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新生大鼠纹状体中等棘状神经元的两种不同谷氨酸能突触输入与双脉冲抑制

Two distinct glutamatergic synaptic inputs to striatal medium spiny neurones of neonatal rats and paired-pulse depression.

作者信息

Mori A, Takahashi T, Miyashita Y, Kasai H

机构信息

Department of Physiology, Faculty of Medicine, University of Tokyo, Japan.

出版信息

J Physiol. 1994 Apr 15;476(2):217-28. doi: 10.1113/jphysiol.1994.sp020125.

Abstract

Excitatory postsynaptic currents (EPSCs) were recorded from the medium spiny neurones of neonatal rat striatal slices using the whole-cell patch clamp method. EPSCs were selectively elicited in the presence of picrotoxin with a glass stimulating pipette placed in the striatum. We found two distinct unitary EPSCs that were evoked by stimulation of single presynaptic fibres. The major type of EPSC, termed 'S-type', failed frequently and had a small mean amplitude (2.05 pA). They probably represented cortical afferents. The other type of unitary EPSC, the 'H-type', seldom failed and was 13 times larger than the S-type. Spontaneous EPSCs with amplitudes similar to those of H-type EPSCs could be induced. H-type EPSCs were mediated by both non-NMDA and NMDA receptors. The two types of EPSCs could be evoked in the same neurons. The intensity of stimulation for H-type EPSCs was higher than that for S-type EPSCs. H-type EPSCs could be polysynaptically activated, suggesting the presence of glutamatergic interneurones in the striatum that generated H-type EPSCs. H-type EPSCs displayed particularly long-lasting paired-pulse depression, while that displayed by the S-type EPSCs was short. The paired-pulse depression of both EPSCs was Ca2+ dependent and involved presynaptic mechanisms. We have demonstrated that the medium spiny neurones of neonatal rats receive two different glutamatergic input systems having different amplitudes, origins and paired-pulse depression, reminiscent of cerebellar Purkinje cells. This suggests that the two types of EPSCs also play distinctive roles in striatal neuronal circuitry.

摘要

采用全细胞膜片钳方法,从新生大鼠纹状体切片的中等棘状神经元记录兴奋性突触后电流(EPSCs)。在存在苦味毒的情况下,用置于纹状体的玻璃刺激微电极选择性地诱发EPSCs。我们发现刺激单个突触前纤维可诱发两种不同的单位EPSCs。主要类型的EPSC,称为“S型”,经常失败且平均幅度较小(2.05 pA)。它们可能代表皮质传入纤维。另一种单位EPSC类型,“H型”,很少失败,比S型大13倍。可以诱导出幅度与H型EPSCs相似的自发性EPSCs。H型EPSCs由非NMDA和NMDA受体介导。两种类型的EPSCs可在同一神经元中诱发。H型EPSCs的刺激强度高于S型EPSCs。H型EPSCs可通过多突触激活,提示纹状体中存在产生H型EPSCs的谷氨酸能中间神经元。H型EPSCs表现出特别持久的双脉冲抑制,而S型EPSCs表现出的双脉冲抑制则较短。两种EPSCs的双脉冲抑制均依赖于Ca2+,且涉及突触前机制。我们已经证明,新生大鼠的中等棘状神经元接受两种不同的谷氨酸能输入系统,它们具有不同的幅度、起源和双脉冲抑制,这让人联想到小脑浦肯野细胞。这表明这两种类型的EPSCs在纹状体神经元回路中也发挥着独特的作用。

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