Mori A, Takahashi T, Miyashita Y, Kasai H
Department of Physiology, Faculty of Medicine, University of Tokyo, Japan.
J Physiol. 1994 Apr 15;476(2):217-28. doi: 10.1113/jphysiol.1994.sp020125.
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.
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。