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1.
Biosci Biotechnol Biochem ; 69(3): 620-2, 2005 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15784992

RESUMEN

We examined antioxidants exhibiting no effects on DNA cross-linking, which is the basis of psoralen and ultraviolet-A therapy for skin diseases, and suppressing oxidative DNA damage incidental to the therapy. Epigallocatechin gallate and esculetin effectively suppressed oxidative DNA damage with little effect on the formation of DNA cross-linking. These antioxidants might be useful in suppressing the adverse reaction induced by this therapy.


Asunto(s)
Catequina/análogos & derivados , Daño del ADN , Ficusina/farmacología , Estrés Oxidativo , Terapia PUVA , Umbeliferonas/farmacología , Catequina/farmacología
2.
Chem Biol Interact ; 142(3): 239-54, 2003 Jan 06.
Artículo en Inglés | MEDLINE | ID: mdl-12453663

RESUMEN

Coumarins comprise a group of natural phenolic compounds found in a variety of plant sources. Protective effects of coumarins against cytotoxicity induced by linoleic acid hydroperoxide were examined in cultured human umbilical vein endothelial cells. When the cells were incubated in medium supplemented with linoleic acid hydroperoxide and coumarins, esculetin (6,7-dihydroxycoumarin) and 4-methylesculetin protected cells from injury by linoleic acid hydroperoxide. Fraxetin and caffeic acid showed weak, but significant, protection. Esculin as well as esculetin and 4-methylesculetin were effective for protecting cells against linoleic acid hydroperoxide-induced cytotoxicity in the case of pretreatment for 24 h, however fraxetin and caffeic acid showed no protection. Since esculetin was detected after 24 h treatment with esculin, a sugar moiety in the esculin molecule appears to be hydrolyzed during pretreatment. Coumarins such as umbelliferone containing only one hydroxyl group showed no protective effect in pretreatment or concurrent treatment. Esculetin and 4-methylesculetin provided synergistic protection against cytotoxicity induced by linoleic acid hydroperoxide with alpha-tocopherol. Furthermore, the radical-scavenging ability of coumarins was examined in electron spin resonance spectrometry. Esucletin, 4-methylesculetin, fraxetin, and caffeic acid showed the quenching effect on the 1,1-diphenyl-2-picrylhydrazyl radical. These results indicate that the presence of an ortho catechol moiety in the coumarin molecules plays an important role in the protective activities against linoleic acid hydroperoixde-induced cytotoxicity.


Asunto(s)
Cumarinas/farmacología , Ácidos Linolénicos/antagonistas & inhibidores , Ácidos Linolénicos/toxicidad , Peróxidos Lipídicos/antagonistas & inhibidores , Peróxidos Lipídicos/toxicidad , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Cinamatos/farmacología , Cumarinas/química , Sinergismo Farmacológico , Espectroscopía de Resonancia por Spin del Electrón , Endotelio Vascular/citología , Endotelio Vascular/efectos de los fármacos , Depuradores de Radicales Libres/química , Depuradores de Radicales Libres/farmacología , Humanos , Umbeliferonas/farmacología
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