Original Contribution
Efficient nitrosation of glutathione by nitric oxide

https://doi.org/10.1016/j.freeradbiomed.2013.04.034Get rights and content
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Highlights

  • The mechanism of aerobic nonenzymatic S-nitrosation is revisited.

  • Nitrosothiol formation is not autoxidation-mediated at physiological NO levels.

  • Direct S-nitrosation is stimulated by divalent cations such as Mg2+.

  • Direct nonenzymatic S-nitrosation is fast enough to be physiologically relevant.

Abstract

Nitrosothiols are increasingly regarded as important participants in a range of physiological processes, yet little is known about their biological generation. Nitrosothiols can be formed from the corresponding thiols by nitric oxide in a reaction that requires the presence of oxygen and is mediated by reactive intermediates (NO2 or N2O3) formed in the course of NO autoxidation. Because the autoxidation of NO is second order in NO, it is extremely slow at submicromolar NO concentrations, casting doubt on its physiological relevance. In this paper we present evidence that at submicromolar NO concentrations the aerobic nitrosation of glutathione does not involve NO autoxidation but a reaction that is first order in NO. We show that this reaction produces nitrosoglutathione efficiently in a reaction that is strongly stimulated by physiological concentrations of Mg2+. These observations suggest that direct aerobic nitrosation may represent a physiologically relevant pathway of nitrosothiol formation.

Abbreviations:

GSNO
S-nitrosoglutathione
DTPA
diethylenetriaminepentaacetic acid
DEA/NO
diethylamine NONOate (diethylammonium (Z)-1-(N,N-diethylamino)diazen-1-ium-1,2-diolate)
PROLI/NO
proline NONOate (1-(hydroxyl-N,N,O-azoxy)-l-proline, disodium salt)
DNIC
dinitrosyl–iron complex
SOD
superoxide dismutase
oxy-Hb
oxyhemoglobin
met-Hb
methemoglobin
TEA
triethanolamine
DAN
2,3-diaminonaphthalene
DTT
dithiothreitol
NAC
N-acetylcysteine
β-ME
β-mercaptoethanol

Keywords

S-nitrosation
Nitrosoglutathione
Nitric oxide
Free radicals

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