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兴奋性氨基酸对纹状体神经元中肌醇磷酸代谢的双重作用。

Dual action of excitatory amino acids on the metabolism of inositol phosphates in striatal neurons.

作者信息

Schmidt B H, Weiss S, Sebben M, Kemp D E, Bockaert J, Sladeczek F

机构信息

Centre CNRS-INSERM de Pharmacologie-Endocrinologie, Montpellier, France.

出版信息

Mol Pharmacol. 1987 Sep;32(3):364-8.

PMID:2890092
Abstract

Glutamate is able to stimulate inositol phosphate (IP) formation in striatal neurons in primary culture, mainly via an excitatory amino acid receptor of the quisqualate subtype. In the present study we show that carbachol (Carb)-(a cholinergic agonist), but not neurotensin or norepinephrine-induced IP production could be reduced by 40% when measured in the presence of Glu. The inhibition of the Carb response by Glu was dose dependent and reproduced by N-methyl-D-aspartate (NMDA). Quisqualate elicited an additive response with Carb. 2-Amino-5-phosphonovalerate (APV) completely reversed the NMDA-induced inhibition. APV had no significant effect on Glu- or kainate-induced inhibition. Therefore, striatal neurons contain at least three different excitatory amino acid receptors: a quisqualate receptor triggering the stimulation of IP metabolism, and an NMDA and a kainate receptor, both able to decrease the Carb-induced IP formation.

摘要

谷氨酸能够刺激原代培养的纹状体神经元中肌醇磷酸(IP)的生成,主要是通过quisqualate亚型的兴奋性氨基酸受体。在本研究中,我们发现,当在谷氨酸存在的情况下进行测量时,卡巴胆碱(Carb)(一种胆碱能激动剂)诱导的IP生成,而非神经降压素或去甲肾上腺素诱导的IP生成,可减少40%。谷氨酸对卡巴胆碱反应的抑制呈剂量依赖性,且N-甲基-D-天冬氨酸(NMDA)可重现这种抑制作用。quisqualate与卡巴胆碱引发相加反应。2-氨基-5-磷酸戊酸(APV)完全逆转了NMDA诱导的抑制作用。APV对谷氨酸或海人藻酸诱导的抑制作用无显著影响。因此,纹状体神经元至少含有三种不同的兴奋性氨基酸受体:一种触发IP代谢刺激的quisqualate受体,以及一种NMDA受体和一种海人藻酸受体,这两种受体均能够减少卡巴胆碱诱导的IP生成。

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