Abstract
Organic nitrates, such as nitroglycerin, are commonly used in the therapy of cardiovascular disease. Long-term therapy with these drugs, however, results in the rapid development of nitrate tolerance, limiting their hemodynamic and anti-ischemic efficacy. In addition, nitrate tolerance is associated with the expression of potentially deleterious modifications such as increased oxidative stress, endothelial dysfunction, and sympathetic activation. In this review we discuss current concepts regarding the mechanisms of organic nitrate bioactivation, nitrate tolerance, and nitrate-mediated oxidative stress and endothelial dysfunction. We also examine how hydralazine may prevent nitrate tolerance and related endothelial dysfunction.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Aldehyde Dehydrogenase / metabolism
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Biotransformation
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Drug Therapy, Combination
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Drug Tolerance*
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Endothelium, Vascular / drug effects*
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Endothelium, Vascular / metabolism
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Endothelium, Vascular / physiopathology
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Ethanol / metabolism
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Humans
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Hydralazine / therapeutic use
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Mitochondria / enzymology
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Nitrates / adverse effects
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Nitrates / metabolism
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Nitrates / therapeutic use*
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Oxidative Stress / drug effects*
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Reactive Oxygen Species / metabolism
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Sympathetic Nervous System / drug effects*
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Sympathetic Nervous System / physiopathology
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Tachyphylaxis
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Vasodilation / drug effects*
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Vasodilator Agents / adverse effects
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Vasodilator Agents / metabolism
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Vasodilator Agents / therapeutic use*
Substances
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Nitrates
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Reactive Oxygen Species
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Vasodilator Agents
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Hydralazine
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Ethanol
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Aldehyde Dehydrogenase