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大鼠新皮质中N-甲基-D-天冬氨酸受体结合位点随年龄的保留情况。

Preservation of N-methyl-D-aspartate receptor binding sites with age in rat neocortex.

作者信息

Palmer A M

机构信息

Department of Psychiatry, University of Pittsburgh School of Medicine, Pennsylvania, USA.

出版信息

J Gerontol A Biol Sci Med Sci. 2000 Nov;55(11):B530-2. doi: 10.1093/gerona/55.11.b530.

Abstract

This study used [3H]dizocilpine ([3H]MK-801) binding to examine glycine, polyamine, and zinc subsites of the N-methyl-D-aspartate (NMDA) receptor in well-washed membranes derived from the neocortex of Fischer 344/Norwegian brown rats aged 3, 12, 24 and 37 months. [3H]dizocilpine binding in the presence of 100 microM glutamate was enhanced by the addition of 30 microM glycine. Binding in the presence of both glutamate and glutamate plus glycine were unaffected by age. The competitive polyamine site antagonist arcaine inhibited [3H]dizocilpine binding in a dose-dependent fashion and 50 microM spermidine caused a rightward shift in this dose response curve. IC50 values derived from these plots were not significantly affected by age. Similarly, zinc inhibited binding in a dose-dependent fashion and was also unaffected by age. These data indicate that the NMDA receptor is spared in aging.

摘要

本研究使用[3H]地卓西平([3H]MK - 801)结合实验,来检测来自3、12、24和37月龄Fischer 344/挪威棕大鼠新皮质的充分洗涤过的膜中N - 甲基 - D - 天冬氨酸(NMDA)受体的甘氨酸、多胺和锌亚位点。在100微摩尔谷氨酸存在的情况下,添加30微摩尔甘氨酸可增强[3H]地卓西平的结合。在单独谷氨酸以及谷氨酸加甘氨酸存在的情况下的结合不受年龄影响。竞争性多胺位点拮抗剂阿卡因以剂量依赖性方式抑制[3H]地卓西平的结合,50微摩尔亚精胺使该剂量反应曲线向右移动。从这些图得出的半数抑制浓度(IC50)值不受年龄显著影响。同样,锌以剂量依赖性方式抑制结合,且也不受年龄影响。这些数据表明NMDA受体在衰老过程中未受影响。

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