Okamoto H, Takahashi K, Yoshii M
J Physiol. 1976 Feb;255(2):527-61. doi: 10.1113/jphysiol.1976.sp011294.
The Ca current of the egg cell membrane of a certain tunicate, Halocynthia roretzi Drasche, was studied by the voltage-clamp technique. 2. The Ca current in the standard artificial sea water (ASW) was produced at the critical membrane potential of -10 mV after inactivating the Na current by conditioning depolarization, -30 to -15 mV. The Ca current was abolished by replacing Ca in ASW with Mg2+ or Mn2+. The Ca current was not significantly influenced by replacing Na in ASW with choline or Cs. 3. The relation of Ca current to the external Ca concentration was a monotonously increasing function, but was not linear. The current tended to saturate above 50 mM-Ca. In 100 mM-Ca ASW, the maximum peak inward current of Ca ranged from 1 to 7 X 10(-9) A. 4. The kinetics of Ca current was accurately analysed because of the small contribution of K outward current and was found to be relatively slow in comparison with the Na current. The peak time and the half-decay time of the maximum Ca current at about 25 mV were about 25 and 100 msec respectively in 100 mM-Ca ASW at 15 degrees C. 5. Addition of 20 mM-Co2+ to 100 mM-Ca ASW reduced Ca current to one fourth and 1 mM-La3+ to 100 mM-Ca ASW abolished the current. 6. Sr and Ba could substitute for Ca in Ca channels. The selectivity ratios for the 'Ca channels's were Ca (1-00):Sr(1-17):Ba(0-71) at a potential level of +40 mV. The Ca current in the egg cell membrane appeared to be essentially the same as the Ca current in the common excitable membranes, such as the crustacean muscle fibre. 7. The polyvalent cations including Ca ion and monovalent H+ ion showed the stabilizing effect upon both Na and Ca currents, by shifting V-I relations along the voltage axis. From the prediction of a theory of the diffuse double layer, the shift in the V-I relation induced by those cations should be directly related to their binding powers to the membrane. Thus, the sequence of the binding powers was inferred as H+ greater than La3+ greater than Co2+ greater than Mn2+ greater than Ca2+ greater than Sr2+ larger than or equal to Ba2+ greater than Mg2+. 9. In Na-free ASW, such as isotonic Ca ASW, Ca current was composed of two components. The one component was the Ca current described in 1 to 6. The other was also dependent upon the external Ca concentration, but showed the more negative critical membrane potential and the faster kinetics. It was concluded that this component should be the Ca current through Na channels. 10. The selectivity among Ca, Sr and Ba for 'Ca' current through 'Na channels' was significantly different from that of 'Ca' current through 'Ca channels', being Ca greater than Sr larger than or equal to Ba = 0.
采用电压钳技术研究了某种被囊动物(柄海鞘)卵细胞的钙电流。
在通过预处理去极化(-30至-15mV)使钠电流失活后,在-10mV的临界膜电位下,标准人工海水(ASW)中产生了钙电流。用Mg2+或Mn2+替代ASW中的Ca可使钙电流消失。用胆碱或Cs替代ASW中的Na对钙电流无显著影响。
钙电流与细胞外钙浓度的关系是单调递增函数,但不是线性关系。当钙浓度高于50mM时,电流趋于饱和。在100mM - Ca的ASW中,钙的最大内向峰值电流范围为1至7×10(-9)A。
由于钾外向电流的贡献较小,因此能够准确分析钙电流的动力学,并且发现与钠电流相比,钙电流相对较慢。在15℃下,100mM - Ca的ASW中,约25mV时最大钙电流的峰值时间和半衰减时间分别约为25和100毫秒。
在100mM - Ca的ASW中添加20mM - Co2+可使钙电流降低至四分之一,添加1mM - La3+可使电流消失。
Sr和Ba可在钙通道中替代Ca。在+40mV的电位水平下,“钙通道”对Ca、Sr、Ba的选择性比率为Ca(1.00):Sr(1.17):Ba(0.71)。卵细胞中的钙电流似乎与常见可兴奋膜(如甲壳类动物肌肉纤维)中的钙电流基本相同。
包括Ca离子的多价阳离子和单价H+离子通过沿电压轴移动V - I关系,对钠电流和钙电流均表现出稳定作用。根据扩散双层理论的预测,这些阳离子引起的V - I关系的变化应与其与膜的结合能力直接相关。因此,推断结合能力的顺序为H+>La3+>Co2+>Mn2+>Ca2+>Sr2+≥Ba2+>Mg2+。
在无钠的ASW(如等渗钙ASW)中,钙电流由两个成分组成。一个成分是1至6中描述的钙电流。另一个成分也依赖于细胞外钙浓度,但具有更负的临界膜电位和更快的动力学。得出的结论是,该成分应为通过钠通道的钙电流。
Ca、Sr和Ba对通过“钠通道”的“钙”电流的选择性与通过“钙通道”的“钙”电流的选择性显著不同,为Ca>Sr≥Ba = 0。