Teramoto N, Creed K E, Brading A F
University Department of Pharmacology, Oxford, UK.
Naunyn Schmiedebergs Arch Pharmacol. 1997 Sep;356(3):418-24. doi: 10.1007/pl00005071.
The membrane potential in pig proximal urethra was examined by use of the microelectrode technique. In cells 1-2 cm from the bladder neck the membrane potential was quiescent, with a value of -37.2+/-2.5 mV (n = 16). In some cells small spontaneous de- and hyperpolarizations were seen. Glibenclamide (1 microM) caused a small but significant depolarization in tissue strips (12+/-3 mV, n = 3) and also in dispersed cells using whole-cell patch electrodes (13+/-3 mV, n = 5). In the conventional whole-cell voltage-clamp configuration, glibenclamide reduced the noise level of the basal membrane current at -50 mV and inhibited the membrane current in symmetrical 140 mM K+ conditions. In cell-attached patches, brief openings of a glibenclamide-sensitive 43 pS K+ channel (K(GS)-43 pS) were seen even under unstimulated conditions and greater activation occurred in the same membrane patch on subsequent application of 100 microM levcromakalim. These results provide direct evidence that glibenclamide-sensitive K+ channels may play a role in maintaining the resting membrane potential of pig proximal urethra under unstimulated conditions.
采用微电极技术检测猪近端尿道的膜电位。在距膀胱颈1 - 2厘米处的细胞中,膜电位处于静息状态,其值为-37.2±2.5毫伏(n = 16)。在一些细胞中可观察到小的自发性去极化和超极化。格列本脲(1微摩尔)在组织条中引起小幅度但显著的去极化(12±3毫伏,n = 3),在使用全细胞膜片钳电极的分散细胞中也引起去极化(13±3毫伏,n = 5)。在传统的全细胞电压钳配置中,格列本脲降低了-50毫伏时基底膜电流的噪声水平,并在对称的140毫摩尔钾离子条件下抑制膜电流。在细胞贴附式膜片中,即使在未受刺激的条件下也可观察到格列本脲敏感的43皮西门子钾离子通道(K(GS)-43 pS)的短暂开放,在随后施加100微摩尔的左旋克罗卡林时,同一膜片中会出现更大程度的激活。这些结果提供了直接证据,表明格列本脲敏感的钾离子通道可能在未受刺激的条件下维持猪近端尿道静息膜电位中发挥作用。