Vascular endothelial growth factor protects cultured rat hippocampal neurons against hypoxic injury via an antiexcitotoxic, caspase-independent mechanism

被引:110
作者
Svensson, B
Peters, M
König, HG
Poppe, M
Levkau, B
Rothermundt, M
Arolt, T
Kögel, D
Prehn, JHM
机构
[1] Univ Munster, Fac Med, Interdisciplinary Ctr Clin Res, Res Grp Apoptosis & Cell Death, D-48149 Munster, Germany
[2] Univ Munster, Fac Med, Dept Psychiat & Psychotherapy, D-48149 Munster, Germany
[3] Univ Munster, Fac Med, Inst Arteriosclerosis Res, D-48149 Munster, Germany
关键词
vascular endothelial growth factor (VEGF); hypoxia; hippocampal neurons; N-miethyl-D-aspartate (NMDA); excitotoxicity; caspases;
D O I
10.1097/01.wcb.0000037988.07114.98
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The authors investigated the effect of vascular endothelial growth factor (VEGF) on hypoxic injury of cultured rat hippocampal neurons. Treatment with glutamate receptor antagonists prevented hypoxic neuron death. The same magnitude of protection was observed in Cultures treated with VEGF, which also reduced excitotoxic neuron death induced directly by an exposure to N-methyl-D-aspartate. Vascular endothelial growth factor did not alter the activation of the transcription factor nuclear factor-kappaB during hypoxia and protected cells in a PI-3-kinase-independent manner. Vascular endothelial growth factor failed to protect against staurosporine-induced, caspase-de pendent apoptosis. These data suggest that VEGF-induced protection against hypoxic injury primarily involves the inhibition of excitotoxic processes.
引用
收藏
页码:1170 / 1175
页数:6
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