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深小脑核神经元反弹刺发放电中明显短程和长程成分的分析。

Analysis of distinct short and prolonged components in rebound spiking of deep cerebellar nucleus neurons.

机构信息

Department of Biology, Emory University, Atlanta, GA, USA.

出版信息

Eur J Neurosci. 2010 Nov;32(10):1646-57. doi: 10.1111/j.1460-9568.2010.07408.x. Epub 2010 Oct 8.

Abstract

Deep cerebellar nucleus (DCN) neurons show pronounced post-hyperpolarization rebound burst behavior, which may contribute significantly to responses to strong inhibitory inputs from cerebellar cortical Purkinje cells. Thus, rebound behavior could importantly shape the output from the cerebellum. We used whole-cell recordings in brain slices to characterize DCN rebound properties and their dependence on hyperpolarization duration and depth. We found that DCN rebounds showed distinct fast and prolonged components, with different stimulus dependence and different underlying currents. The initial depolarization leading into rebound spiking was carried by hyperpolarization-activated cyclic nucleotide-gated current, and variable expression of this current could lead to a control of rebound latency. The ensuing fast rebound burst was due to T-type calcium current, as previously described. It was highly variable between cells in strength, and could be expressed fully after short periods of hyperpolarization. In contrast, a subsequent prolonged rebound component required longer and deeper periods of hyperpolarization before it was fully established. We found using voltage-clamp and dynamic-clamp analyses that a slowly inactivating persistent sodium current fits the conductance underlying this prolonged rebound component, resulting in spike rate increases over several seconds. Overall, our results demonstrate that multiphasic DCN rebound properties could be elicited differentially by different levels of Purkinje cell activation, and thus create a rich repertoire of potential rebound dynamics in the cerebellar control of motor timing.

摘要

小脑深部核(DCN)神经元表现出明显的超极化后复发性爆发行为,这可能对来自小脑皮质浦肯野细胞的强抑制性输入的反应有重要贡献。因此,复发性行为可能会重要地塑造小脑的输出。我们使用脑切片中的全细胞记录来描述 DCN 复发性特征及其对超极化持续时间和深度的依赖性。我们发现 DCN 复发性表现出明显的快速和持续成分,具有不同的刺激依赖性和不同的潜在电流。导致复发性尖峰进入的初始去极化是由超极化激活环核苷酸门控电流携带的,并且这种电流的可变表达可能导致复发性潜伏期的控制。随后的快速复发性爆发归因于 T 型钙电流,如前所述。它在细胞之间的强度上差异很大,并且可以在短时间的超极化后完全表达。相比之下,随后的持续时间较长的复发性成分需要更长和更深的超极化期才能完全建立。我们通过电压箝位和动态箝位分析发现,一种缓慢失活的持续钠电流适合于该持续复发性成分的基础电导,从而导致在几秒钟内增加尖峰率。总体而言,我们的结果表明,不同水平的浦肯野细胞激活可以引发多相 DCN 复发性特征,从而在小脑对运动定时的控制中产生丰富的潜在复发性动力学。

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