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NMDA受体拮抗剂对大鼠内嗅皮层及培养的内嗅皮层神经元的兴奋作用。

Excitatory actions of NMDA receptor antagonists in rat entorhinal cortex and cultured entorhinal cortical neurons.

作者信息

Väisänen J, Lindén A M, Lakso M, Wong G, Heinemann U, Castrén E

机构信息

A.I. Virtanen Institute, University of Kuopio, Finland.

出版信息

Neuropsychopharmacology. 1999 Jul;21(1):137-46. doi: 10.1016/S0893-133X(99)00006-8.

Abstract

We have characterized excitatory effects of non-competitive NMDA receptor antagonists MK-801, PCP, and ketamine in the rat entorhinal cortex and in cultured primary entorhinal cortical neurons using expression of immediate early gene c-fos as an indicator. NMDA receptor antagonists produced a strong and dose-dependent increase in c-fos mRNA and protein expression confined to neurons in the layer III of the caudal entorhinal cortex. Induction of c-fos mRNA is delayed and it is inhibited by antipsychotic drugs. Cultured entorhinal neurons are killed by high doses of MK-801 and PCP but c-fos expression is not induced in these neurons indicating that this in vitro model does not fully replicate the in vivo effects of PCP-like drugs in the entorhinal cortex. Excitatory effects of the NMDA receptor antagonists may be connected with the psychotropic side effects of these drugs and might become a useful model system to investigate neurobiology of psychosis.

摘要

我们利用即刻早期基因c-fos的表达作为指标,在大鼠内嗅皮层及原代培养的内嗅皮层神经元中,对非竞争性NMDA受体拮抗剂MK-801、苯环己哌啶(PCP)和氯胺酮的兴奋作用进行了特征描述。NMDA受体拮抗剂使局限于尾侧内嗅皮层III层神经元的c-fos mRNA和蛋白表达呈强烈且剂量依赖性增加。c-fos mRNA的诱导延迟,且受抗精神病药物抑制。高剂量的MK-801和PCP可杀死培养的内嗅神经元,但这些神经元中未诱导出c-fos表达,这表明该体外模型不能完全复制PCP类药物在内嗅皮层的体内效应。NMDA受体拮抗剂的兴奋作用可能与这些药物的精神副作用有关,并且可能成为研究精神病神经生物学的有用模型系统。

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