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与突触前轴突传导阻滞相关的突触抑制

Synaptic depression related to presynaptic axon conduction block.

作者信息

Hatt H, Smith D O

出版信息

J Physiol. 1976 Jul;259(2):367-93. doi: 10.1113/jphysiol.1976.sp011471.

Abstract
  1. The depression of synaptic transmission, which occurs during prolonged repetitive activation, was examined in the opener muscle of the crayfish walking leg. 2. Excitatory post-synaptic potentials (e.p.s.p.s) initially facilitated but then declined to low amplitudes after about 4000 stimulus pulses had been delivered; this depression is presynaptic in origin; 3. Axon conduction blocks occured at points of bifurcation along the entire length of the presynaptic nerve. This resulted in failure of the nerve impulse to invade some branches of the terminal arborization. 4. Nerve terminal invasion failure caused either intermittent or complete inactiviation of some synaptic release sites; this was associated with depression of the post-synaptic response. 5. The statistics of transmitter release during prolonged repetitive stimulation were examined by focal extracellular recording methods. Transmitter release could be described by binomial statistics, and depression involved a drop in m, n and p. 6. The rate of spontaneous quantal release did not decrease, however, arguing against transmitter depletion. 7. It is concluded that repetitive stimulation eventually leads to depolarization of the axon membrane. This causes impulse propagation failure which reduces the number of synaptic release sites that are activated and mimics a drop in the effective stimulation rate; both effects cause synaptic depression.
摘要
  1. 在小龙虾步行腿的开肌中,研究了长时间重复激活期间发生的突触传递抑制。2. 兴奋性突触后电位(e.p.s.p.s)最初增强,但在传递约4000个刺激脉冲后降至低幅度;这种抑制起源于突触前;3. 轴突传导阻滞发生在突触前神经全长的分支点处。这导致神经冲动无法侵入终末分支的一些分支。4. 神经终末侵入失败导致一些突触释放位点间歇性或完全失活;这与突触后反应的抑制有关。5. 通过局部细胞外记录方法研究了长时间重复刺激期间递质释放的统计学。递质释放可用二项式统计学描述,抑制涉及m、n和p的下降。6. 然而,自发量子释放率并未降低,这与递质耗竭的观点相悖。7. 得出的结论是,重复刺激最终导致轴突膜去极化。这导致冲动传播失败,减少了被激活的突触释放位点的数量,并模拟有效刺激率的下降;这两种效应都导致突触抑制。

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