2), pp. 300-305. https://doi.org/10.1097/HJH.0000000000000016
APA-Zitierstil: Schulz, R., Murzabekova, G., Egemnazarov, B., Kraut, S., Eisele, H., Dumitrascu, R., Heitmann, J., Seimetz, M., Witzenrath, M., Ghofrani, H., Schermuly, R., Grimminger, F., Seeger, W., & Weissmann, N. (2014). Arterial hypertension in a murine model of sleep apnea: role of NADPH oxidase 2. Journal of Hypertension. 32(2), 300-305. https://doi.org/10.1097/HJH.0000000000000016
Schlagwörter
Arterial hypertension; BLOOD-PRESSURE; CHRONIC EPISODIC HYPOXIA; DINUCLEOTIDE PHOSPHATE OXIDASE; IMPROVES ENDOTHELIAL FUNCTION; INTERMITTENT HYPOXIA; NADPH OXIDASE; POSITIVE AIRWAY PRESSURE; sleep apnea; SUPEROXIDE-PRODUCTION; SYMPATHETIC-NERVOUS-SYSTEM