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大鼠脑突触体对钙的摄取与释放

Uptake and release of calcium by rat brain synaptosomes.

作者信息

Goddard G A, Robinson J D

出版信息

Brain Res. 1976 Jul 9;110(2):331-50. doi: 10.1016/0006-8993(76)90406-6.

Abstract

Rat brain synaptosomes, prepared by discontinuous Ficoll density gradient centrifugation, accumulated 45Ca during brief incubations in modified Krebs-Ringer media. Uptake of 45Ca was increased by 5 mM glutamate and 50 mM KCl, conditions that depolarize nerve cells; uptake of 22Na was also increased by these agents. With 0.2 mM diphenylhydantoin, the increased 45Ca uptake due to KCl was diminished, whereas that due to glutamate was less affected; conversely, with 0.15 muM tetrodotoxin the increased 45Ca uptake due to glutamate was diminished, whereas that due to KCl was less affected. Both diphenylhydantoin and tetrodotoxin diminished the augmented uptake of 22Na due to KCl and glutamate; thus the increased uptake of 45Ca under depolarizing conditions may be dissociated from the increased influx of sodium. Ruthenium red decreased the uptake of 45Ca under all conditions, as did procaine and the lanthanide Pr3+. Neither 5 mM glutamate nor 50 mM KCl increased 45Ca uptake by brain mitochondria under comparable experimental conditions, whereas ATP increased the uptake by mitochondria but not that by these synaptosomes. Altering the sodium gradient by equimolar substitution of lithium or choline for sodium in the medium increased 45Ca uptake, whereas 22Na uptake was decreased. Inhibiting the sodium pump by ouabain or strophanthidin also increased 45Ca uptake, and increased 22Na uptake as well. The increased uptake of 45Ca induced by ouabain was inhibited by diphenylhydantoin and tetrodotoxin. Measurements of the total calcium content showed that conditions producing an increased uptake of 45Ca also produced a net uptake of calcium, rather than merely accelerating a 45Ca-40Ca exchange. Experiments measuring the loss of previously accumulated 45Ca showed that directly decreasing the sodium gradient or inhibiting the sodium pump slowed the loss of 45Ca. These data are considered in terms of calcium influx through 'leak' pathways and gated channels (sensitive to membrane depolarization) and of net efflux dependent on a coupled sodium-calcium exchange mechanism.

摘要

通过不连续的Ficoll密度梯度离心法制备的大鼠脑突触体,在改良的Krebs-Ringer培养基中短暂孵育期间积累了45Ca。5 mM谷氨酸和50 mM KCl可增加45Ca的摄取,这两种条件会使神经细胞去极化;这些试剂也会增加22Na的摄取。使用0.2 mM苯妥英时,KCl引起的45Ca摄取增加减少,而谷氨酸引起的增加受影响较小;相反,使用0.15 μM河豚毒素时,谷氨酸引起的45Ca摄取增加减少,而KCl引起的增加受影响较小。苯妥英和河豚毒素均减少了KCl和谷氨酸引起的22Na摄取增加;因此,去极化条件下45Ca摄取的增加可能与钠内流的增加无关。钌红在所有条件下均降低了45Ca的摄取,普鲁卡因和镧系元素Pr3+也是如此。在可比的实验条件下,5 mM谷氨酸和50 mM KCl均未增加脑线粒体对45Ca的摄取,而ATP增加了线粒体对45Ca的摄取,但未增加这些突触体对45Ca的摄取。通过在培养基中用锂或胆碱等摩尔替代钠来改变钠梯度会增加45Ca的摄取,而22Na的摄取则减少。用哇巴因或毒毛花苷抑制钠泵也会增加45Ca的摄取,同时增加22Na的摄取。哇巴因诱导的45Ca摄取增加受到苯妥英和河豚毒素的抑制。总钙含量的测量表明,导致45Ca摄取增加的条件也导致了钙的净摄取,而不仅仅是加速了45Ca-40Ca交换。测量先前积累的45Ca损失的实验表明,直接降低钠梯度或抑制钠泵会减缓45Ca的损失。这些数据是根据通过“渗漏”途径和门控通道(对膜去极化敏感)的钙内流以及依赖于耦合钠钙交换机制的净外流来考虑的。

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