M. Nakano et al., A SIMPLE LUMINESCENCE METHOD FOR DETECTING LIPID-PEROXIDATION AND ANTIOXIDANT ACTIVITY IN-VITRO, Biochemical and biophysical research communications, 202(2), 1994, pp. 940-946
The excited carbonyl species formed during lipid peroxidation may tran
sfer their energy to dye molecules containing heavy atoms such as rose
bengal to produce excited singlet state dye molecules. The excited dy
e then emits photons to return to its ground state. The aim of the pre
sent study was to investigate the relationship between methemoglobin (
metHb)-induced lipid peroxidation, rose bengal luminescence, and O-2 c
onsumption in a system containing 0-850 mu M phospholipid and 1 mu M m
etHb and 1 mu M rose bengal in Tris-HCl buffer, pH 7.4. The rapid rise
in rose bengal luminescence was accompanied by a rapid rise in O-2 co
nsumption. Further, the luminescence of rose bengal could be quenched
by alpha-tocopherol or probucol present in the phospholipid liposomes,
with the latter being strikingly more effective than the former. This
simple luminescence method is a useful practical approach to detect l
ipid peroxidation and determine antioxidant effects of water insoluble
compounds in vitro. (C) 1994 Academic Press, Inc.