首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Modulatory effects of NMDA on phosphoinositide responses evoked by the metabotropic glutamate receptor agonist 1S3R-ACPD in neonatal rat cerebral cortex.
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Modulatory effects of NMDA on phosphoinositide responses evoked by the metabotropic glutamate receptor agonist 1S3R-ACPD in neonatal rat cerebral cortex.

机译:NMDA对代谢型谷氨酸受体激动剂1S3R-ACPD诱发的新生大鼠大脑皮层中磷酸肌醇反应的调节作用。

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摘要

1. The effect of NMDA-receptor stimulation on phosphoinositide signalling in response to the metabotropic glutamate receptor agonist 1-aminocyclopentane-1S,3R-dicarboxylic acid (1S,3R-ACPD) has been examined in neonatal rat cerebral cortex slices. 2. Total [3H]-inositol phosphate ([3H]-InsPx) accumulation, in the presence of 5 mM LiCl, in [3H]-inositol pre-labelled slices was concentration-dependently increased by 1S,3R-ACPD (EC50 16.6 microM) and, at a maximally effective concentration, 1S,3R-ACPD (300 microM) increased [3H]-InsPx accumulation by 12.8 fold over basal values. 3. [3H]-InsPx accumulation stimulated by 1S,1R-ACPD was enhanced by low concentrations of NMDA (3-30 microM), but not by higher concentrations (> 30 microM). [3H]-InsPx accumulations stimulated by 1S,3R-ACPD in the absence or presence of 10 microM NMDA were linear with time, at least over the 15 min period examined; however, in the presence of 100 microM NMDA the initial enhancement of 1S,3R-ACPD-stimulated phosphoinositide hydrolysis progressively decreased with time. 4. In the presence of a maximal enhancing concentration of NMDA (10 microM), the response to 1S,3R-ACPD (300 microM) was increased 1.9 fold and the EC50 for agonist-stimulated [3H]-InsPx accumulation decreased about 4 fold. The enhanced response to the metabotropic agonist was concentration-dependently inhibited by competitive and uncompetitive antagonists of NMDA-receptor activation. 5. 1S,3R-ACPD also stimulated inositol 1,4,5-trisphosphate (Ins(1,4,5)P3) mass accumulation with an initial peak response (5-6 fold over basal) at 15 s decaying to a smaller (2 fold), but persistent elevated accumulation (1-10 min).(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在新生大鼠大脑皮层切片中检查了NMDA受体刺激对代谢型谷氨酸受体激动剂1-氨基环戊烷-1S,3R-二羧酸(1S,3R-ACPD)响应的磷酸肌醇信号的影响。 2.在[3H]-肌醇预标记的切片中,在5 mM LiCl存在下,[3H]-肌醇磷酸([3H] -InsPx)的总积累浓度依赖性地增加了1S,3R-ACPD(EC50 16.6 microM),并且在最大有效浓度下,1S,3R-ACPD(300 microM)使[3H] -InsPx积累比基础值增加了12.8倍。 3.低浓度的NMDA(3-30 microM)增强了1S,1R-ACPD刺激的[3H] -InsPx积累,但较高的浓度(> 30 microM)没有增强。在不存在或存在10 microM NMDA的情况下,由1S,3R-ACPD刺激的[3H] -InsPx积累至少在15分钟内与时间呈线性关系。但是,在存在100 microM NMDA的情况下,1S,3R-ACPD刺激的磷酸肌醇水解的初始增强随时间逐渐降低。 4.在最大浓度的NMDA(10 microM)存在下,对1S,3R-ACPD(300 microM)的响应增加1.9倍,激动剂刺激的[3H] -InsPx积聚的EC50降低约4倍。 。 NMDA受体激活的竞争性和非竞争性拮抗剂可浓度依赖性地抑制对代谢型激动剂的增强反应。 5. 1S,3R-ACPD还刺激了肌醇1,4,5-三磷酸(Ins(1,4,5)P3)质量积累,并在15 s时出现了初始峰值响应(比基础值高5-6倍),并逐渐减小(2折),但持续的累积积累(1-10分钟)。(摘要以250字截断)

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