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苯甲脒抑制神经元和异源表达的小电导钙激活钾通道。

Benzamil inhibits neuronal and heterologously expressed small conductance Ca-activated K channels.

机构信息

Research Department of Neuroscience, Physiology and Pharmacology, University College London, London, UK; Kinases and Brain Development Laboratory, The Francis Crick Institute, London, UK.

Research Department of Neuroscience, Physiology and Pharmacology, University College London, London, UK; Neuromodulation of Cortical and Subcortical Circuits Laboratory, Fondazione Istituto Italiano di Tecnologia, Genova, Italy.

出版信息

Neuropharmacology. 2019 Nov 1;158:107738. doi: 10.1016/j.neuropharm.2019.107738. Epub 2019 Aug 20.

Abstract

Small conductance Ca-activated K (SK) channels are expressed throughout the soma and dendrites of pyramidal neurons in the neocortex and hippocampal formation, where they participate in the local regulation of membrane excitability and synaptic signals. Through their inter-play with Ca channels, SK channels regulate Ca influx triggered by back-propagating action potentials in dendrites. Inhibition of SK channels affects both the amplitude and duration of Ca transients, but the role of Ca clearance mechanisms and their link to SK channel activity has not been established. Here we report the effect of the Na/Ca exchanger (NCX) inhibitor benzamil on Ca extrusion and SK channels in the regulation of dendritic Ca signals. Benzamil increased the duration and amplitude of dendritic Ca transients elicited by back-propagating action potentials in hippocampal pyramidal neurons. This data is consistent with previous studies with SK channel blockers and suggests that benzamil inhibits SK channels in addition to the Na/Ca exchanger. Here we show that indeed both the neuronal SK-mediated I current and the currents mediated by heterologously expressed SK channels were inhibited by benzamil. The inhibition of recombinant SK channels was seen with different K concentration gradients, and was stronger at negative voltages. The suppression of SK channels by benzamil is consistent with previous findings on the modulation of Ca signals by SK channels in neurons. We additionally show that benzamil inhibits neuronal voltage-gated calcium currents. The results prompt a careful reassessment of the effects of benzamil on Ca transients in native systems, given the spectrum of ion channels and exchangers this compound targets within a similar range of concentrations.

摘要

小电导钙激活钾 (SK) 通道广泛表达于新皮质和海马结构中的锥体神经元的胞体和树突,在那里它们参与膜兴奋性和突触信号的局部调节。通过与钙通道的相互作用,SK 通道调节由树突中的逆行动作电位触发的钙内流。SK 通道的抑制作用会影响 Ca 瞬变的幅度和持续时间,但 Ca 清除机制的作用及其与 SK 通道活性的联系尚未确定。本文报道了 Na/Ca 交换器 (NCX) 抑制剂苯甲脒对调节树突 Ca 信号的 SK 通道和 Ca 外排的影响。苯甲脒增加了海马锥体神经元中逆行动作电位引发的树突 Ca 瞬变的持续时间和幅度。这一数据与之前使用 SK 通道阻滞剂的研究结果一致,表明苯甲脒除了抑制 Na/Ca 交换器外,还抑制 SK 通道。本文显示,神经元 SK 介导的 I 电流和异源表达的 SK 通道介导的电流确实都被苯甲脒抑制。不同的 K 浓度梯度下均可观察到重组 SK 通道的抑制,而在负电压下抑制作用更强。苯甲脒对 SK 通道的抑制作用与之前关于 SK 通道对神经元 Ca 信号的调制的研究结果一致。我们还表明,苯甲脒抑制神经元电压门控钙电流。鉴于该化合物在类似浓度范围内针对的离子通道和交换器的范围,因此需要仔细重新评估苯甲脒对天然系统中 Ca 瞬变的影响。

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