Synaptic and cellular properties of the feedforward inhibitory circuit within the input layer of the cerebellar cortex.

Synaptic and cellular properties of the feedforward inhibitory circuit within the input layer of the cerebellar cortex.
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DOI:
10.1523/jneurosci.5469-07.2008
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发表时间:
2008-09-03
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
通讯作者:
Silver RA
Silver RA
中科院分区:
其他
文献类型:
--
作者:
Kanichay RT;Silver RA

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Precise representation of the timing of sensory stimuli is essential for rapid motor coordination, a core function of the cerebellum. Feed-forward inhibition has been implicated in precise temporal signalling in several regions of the brain, but little is known about this type of inhibitory circuit within the input layer of the cerebellar cortex. We have investigated the synaptic properties of feed-forward inhibition at near physiological temperatures (35°C) in rat cerebellar slices. We establish that the previously uncharacterized mossy fibre–Golgi cell–granule cell pathway can act as a functional feed-forward inhibitory circuit. The synchronous activation of 4 mossy fibres, releasing a total of 6 quanta onto a Golgi cell, can reset spontaneous Golgi cell firing with high temporal precision (200μs). However, only modest increases in Golgi cell firing rate were observed during trains of high frequency mossy fibre stimulation. This decoupling of Golgi cell activity from mossy fibre firing rate was due to a strong after-hyperpolarization following each action potential, preventing mossy fibre–Golgi cell signalling for ~50 ms. Feed-forward excitation of Golgi cells induced a temporally precise inhibitory conductance in granule cells that curtailed the excitatory action of the mossy fibre EPSC. The synaptic and cellular properties of this feed-forward circuit appear tuned to trigger a fast inhibitory conductance in granule cells at the onset of stimuli that produce intense bursts of activity in multiple mossy fibres, thereby conserving the temporal precision of the initial granule cell response.