Noulin J F, Brochiero E, Lapointe J Y, Laprade R
Groupe de Recherche en Transport Membranaire, Université de Montréal, Montreal, Quebec, Canada H3C 3J7.
Am J Physiol. 1999 Aug;277(2):F290-7. doi: 10.1152/ajprenal.1999.277.2.F290.
The cell-attached configuration of the patch-clamp technique was used to investigate the effects of taurine on the basolateral potassium channels of rabbit proximal convoluted tubule. In the absence of taurine, the previously reported ATP-blockable channel, K(ATP), was observed in 51% of patches. It is characterized by an inwardly rectifying current-voltage curve with an inward slope conductance of 49 +/- 5 pS (n = 15) and an outward slope conductance of 13 +/- 6 pS (n = 15). The K(ATP) channel open probability (P(o)) is low, 0.15 +/- 0.06 (n = 15) at a -V(p) = -100 mV (V(p) is the pipette potential), and increases slightly with depolarization. The gating kinetics are characterized by one open time constant (tau(o) = 5.0 +/- 1.9 ms, n = 6) and two closed time constants (tau(C1) = 5. 2 +/- 1.5 ms, tau(C2) = 140 +/- 40 ms; n = 6). In 34% of patches, a second type of potassium channel, sK, with distinct properties was recorded. Its current-voltage curve is characterized by a sigmoidal shape, with an inward slope conductance of 12 +/- 2 pS (n = 4). Its P(o) is voltage independent and averages 0.67 +/- 0.03 (n = 4) at -V(p) = -80 mV. Both its open time and closed time distributions are described by a single time constant (tau(o) = 96 +/- 19 ms, tau(C) = 10.5 +/- 3.6 ms; n = 4). Extracellular perfusion of 40 mM taurine fails to affect sK channels, whereas K(ATP) channel P(o) decreases by 75% (from 0.17 +/- 0.06 to 0.04 +/- 0.02, n = 7, P < 0.05). In conclusion, the absolute basolateral potassium conductance of rabbit proximal tubules is the resulting combination of, at least, two types of potassium channels of roughly equal importance: a high-conductance low-open probability K(ATP) channel and a low-conductance high-open probability sK channel. The previously described decrease in the basolateral absolute potassium conductance by taurine is, however, mediated by a single type of K channel: the ATP-blockable K channel.
采用膜片钳技术的细胞贴附式记录模式,研究牛磺酸对兔近端肾小管基底外侧钾通道的影响。在无牛磺酸情况下,在51%的膜片中观察到先前报道的可被ATP阻断的通道,即K(ATP)通道。其特征为内向整流的电流-电压曲线,内向斜率电导为49±5 pS(n = 15),外向斜率电导为13±6 pS(n = 15)。K(ATP)通道的开放概率(P(o))较低,在-V(p)= -100 mV时为0.15±0.06(n = 15)(V(p)为微电极电位),且随去极化略有增加。门控动力学特征为一个开放时间常数(tau(o)= 5.0±1.9 ms,n = 6)和两个关闭时间常数(tau(C1)= 5.2±1.5 ms,tau(C2)= 140±40 ms;n = 6)。在34%的膜片中,记录到另一种具有不同特性的钾通道,即sK通道。其电流-电压曲线呈S形,内向斜率电导为12±2 pS(n = 4)。其P(o)与电压无关,在-V(p)= -80 mV时平均为0.67±0.03(n = 4)。其开放时间和关闭时间分布均由一个时间常数描述(tau(o)= 96±19 ms,tau(C)= 10.5±3.6 ms;n = 4)。细胞外灌注40 mM牛磺酸对sK通道无影响,而K(ATP)通道的P(o)降低75%(从0.17±0.06降至0.04±0.02,n = 7,P<0.05)。总之,兔近端肾小管基底外侧钾电导至少是由两种重要性大致相当的钾通道共同作用的结果:一种是高电导、低开放概率的K(ATP)通道,另一种是低电导、高开放概率的sK通道。然而,先前描述的牛磺酸引起的基底外侧绝对钾电导降低是由单一类型的钾通道介导的:即ATP可阻断的钾通道。