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PMID: 12757846 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Superoxide reacts with hydroethidine but forms a fluorescent product that is distinctly different from ethidium: potential implications in intracellular fluorescence detection of superoxide.

Free radical biology & medicine ·Vol. 34 ·No. 11 ·2003-06-01 ·Pages 1359-68

Zhao H, Kalivendi S, Zhang H, Joseph J, Nithipatikom K, Vásquez-Vivar J, Kalyanaraman B

Abstract

Hydroethidine (HE) or dihydroethidium (DHE), a redox-sensitive probe, has been widely used to detect intracellular superoxide anion. It is a common assumption that the reaction between superoxide and HE results in the formation of a two-electron oxidized product, ethidium (E+), which binds to DNA and leads to the enhancement of fluorescence (excitation, 500-530 nm; emission, 590-620 nm). However, the mechanism of oxidation of HE by the superoxide anion still remains unclear. In the present study, we show that superoxide generated in several enzymatic or chemical systems (e.g., xanthine/xanthine oxidase, endothelial nitric oxide synthase, or potassium superoxide) oxidizes HE to a fluorescent product (excitation, 480 nm; emission, 567 nm) that is totally different from E+. HPLC measurements revealed that the HE/superoxide reaction product elutes differently from E+. This new product exhibited an increase in fluorescence in the presence of DNA. Mass spectral data indicated that the molecular weight of the HE/superoxide reaction product is 330, while ethidium has a molecular weight of 314. We conclude that the reaction between superoxide and HE forms a fluorescent marker product that is different from ethidium. Potential implications of this finding in intracellular detection and imaging of superoxide are discussed.

MeSH Terms
Chromatography, High Pressure Liquid DNA/metabolism Ethidium/chemistry,metabolism Fluorescence Fluorescent Dyes Hydrazines/pharmacology Mass Spectrometry Nitric Oxide Nitric Oxide Donors/pharmacology Nitric Oxide Synthase/metabolism Nitric Oxide Synthase Type III Nitrogen Oxides Oxidation-Reduction Phenanthridines/chemistry,metabolism Superoxide Dismutase/metabolism Superoxides/chemistry,metabolism Xanthine/metabolism Xanthine Oxidase/metabolism
Chemicals
Fluorescent Dyes Hydrazines Nitric Oxide Donors Nitrogen Oxides Phenanthridines Superoxides potassium superoxide Xanthine Nitric Oxide hydroethidine 1,1-diethyl-2-hydroxy-2-nitrosohydrazine DNA Nitric Oxide Synthase Nitric Oxide Synthase Type III Superoxide Dismutase Xanthine Oxidase Ethidium
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Zhao Hongtao
Biophysics Research Institute and Free Radical Research Center, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.
Kalivendi Shasi
Zhang Hao
Joseph Joy
Nithipatikom Kasem
Vásquez-Vivar Jeannette
Kalyanaraman B
Article Info
Journal
Free radical biology & medicine
Abbr.
Free Radic Biol Med
ISSN
0891-5849
Published
2003-06-01
Pages
1359-68
Language
English
Region
United States
NLM ID
8709159
Subset
IM
Grants
NHLBI NIH HHS · 1P1 HL 68769-01 · United States
NCI NIH HHS · CA 77822 · United States
NHLBI NIH HHS · HL 067244 · United States
NINDS NIH HHS · NS 39958 · United States
NINDS NIH HHS · NS 40494 · United States
NCRR NIH HHS · RR 01008 · United States
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