Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1982 Dec;70(6):1253-9.
doi: 10.1172/jci110724.

Spontaneous oxygen radical generation by sickle erythrocytes

Spontaneous oxygen radical generation by sickle erythrocytes

R P Hebbel et al. J Clin Invest. 1982 Dec.

Abstract

Since the various membrane abnormalities of sickle erythrocytes might result from excessive accumulation of oxidant damage, we have measured the generation of superoxide, peroxide, and hydroxyl radical by normal and sickle erythrocytes using assays involving reduction of cytochrome c, aminotriazole inhibition of catalase, and methane evolution from dimethyl sulfoxide, respectively. Compared with normal erythrocytes, sickle erythrocytes spontaneously generate approximately twice as much superoxide, peroxide, and hydroxyl radical. One possible source of hydroxyl radical generation was identified as hemichrome, excessive amounts of which are bound to sickle erythrocyte membranes. Hemichrome did not generate hydroxyl radical when exposed to superoxide alone or peroxide alone. However, in the presence of both superoxide and peroxide, hemichrome greatly facilitated hydroxyl radical generation. Supporting this, normal erythrocyte membranes induced to acquire sickle hemichrome concomitantly acquired an enhanced ability to mediate hydroxyl radical generation. Finally, sickle erythrocyte membranes greatly enhanced superoxide/peroxide-driven hydroxyl radical generation as compared with normal erythrocyte membranes. These data suggest that an excessive accumulation of oxidant damage in sickle erythrocyte membranes might contribute to the accelerated membrane senescence of these cells. They further indicate that accumulation of oxidant damage could be a determinant of normal erythrocyte membrane senescence.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Science. 1970 Apr 10;168(3928):255-7 - PubMed
    1. Proc Natl Acad Sci U S A. 1970 Dec;67(4):1846-53 - PubMed
    1. J Biol Chem. 1972 Nov 10;247(21):6960-2 - PubMed
    1. Br J Haematol. 1972 Dec;23(6):713-24 - PubMed
    1. N Engl J Med. 1974 Mar 14;290(11):593-7 - PubMed

Publication types