Intraneuronal aluminum potentiates iron-induced oxidative stress in cultured rat hippocampal neurons

被引:60
作者
Xie, CX
Mattson, MP
Lovell, MA
Yokel, RA
机构
[1] UNIV KENTUCKY,GRAD CTR TOXICOL,LEXINGTON,KY 40506
[2] UNIV KENTUCKY,DEPT ANAT & NEUROBIOL,LEXINGTON,KY 40536
[3] UNIV KENTUCKY,SANDERS BROWN CTR AGING,LEXINGTON,KY 40536
[4] UNIV KENTUCKY,DEPT CHEM,LEXINGTON,KY 40536
[5] UNIV KENTUCKY,COLL PHARM,LEXINGTON,KY 40536
关键词
aluminum; confocal laser scanning microscopy; 2,7-dichlorofluorescin diacetate; laser microprobe mass spectrometry; hippocampal neuron; iron; oxidative stress; reactive oxygen species;
D O I
10.1016/S0006-8993(96)01055-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Aluminum can facilitate Fe-mediated oxidative injury, which may contribute to Al neurotoxicity. It has been reported that Al potentiates Fe-induced oxidative stress in cultured granule cells, suggesting a mechanism for Al facilitation of Fe-mediated oxidative injury. However, the relationship of intracellular Al concentration to Fe-induced oxidative stress has not been reported. In the present study, neuronal oxidative stress and survival were investigated. Embryo rat hippocampal neuron cultures were treated with Al-2(SO4)(3) and/or FeSO4. An ionophore, A23187, was utilized to facilitate cellular Al uptake. Intraneuronal Al concentration was ascertained by laser microprobe mass spectrometry (LMMS). Neuronal oxidative stress was measured by confocal laser scanning microscopy, using 2,7-dichlorofluorescin diacetate (DCFH-DA) as a probe. The study showed that neuronal Al uptake was facilitated by the ionophore and that an increase of intraneuronal Al concentration potentiated Fe-induced oxidative stress and neuronal death. The results indicate that Al potentiation of Fe-induced oxidative stress might contribute to Al facilitation of oxidative injury, and thus to Al neurotoxicity.
引用
收藏
页码:271 / 277
页数:7
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