Proton-induced Dismutation of Superoxide in Aprotic Media by Bile Pigments
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Abstract
Cyclic voltammetry of molecular oxygen in aprotic media (dimethylformamide) and in the presence of bilirubin and other bile pigments shows that superoxide anion (O2-.) undergoes proton-induced dismutation. Lactam hydrogens of bile pigments are sufficiently acid to induce (O2-.) disproportionation to O2 and H2O2. Because of its characteristic lipophilic behavior, a biological role for natural bilirubin similar to that of other non-enzymatic lipophilic scavengers of (O2-.) is suggested.
References
1.
KUENZLE C, Weibel M, Pelloni R
. The reaction of bilirubin with diazomethane. Biochem J. 1973; 133(2):357-64.
PMC: 1177705.
DOI: 10.1042/bj1330357.
View
2.
KRENITSKY T, Tuttle J, Cattau Jr E, Wang P
. A comparison of the distribution and electron acceptor specificities of xanthine oxidase and aldehyde oxidase. Comp Biochem Physiol B. 1974; 49(4):687-703.
DOI: 10.1016/0305-0491(74)90256-9.
View
3.
Cofre P, Sawyer D
. Electrochemical reduction of dioxygen to perhydroxyl (HO2.) in aprotic solvents that contain Brønsted acids. Anal Chem. 1986; 58(6):1057-62.
DOI: 10.1021/ac00297a017.
View
4.
Kaul R, Kaul H, Murti C
. An alternate pathway for bilirubin catabolism. FEBS Lett. 1980; 111(1):240-2.
DOI: 10.1016/0014-5793(80)80802-7.
View
5.
Cerutti P
. Prooxidant states and tumor promotion. Science. 1985; 227(4685):375-81.
DOI: 10.1126/science.2981433.
View