高红, 冯亦璞. 用Fura-2测定突触体内游离Ca2+浓度及Ca2+通道激动剂和阻断剂的影响J. 药学学报, 1993, 28(6): 404-409.
引用本文: 高红, 冯亦璞. 用Fura-2测定突触体内游离Ca2+浓度及Ca2+通道激动剂和阻断剂的影响J. 药学学报, 1993, 28(6): 404-409.
H Gao, YP Feng. ESTIMATION OF FREE CALCIUM LEVEL WITHIN SYNAPTOSOMES BY USING FURA—2 AND THE EFFECT OF CALCIUM CHANNEL AGONIST AND ANTAGONISTJ. Acta Pharmaceutica Sinica, 1993, 28(6): 404-409.
Citation: H Gao, YP Feng. ESTIMATION OF FREE CALCIUM LEVEL WITHIN SYNAPTOSOMES BY USING FURA—2 AND THE EFFECT OF CALCIUM CHANNEL AGONIST AND ANTAGONISTJ. Acta Pharmaceutica Sinica, 1993, 28(6): 404-409.

用Fura-2测定突触体内游离Ca2+浓度及Ca2+通道激动剂和阻断剂的影响

ESTIMATION OF FREE CALCIUM LEVEL WITHIN SYNAPTOSOMES BY USING FURA—2 AND THE EFFECT OF CALCIUM CHANNEL AGONIST AND ANTAGONIST

  • 摘要: 用Fura-2测定大鼠突触体内游离Ca2+浓度,探讨Ca2+通道激动剂和阻断剂对突触体内钙浓度的影响。测得突触体内Ca2+浓度为200~400 nmol/L。观察了不同浓度KCl,CaCl2,NMDA和谷氨酸对突触体内Ca2+增加的影响以及维拉帕米及MgCl2对KCl和NMDA引起钙内流的阻断作用。本实验提供一个研究突触体内Ca2+变化的准确而稳定的方法,并对测定中几个影响因素加以讨论。

     

    Abstract: The cytosolic free calcium concentration Ca2+i in synaptosomes was determined with the fluorescent indicator fura-2, the effects of calcium channel agonist and antagonist on intracellular Ca2+ level were studied. The cytosolic ionized calcium concentrations in resting status were between 200 nmol/L and 400 nmol/L. Cytosolic Ca2+ was elevated following increases in Ca2+ concentration in the medium, plasma membrane depolarizations induced by KC1, and the addition of glutamate and NMDA. On the other hand, the increase of cytosolic Ca2+ induced by KCI was decreased by verapamil and that induced by NMDA was decreased by MgCl2.A few critical problems in Ca2+i detection were also discussed.

     

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