Photodynamic degradation of vitamin E induced by psoralens
Psoralens and other furocoumarins currently used in PUVA photochemotherapy are shown to have, to a variable extent, the ability to hasten the rate of ultraviolet-induced photooxidation of α-tocopherol (α-T) in ethanol or ethanol-phosphate buffer (pH 6.8). The sensitizing effect varies significantly...
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Published in | Biochimica et biophysica acta Vol. 1116; no. 3; pp. 291 - 296 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
12.06.1992
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 0304-4165 0006-3002 1872-8006 |
DOI | 10.1016/0304-4165(92)90042-S |
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Abstract | Psoralens and other furocoumarins currently used in PUVA photochemotherapy are shown to have, to a variable extent, the ability to hasten the rate of ultraviolet-induced photooxidation of α-tocopherol (α-T) in ethanol or ethanol-phosphate buffer (pH 6.8). The sensitizing effect varies significantly with the substrate concentration and the nature of the furocoumarin used, and is dependent on the presence of oxygen. Scavengers of singlet oxygen, e.g., sodium azide, markedly inhibit the psoralen-sensitized photooxidation of α-T, whereas superoxide dismutase exerts an opposite, accelerating effect on the reaction rate. Catalase has no significant influence on the kinetics of α-T decay. Analysis of the products formed by psoralen-sensitized photooxidation of α-T in ethanol-phosphate buffer showed the presence of α-tocopherolquinone, its 2,3-epoxide and two related compounds containing the 7-oxaspiro[4,5]dec-1-ene-3,6-dione ring system. The nature of these products, coupled with the results of the kinetic experiments, suggest that psoralens induce a type II, oxygen-dependent photodegradation of α-T primarily mediated by singlet oxygen. |
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AbstractList | Psoralens and other furocoumarins currently used in PUVA photochemotherapy are shown to have, to a variable extent, the ability to hasten the rate of ultraviolet-induced photooxidation of alpha-tocopherol (alpha-T) in ethanol or ethanol-phosphate buffer (pH 6.8). The sensitizing effect varies significantly with the substrate concentration and the nature of the furocoumarin used, and is dependent on the presence of oxygen. Scavengers of singlet oxygen, e.g., sodium azide, markedly inhibit the psoralen-sensitized photooxidation of alpha-T, whereas superoxide dismutase exerts an opposite, accelerating effect on the reaction rate. Catalase has no significant influence on the kinetics of alpha-T decay. Analysis of the products formed by psoralen-sensitized photooxidation of alpha-T in ethanol-phosphate buffer showed the presence of alpha-tocopherolquinone, its 2,3-epoxide and two related compounds containing the 7-oxaspiro[4.5]dec-1-ene-3,6-dione ring system. The nature of these products, coupled with the results of the kinetic experiments, suggest that psoralens induce a type II, oxygen-dependent photodegradation of alpha-T primarily mediated by singlet oxygen.Psoralens and other furocoumarins currently used in PUVA photochemotherapy are shown to have, to a variable extent, the ability to hasten the rate of ultraviolet-induced photooxidation of alpha-tocopherol (alpha-T) in ethanol or ethanol-phosphate buffer (pH 6.8). The sensitizing effect varies significantly with the substrate concentration and the nature of the furocoumarin used, and is dependent on the presence of oxygen. Scavengers of singlet oxygen, e.g., sodium azide, markedly inhibit the psoralen-sensitized photooxidation of alpha-T, whereas superoxide dismutase exerts an opposite, accelerating effect on the reaction rate. Catalase has no significant influence on the kinetics of alpha-T decay. Analysis of the products formed by psoralen-sensitized photooxidation of alpha-T in ethanol-phosphate buffer showed the presence of alpha-tocopherolquinone, its 2,3-epoxide and two related compounds containing the 7-oxaspiro[4.5]dec-1-ene-3,6-dione ring system. The nature of these products, coupled with the results of the kinetic experiments, suggest that psoralens induce a type II, oxygen-dependent photodegradation of alpha-T primarily mediated