Probe-assisted flow cytometric analysis of erythrocyte membrane response to site-specific oxidant stress

被引:0
|
作者
Chung, WY [1 ]
Benzie, IFF [1 ]
机构
[1] Hong Kong Polytech Univ, Dept Nursing & Hlth Sci, Kowloon, Hong Kong, Peoples R China
来源
CYTOMETRY | 2000年 / 40卷 / 03期
关键词
lipid peroxidation; oxidant stress; antioxidants; fluorescence; flow cytometry; cumene hydroperoxide; fluorophore; urate; ascorbate; alpha tocopherol;
D O I
10.1002/1097-0320(20000701)40:3<182::AID-CYTO2>3.0.CO;2-G
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Probe-assisted flow cytometry was used to monitor the response of membranes of living cells to oxidant stress in the presence and absence of antioxidants. Test conditions (fluorophore loading, oxidant concentration) were investigated and storage-related changes in erythrocyte response to oxidant stress explored. Methods: Erythrocytes were incubated with a lipophilic fluorescent probe and exposed to site-specific oxidant challenge, induced by cumene hydroperoxide, in the presence and absence of urate, ascorbate, or alpha tocopherol in physiological amounts. Fluorescence of labeled and treated erythrocytes was measured for 120 min using a Coulter EPICS Elite ESP flow cytometer. Results: Probe loading was dose and time dependent. Cumene hydroperoxide exhibited a potent and dose-dependent oxidant effect on erythrocyte membranes. Alpha tocopherol slowed, but did not prevent, membrane oxidation. Ascorbate appeared to have no effect on peroxidation initially, but then slowed and stopped propagation of membrane oxidation. The effect of urate was slight. Conclusions: This technique can provide insight into oxidative processes at the cellular level. Results indicated that lipophilic alpha tocopherol was the most effective antioxidant in slewing membrane peroxidation, but ascorbate appears to stop chain propagation. This effect may be owing to vitamin C/E interaction. Further study is needed. (C) 2000 Wiley-Liss, Inc.
引用
收藏
页码:182 / 188
页数:7
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