Volume 7, Issue 1 pp. 13-19
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Bilirubin chemiluminescence induced by the attack of active oxygen species

Haruo Watanabe

Corresponding Author

Haruo Watanabe

Biophoton Project, Research Development Corporation of Japan, 2-1-1, Yagiyama-minami, Taihaku-ku, Sendai 982, Japan

Biophoton Project, Research Development Corporation of Japan, 2-1-1, Yagiyama-minami, Taihaku-ku, Sendai 982, JapanSearch for more papers by this author
Toshiyuki Nagoshi

Toshiyuki Nagoshi

Biophoton Project, Research Development Corporation of Japan, 2-1-1, Yagiyama-minami, Taihaku-ku, Sendai 982, Japan

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Shinichi Agatsuma

Shinichi Agatsuma

Biophoton Project, Research Development Corporation of Japan, 2-1-1, Yagiyama-minami, Taihaku-ku, Sendai 982, Japan

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Masaki Kobayashi

Masaki Kobayashi

Biophoton Project, Research Development Corporation of Japan, 2-1-1, Yagiyama-minami, Taihaku-ku, Sendai 982, Japan

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Humio Inaba

Humio Inaba

Biophoton Project, and Research Institute of Electrical Communication, Tohoku University, 2-1-1, Katahira, Aoba-ku, Sendai 980, Japan

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First published: January 1992
Citations: 5

Abstract

Ultraweak chemiluminescence (CL) from bilirubin occurs in the presence of triplet oxygen and is stimulated by the addition of aldehydes. Active oxygen species also enhance bilirubin CL, in the absence of aldehydes. An inhibitory effect of active oxygen scavengers on the CL indicated that active oxygens generated from the decomposition of added hydrogen peroxide or from the xanthine-xanthine oxidase reaction contributed to the CL from bilirubin molecules. However, the contribution of singlet oxygen to the CL disappeared in the presence of formaldehyde. This suggested that the scission of tetrapyrrole bonds via a dioxetane intermediate or the production of triplet carbonyls from the oxidation of aldehydes by singlet oxygen was not involved in the CL, at least in the presence of formaldehyde. The spectrum of CL induced by the generation of active oxygen was the same as that from the aldehyde-enhanced CL reaction. We propose that the formation of a hydroperoxide (and/or hydroxide) bilirubin intermediate, but not a dioxetane, may be involved in the excitation of bilirubin molecules for CL.

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