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两种不同的使君子氨酸受体在体外调节海马神经元中的钙离子稳态。

Two distinct quisqualate receptors regulate Ca2+ homeostasis in hippocampal neurons in vitro.

作者信息

Murphy S N, Miller R J

机构信息

Department of Pharmacological and Physiological Sciences, University of Chicago, Illinois 60637.

出版信息

Mol Pharmacol. 1989 May;35(5):671-80.

PMID:2566904
Abstract

Addition of quisqualate to mouse hippocampal neurons in vitro elicited two types of changes in [Ca2+]i as assessed by fura-2-based microfluorimetry. The first was a transient spike or group of oscillations and the second was a long lasting "plateau" response. The long-lasting response was abolished on removal of either Ca2+ or Na+ from the external medium or by blocking voltage-sensitive Ca2+ channels. Furthermore, the novel glutamate antagonist 6-nitro-7-cyano-quinoxaline-2,3-dione was a competitive inhibitor of this response. In contrast, none of these manipulations abolished the transient [Ca2+]i spike. Transient [Ca2+]i spikes or oscillations could also be produced by the alpha 1-adrenergic agonist phenylephrine. Production of such an alpha 1-response reduced the size of a subsequently elicited quisqualate response. However production of transient [Ca2+]i spikes with caffeine did not alter the size of the quisqualate-induced spike. We conclude that hippocampal neurons possess two different types of quisqualate receptors. The first mediates quisqualate-induced depolarization and the second mediates Ca2+ mobilization from intracellular stores.

摘要

在体外向小鼠海马神经元添加喹啉酸后,通过基于fura - 2的显微荧光测定法评估,[Ca2+]i出现了两种变化。第一种是短暂的尖峰或一组振荡,第二种是持久的“平台”反应。当从外部培养基中去除Ca2+或Na+或通过阻断电压敏感性Ca2+通道时,这种持久反应就会消失。此外,新型谷氨酸拮抗剂6 - 硝基 - 7 - 氰基 - 喹喔啉 - 2,3 - 二酮是这种反应的竞争性抑制剂。相比之下,这些操作均未消除短暂的[Ca2+]i尖峰。α1 - 肾上腺素能激动剂去氧肾上腺素也可产生短暂的[Ca2+]i尖峰或振荡。这种α1反应的产生会减小随后引发的喹啉酸反应的大小。然而,用咖啡因产生短暂的[Ca2+]i尖峰并不会改变喹啉酸诱导的尖峰大小。我们得出结论,海马神经元拥有两种不同类型的喹啉酸受体。第一种介导喹啉酸诱导的去极化,第二种介导从细胞内储存库中动员Ca2+。

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