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Dysregulation of Antioxidant Mechanisms Contributes to Increased Oxidative Stress in Calcific Aortic Valvular Stenosis in Humans
Journal article   Open access   Peer reviewed

Dysregulation of Antioxidant Mechanisms Contributes to Increased Oxidative Stress in Calcific Aortic Valvular Stenosis in Humans

Jordan D Miller, Yi Chu, Robert M Brooks, Wayne E Richenbacher, Ricardo Peña-Silva and Donald D Heistad
Journal of the American College of Cardiology, Vol.52(10), pp.843-850
09/02/2008
DOI: 10.1016/j.jacc.2008.05.043
PMCID: PMC2748760
PMID: 18755348
url
https://doi.org/10.1016/j.jacc.2008.05.043View
Published (Version of record) Open Access

Abstract

Dysregulation of Antioxidant Mechanisms Contributes to Increased Oxidative Stress in Calcific Aortic Valvular Stenosis in Humans Jordan D. Miller, Yi Chu, Robert M. Brooks, Wayne E. Richenbacher, Ricardo Peña-Silva, Donald D. Heistad Oxidative stress plays an important role in development of atherosclerotic lesions. We report that superoxide and H2O2 levels are increased in calcified and peri-calcified regions of stenotic aortic valves and are associated with increases in myofibroblast activation and pro-osteogenic gene expression. In striking contrast to atherosclerotic plaques, increases in oxidative stress in aortic valves are not due to increases in nicotinamide adenine dinucleotide phosphate oxidase activity but seem to be due to reductions in antioxidant defense mechanisms and increases in uncoupling of nitric oxide synthase. We propose that oxidative stress might play an important role in driving calcification in aortic valve stenosis. The aim of this study was to determine whether oxidative stress is increased in calcified, stenotic aortic valves and to examine mechanisms that might contribute to increased oxidative stress. Oxidative stress is increased in atherosclerotic lesions and might play an important role in plaque progression and calcification. The role of oxidative stress in valve disease is not clear. Superoxide (dihydroethidium fluorescence and lucigenin-enhanced chemiluminescence), hydrogen peroxide (H2O2) (dichlorofluorescein fluorescence), and expression and activity of pro- and anti-oxidant enzymes were measured in normal valves from hearts not suitable for transplantation and stenotic aortic valves that were removed during surgical replacement of the valve. In normal valves, superoxide levels were relatively low and distributed homogeneously throughout the valve. In stenotic valves, superoxide levels were increased 2-fold near the calcified regions of the valve (p < 0.05); noncalcified regions did not differ significantly from normal valves. Hydrogen peroxide levels were also markedly elevated in calcified regions of stenotic valves. Nicotinamide adenine dinucleotide phosphate oxidase activity was not increased in calcified regions of stenotic valves. Superoxide levels in stenotic valves were significantly reduced by inhibition of nitric oxide synthases (NOS), which suggests uncoupling of the enzyme. Antioxidant mechanisms were reduced in calcified regions of the aortic valve, because total superoxide dismutase (SOD) activity and expression of all 3 SOD isoforms was significantly decreased. Catalase expression also was reduced in pericalcific regions. This study provides the first evidence that oxidative stress is increased in calcified regions of stenotic aortic valves from humans. Increased oxidative stress is due at least in part to reduction in expression and activity of antioxidant enzymes and perhaps to uncoupled NOS activity. Thus, mechanisms of oxidative stress differ greatly between stenotic aortic valves and atherosclerotic arteries.
 Oxidative Stress aortic valve calcification stenosis

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