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钙在运动神经末梢去极化-分泌偶联中的作用。

The role of calcium in depolarization-secretion coupling at the motor nerve terminal.

作者信息

Cooke J D, Okamoto K, Quastel D M

出版信息

J Physiol. 1973 Jan;228(2):459-97. doi: 10.1113/jphysiol.1973.sp010095.

DOI:10.1113/jphysiol.1973.sp010095
PMID:4346994
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1331306/
Abstract
  1. The relation between m.e.p.p. frequency (F) and [Ca] was studied at the mouse neuromuscular junction, at varied concentrations of K(+) and at nerve terminals depolarized by focal depolarization.2. Under all conditions the relation between log F and log [Ca] was sigmoid, with a maximum slope that increased with depolarization or raised [K(+)]. In addition, depolarization or raised K(+) caused a progressive shift of the sigmoid curve upward and to the left (to reduced log [Ca]) and increased the range over which log F could be altered by [Ca].3. Reduction of osmotic pressure changed the relation between log F and log [Ca] in the same way as increase of depolarization, while increase of osmotic pressure did the opposite.4. Raised [Mg] acted in two ways: (a) to shift the curve of log F vs. log [Ca] to the right and (b) to reduce maximum Delta log F/Delta log [Ca] without altering the range of log F sensitive to [Ca].5. The relation between log quantal content of e.p.p.s and log [Ca] was similar to that between log m.e.p.p. frequency and log [Ca].6. Individual nerve terminals varied in both Ca-dependent and Ca-independent fractions of log F; a large Ca-independent portion appears to be associated with a low Ca-dependent portion and vice versa. With large prolonged depolarization the Ca-independent portion was increased, apparently at the expense of the Ca-dependent portion.7. The results of all experiments were summarized in terms of parameters found by fitting the observed log release -log [Ca] curves to two theoretical equations, each derived on the basis of a model: (a) all-or-nothing activation of release probability by Ca-complex(es) and (b) graded activation of release probability by Ca complex(es).8. On the basis of the all-or-nothing model, from which follows alinear relation between F and amounts of Ca complex(es), the number of Ca(2+) atoms that ;cooperate' to mediate release appeared to increase progressively with presynaptic depolarization, to a value of 4 or more with a presynaptic action potential.9. On the basis of the graded activation model, which predicts an exponential relation between F and amount of Ca complex, the number of Ca(2+) atoms that combine with Ca receptor appears to be independent of presynaptic depolarization.10. Various models which could account for the data are discussed. It was concluded that all the data are consistent with a model in which:(i) quantal release probability is continuously graded with the amount of a simple Ca complex (CaX) inside the nerve terminal.(ii) Ca entry is governed by presynaptic membrane potential (increasing exponentially with depolarization) and by the amount of a Ca complex (Ca(2)Y) on or in the membrane.(iii) Mg(2+) competes with Ca(2+) at both receptors, X and Y.(iv) The internal Ca receptor X is also increased by presynaptic depolarization.
摘要
  1. 在小鼠神经肌肉接头处,研究了微小终板电位频率(F)与[Ca]之间的关系,实验采用了不同浓度的K(+)以及通过局部去极化使神经末梢去极化的条件。

  2. 在所有条件下,log F与log [Ca]之间的关系呈S形,最大斜率随去极化或升高的[K(+)]而增加。此外,去极化或升高的K(+)导致S形曲线逐渐向上和向左移动(至降低的log [Ca]),并增加了log F可被[Ca]改变的范围。

  3. 渗透压降低对log F与log [Ca]关系的影响与去极化增加相同,而渗透压增加则产生相反的效果。

  4. 升高的[Mg]有两种作用方式:(a)将log F与log [Ca]的曲线向右移动;(b)降低最大Δlog F/Δlog [Ca],而不改变对[Ca]敏感的log F范围。

  5. 终板电位的log量子含量与log [Ca]之间的关系类似于微小终板电位频率的log与log [Ca]之间的关系。

  6. 各个神经末梢在log F的钙依赖性和非钙依赖性部分均存在差异;较大的非钙依赖性部分似乎与较低的钙依赖性部分相关,反之亦然。长时间的大去极化会增加非钙依赖性部分,显然是以牺牲钙依赖性部分为代价。

  7. 通过将观察到的log释放-log [Ca]曲线拟合到两个理论方程所得到的参数,总结了所有实验结果,每个方程均基于一个模型推导得出:(a)钙复合物对释放概率的全或无激活;(b)钙复合物对释放概率的分级激活。

  8. 根据全或无模型(由此得出F与钙复合物量之间的线性关系),参与介导释放的Ca(2+)原子数量似乎随着突触前去极化而逐渐增加,在突触前动作电位时达到4个或更多。

  9. 根据分级激活模型(该模型预测F与钙复合物量之间呈指数关系),与钙受体结合的Ca(2+)原子数量似乎与突触前去极化无关。

  10. 讨论了各种能够解释这些数据的模型。得出的结论是,所有数据都与以下模型一致:

(i)量子释放概率随神经末梢内简单钙复合物(CaX)的量连续分级。

(ii)Ca的进入受突触前膜电位(随去极化呈指数增加)和膜上或膜内钙复合物(Ca(2)Y)量的控制。

(iii)Mg(2+)在受体X和Y处与Ca(2+)竞争。

(iv)突触前去极化也会增加内部钙受体X。

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本文引用的文献

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