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The calcium dependence of spontaneous and evoked quantal release at the frog neuromuscular junction.青蛙神经肌肉接头处自发和诱发量子释放的钙依赖性。
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10
An excitatory action of iontophoretically administered lithium on mammalian central neurones.离子电渗法施加锂对哺乳动物中枢神经元的兴奋作用。
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本文引用的文献

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The effect of sodium ions on the electrical activity of giant axon of the squid.钠离子对鱿鱼巨大轴突电活动的影响。
J Physiol. 1949 Mar 1;108(1):37-77. doi: 10.1113/jphysiol.1949.sp004310.
2
Interaction between sodium and calcium ions in the process of transmitter release at the neuromuscular junction.神经肌肉接头处递质释放过程中钠离子与钙离子之间的相互作用。
J Physiol. 1968 Sep;198(1):203-18. doi: 10.1113/jphysiol.1968.sp008602.
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Cation control in human erythrocytes.人类红细胞中的阳离子控制
J Physiol. 1949 Dec;110(3-4):301-18. doi: 10.1113/jphysiol.1949.sp004440.
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Spontaneous subthreshold activity at motor nerve endings.运动神经末梢的自发性阈下活动。
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Effect of potassium and sodium on resting and action potentials of single myelinated nerve fibers.钾和钠对单根有髓神经纤维静息电位和动作电位的影响。
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The electromotive action of acetylcholine at the motor end-plate.乙酰胆碱在运动终板处的电动力作用。
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The effect of external sodium concentration on the sodium fluxes in frog skeletal muscle.外部钠浓度对青蛙骨骼肌钠通量的影响。
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The chloride conductance of frog skeletal muscle.青蛙骨骼肌的氯离子电导率。
J Physiol. 1960 Apr;151(1):89-102.
9
PROPAGATION OF ELECTRIC ACTIVITY IN MOTOR NERVE TERMINALS.运动神经末梢电活动的传播
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10
ANTAGONISM BETWEEN NA+ AND CA2+ AT THE NEUROMUSCULAR JUNCTION.神经肌肉接头处钠离子与钙离子之间的拮抗作用。
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锂离子与青蛙神经肌肉接头处神经递质的释放

Lithium ions and the release of transmitter at the frog neuromuscular junction.

作者信息

Crawford A C

出版信息

J Physiol. 1975 Mar;246(1):109-42. doi: 10.1113/jphysiol.1975.sp010882.

DOI:10.1113/jphysiol.1975.sp010882
PMID:237119
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1309406/
Abstract
  1. Transmitter release has been examined at the frog neuromuscular junction when all or part of the Na of the Ringer is replaced by Li ions. 2. No immediate change occurs in either the mean quantal content of the end-plate potential or the miniature end-plate potential frequency on changing to Li Ringer but over the following hour both these quantities increase by more than two orders of magnitude. 3. During thefirst 30-40 min of an exposure to Li-Ringer the m.e.p.p. frequency rises exponentially with a time constant of 10 min, and the mean quantal content of the e.p.p. grows by addition of extra evoked quanta, the increment rising exponentially with a time constant the same as that of the m.e.p.p. frequency. 4. Following this initial period in Li-Ringer the m. e.p.p. frequency accelerates to a peak of several hundred quanta per second and then declines slowly over the next few hours. Just before the m.e.p.p.frequency peak the conduction velocity of the presynaptic action potential declines and shortly afterwards synaptic transmission fails as the action potential no longer conducts into the terminals. 5. The rise in the m.e.p.p. frequency during the first 30-40 min is independent of the [Ca-2+]o. At subsequent times before the peak external Cabecomes progressively more effective in accelerating the m.e.p.p. frequency and in the presence of 1mM-EGTA spontaneous release stabilizes at 60-80 quanta/sec. 6. The [Li-+]o strongly influences the rate of increases in both evoked and spontaneous release but not their extent; replacing only half the Na of the Ringer by Li increases the time constants of the increases to about 30 min. 7. Rises in the m.e.p.p. frequency can be irreversibly accelerated by tetanizing the nerve in a Li-Ringer in which the Ca has been chelated by EGTA. The extent of the increases in the m.e.p.p. frequency is dependent on the number of pulses in the tetanus and is little affected by the frequency of stimulation. Accumulation of Li ions inside the presynaptic terminals probably underlies the changes in spontaneous release. 8. When only 10 percent of the Na of the Ringer is replaced by Li-+ ions the magnitude of post-tetanic potentiation of the e.p.p. and of the post-tetanic rise in the m.e.p.p. frequency is increased. Under these conditions changes in facilitation of the e.p.p. are small. 9. Various mechanisms by which Li could alter transmitter release are discussed and it is suggested that intracellular Ca sequestering mechanisms of the presynaptic terminals are affected when an end-plate is exposed to Li-Ringer.
摘要
  1. 当任氏液中的全部或部分钠离子被锂离子取代时,已对青蛙神经肌肉接头处的递质释放进行了研究。2. 换成锂任氏液时,终板电位的平均量子含量或微小终板电位频率均无立即变化,但在接下来的一小时内,这两个量均增加了两个以上的数量级。3. 在暴露于锂任氏液的最初30 - 40分钟内,微小终板电位频率呈指数上升,时间常数为10分钟,终板电位的平均量子含量通过额外诱发量子的添加而增加,增量也呈指数上升,时间常数与微小终板电位频率相同。4. 在锂任氏液中的这个初始阶段之后,微小终板电位频率加速至每秒数百个量子的峰值,然后在接下来的几个小时内缓慢下降。就在微小终板电位频率达到峰值之前,突触前动作电位的传导速度下降,不久之后,由于动作电位不再传入终末,突触传递失效。5. 在最初的30 - 40分钟内微小终板电位频率的上升与细胞外钙离子浓度无关。在随后达到峰值之前的时间里,外部钙离子在加速微小终板电位频率方面变得越来越有效,并且在存在1mM乙二醇双四乙酸(EGTA)的情况下,自发释放稳定在60 - 80个量子/秒。6. 细胞外锂离子浓度强烈影响诱发释放和自发释放的增加速率,但不影响其程度;仅将任氏液中一半的钠离子换成锂离子,会使增加的时间常数增加到约30分钟。7. 在钙离子已被EGTA螯合的锂任氏液中对神经进行强直刺激,可使微小终板电位频率的上升不可逆地加速。微小终板电位频率增加的程度取决于强直刺激中的脉冲数,且受刺激频率的影响较小。突触前终末内锂离子的积累可能是自发释放变化的基础。8. 当任氏液中只有10%的钠离子被锂离子取代时,终板电位的强直后增强以及微小终板电位频率的强直后上升幅度会增加。在这些条件下,终板电位易化的变化很小。9. 讨论了锂可能改变递质释放的各种机制,并提出当终板暴露于锂任氏液时,突触前终末的细胞内钙螯合机制会受到影响。