| |
|
|
|
|
|
|
|||
|
MA Beilke, C Collins-Lech and PG Sohnle
Department of Medicine, Medical College of Wisconsin, Milwaukee.
Excessive concentrations of hydrogen peroxide inhibit the neutrophil
myeloperoxidase system, presumably by inactivating the hypochlorous acid
produced by this system. Ammonium ion generated by neutrophils and other
cells can react with hypochlorous acid to produce monochloramine, an
oxidant with good microbicidal activity, but relative resistance to
inactivation by other compounds. In an assay based on the oxidation of
5-thio-2-nitrobenzoic acid, hydrogen peroxide reacted more readily with
sodium hypochlorite (used as a source of hypochlorous acid) than with
monochloramine. Also, in this assay Candida albicans yeast inactivated the
oxidant activity of hypochlorous acid more completely than they did that of
monochloramine. The killing of Candida by sodium hypochlorite, as
determined in a standard colony count microbicidal assay, was inhibited by
equimolar and greater concentrations of hydrogen peroxide; killing of this
organism by monochloramine was not affected by a tenfold excess
concentration of hydrogen peroxide. In microbicidal assays using 4 mU of
myeloperoxidase and optimal or excessive concentrations of hydrogen
peroxide or glucose and glucose oxidase to generate hydrogen peroxide, the
excessive concentrations inhibited killing of Candida, but not
Staphylococcus aureus. The inhibition of Candida killing could be reversed
by addition of ammonium ion to convert hypochlorous acid to monochloramine.
These results indicate that for certain organisms such as C albicans,
conversion of hypochlorous acid to monochloramine by reactions with
ammonium ion may extend the range of hydrogen peroxide concentrations under
which killing by the myeloperoxidase system can occur by protecting the
necessary microbicidal oxidants from inactivation by excess hydrogen
peroxide.
This article has been cited by other articles:
| |||||||||||
| Copyright © 1989 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||