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单电极电压钳的设计

Design of a single electrode voltage clamp.

作者信息

Merickel M

出版信息

J Neurosci Methods. 1980 Feb;2(1):87-96. doi: 10.1016/0165-0270(80)90047-3.

Abstract

The detailed schematic diagrams and construction techniques are presented for a single microelectrode voltage clamp. The devices is used to study the membrane processes of small cells not able to be penetrated with the traditional two microelectrode system. The technique utilizes the same microelectrode alternately for current injection and membrane potential sampling on a time-sharing basis controlled by electronic switching circuitry. Current is injected in pulses and the membrane potential is sampled after an individual current pulse discharges from the microelectrode capacitance to the true membrane potential. The device can either measure the voltage response to an injected current waveform (current injection mode) or the membrane currents generated during a controlled change in membrane potential (voltage clamp mode). In voltage clamp mode, the membrane potential reaches steady-state within 2 msec (maximum time) in response to a 40 mV step command. The single electrode voltage clamp is potentially very important to the investigation of slow current processes within electrically excitable cells too small to be previously studied with traditional voltage clamp technology.

摘要

本文介绍了单微电极电压钳的详细示意图和构建技术。该装置用于研究传统双微电极系统无法穿透的小细胞的膜过程。该技术利用同一个微电极,在电子开关电路控制的分时基础上交替进行电流注入和膜电位采样。电流以脉冲形式注入,在单个电流脉冲从微电极电容放电到真实膜电位后对膜电位进行采样。该装置既可以测量对注入电流波形的电压响应(电流注入模式),也可以测量在膜电位受控变化期间产生的膜电流(电压钳模式)。在电压钳模式下,响应40 mV阶跃指令,膜电位在2毫秒(最长时间)内达到稳态。单电极电压钳对于研究电兴奋性细胞内的缓慢电流过程可能非常重要,这些细胞太小,以前无法用传统电压钳技术进行研究。

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