Neuroprotective effects of brain-derived neurotrophic factor in eyes with NMDA-induced neuronal death

被引:68
作者
Kido, N
Tanihara, H
Honjo, M
Inatani, M
Tatsuno, T
Nakayama, C
Honda, Y
机构
[1] Tenri Hosp, Dept Ophthalmol, Tenri, Nara 6328552, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Ophthalmol & Visual Sci, Kyoto, Japan
[3] Sumitomo Pharmaceut Res Ctr, Osaka, Japan
关键词
glutamate; retina; flat mount; retinal ganglion cell; cell death; brain-derived neurotrophic factor; N-methyl-D-aspartate;
D O I
10.1016/S0006-8993(00)02887-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Purpose: To determine if brain-derived neurotrophic factor (BDNF) has a neuroprotective effect against N-methyl-D-aspartate (NMDA)-induced cell death in retina. Methods: NMDA was injected into the vitreous of rat eyes. NMDA-induced neuronal death was measured by morphometric analyses on cell counts of ganglion cell layer cells and thickness of retinal layers. Also, we conducted additional experiment using retrograde labeling with a fluorescent tracer (Fluoro-Gold) for exact counting of retinal ganglion cells (RGCs). In addition, intravitreal glutamate levels were measured with the use of a high-performance liquid chromatography (HPLC) system. Results: Morphometric analysis of retinal damage in NMDA-injected eyes showed that BDNF could protect inner retinal cells from glutamate receptor-mediated neuronal death. Also, counts of RGCs labeled with a fluorescent tracer showed that BDNF could protect RGCs from glutamate receptor-mediated neuronal death. Furthermore, measurements of intravitreal glutamate levels indicated an increase in this excitatory amino acid in the vitreous after NMDA injection. Conclusions: Exogenous BDNF can protect inner retinal cells (possible RGCs and amacrine cells) from NMDA-induced neuronal death. However, increased intravitreal glutamate levels in response to NMDA-mediated neurotoxicity may augment retinal degeneration. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:59 / 67
页数:9
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