A Reassessment of the Peroxynitrite Scavenging Activity of Uric Acid

: Peroxynitrite is implicated in numerous human diseases. Hence, there is considerable interest in potential therapeutic peroxynitrite scavengers. It has been claimed that uric acid is a powerful peroxynitrite scavenger. We previously observed that uric acid is a powerful inhibitor of tyrosine nitra...

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Veröffentlicht in:Annals of the New York Academy of Sciences 2002-05, Vol.962 (1), p.242-259
Hauptverfasser: WHITEMAN, M., KETSAWATSAKUL, U., HALLIWELL, B.
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KETSAWATSAKUL, U.
HALLIWELL, B.
description : Peroxynitrite is implicated in numerous human diseases. Hence, there is considerable interest in potential therapeutic peroxynitrite scavengers. It has been claimed that uric acid is a powerful peroxynitrite scavenger. We previously observed that uric acid is a powerful inhibitor of tyrosine nitration induced by peroxynitrite, but fails to prevent α1‐antiproteinase (α1‐AP) inactivation induced by peroxynitrite. However, the reactivity of peroxynitrite is significantly modified by bicarbonate and this has not been considered in evaluating the scavenging activity of uric acid and other endogenous antioxidant compounds. In the presence of bicarbonate (25 mM), the ability of uric acid, ascorbate, Trolox, and GSH to inhibit peroxynitrite‐mediated tyrosine and guanine nitration is decreased. Protection against peroxynitrite‐mediated α1‐AP inactivation is also decreased by ascorbate, Trolox, and GSH, but it is enhanced by uric acid. Bicarbonate also inhibits the ability of these compounds to prevent peroxynitrite‐mediated ABTS radical cation formation. However, the abilities of these antioxidants to prevent peroxynitrite‐mediated bleaching of pyrogallol red are enhanced by bicarbonate. These results show that physiologic concentrations of bicarbonate substantially modify the ability of uric acid to prevent peroxynitrite‐mediated reactions. This study highlights the need to use several different assays in the presence of physiologically relevant concentrations of bicarbonate when assessing compounds for peroxynitrite scavenging, in order to avoid misleading results.
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Hence, there is considerable interest in potential therapeutic peroxynitrite scavengers. It has been claimed that uric acid is a powerful peroxynitrite scavenger. We previously observed that uric acid is a powerful inhibitor of tyrosine nitration induced by peroxynitrite, but fails to prevent α1‐antiproteinase (α1‐AP) inactivation induced by peroxynitrite. However, the reactivity of peroxynitrite is significantly modified by bicarbonate and this has not been considered in evaluating the scavenging activity of uric acid and other endogenous antioxidant compounds. In the presence of bicarbonate (25 mM), the ability of uric acid, ascorbate, Trolox, and GSH to inhibit peroxynitrite‐mediated tyrosine and guanine nitration is decreased. Protection against peroxynitrite‐mediated α1‐AP inactivation is also decreased by ascorbate, Trolox, and GSH, but it is enhanced by uric acid. Bicarbonate also inhibits the ability of these compounds to prevent peroxynitrite‐mediated ABTS radical cation formation. However, the abilities of these antioxidants to prevent peroxynitrite‐mediated bleaching of pyrogallol red are enhanced by bicarbonate. These results show that physiologic concentrations of bicarbonate substantially modify the ability of uric acid to prevent peroxynitrite‐mediated reactions. 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Hence, there is considerable interest in potential therapeutic peroxynitrite scavengers. It has been claimed that uric acid is a powerful peroxynitrite scavenger. We previously observed that uric acid is a powerful inhibitor of tyrosine nitration induced by peroxynitrite, but fails to prevent α1‐antiproteinase (α1‐AP) inactivation induced by peroxynitrite. However, the reactivity of peroxynitrite is significantly modified by bicarbonate and this has not been considered in evaluating the scavenging activity of uric acid and other endogenous antioxidant compounds. In the presence of bicarbonate (25 mM), the ability of uric acid, ascorbate, Trolox, and GSH to inhibit peroxynitrite‐mediated tyrosine and guanine nitration is decreased. Protection against peroxynitrite‐mediated α1‐AP inactivation is also decreased by ascorbate, Trolox, and GSH, but it is enhanced by uric acid. Bicarbonate also inhibits the ability of these compounds to prevent peroxynitrite‐mediated ABTS radical cation formation. However, the abilities of these antioxidants to prevent peroxynitrite‐mediated bleaching of pyrogallol red are enhanced by bicarbonate. These results show that physiologic concentrations of bicarbonate substantially modify the ability of uric acid to prevent peroxynitrite‐mediated reactions. 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Hence, there is considerable interest in potential therapeutic peroxynitrite scavengers. It has been claimed that uric acid is a powerful peroxynitrite scavenger. We previously observed that uric acid is a powerful inhibitor of tyrosine nitration induced by peroxynitrite, but fails to prevent α1‐antiproteinase (α1‐AP) inactivation induced by peroxynitrite. However, the reactivity of peroxynitrite is significantly modified by bicarbonate and this has not been considered in evaluating the scavenging activity of uric acid and other endogenous antioxidant compounds. In the presence of bicarbonate (25 mM), the ability of uric acid, ascorbate, Trolox, and GSH to inhibit peroxynitrite‐mediated tyrosine and guanine nitration is decreased. Protection against peroxynitrite‐mediated α1‐AP inactivation is also decreased by ascorbate, Trolox, and GSH, but it is enhanced by uric acid. Bicarbonate also inhibits the ability of these compounds to prevent peroxynitrite‐mediated ABTS radical cation formation. However, the abilities of these antioxidants to prevent peroxynitrite‐mediated bleaching of pyrogallol red are enhanced by bicarbonate. These results show that physiologic concentrations of bicarbonate substantially modify the ability of uric acid to prevent peroxynitrite‐mediated reactions. This study highlights the need to use several different assays in the presence of physiologically relevant concentrations of bicarbonate when assessing compounds for peroxynitrite scavenging, in order to avoid misleading results.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>12076979</pmid><doi>10.1111/j.1749-6632.2002.tb04072.x</doi><tpages>18</tpages></addata></record>
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subjects 3-nitrotyrosine
alpha 1-Antitrypsin - metabolism
Antioxidants - metabolism
Ascorbic Acid - metabolism
Benzothiazoles
Bicarbonates - metabolism
Chromans - metabolism
Coloring Agents - metabolism
Glutathione - metabolism
Guanine - metabolism
Humans
Indicators and Reagents - metabolism
nitric oxide
nitrosative stress
oxidative stress
peroxynitrite
Peroxynitrous Acid - metabolism
Pyrogallol - analogs & derivatives
Pyrogallol - metabolism
Reactive Nitrogen Species - metabolism
Serine Proteinase Inhibitors - metabolism
Sulfonic Acids - metabolism
Tyrosine - metabolism
uric acid
Uric Acid - metabolism
title A Reassessment of the Peroxynitrite Scavenging Activity of Uric Acid
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