Lee K S, Tsien R W
J Physiol. 1984 Sep;354:253-72. doi: 10.1113/jphysiol.1984.sp015374.
Membrane currents and action potentials were recorded in single ventricular cells obtained from guinea-pig hearts by enzymatic dissociation. Ca2+ channel currents carried by Ba2+ or Ca2+ were recorded with a suction pipette (5-10 microns diameter) for voltage clamp and internal dialysis. Currents through Na+, K+ and non-selective monovalent cation channels were suppressed by suitable holding potentials and external and internal solutions. The dialysis method allowed exchange within minutes of alkali metal cations (e.g. Cs+) and small molecules (e.g. quaternary derivatives of lidocaine and verapamil). Nevertheless, Ca2+ channels remained functional for considerable periods, typically 20 min and sometimes more than 1 h. With Ba2+ outside and Cs+ inside, current flow through Ca2+ channels changed from inward to outward at strongly positive levels beyond a clear-cut reversal potential Erev. Several methods for defining Erev were in close agreement: (1) zero-crossing of leak-subtracted peak current, (2) inversion of time-dependent current changes during channel activation or inactivation, (3) inversion of drug-sensitive current as defined by channel blockers such as Cd2+ or D-600. Erev varied with external Ba2+ or internal Cs+. Erev increased by 29 mV per 10-fold increase in Ba2+. Interpreted with constant-field theory, Erev values correspond to PBa/PCs of approximately 1360. With 5 mM-Ca2+ outside and 151 mM-Cs+ inside, Ca2+ channel current reversed near + 75 mV, corresponding to PCa/PCs approximately 6000. Earlier measurements of Erev (Lee & Tsien, 1982) suggest that PCa/PK greater than 1000. At strongly positive membrane potentials where channel activation is maximal, the Ca2+ channel current-voltage relationship is strongly non-linear, with conductance increasing on either side of an inflexion point near Erev. Activation of inward or outward currents through Ca2+ channels follows a sigmoid time course, as expected if activation were a multi-step process.
采用酶解法从豚鼠心脏获取单个心室细胞,记录其膜电流和动作电位。用吸管(直径5 - 10微米)进行电压钳制和内部透析,记录Ba²⁺或Ca²⁺携带的Ca²⁺通道电流。通过合适的钳制电位以及外部和内部溶液抑制通过Na⁺、K⁺和非选择性单价阳离子通道的电流。透析方法可在数分钟内实现碱金属阳离子(如Cs⁺)和小分子(如利多卡因和维拉帕米的季铵衍生物)的交换。尽管如此,Ca²⁺通道在相当长的时间内仍保持功能,通常为20分钟,有时超过1小时。外部为Ba²⁺且内部为Cs⁺时,通过Ca²⁺通道的电流在强正电位超过明确的反转电位Erev时从内向电流变为外向电流。定义Erev的几种方法结果相近:(1)减去漏电流后的峰值电流过零;(2)通道激活或失活期间时间依赖性电流变化的反转;(3)由通道阻滞剂如Cd²⁺或D - 600定义的药物敏感性电流的反转。Erev随外部Ba²⁺或内部Cs⁺而变化。Ba²⁺浓度每增加10倍,Erev增加29 mV。用恒定场理论解释,Erev值对应于PBa/PCs约为1360。外部为5 mM - Ca²⁺且内部为151 mM - Cs⁺时,Ca²⁺通道电流在 + 75 mV附近反转,对应于PCa/PCs约为6000。早期对Erev的测量(Lee和Tsien,1982)表明PCa/PK大于1000。在通道激活最大的强正膜电位处,Ca²⁺通道电流 - 电压关系呈强非线性,在接近Erev的拐点两侧电导增加。通过Ca²⁺通道的内向或外向电流激活呈S形时间进程,这符合激活为多步过程的预期。