Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation Research
Search: search_blue_button Advanced Search
Circulation Research. 2001;89:e46

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Afanas’ev, I. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Afanas’ev, I. B.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Hazardous Substances DB
*ACRIDINE
(Circulation Research. 2001;89:e46.)
© 2001 American Heart Association, Inc.


Letter to the Editor

Lucigenin Chemiluminescence Assay for Superoxide Detection

Igor B. Afanas’ev

Vitamin Research Institute, Moscow, Russia, iafan@aha.ru

To the Editor:

The recent review by Tarpey and Fridovich published in Circulation Research1 mostly contains interesting and sound material; however, I would like to comment on the section entitled, "Superoxide Detection, Chemiluminescence Reactions." Basing mainly on their own data,2 authors maintain that lucigenin-amplified chemiluminescence (LucCL) overestimates the rate of superoxide production due to the redox cycling of lucigenin. Taking into account that LucCL is the most sensitive method of superoxide detection, which is especially useful for the detection of low superoxide concentrations in vascular systems (see, for example, References 3 through 5), such an assertion (if true) devalues numerous previous experimental findings.

Fortunately, it is not true. And our conclusion is not due to "the triumph of hope over reality"1 (page 229) but is based on reliable experimental data. We have shown earlier6 that lucigenin cannot take part in redox cycling with molecular oxygen because of its positive one-electron reduction potential (about 0.19 V). (Spasojevic et al7 recently measured the two-electron reduction potential of lucigenin as -0.14 V. However, it was shown long ago that two-electron reduction potentials are not equal to one-electron reduction potentials.8) In addition to theoretical considerations, it is possible to demonstrate the reliability of the LucCL method on the basis of experimental data. We9 compared the results of superoxide measurement by LucCL and cytochrome c reduction in several enzymatic and cellular systems, and we found out that there are excellent correlations among the results obtained for the xanthine- and NADH-xanthine oxidase systems, neutrophils, and monocytes (correlation coefficients are of . . . [Full Text of this Article]