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亚精胺增强[3H]MK-801与人皮层膜中NMDA受体复合物的结合。

Spermidine enhancement of [3H]MK-801 binding to the NMDA receptor complex in human cortical membranes.

作者信息

Steele J E, Bowen D M, Francis P T, Green A R, Cross A J

机构信息

Department of Neurochemistry, Institute of Neurology, London, U.K.

出版信息

Eur J Pharmacol. 1990 Sep 18;189(2-3):195-200. doi: 10.1016/0922-4106(90)90023-q.

Abstract

The effects of spermidine on the binding of [3H]MK-801 to the N-methyl-D-aspartate (NMDA) receptor complex was studied in human cerebral cortical membranes. [3H]MK-801 binding was increased from 56 +/- 5 fmol/mg protein (mean +/- S.E.M., n = 7) to 319 +/- 71 fmol/mg protein in the presence of 200 microM spermidine. The ED50 for spermidine stimulation of [3H]MK-801 binding was 89 +/- 22 microM (mean +/- S.E.M., n = 6). In the presence of glutamate (1 microM) plus glycine (1 microM) the ED50 was reduced to 5.5 +/- 0.7 microM. The increase in binding in the presence of spermidine was characterised by an increase in the rate of association of [3H]MK-801. In the presence of spermidine. [3H]MK-801 was inhibited by AP5. 7-chlorokynurenic acid and ifenprodil with IC50 values of 0.5 +/- 0.3 24 +/- 19 and 91 +/- 28 microM, respectively. None of these antagonists was a competitive inhibitor of the spermidine stimulation of [3H]MK-801 binding. Thus spermidine modulates the NMDA receptor complex in human brain, providing further evidence that the complex is similar in rat and human cortex.

摘要

在人脑皮质膜中研究了亚精胺对[3H]MK-801与N-甲基-D-天冬氨酸(NMDA)受体复合物结合的影响。在存在200微摩尔亚精胺的情况下,[3H]MK-801结合量从56±5飞摩尔/毫克蛋白质(平均值±标准误,n = 7)增加到319±71飞摩尔/毫克蛋白质。亚精胺刺激[3H]MK-801结合的半数有效浓度(ED50)为89±22微摩尔(平均值±标准误,n = 6)。在存在谷氨酸(1微摩尔)加甘氨酸(1微摩尔)的情况下,ED50降至5.5±0.7微摩尔。在存在亚精胺的情况下结合增加的特征是[3H]MK-801结合速率增加。在存在亚精胺的情况下,[3H]MK-801被AP5、7-氯犬尿氨酸和ifenprodil抑制,其半数抑制浓度(IC50)值分别为0.5±0.3、24±19和91±28微摩尔。这些拮抗剂均不是亚精胺刺激[3H]MK-801结合的竞争性抑制剂。因此,亚精胺调节人脑NMDA受体复合物,进一步证明该复合物在大鼠和人类皮质中相似。

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