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静水椎实螺内部灌注神经细胞体中的钙电流

Calcium currents in internally perfused nerve cell bodies of Limnea stagnalis.

作者信息

Byerly L, Hagiwara S

出版信息

J Physiol. 1982 Jan;322:503-28. doi: 10.1113/jphysiol.1982.sp014052.

Abstract
  1. When K(+) is removed from both sides of the somal membrane of Limnea neurones, time-dependent, voltage-dependent outward currents are observed at positive potentials. These currents can be carried by Tris(+) and tetraethylammonium (TEA(+)), as well as Cs(+), but the Cs currents are several times larger. The Cs currents are not affected by external or internal TEA, but are strongly reduced by 4-aminopyridine (4-AP) and all Ca blockers tried.2. The presence of these non-specific outward currents and their sensitivity to all treatments that eliminate the Ca currents prevent the complete isolation of Ca currents. The non-specific outward currents are most prominent at large positive potentials and as slow tail currents on stepping back to the holding potential.3. Ca currents are ;washed out' in well perfused cells. Typically the Ca current has decayed to less than one tenth of its original size after (1/2) h of perfusion. This wash-out is specific for the Ca current; Na and K currents persist for several hours.4. Once the Ca current has completely decayed, it is possible to study one type of non-specific current without overlapping inward currents. This current activates between 0 and +30 mV and appears to reverse near 0 mV.5. In spite of the probable presence of slowly activating outward currents, the net inward currents measured show little apparent inactivation. In all the cells studied the inward current evoked at +20 mV has never decayed by more than 50% during a 60 ms pulse. So the true inactivation of these Ca currents must be quite slow, with time constants of the order of 100 ms and larger.6. The activation of the Ca current agrees with m(2) kinetics. The rate of activation is the same for Ba currents as for Ca currents.7. When the membrane potential is stepped back to the holding level (-50 mV), the Ca current turns off quite rapidly with a time constant of about 100 mus (25 degrees C). The time constant for turning off the Ca current is not related to the time constant for turning on the Ca current at the same voltage as expected for m(2) kinetics in the Hodgkin and Huxley model. At -30 mV the tau(m) for turn-on is eight times larger than the tau(m) for turn-off.
摘要
  1. 当从扁卷螺神经元的胞体膜两侧移除K⁺时,在正电位下可观察到时间依赖性和电压依赖性外向电流。这些电流可由Tris⁺、四乙铵(TEA⁺)以及Cs⁺携带,但Cs电流要大几倍。Cs电流不受细胞外或细胞内TEA的影响,但会被4-氨基吡啶(4-AP)和所有试过的钙通道阻滞剂强烈减弱。

  2. 这些非特异性外向电流的存在及其对消除钙电流的所有处理的敏感性妨碍了钙电流的完全分离。非特异性外向电流在大的正电位时最为显著,并且在回到静息电位时作为缓慢的尾电流出现。

  3. 在充分灌流的细胞中钙电流会“被洗脱”。通常,灌流(1/2)小时后钙电流已衰减至其原始大小的十分之一以下。这种洗脱对钙电流是特异性的;钠电流和钾电流会持续数小时。

  4. 一旦钙电流完全衰减,就有可能研究一种类型的非特异性电流而不会有重叠的内向电流。这种电流在0至 +30 mV之间激活,并且似乎在接近0 mV时反转。

  5. 尽管可能存在缓慢激活的外向电流,但所测量的净内向电流几乎没有明显的失活。在所有研究的细胞中,在 +20 mV诱发的内向电流在60 ms脉冲期间从未衰减超过50%。因此这些钙电流的真正失活一定相当缓慢,时间常数约为100 ms或更大。

  6. 钙电流的激活符合m²动力学。Ba电流的激活速率与钙电流相同。

  7. 当膜电位回到静息水平(-50 mV)时,钙电流以约100 μs(25℃)的时间常数相当迅速地关闭。关闭钙电流的时间常数与在相同电压下开启钙电流的时间常数无关,这与霍奇金和赫胥黎模型中m²动力学的预期情况不同。在 -30 mV时,开启的τm比关闭的τm大八倍。

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