Nachshen D A
J Physiol. 1985 Jun;363:87-101. doi: 10.1113/jphysiol.1985.sp015697.
The regulation of cytosolic Ca concentration ([Ca]i) was studied with the fluorescent Ca indicator, quin2, in pinched-off presynaptic nerve endings (synaptosomes) isolated from rat brain. The resting [Ca]i is 0.1-0.2 microM, in solutions containing 1-2 mM-Ca. [Ca]i increases by only 100-150 nM when the external Ca concentration is increased from 0.02 to 2 mM. The mitochondrial inhibitors valinomycin and fluoro-carbonyl cyanide phenylhydrazone (FCCP) increase [Ca]i by 100-200 nM. This increase is not correlated with the resting level of [Ca]i prior to the addition of inhibitors, but it is dependent on the presence of external Ca. It seems likely that the effect of these inhibitors on [Ca]i is a secondary consequence of metabolic inhibition. [Ca]i increases by about 2-fold when the external Na concentration is lowered from 145 to 5 mM, and returns to its initial level when external Na is restored. This recovery occurs also in the presence of FCCP. These results suggest that Na/Ca exchange, but not mitochondrial Ca uptake, plays a role in regulating [Ca]i and in allowing the nerve terminals to recover from Ca loading.
利用荧光钙指示剂喹啉-2,对从大鼠脑部分离出的钳断型突触前神经末梢(突触体)中的胞质钙浓度([Ca]i)调节进行了研究。在含有1-2 mM钙的溶液中,静息[Ca]i为0.1-0.2 microM。当外部钙浓度从0.02 mM增加到2 mM时,[Ca]i仅增加100-150 nM。线粒体抑制剂缬氨霉素和氟代羰基氰化物苯腙(FCCP)使[Ca]i增加100-200 nM。这种增加与添加抑制剂之前的[Ca]i静息水平无关,但依赖于外部钙的存在。这些抑制剂对[Ca]i的作用似乎是代谢抑制的次要后果。当外部钠浓度从145 mM降低到5 mM时,[Ca]i增加约2倍,当恢复外部钠时,[Ca]i恢复到初始水平。在FCCP存在的情况下也会发生这种恢复。这些结果表明,钠/钙交换而非线粒体钙摄取在调节[Ca]i以及使神经末梢从钙负荷中恢复方面发挥作用。