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青蛙神经肌肉接头处自发和诱发量子释放的钙依赖性。

The calcium dependence of spontaneous and evoked quantal release at the frog neuromuscular junction.

作者信息

Barton S B, Cohen I S, van der Kloot W

出版信息

J Physiol. 1983 Apr;337:735-51. doi: 10.1113/jphysiol.1983.sp014652.

Abstract
  1. The quantal output from stimulated nerve terminals in the frog sciatic nerve-sartorius muscle preparation in low-Ca(2+) Ringer solution was measured by the coefficient of variation and the failures methods. Adding sucrose to the Ringer to increase the tonicity or adding ethanol increased miniature end-plate potential (m.e.p.p.) frequency and also the end-plate potential (e.p.p.) amplitude. Earlier reports suggested that increases in tonicity did not increase evoked quantal release.2. Concanavalin A has been reported to block the increase in m.e.p.p. frequency caused by increasing the tonicity of the Ringer (Gorio & Mauro, 1979). This effect was confirmed. The lectin-treated preparations also failed to show an increase in evoked quantal release when the tonicity was increased.3. A model in which both spontaneous and evoked quantal releases depend on some power of the intracellular [Ca(2+)] is presented. The model predicts that rises in m.e.p.p. frequency will be accompanied by increased quantal output from stimulated nerve terminals. The maximum slope of the relationship between log (evoked quantal output) and log (Ca(2+)) will be less than the true power. A theoretical analysis shows that, as the true power approaches infinity, the maximum slope will be slightly above 4. The value for the slope usually found experimentally at the frog neuromuscular junction is also about 4.4. The model does not fit the experimental data. The observed increases in evoked quantal release are higher than those predicted for the observed increases in spontaneous release. There are several possible explanations for the discrepancy. Treatments that increase m.e.p.p. frequency may also increase Ca(2+) influx into the stimulated terminal. However, we prefer the explanation that there is a fraction of spontaneous release that is independent of the [Ca(2+)] in the terminal; if this is true the model might account for the data.5. The model can account for a variety of puzzling experimental observations, including: (a) the effect of hypertonic solutions and of diamine in decreasing the slope in the relation between log (evoked quantal output) and log (Ca(2+)); (b) the slope of near 1 observed at the crustacean neuromuscular junction; (c) the decrease in the slope produced by treatment with botulinum toxin.
摘要
  1. 在低钙任氏液中,采用变异系数法和失败率法测定了蛙坐骨神经 - 缝匠肌标本中受刺激神经末梢的量子释放量。向任氏液中添加蔗糖以增加张力或添加乙醇可增加微小终板电位(m.e.p.p.)频率以及终板电位(e.p.p.)幅度。早期报告表明,张力增加并不会增加诱发的量子释放。

  2. 据报道,伴刀豆球蛋白A可阻断因任氏液张力增加而导致的m.e.p.p.频率增加(戈里奥和毛罗,1979年)。这一效应得到了证实。经凝集素处理的标本在张力增加时也未表现出诱发量子释放的增加。

  3. 提出了一个模型,其中自发和诱发的量子释放均取决于细胞内[Ca(2+)]的某种幂次。该模型预测,m.e.p.p.频率的升高将伴随着受刺激神经末梢量子释放量的增加。log(诱发量子释放量)与log(Ca(2+))之间关系的最大斜率将小于真实幂次。理论分析表明,当真实幂次趋近于无穷大时,最大斜率将略高于4。在蛙神经肌肉接头处实验中通常发现的斜率值也约为4。

  4. 该模型与实验数据不符。观察到的诱发量子释放增加高于根据自发释放增加所预测的值。对于这种差异有几种可能的解释。增加m.e.p.p.频率的处理可能也会增加Ca(2+)流入受刺激的末梢。然而,我们更倾向于这样的解释,即存在一部分自发释放与末梢中的[Ca(2+)]无关;如果这是真的,该模型或许可以解释这些数据。

  5. 该模型可以解释各种令人困惑的实验观察结果,包括:(a)高渗溶液和二胺对log(诱发量子释放量)与log(Ca(2+))之间关系斜率的降低作用;(b)在甲壳类神经肌肉接头处观察到的接近1的斜率;(c)肉毒杆菌毒素处理导致的斜率降低。

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