Hypotaurine (HTAU) and cysteine sulfinic acid (CSA) are the metabolic intermediates in the mammalian pathway leading from cysteine to taurine. Strong evidence has been presented that the formation of taurine (TAU) and cysteic acid (CA) is the result of the interaction of both sulfinates with various oxidizing agents that may be present in biological systems. The purpose of the present study is to investigate the oxidation of sulfinates, HTAU and CSA, by peroxidase-generated reactive species. Reactive nitrogen and oxygen species can be produced during the process of nitrite oxidation catalyzed by heme peroxidases, such as horseradish peroxidase (HRP) or myeloperoxidase, in the presence of hydrogen peroxide (H2O2). Nitrite is the major end product of nitric oxide (NO) metabolism. Oxidation of nitrite by such mechanisms could be important at sites of inflammatory processes. The formation of reactive nitrogen species (RNS) via peroxidase-catalyzed oxidation of nitrite could represent an ad
Oxidation of hypotaurine and cysteine sulfinic acid by peroxidase-generated reactive species / BASEGGIO CONRADO, Alessia; Pecci, Laura; Capuozzo, Elisabetta; Fontana, Mario. - STAMPA. - 803(2015), pp. 41-51. - ADVANCES IN EXPERIMENTAL MEDICINE AND BIOLOGY. [10.1007/978-3-319-15126-7_4].
Oxidation of hypotaurine and cysteine sulfinic acid by peroxidase-generated reactive species
BASEGGIO CONRADO, ALESSIA;PECCI, Laura;CAPUOZZO, Elisabetta;FONTANA, Mario
2015
Abstract
Hypotaurine (HTAU) and cysteine sulfinic acid (CSA) are the metabolic intermediates in the mammalian pathway leading from cysteine to taurine. Strong evidence has been presented that the formation of taurine (TAU) and cysteic acid (CA) is the result of the interaction of both sulfinates with various oxidizing agents that may be present in biological systems. The purpose of the present study is to investigate the oxidation of sulfinates, HTAU and CSA, by peroxidase-generated reactive species. Reactive nitrogen and oxygen species can be produced during the process of nitrite oxidation catalyzed by heme peroxidases, such as horseradish peroxidase (HRP) or myeloperoxidase, in the presence of hydrogen peroxide (H2O2). Nitrite is the major end product of nitric oxide (NO) metabolism. Oxidation of nitrite by such mechanisms could be important at sites of inflammatory processes. The formation of reactive nitrogen species (RNS) via peroxidase-catalyzed oxidation of nitrite could represent an adFile | Dimensione | Formato | |
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Baseggio Conrado_Oxidation_2015.pdf
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