首页> 美国卫生研究院文献>The Journal of Physiology >Separation of sodium and calcium currents in the somatic membrane of mollusc neurones. With an Appendix by Yu A. Shakhovalov
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Separation of sodium and calcium currents in the somatic membrane of mollusc neurones. With an Appendix by Yu A. Shakhovalov

机译:软体动物神经元体膜中钠和钙电流的分离。附Yu A. Shakhovalov的附录

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摘要

1. Characteristics of the transmembrane ionic currents under controlled changes in ionic composition of extra- and intracellular medium were studied in isolated neurones from the ganglia of molluscs, Helix pomatia, Limnea stagnalis and Planorbis corneus. The neurones were investigated by a new technique which allows for dialysis of their interior and for clamping of the potential at the surface membrane without using micro-electrodes.2. Replacement of K ions by Tris inside the neurones eliminated the outward K current so that the actual time course of the inward current could be measured. The latter was separated into two additive components, one of which was carried by Na ions and the other one by Ca ions.3. Both inward currents were unaltered by tetrodotoxin (TTX); however, Ca current could be separately blocked by externally applied Cd ions (Kd = 7·2 × 10-5 M) and by the use of fluoride as an intracellular anion.4. No reversal of Na inward current could be achieved in neurones dialysed with Na-free solution, indicating the absence of outward current carrying ions through the corresponding channels. With 5 mM-Na inside the cell, the equilibrium potential was close to the value predicted by the Nernst equilibrium.5. A non-specific outward current could be detected in K-free cells at membrane potentials exceeding 20-40 mV. Its time course was proportional to 1 — exp (—t/τns). Cd ions depressed this current. The presence of the non-specific outward current made an exact measurement of the equilibrium potential for the Ca inward current impossible.6. The kinetics of Na inward currents could be described by m3h and those of the Ca current by m2h law. The corresponding values for Vm = 0 are: τm(Na) = 1·1 ± 0·5 msec, τm(Ca) = 2·4 ± 1·0 msec, τh(Na) = 7·9 ± 2·0 msec. The inactivation of Ca current included two first-order kinetic processes with τh1 = 50 ± 10 msec and τh = 320 ± 30 msec.7. The data presented are considered to be a proof of the existence of separate systems of Na and Ca ion-conducting channels in the nerve cell membrane.
机译:1.在软体动物神经节,螺旋性血球,stagnalis和角膜炎的神经节中分离出的神经元中研究了在细胞外和细胞内离子组成受控变化下的跨膜离子电流特性。通过一种新技术对神经元进行了研究,该技术允许在不使用微电极的情况下对其内部进行透析并在表面膜处钳制电位。2。神经元内部的Tris替代K离子消除了向外的K电流,因此可以测量向内电流的实际时间过程。后者被分为两种添加剂成分,一种由Na离子携带,另一种由Ca离子携带。3。河豚毒素(TTX)并没有改变这两种流入电流。然而,Ca电流可以被外部施加的Cd离子(Kd = 7·2×10 -5 M)和使用氟化物作为细胞内阴离子分别阻止。4。在用无钠溶液透析的神经元中,无法实现Na内向电流的逆转,这表明没有通过相应通道携带离子的外向电流。电池内部有5 mM-Na时,平衡电位接近能斯特平衡所预测的值。5。在膜电位超过20-40 mV的无K细胞中可以检测到非特异性向外电流。它的时间过程与1 exp(-t /τns)成正比。镉离子抑制了这种电流。非特定的外向电流的存在使得无法精确测量Ca内向电流的平衡电位。6。 Na向内流动的动力学可以用m 3 h描述,而Ca向内流动的动力学可以通过m 2 h定律描述。 Vm = 0的相应值为:τm(Na)= 1·1±0·5毫秒,τm(Ca)= 2·4±1·0毫秒,τh(Na)= 7·9±2·0毫秒。 Ca电流的失活包括两个一级动力学过程,τh1= 50±10毫秒和τh= 320±30毫秒。7。所提供的数据被认为是神经细胞膜中存在单独的Na和Ca离子传导通道系统的证据。

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