Photosensitized lipid peroxidation and enzyme inactivation by membrane-bound merocyanine 540: reaction mechanisms in the absence and presence of ascorbate

• Published in: Photochemistry and photobiology Vol. 53; no. 4; p. 481
• Main Authors: Bachowski, G J, Pintar, T J, Girotti, A W
• Format: Journal Article
• Language: English
• Published: United States 01-04-1991
• Subjects: Ascorbic Acid - pharmacology; Cholesterol - radiation effects; Erythrocyte Membrane - drug effects; Erythrocyte Membrane - radiation effects; Free Radicals; Humans; In Vitro Techniques; L-Lactate Dehydrogenase - antagonists & inhibitors; Lipid Peroxidation - drug effects; Lipid Peroxidation - radiation effects; Photochemistry; Pyrimidinones - pharmacology; Radiation-Sensitizing Agents - pharmacology
• ISSN: 0031-8655
• DOI: 10.1111/j.1751-1097.1991.tb03660.x

The lipophilic photosensitizing dye merocyanine 540 (MC540) is being studied intensively as an antitumor and antiviral agent. Since plasma membranes are believed to be the principal cellular targets of MC540-mediated photodamage, we have studied membrane damage in a well characterized test system, the human erythrocyte ghost. When irradiated with white light, MC540-sensitized ghosts accumulated lipid hydroperoxides (LOOHs derived from phospholipids and cholesterol) at a rate dependent on initial dye concentration. Neither desferrioxamine nor butylated hydroxytoluene inhibited LOOH formation, suggesting that Type I (iron-mediated free radical) chemistry is not important. By contrast, azide inhibited the reaction in a dose-dependent fashion, implicating a Type II (singlet oxygen, 1O2) mechanism. Stern-Volmer analysis of the data gave a 1O2 quenching constant approximately 50 times lower than that determined for an extramembranous target, lactate dehydrogenase (the latter value agreeing with literature values). This suggests that 1O2 reacts primarily at its membrane sites of origin and that azide has limited access to these sites. Using [14C]cholesterol-labeled membranes and HPLC with radiodetection, we identified 3 beta-hydroxy-5 alpha-cholest-6-ene-5-hydroperoxide as the major cholesterol photoproduct, thereby confirming 1O2 intermediacy. Irradiation of MC540-sensitized membranes in the presence of added iron and ascorbate resulted in a large burst of lipid peroxidation, as shown by thiobarbituric acid reactivity and appearance of 7-hydroperoxycholesterol and 7-hydroxycholesterol as major oxidation products. Amplification of MC540-initiated lipid peroxidation by iron/ascorbate (attributed to light-independent reduction of nascent photoperoxides, with ensuing free radical chain reactions) could prove useful in augmenting MC540's phototherapeutic effects.