Protection by rapid chemical preconditioning of stressed hippocampal slice: a study of cellular swelling using optical scatter imaging

被引:5
作者
Bandyopadhyay, A [1 ]
Johnson, L [1 ]
Chung, W [1 ]
Thakor, NV [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
关键词
chemical preconditioning; excitoxicity; ischemia; hippocampal slice; scatter theory; light scatter; cellular swelling; imaging;
D O I
10.1016/S0006-8993(02)02693-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It has been demonstrated that anoxic preconditioning protects against a subsequent 'lethal' injury in the hippocampal slice. The goal of this paper was to test the hypothesis that chemical preconditioning could help reduce the cellular swelling observed in excitotoxically injured hippocampal slices. The control slice was given a 10-min insult of 100 muM N-methyl-D-aspartate (NMDA) to simulate ischemic injury, followed by 30-min perfusion of standard Ringers solution. Cellular swelling was observed with a microscope designed to image light scatter changes resulting from cellular swelling. After the control NMDA injury, the average peak scatter change for CA1, CA3 and DG regions was 31.0+/-3.4, 22.4+/-4.8 and 27.6+/-4.6%, respectively. The peak scatter change of the overall slice was 26.0+/-3.6%. The experimental slices were preconditioned by three short 100 muM NMDA insults of 15 s each separated by 10 min of standard Ringers solution perfusion. The slices then received 10 min of 'lethal' injury by 100 muM NMDA. It was observed that the overall scatter signal, as a measure of cellular swelling, was reduced by 8.0% (P<0.05, n=11) after preconditioning. A regional heterogeneity in the responses was also observed. Cellular swelling in CA1, CA3 and DG were reduced by 9.8% (P<0.001, n=11), 9.2% (P<0.005, n=11) and 7.7% (P<0.05, n=11), respectively, when. compared to the control. This study presents experimental evidence that short episodes of preconditioning may protect against acute cellular swelling under ischemic conditions. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:79 / 87
页数:9
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