Bicarbonate Inhibits N-Nitrosation in Oxygenated Nitric Oxide Solutions

N -Nitrosation in oxygenated nitric oxide (NO·) solutions was previously shown to be significantly inhibited by phosphate and chloride presumably by anion scavenging of the nitrosating agent nitrous anhydride, N 2 O 3 (Lewis, R. S., Tannenbaum, S. R., and Deen, W. M. (1995) J. Am. Chem. Soc. 117, 3...

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Veröffentlicht in:The Journal of biological chemistry 1996-10, Vol.271 (42), p.25859-25863
Hauptverfasser: Caulfield, J L, Singh, S P, Wishnok, J S, Deen, W M, Tannenbaum, S R
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Sprache:eng
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Zusammenfassung:N -Nitrosation in oxygenated nitric oxide (NO·) solutions was previously shown to be significantly inhibited by phosphate and chloride presumably by anion scavenging of the nitrosating agent nitrous anhydride, N 2 O 3 (Lewis, R. S., Tannenbaum, S. R., and Deen, W. M. (1995) J. Am. Chem. Soc. 117, 3933-3939). Here, bicarbonate is shown to exhibit this same inhibitory effect. Rate constants for reaction of morpholine, phosphate, and bicarbonate with N 2 O 3 relative to N 2 O 3 hydrolysis at pH 8.9 were determined to be (3.7 ± 0.2) × 10 4 M −1 , (4.0 ± 0.9) × 10 2 M −1 , and (9.3 ± 1.5) × 10 2 M −1 , respectively. The morpholine and phosphate rate constants at pH 8.9 are similar to those reported at pH 7.4 assuring that these results are relevant to physiological conditions. The rate constant for this previously unrecognized reaction of bicarbonate with N 2 O 3 suggests the strong scavenging ability of bicarbonate; accordingly, bicarbonate may contribute to reducing deleterious effects of N 2 O 3 . This is biologically important due to substantial bicarbonate concentrations in vivo , approximately 30 m M . Bicarbonate was previously shown to alter peroxynitrite reactivity; however, carbon dioxide is the probable reactive species. Bicarbonate is therefore potentially important in determining the fate of two reactive species generated from nitric oxide, N 2 O 3 and ONOO − , and may thus act as a regulator of NO·-induced toxicity.
ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.271.42.25859