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A 型钾通道阻碍了 3 层新皮层锥体神经元中聚集谷氨酸能输入的超线性总和。

A-type K channels impede supralinear summation of clustered glutamatergic inputs in layer 3 neocortical pyramidal neurons.

机构信息

UCL School of Pharmacy, Brunswick Square, London WC1N 1AX, United Kingdom.

UCL School of Pharmacy, Brunswick Square, London WC1N 1AX, United Kingdom.

出版信息

Neuropharmacology. 2018 Sep 15;140:86-99. doi: 10.1016/j.neuropharm.2018.07.005. Epub 2018 Jul 6.

Abstract

A-type K channels restrain the spread of incoming signals in tufted and apical dendrites of pyramidal neurons resulting in strong compartmentalization. However, the exact subunit composition and functional significance of K channels expressed in small diameter proximal dendrites remain poorly understood. We focus on A-type K channels expressed in basal and oblique dendrites of cortical layer 3 pyramidal neurons, in ex vivo brain slices from young adult mice. Blocking putative Kv4 subunits with phrixotoxin-2 enhances depolarizing potentials elicited by uncaging RuBi-glutamate at single dendritic spines. A concentration of 4-aminopyridine reported to block Kv1 has no effect on such responses. 4-aminopyridine and phrixotoxin-2 increase supralinear summation of glutamatergic potentials evoked by synchronous activation of clustered spines. The effect of 4-aminopyridine on glutamate responses is simulated in a computational model where the dendritic A-type conductance is distributed homogeneously or in a linear density gradient. Thus, putative Kv4-containing channels depress excitatory inputs at single synapses. The additional recruitment of Kv1 subunits might require the synchronous activation of multiple inputs to regulate the gain of signal integration.

摘要

A 型钾通道抑制传入信号在锥形神经元树突和顶树突中的传播,从而导致强烈的区室化。然而,在小直径近端树突中表达的 K 通道的确切亚基组成和功能意义仍知之甚少。我们关注的是在年轻成年小鼠的体外脑片中表达的皮质第 3 层锥形神经元的基底和斜形树突中的 A 型 K 通道。用 phrixotoxin-2 阻断假定的 Kv4 亚基可增强 RuBi-谷氨酸在单个树突棘上光解时产生的去极化电位。据报道,4-氨基吡啶可阻断 Kv1 的浓度对这种反应没有影响。4-氨基吡啶和 phrixotoxin-2 增加了同步激活簇状棘突引起的谷氨酸能电位的超线性总和。在一个计算模型中模拟了 4-氨基吡啶对谷氨酸反应的影响,其中树突 A 型电导均匀分布或呈线性密度梯度分布。因此,假定包含 Kv4 的通道会抑制单个突触处的兴奋性输入。Kv1 亚基的额外募集可能需要多个输入的同步激活来调节信号整合的增益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a580/6137074/a4a6fb4b0051/egi105JXBV812F.jpg

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