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氯异吲哚铵对甲壳类动物肌肉中胆碱能通道的阻断作用。

Blockade of cholinergic channels by chlorisondamine on a crustacean muscle.

作者信息

Lingle C

出版信息

J Physiol. 1983 Jun;339:395-417. doi: 10.1113/jphysiol.1983.sp014723.

Abstract

Details of the blocking action of chlorisondamine, a ganglionic nicotinic blocker, on the excitatory cholinergic currents of the spiny lobster gastric mill 1 (g.m.1) muscle are described. The steady-state block of cholinergic ionophoretic currents produced by chlorisondamine is strongly voltage-dependent. During a hyperpolarizing voltage step, a sequence of ionophoretic agonist pulses in the presence of chlorisondamine shows a large interpulse interaction manifested as a gradual diminution in response amplitude. The extent of diminution is dependent on the number of the pulse in a series and not on the duration of the interval between pulses. The slowly developing blockade is entirely dependent on agonist application. If agonist application is suspended for various time intervals following the development of a given blocked level in chlorisondamine, no recovery from the block is observed whether the rest interval is at the step potential or at more depolarized potentials. Recovery from a given blocked level can be observed if, during a depolarizing voltage step (to -60 mV) away from the potential at which the block was established (-140 mV), agonist is applied before return to the initial potential (-140 mV). Chlorisondamine produces a dose-dependent reduction in excitatory junctional current (e.j.c.) decay rate that is linear with chlorisondamine concentration and markedly dependent on voltage (approximately equal to 35 mV/e-fold change). Reduction in the amplitude of e.j.c.s occurred at concentrations of chlorisondamine that produced no detectable effect on e.j.c. decay. Alterations in e.j.c. amplitude showed time- and use-dependent aspects similar to those observed for ionophoretic currents. These results are discussed primarily in terms of a sequential model in which, following the binding of chlorisondamine to the opened ion channel, the channel can undergo a transition to a stable-blocked state that requires reactivation by agonist to become unblocked. This stable-blocked state is considered a closed-blocked channel.

摘要

本文描述了神经节烟碱阻滞剂氯异吲哚铵对刺龙虾胃磨1(g.m.1)肌肉兴奋性胆碱能电流的阻断作用细节。氯异吲哚铵产生的胆碱能离子电泳电流的稳态阻断具有强烈的电压依赖性。在超极化电压阶跃期间,在氯异吲哚铵存在下的一系列离子电泳激动剂脉冲显示出较大的脉冲间相互作用,表现为反应幅度逐渐减小。减小的程度取决于系列脉冲的数量,而不取决于脉冲之间间隔的持续时间。缓慢发展的阻断完全依赖于激动剂的应用。如果在氯异吲哚铵达到给定阻断水平后,将激动剂应用暂停不同的时间间隔,无论静息间隔是在阶跃电位还是在更去极化的电位,都观察不到阻断的恢复。如果在从建立阻断的电位(-140 mV)进行去极化电压阶跃(至-60 mV)期间,在回到初始电位(-140 mV)之前应用激动剂,则可以观察到从给定阻断水平的恢复。氯异吲哚铵使兴奋性接头电流(e.j.c.)衰减率呈剂量依赖性降低,该降低与氯异吲哚铵浓度呈线性关系,并且明显依赖于电压(约等于35 mV/ e倍变化)。在对e.j.c.衰减没有可检测到影响的氯异吲哚铵浓度下,e.j.c.s的幅度出现了降低。e.j.c.幅度的变化表现出与离子电泳电流观察到的类似的时间和使用依赖性方面。这些结果主要根据一个顺序模型进行讨论,在该模型中,氯异吲哚铵与开放的离子通道结合后,通道可以转变为稳定阻断状态,该状态需要激动剂重新激活才能解除阻断。这种稳定阻断状态被认为是一个封闭的阻断通道。

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