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Transients in global Ca2+ concentration induced by electrical activity in a giant nerve terminal

机译:巨神经末梢电活动引起的整体Ca2 +浓度瞬变

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摘要

Giant nerve terminals offer a unique opportunity to learn about dynamic changes in intracellular global Ca2+ concentration ([Ca2+]i) because this quantity can be measured precisely with indicator dyes and the composition of the intra-terminal ionic milieu can be controlled. We review here recent literature on [Ca2+]i signalling in the calyx of Held and discuss what these measurements can tell us about endogenous Ca2+ buffers and Ca2+ extrusion mechanisms. We conclude that in spite of the favourable experimental conditions, some unresolved questions still remain regarding absolute values for the Ca2+-binding ratio, the affinity of the basic fixed buffer and the Ca2+ affinities of the major endogenous Ca2+ binding proteins. Uncertainties about some of these presynaptic properties, including the roles of Mg2+ and ATP (as a Mg2+ buffer), however, extend to the point that mechanisms controlling the decay of [Ca2+]i signals in unperturbed terminals may have to be reconsidered.
机译:巨型神经末梢为了解细胞内全局Ca 2 + 浓度([Ca 2 + ] i)的动态变化提供了独特的机会,因为该量可以用指示剂精确测量染料和末端内离子环境的组成可以控制。我们在这里回顾有关Held花萼中[Ca 2 + ] i信号的最新文献,并讨论这些测量值可以告诉我们有关内源Ca 2 + 缓冲液和Ca 2 + 挤出机制。我们得出的结论是,尽管实验条件良好,但关于Ca 2 + 结合比的绝对值,碱性固定缓冲液的亲和力和Ca 2+的绝对值仍然存在一些未解决的问题主要内源性Ca 2 + 结合蛋白的亲和力。但是,其中一些不确定的突触特性,包括Mg 2 + 和ATP(作为Mg 2 + 缓冲液)的作用,都不确定到控制机理。可能需要重新考虑在不受干扰的终端中[Ca 2 + ] i信号的衰减。

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