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氟西汀对小龙虾运动轴突动作电位的抑制调节作用。

Inhibitory modulation of action potentials in crayfish motor axons by fluoxetine.

机构信息

Department of Biology, Boston University, Boston, Massachusetts, USA.

出版信息

Synapse. 2024 Jul;78(4):e22304. doi: 10.1002/syn.22304.

Abstract

The goal of this report is to explore how K2P channels modulate axonal excitability by using the crayfish ventral superficial flexor preparation. This preparation allows for simultaneous recording of motor nerve extracellular action potentials (eAP) and intracellular excitatory junctional potential (EJP) from a muscle fiber. Previous pharmacological studies have demonstrated the presence of K2P-like channels in crayfish. Fluoxetine (50 µM) was used to block K2P channels in this study. The blocker caused a gradual decline, and eventually complete block, of motor axon action potentials. At an intermediate stage of the block, when the peak-to-peak amplitude of eAP decreased to ∼60%-80% of the control value, the amplitude of the initial positive component of eAP declined at a faster rate than that of the negative peak representing sodium influx. Furthermore, the second positive peak following this sodium influx, which corresponds to the after-hyperpolarizing phase of intracellularly recorded action potentials (iAP), became larger during the intermediate stage of eAP block. Finally, EJP recorded simultaneously with eAP showed no change in amplitude, but did show a significant increase in synaptic delay. These changes in eAP shape and EJP delay are interpreted as the consequence of depolarized resting membrane potential after K2P channel block. In addition to providing insights to possible functions of K2P channels in unmyelinated axons, results presented here also serve as an example of how changes in eAP shape contain information that can be used to infer alterations in intracellular events. This type of eAP-iAP cross-inference is valuable for gaining mechanistic insights here and may also be applicable to other model systems.

摘要

本报告的目的是探讨 K2P 通道如何通过使用螯虾腹侧浅层屈肌制剂来调节轴突兴奋性。该制剂允许同时记录运动神经细胞外动作电位 (eAP) 和来自肌肉纤维的细胞内兴奋性突触后电位 (EJP)。先前的药理学研究表明,螯虾中存在 K2P 样通道。在本研究中,使用氟西汀 (50 µM) 阻断 K2P 通道。该阻断剂导致运动轴突动作电位逐渐下降,最终完全阻断。在阻断的中间阶段,当 eAP 的峰峰值幅度降低到对照值的 60%-80%时,eAP 的初始正相成分的幅度下降速度比代表钠离子内流的负峰更快。此外,在该钠离子内流之后的第二个正峰,对应于细胞内记录的动作电位 (iAP) 的超极化后相,在 eAP 阻断的中间阶段变得更大。最后,同时记录的 EJP 幅度没有变化,但突触延迟显著增加。eAP 形状和 EJP 延迟的这些变化解释为 K2P 通道阻断后去极化静息膜电位的结果。除了为未髓鞘化轴突中 K2P 通道的可能功能提供见解外,这里呈现的结果还作为 eAP 形状变化包含可用于推断细胞内事件改变的信息的示例。这种 eAP-iAP 交叉推断对于获得这里的机制见解是有价值的,并且也可能适用于其他模型系统。

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