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The effect of foreign cations pH and pharmacological agents on the ionic permeability of an excitatory glutamate synapse.

机译:外来阳离子pH和药理剂对兴奋性谷氨酸突触的离子渗透性的影响。

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摘要

1. Voltage clamp studies of the post-synaptic membrane of the insect neuromuscular junction have shown that normal amplitude glutamate currents could be recorded for a limited time when external Na was completely replaced by Ca, Li, ammonium, methylamine and guanidine. No change in the reversal potential of the glutamate current was observed when Na was replaced by these ions. It is suggested that the glutamate ionic channel has a similar permeability to Na and to these foreign cations, although the foreign ions cause a longer-term block of the permeability increase or receptor function. 2. Procaine, pentobarbitone, 2-4-6-triaminopyrimidine, high and low pH and low temperature reduced the synaptic ionic permeability but did not alter the ratio of the conductance increase of Na to K (delta g Na/delta gK). 4-Aminopyridine and TEA did not reduce the synaptic ionic permeability. 3. The 3. The properties of the synaptic ionic channels resemble the tight junction transepithelial ionic channels of the mammalian gall-bladder, but are very different from the Na and K non-synaptic channels of axons. It is suggested that Na and K normally pass through a single relatively large channel containing strong proton accepting acidic ligands which render the channel cation selective.
机译:1.对昆虫神经肌肉接头的突触后膜的电压钳研究表明,当外部Na被Ca,Li,铵,甲胺和胍完全替代时,可以在有限的时间内记录正常幅度的谷氨酸电流。当Na被这些离子替代时,未观察到谷氨酸电流的逆转电位的变化。提示谷氨酸离子通道具有与Na和这些外来阳离子相似的渗透性,尽管外来离子引起通透性增加或受体功能的长期阻断。 2.普鲁卡因,戊巴比妥,2-4-4-6-三氨基嘧啶,高和低pH值和低温降低了突触的离子渗透性,但没有改变Na与K的电导增加比率(δg Na /δgK)。 4-氨基吡啶和TEA不会降低突触的离子通透性。 3. 3.突触离子通道的性质类似于哺乳动物胆囊的紧密连接跨上皮离子通道,但与轴突的Na和K非突触通道非常不同。建议Na和K通常通过单个相对较大的通道,该通道包含强质子接受酸性配体,从而使通道阳离子具有选择性。

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