Carnosine protects against excitotoxic cell death independently of effects on reactive oxygen species

被引:100
作者
Boldyrev, A
Song, R
Lawrence, D
Carpenter, DO [1 ]
机构
[1] SUNY Albany, Sch Publ Hlth, Dept Environm Hlth & Toxicol, Rensselaer, NY 12144 USA
[2] New York State Dept Hlth, Wadsworth Ctr Labs & Res, Albany, NY 12201 USA
[3] Moscow MV Lomonosov State Univ, Int Ctr Biotechnol, Sch Biol, Dept Biochem, Moscow 119899, Russia
[4] Moscow MV Lomonosov State Univ, Ctr Mol Med, Sch Biol, Dept Biochem, Moscow 119899, Russia
关键词
cerebellar granule cells; cell death; flow cytometry; NMDA; kainate; apoptosis;
D O I
10.1016/S0306-4522(99)00273-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The role of carnosine. N-acetylcarnosine and homocarnosine as scavengers of reactive oxygen species and protectors against neuronal cell death secondary to excitotoxic concentrations of kainate and N-methyl-D-aspartate was studied using acutely dissociated cerebellar granule cell neurons and flow cytometry. We find that carnosine, N-acetylcarnosine and homocarnosine at physiological concentrations are all potent in suppressing fluorescence of 2',7'-dichlorofluorescein, which reacts with intracellularly generated reactive oxygen species. However, only carnosine in the same concentration range was effective in preventing apoptotic neuronal cell death, studied using a combination of the DNA binding dye, propidium iodide, and a fluorescent derivative of the phosphatidylserine-binding dye, Annexin-V. Our results indicate that carnosine and related compounds are effective scavengers of reactive oxygen species generated by activation of ionotropic glutamate receptors, but that this action does not prevent excitotoxic cell death. Some other process which is sensitive to carnosine but not the related compounds is a critical factor in cell death. These observations indicate that at least in this system reactive oxygen species generation is not a major contributor to excitotoxic neuronal cell death. (C) 1999 IBRO. Published by Elsevier Science Ltd.
引用
收藏
页码:571 / 577
页数:7
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