Protection by the flavonoids quercetin and luteolin against peroxide- or menadione-induced oxidative stress in MC3T3-E1 osteoblast cells

被引:25
作者
Fatokun, Amos A. [1 ]
Tome, Mercedes [1 ]
Smith, Robert A. [1 ]
Darlington, L. Gail [2 ]
Stone, Trevor W. [1 ]
机构
[1] Univ Glasgow, Coll Med Vet & Life Sci, Inst Neurosci & Psychol, Glasgow G12 8QQ, Lanark, Scotland
[2] Ashtead Hosp, Ashtead KT18 2SB, Surrey, England
关键词
oxidative stress; luteolin; bone; quercetin; osteoblasts; flavonoids; ARYL-HYDROCARBON RECEPTOR; IN-VITRO; BINDING; MODEL; NEURODEGENERATION; PHYTOCHEMICALS; DERIVATIVES; ANTAGONISTS; MECHANISMS; BONE;
D O I
10.1080/14786419.2014.980252
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Potential protective effects of the flavonoids quercetin and luteolin have been examined against the oxidative stress of MC3T3-E1 osteoblast-like cells. Although hydrogen peroxide and menadione reduced cell viability, the toxicity was prevented by desferrioxamine or catalase but not superoxide dismutase, suggesting the involvement of hydrogen peroxide in both cases. Quercetin and luteolin reduced the oxidative damage, especially that caused by hydrogen peroxide. When cultures were pre-incubated with quercetin or luteolin, protection was reduced or lost. Protection was also reduced when a 24h pre-incubation with the flavonoids was followed by exposure to menadione alone. Pretreating cultures with luteolin impaired protection by quercetin, whereas quercetin pretreatment did not affect protection by luteolin. It is concluded that quercetin and luteolin suppress oxidative damage to MC3T3-E1 cells, especially caused by peroxide. The reduction in protection by pretreatment implies a down-regulation of part of the toxic transduction pathway.
引用
收藏
页码:1127 / 1132
页数:6
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