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内部透析的枪乌贼巨大轴突中的钙外流。

Calcium efflux from internally dialyzed squid giant axons.

作者信息

Dipolo R

出版信息

J Gen Physiol. 1973 Nov;62(5):575-89. doi: 10.1085/jgp.62.5.575.

Abstract

Calcium efflux has been studied in squid giant axons under conditions in which the internal composition was controlled by means of a dialysis perfusion technique. The mean calcium efflux from axons dialyzed with 0.3 microM calcium and 5 mM ATP was 0.26 pmol/cm(2).s at 22 degrees C. The curve relating the Ca efflux with the internal Ca concentration had a slope of about one for Ca lower than 0.3microM and a slope smaller than one for higher concentrations. Under the above conditions replacement of Na and Ca by Tris and Mg causes an 80% fall in the calcium efflux. When the axons were dialyzed with a medium free of ATP and containing 2 mM cyanide plus 5microg/ml oligomycin, analysis of the perfusion effluent gave values of 1-4 microM ATP. Under this low ATP condition, replacement of external sodium and calcium causes the same drop in the calcium efflux. The same effect was observed at higher Ca, (80 microM). These results suggest that the Na-Ca exchange component of the calcium efflux is apparently not dependent on the amounts of ATP in the axoplasm. Axons previously depleted of ATP show a significant transient drop in the calcium efflux when ATP is added to the dialysis medium. This effect probably represents the sequestering of calcium by the mitochondrial system. The consumption of calcium by the mitochondria of the axoplasm in dialyzed axons was determined to be of the order of 6.0 x 10(-7) mol Ca(++)/mg of protein with an initial rate of 2.6 x 10(-8) mol Ca(++)/min.mg of protein. Axons dialyzed with 2 mM cyanide after 8-10-min delays show a rise in the calcium efflux in the presence of "normal" amounts of exogenous ATP. This effect seems to indicate that cyanide, per se, can release calcium ions from internal sources.

摘要

在通过透析灌注技术控制内部成分的条件下,对枪乌贼巨大轴突中的钙外流进行了研究。在22℃时,用0.3微摩尔/升钙和5毫摩尔/升ATP透析的轴突的平均钙外流为0.26皮摩尔/平方厘米·秒。当细胞内钙浓度Ca低于0.3微摩尔/升时,钙外流与细胞内钙浓度的曲线斜率约为1,而在较高浓度时斜率小于1。在上述条件下,用Tris和Mg替代NaCa会使钙外流下降80%。当轴突用不含ATP且含有2毫摩尔/升氰化物加5微克/毫升寡霉素的培养基透析时,对灌注流出物的分析给出了1 - 4微摩尔/升ATP的值。在这种低ATP条件下,替代外部钠和钙会使钙外流产生相同程度的下降。在较高的Ca(80微摩尔/升)时也观察到了相同的效果。这些结果表明,钙外流的钠 - 钙交换成分显然不依赖于轴浆中ATP的量。先前耗尽ATP的轴突在向透析培养基中添加ATP时,钙外流会出现明显的瞬时下降。这种效应可能代表线粒体系统对钙的螯合。经测定,透析轴突中轴浆线粒体对钙的消耗量约为6.0×10⁻⁷摩尔Ca²⁺/毫克蛋白质,初始速率为2.6×10⁻⁸摩尔Ca²⁺/分钟·毫克蛋白质。在延迟8 - 10分钟后用2毫摩尔/升氰化物透析的轴突,在存在“正常”量的外源性ATP时,钙外流会增加。这种效应似乎表明,氰化物本身可以从内部来源释放钙离子。

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