by singlet oxygen. Psoralens and other furocoumarins currently used in PUVA photochemotherapy are shown to have, to a variable extent, the ability to hasten the rate of ultraviolet-induced photooxidation of α-tocopherol (α-T) in ethanol or ethanol-phosphate buffer (pH 6.8). The sensitizing effect varies significantly with the substrate concentration and the nature of the furocoumarin used, and is dependent on the presence of oxygen. Scavengers of singlet oxygen, e.g., sodium azide, markedly inhibit the psoralen-sensitized photooxidation of α-T, whereas superoxide dismutase exerts an opposite, accelerating effect on the reaction rate. Catalase has no significant influence on the kinetics of α-T decay. Analysis of the products formed by psoralen-sensitized photooxidation of α-T in ethanol-phosphate buffer showed the presence of α-tocopherolquinone, its 2,3-epoxide and two related compounds containing the 7-oxaspiro[4,5]dec-1-ene-3,6-dione ring system. The nature of these products, coupled with the results of the kinetic experiments, suggest that psoralens induce a type II, oxygen-dependent photodegradation of α-T primarily mediated by singlet oxygen. Psoralens and other furocoumarins currently used in PUVA photochemotherapy are shown to have, to a variable extent, the ability to hasten the rate of ultraviolet-induced photooxidation of alpha-tocopherol (alpha-T) in ethanol or ethanol-phosphate buffer (pH 6.8). The sensitizing effect varies significantly with the substrate concentration and the nature of the furocoumarin used, and is dependent on the presence of oxygen. Scavengers of singlet oxygen, e.g., sodium azide, markedly inhibit the psoralen-sensitized photooxidation of alpha-T, whereas superoxide dismutase exerts an opposite, accelerating effect on the reaction rate. Catalase has no significant influence on the kinetics of alpha-T decay. Analysis of the products formed by psoralen-sensitized photooxidation of alpha-T in ethanol-phosphate buffer showed the presence of alpha-tocopherolquinone, its 2,3-epoxide and two related compounds containing the 7-oxaspiro[4.5]dec-1-ene-3,6-dione ring system. The nature of these products, coupled with the results of the kinetic experiments, suggest that psoralens induce a type II, oxygen-dependent photodegradation of alpha-T primarily mediated by singlet oxygen. |
Author | d'Ischia, Marco Prota, Giuseppe Misuraca, Giovanna Costantini, Claudio Napolitano, Alessandra |
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Cites_doi | 10.1111/j.1751-1097.1982.tb04377.x 10.1021/ja00758a026 10.1016/S0040-4039(01)84235-0 10.1021/ja00751a031 10.1016/0304-4165(84)90018-7 10.1111/1523-1747.ep12455986 10.1111/j.1751-1097.1987.tb08402.x 10.1111/j.1751-1097.1980.tb04061.x 10.1111/j.1751-1097.1982.tb02610.x 10.1515/znc-1974-9-1031 10.1021/ja01025a059 10.1021/bi00754a020 10.1111/j.1751-1097.1979.tb07194.x 10.1021/bi00534a008 10.1021/ja00335a014 10.1111/j.1751-1097.1979.tb07183.x 10.1021/ja00022a023 10.1016/0003-9861(90)90034-V 10.1111/j.1751-1097.1974.tb06610.x 10.1111/j.1751-1097.1979.tb07838.x 10.1111/j.1751-1097.1979.tb07364.x 10.1021/jo00408a041 10.1016/0304-4165(89)90156-6 10.1021/ar00127a001 |
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Keywords | PS SOD TLC AN DABCO Psoralen Singlet oxygen 8-MOP Vitamin E α-T PUVA 5-MOP TMP Photooxidation HPLC Oxygen Ultraviolet irradiation Molecular structure Enzyme Reaction mechanism Superoxide dismutase α-Tocopherol Singlet state Psoralen derivatives |
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Snippet | Psoralens and other furocoumarins currently used in PUVA photochemotherapy are shown to have, to a variable extent, the ability to hasten the rate of... |
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SubjectTerms | Biological and medical sciences Chromatography, High Pressure Liquid Fundamental and applied biological sciences. Psychology Furocoumarins - pharmacology Molecular biophysics Molecular Structure Oxidation-Reduction Photochemistry Photochemistry. Photosynthesis. Bioluminescence Photooxidation Psoralen Radiation-biomolecule interaction Singlet oxygen Vitamin E Vitamin E - metabolism |
Title | Photodynamic degradation of vitamin E induced by psoralens |
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