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哺乳动物神经肌肉接头处递质释放中钠离子与钙离子之间的竞争。

Competition between sodium and calcium ions in transmitter release at mammalian neuromuscular junctions.

作者信息

Gage P W, Quastel D M

出版信息

J Physiol. 1966 Jul;185(1):95-123. doi: 10.1113/jphysiol.1966.sp007974.

Abstract
  1. Frequencies of miniature end-plate potentials (m.e.p.p.s) were recorded at neuromuscular junctions in rat diaphragm-phrenic nerve preparations in vitro.2. In the presence of raised [K] (15-20 mM) lowering [Na] caused a rapid increase in m.e.p.p. frequency whether [Ca] was low or normal. Raising [Na] towards the normal concentration (162 mM) caused a slow fall in frequency and raising [Ca] in the range 0.32-2 mM caused a slow increase in frequency. These effects were less in the normal [K] (5 mM).3. Mean m.e.p.p. frequencies were determined for solutions containing 15 mM-K and combinations of [Ca] and [Na]. M.e.p.p. frequency varied inversely with [Na] when [Ca] was constant. In each of the three Na concentrations used (162, 113 and 65 mM) raising [Ca] in the range 0.32-2 mM increased m.e.p.p. frequency but when raised above 2-3 mM, Ca depressed frequency.4. A model was proposed in which Ca affected transmitter release by changing the concentration in the presynaptic membrane of a complex CaX to which the rate of transmitter release was directly proportional. Higher concentrations of Ca depressed transmitter release by inactivating CaX. Sodium ions competitively depressed release either by competing with calcium ions for association with X or by reducing the affinity of X for Ca.5. When [Na] was lowered in solutions containing raised [Mg] and [Ca], the increase of mean m.e.p.p. frequency was greater than that observed in raised [Ca] and normal [Mg] and was of the same order as the increases seen in low [Ca]. The result was interpreted to indicate either that Na and Mg do not compete with Ca at the same site or that Mg affects the affinity of X for Ca and Na.6. The effect of lowering [Na] on m.e.p.p. frequency was a specific effect of Na ions. When LiCl was substituted for NaCl, the increase of m.e.p.p. frequency persisted. Changes in [Cl] had no effect on m.e.p.p. frequency.7. There was a linear relation between the mean logarithm of m.e.p.p. frequencies and [K], the slope of the relation increasing as [Na] was lowered. Conversely, lowering [Na] caused a greater increase in m.e.p.p. frequency as [K] was raised.8. The variation of m.e.p.p. frequencies in a diaphragm was roughly proportional to a second or higher power of [Na] and inversely proportion to [Ca]. It was thought that this could be due to differences in chelation of Ca which were more apparent at low Ca concentrations.9. The similarities between the effects of Na, Ca and K on m.e.p.p. frequency and the effects of these ions on Ca-influx in heart muscle led to the suggestion that transmitter release is proportional to the concentration of a negatively charged complex of a carrier X with one calcium ion (CaX) at the internal surface of the membrane and that changes in membrane potential affect transmitter release by changing the distribution or location of CaX in the membrane.
摘要
  1. 在体外大鼠膈神经 - 膈肌标本的神经肌肉接头处记录微小终板电位(m.e.p.p.s)的频率。

  2. 在高[K](15 - 20 mM)存在的情况下,降低[Na]会导致m.e.p.p.频率迅速增加,无论[Ca]是低还是正常。将[Na]提高到正常浓度(162 mM)会导致频率缓慢下降,而在0.32 - 2 mM范围内提高[Ca]会导致频率缓慢增加。在正常[K](5 mM)时,这些效应较小。

  3. 测定了含有15 mM - K以及[Ca]和[Na]组合的溶液的平均m.e.p.p.频率。当[Ca]恒定时,m.e.p.p.频率与[Na]呈反比。在使用的三种Na浓度(162、113和65 mM)中的每一种情况下,在0.32 - 2 mM范围内提高[Ca]会增加m.e.p.p.频率,但当Ca升高到2 - 3 mM以上时,会降低频率。

  4. 提出了一个模型,其中Ca通过改变突触前膜中一种复合物CaX的浓度来影响递质释放,递质释放速率与该复合物直接成正比。较高浓度的Ca通过使CaX失活来抑制递质释放。钠离子通过与钙离子竞争与X结合或通过降低X对Ca的亲和力来竞争性地抑制释放。

  5. 当在含有高[Mg]和[Ca]的溶液中降低[Na]时,平均m.e.p.p.频率的增加大于在高[Ca]和正常[Mg]中观察到的增加,并且与在低[Ca]中看到的增加幅度相同。该结果被解释为表明Na和Mg不在同一部位与Ca竞争,或者Mg影响X对Ca和Na的亲和力。

  6. 降低[Na]对m.e.p.p.频率的影响是Na离子的特异性作用。当用LiCl替代NaCl时,m.e.p.p.频率的增加仍然存在。[Cl]的变化对m.e.p.p.频率没有影响。

  7. m.e.p.p.频率的平均对数与[K]之间存在线性关系,随着[Na]的降低,该关系的斜率增加。相反,随着[K]的升高,降低[Na]会导致m.e.p.p.频率有更大的增加。

  8. 膈肌中m.e.p.p.频率的变化大致与[Na] 的二次方或更高次方成正比,与[Ca]成反比。认为这可能是由于Ca螯合的差异在低Ca浓度下更明显。

  9. Na、Ca和K对m.e.p.p.频率的影响与这些离子对心肌Ca内流的影响之间的相似性表明,递质释放与膜内表面载体X与一个钙离子(CaX)的带负电荷复合物的浓度成正比,并且膜电位的变化通过改变CaX在膜中的分布或位置来影响递质释放。

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