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J Biol Chem, Vol. 273, Issue 30, 18709-18713, July 24, 1998
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, and
From the Concentration changes of nitric oxide (NO) were
monitored using an NO-sensitive electrode in phosphate-buffered saline
(PBS) with either free oxyhemoglobin (oxyHb) or red blood cells (RBCs). In aerated PBS, the half-life of 0.9 µM NO is
greater than 4 min. NO is undetectable (<50 nM) when added
to a solution of oxyHb because the reaction of NO with oxyHb is rapid.
The disappearance rate of NO in PBS containing RBCs is rapid, compared
with PBS, but it is much slower (by a factor of approximately 650) than with an equivalent solution of free oxyHb. The half-life of NO is
inversely proportional to the concentration of RBCs, independent of
oxyHb concentration inside RBCs, and the disappearance rate of NO is
first order in NO concentration and first order in the concentration of
RBCs. After all the oxyHb reacts with NO to form methemoglobin, the
disappearance rate of NO slows greatly. These data indicate that the
reaction of NO with oxyhemoglobin within RBCs is limited by the
diffusion of NO into the cell, which has also been shown previously for
the reaction of O2 with deoxyhemoglobin. Experimental data
show that the half-life of NO in the presence of 2.1 × 106 RBCs/ml is 4.2 s. From this value, we estimate
that the half-life of NO in whole blood (5 × 109
RBCs/ml) will be 1.8 ms. A simple analytical expression for the half-life of NO in PBS with RBCs was derived in this study based on a
spherical diffusion model. The calculated half-life of NO from the
expression is in good agreement with the experimental values.
Department of Pediatrics, ¶ Department
of Physiology, and
Department of Medicine, Louisiana State
University School of Medicine, New Orleans, Louisiana 70112
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