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Direct demonstration of persistent Na+ channel activity in dendritic processes of mammalian cortical neurones

机译:在哺乳动物皮质神经元的树突状过程中直接显示持续的Na +通道活性

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摘要

class="enumerated" style="list-style-type:decimal">Single Na+ channel activity was recorded in patch-clamp, cell-attached experiments performed on dendritic processes of acutely isolated principal neurones from rat entorhinal-cortex layer II. The distances of the recording sites from the soma ranged from ≈20 to ≈100 μm.Step depolarisations from holding potentials of −120 to −100 mV to test potentials of −60 to +10 mV elicited Na+ channel openings in all of the recorded patches (n= 16).In 10 patches, besides transient Na+ channel openings clustered within the first few milliseconds of the depolarising pulses, prolonged and/or late Na+ channel openings were also regularly observed. This ‘persistent’ Na+ channel activity produced net inward, persistent currents in ensemble-average traces, and remained stable over the entire duration of the experiments (≈9 to 30 min).Two of these patches contained <= 3 channels. In these cases, persistent Na+ channel openings could be attributed to the activity of one single channel.The voltage dependence of persistent-current amplitude in ensemble-average traces closely resembled that of whole-cell, persistent Na+ current expressed by the same neurones, and displayed the same characteristic low threshold of activation.Dendritic, persistent Na+ channel openings had relatively high single-channel conductance (≈20 pS), similar to what is observed for somatic, persistent Na+ channels.We conclude that a stable, persistent Na+ channel activity is expressed by proximal dendrites of entorhinal-cortex layer II principal neurones, and can contribute a significant low-threshold, persistent Na+ current to the dendritic processing of excitatory synaptic inputs.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 在从大鼠内嗅皮层II急性分离的主要神经元的树突过程中进行的膜片钳,细胞附着实验中记录了单个Na + 通道活性。记录部位距躯体的距离在≈20至≈100μm之间。 阶跃去极化从-120至-100 mV的保持电势到−60至+10 mV的测试电势引起的Na <所有记录的色块中都有sup> + 通道开口(n = 16)。 在10个色块中,除了前几个簇内的瞬态Na + 通道开口以外还定期观察到毫秒级的去极化脉冲,延长的和/或较晚的Na + 通道开口。这种“持续的” Na + 通道活动在整体平均迹线中产生净内向,持续的电流,并在整个实验过程中(约9至30分钟)保持稳定。 < li>其中两个补丁包含<= 3个频道。在这种情况下,持续的Na + 通道开口可能归因于单个通道的活动。 整体平均迹线中持续电流幅度的电压依赖性与之相似,即相同神经元表达的全细胞持久性Na + 电流,并表现出相同的特征性低激活阈值。 树突状持久性Na + 通道开口具有相对较高的单通道电导(≈20pS),类似于在体细胞,持久性Na + 通道中观察到的情况。 我们得出的结论是,稳定,持久Na + 通道的活性由内嗅皮质第二层主要神经元的近端树突表达,并且可以为低密度,持续性Na + 电流贡献显着的树突状过程。兴奋性突触输入。

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