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在青蛙神经肌肉接头处存在掩盖性抑制的情况下,增强作用会增加囊泡释放概率。

Augmentation increases vesicular release probability in the presence of masking depression at the frog neuromuscular junction.

作者信息

Kalkstein Jonathan M, Magleby Karl L

机构信息

Department of Physiology and Biophysics and Neuroscience Program, University of Miami School of Medicine, Miami, Florida 33136, USA.

出版信息

J Neurosci. 2004 Dec 15;24(50):11391-403. doi: 10.1523/JNEUROSCI.2756-04.2004.

Abstract

Synaptic augmentation is a short-term component of synaptic plasticity that increases transmitter release during repetitive stimulation and decays thereafter with a time constant of approximately 7 sec. Augmentation has typically been observed under conditions where there is little or no depression because of depletion of synaptic vesicles from the readily releasable pool (RRP) of transmitter. We now study augmentation under conditions of pronounced depression at the frog neuromuscular junction to gain additional insight into mechanism. If augmentation reflects an increase in the size of the RRP of transmitter, then augmentation should not be present with depression. Our findings using four different experimental approaches suggested that augmentation was still present in the presence of pronounced depression: mathematical extraction of augmentation from the changes in transmitter release after repetitive stimulation, identification of augmentation with Ba2+, correction of the data for the measured depletion of the RRP, and identification of an augmentation component of residual Ca2+. We conclude that the augmentation machinery still acts to increase transmitter release when depression reduces the RRP sufficiently to mask obvious augmentation. The masked augmentation was found to increase transmitter release by increasing the probability of releasing individual vesicles from the depressed RRP, countering the effects of depression. Because augmentation and depression have similar time courses, either process can mask the other, depending on their relative magnitudes. Consequently, the apparent absence of one of the processes does not exclude that it is still contributing to short-term synaptic plasticity.

摘要

突触增强是突触可塑性的一个短期组成部分,在重复刺激期间会增加递质释放,之后以约7秒的时间常数衰减。增强现象通常在由于递质的易释放池(RRP)中突触小泡耗尽而几乎没有或没有抑制的条件下观察到。我们现在在青蛙神经肌肉接头处明显抑制的条件下研究增强现象,以进一步深入了解其机制。如果增强反映了递质RRP大小的增加,那么在存在抑制的情况下就不应出现增强。我们使用四种不同实验方法的研究结果表明,在明显抑制的情况下增强现象仍然存在:从重复刺激后递质释放的变化中数学提取增强,用Ba2+鉴定增强,对RRP测量耗尽的数据进行校正,以及鉴定残余Ca2+的增强成分。我们得出结论,当抑制充分降低RRP以掩盖明显的增强时,增强机制仍会增加递质释放。发现被掩盖的增强通过增加从受抑制的RRP中释放单个小泡的概率来增加递质释放,从而抵消抑制的影响。由于增强和抑制具有相似的时间进程,这两个过程中的任何一个都可以掩盖另一个,这取决于它们的相对大小。因此,一个过程看似不存在并不排除它仍在对短期突触可塑性起作用。

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