IRIS publication 43338762
Mechanism of protection by the flavonoids, quercetin and rutin, against tert-butylhydroperoxide- and menadione induced DNA single strand breaks in Caco-2 cells
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TY - JOUR - Aherne, SA,O'Brien, NM - 2000 - July - Free Radical Biology and Medicine - Mechanism of protection by the flavonoids, quercetin and rutin, against tert-butylhydroperoxide- and menadione induced DNA single strand breaks in Caco-2 cells - Validated - () - flavonoids tert-butylhydroperoxide menadione DNA damage Caco-2 cells BHT 1,10-phenanthroline deferoxamine mesylate free radicals ANTIOXIDANT ACTIVITY HYDROGEN-PEROXIDE RAT HEPATOCYTES CULTURED-HEPATOCYTES OXIDATIVE STRESS DAMAGE RADICALS TOXICITY IRON HYDROPEROXIDES - 29 - 507 - 514 - Protection by the flavonoids, quercetin and rutin, against tert-butylhydroperoxide (tert-BOOH)- and menadione-induced DNA single strand breaks was investigated in Caco-2 cells. Both tert-BOOH and menadione induced DNA single strand breaks in a concentration-dependent manner. Pre-incubation of Caco-2 cells with either quercetin or rutin for 24 h significantly decreased the formation of DNA single strand breaks evoked by tert-BOOH (P < .05). Iron chelators, 1,10-phenanthroline (o-Phen) and deferoxamine mesylate (DFO), also protected against tert-BOOH-induced DNA damage, whereas butylated hydroxytoluene (BHT) had no effect. Quercetin, and not rutin, decreased the extent of menadione-induced DNA single strand breaks. DFO and BHT, and not o-Phen, protected against menadione-induced DNA strand break formation (P < .05). From the results of this study, iron ions were involved in tert-BOOH-induced DNA single strand break formation in Caco-2 cells, whereas DNA damage evoked by menadione was far more complex. We demonstrated that the flavonoids, quercetin and rutin, protected against tert-BOOH-induced DNA strand breaks by way of their metal ion chelating mechanism. However, quercetin, and not rutin, protected against menadione-induced DNA single strand breaks by acting as both a metal chelator and radical scavenger. (C) 2000 Elsevier Science Inc. DA - 2000/07 ER -
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@article{V43338762, = {Aherne, SA and O'Brien, NM }, = {2000}, = {July}, = {Free Radical Biology and Medicine}, = {Mechanism of protection by the flavonoids, quercetin and rutin, against tert-butylhydroperoxide- and menadione induced DNA single strand breaks in Caco-2 cells}, = {Validated}, = {()}, = {flavonoids tert-butylhydroperoxide menadione DNA damage Caco-2 cells BHT 1,10-phenanthroline deferoxamine mesylate free radicals ANTIOXIDANT ACTIVITY HYDROGEN-PEROXIDE RAT HEPATOCYTES CULTURED-HEPATOCYTES OXIDATIVE STRESS DAMAGE RADICALS TOXICITY IRON HYDROPEROXIDES}, = {29}, pages = {507--514}, = {{Protection by the flavonoids, quercetin and rutin, against tert-butylhydroperoxide (tert-BOOH)- and menadione-induced DNA single strand breaks was investigated in Caco-2 cells. Both tert-BOOH and menadione induced DNA single strand breaks in a concentration-dependent manner. Pre-incubation of Caco-2 cells with either quercetin or rutin for 24 h significantly decreased the formation of DNA single strand breaks evoked by tert-BOOH (P < .05). Iron chelators, 1,10-phenanthroline (o-Phen) and deferoxamine mesylate (DFO), also protected against tert-BOOH-induced DNA damage, whereas butylated hydroxytoluene (BHT) had no effect. Quercetin, and not rutin, decreased the extent of menadione-induced DNA single strand breaks. DFO and BHT, and not o-Phen, protected against menadione-induced DNA strand break formation (P < .05). From the results of this study, iron ions were involved in tert-BOOH-induced DNA single strand break formation in Caco-2 cells, whereas DNA damage evoked by menadione was far more complex. We demonstrated that the flavonoids, quercetin and rutin, protected against tert-BOOH-induced DNA strand breaks by way of their metal ion chelating mechanism. However, quercetin, and not rutin, protected against menadione-induced DNA single strand breaks by acting as both a metal chelator and radical scavenger. (C) 2000 Elsevier Science Inc.}}, source = {IRIS} }
Data as stored in IRIS
AUTHORS | Aherne, SA,O'Brien, NM | ||
YEAR | 2000 | ||
MONTH | July | ||
JOURNAL_CODE | Free Radical Biology and Medicine | ||
TITLE | Mechanism of protection by the flavonoids, quercetin and rutin, against tert-butylhydroperoxide- and menadione induced DNA single strand breaks in Caco-2 cells | ||
STATUS | Validated | ||
TIMES_CITED | () | ||
SEARCH_KEYWORD | flavonoids tert-butylhydroperoxide menadione DNA damage Caco-2 cells BHT 1,10-phenanthroline deferoxamine mesylate free radicals ANTIOXIDANT ACTIVITY HYDROGEN-PEROXIDE RAT HEPATOCYTES CULTURED-HEPATOCYTES OXIDATIVE STRESS DAMAGE RADICALS TOXICITY IRON HYDROPEROXIDES | ||
VOLUME | 29 | ||
ISSUE | |||
START_PAGE | 507 | ||
END_PAGE | 514 | ||
ABSTRACT | Protection by the flavonoids, quercetin and rutin, against tert-butylhydroperoxide (tert-BOOH)- and menadione-induced DNA single strand breaks was investigated in Caco-2 cells. Both tert-BOOH and menadione induced DNA single strand breaks in a concentration-dependent manner. Pre-incubation of Caco-2 cells with either quercetin or rutin for 24 h significantly decreased the formation of DNA single strand breaks evoked by tert-BOOH (P < .05). Iron chelators, 1,10-phenanthroline (o-Phen) and deferoxamine mesylate (DFO), also protected against tert-BOOH-induced DNA damage, whereas butylated hydroxytoluene (BHT) had no effect. Quercetin, and not rutin, decreased the extent of menadione-induced DNA single strand breaks. DFO and BHT, and not o-Phen, protected against menadione-induced DNA strand break formation (P < .05). From the results of this study, iron ions were involved in tert-BOOH-induced DNA single strand break formation in Caco-2 cells, whereas DNA damage evoked by menadione was far more complex. We demonstrated that the flavonoids, quercetin and rutin, protected against tert-BOOH-induced DNA strand breaks by way of their metal ion chelating mechanism. However, quercetin, and not rutin, protected against menadione-induced DNA single strand breaks by acting as both a metal chelator and radical scavenger. (C) 2000 Elsevier Science Inc. | ||
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