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Patch-clamp studies of slow potential-sensitive potassium channels in longitudinal smooth muscle cells of rabbit jejunum

机译:膜片钳研究家兔空肠纵向平滑肌细胞中缓慢的电位敏感钾通道

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摘要

1. The patch-clamp technique was used to study single channel currents in membrane patches of longitudinal smooth muscle cells of rabbit jejunum dispersed by collagenase treatment. Recordings were made from both cell-attached and isolated patches.2. The predominant unit currents observed were outward at membrane potentials positive to the potassium equilibrium potential (EK) and they were rapidly and reversibly blocked by tetraethylammonium (TEA). Their size varied as EK was changed but was not noticeably affected by changing ENa, ECl or ECa; it was little altered in calcium-free EGTA solution. Thus, these currents apparently result mainly, if not exclusively, from the movements of potassium ions through channels insensitive to the calcium ion concentration. The present study describes the properties of these potassium channels.3. The unit conductance varied slightly with potential in most experiments; around zero potential it was about 50 pS. The conductance was dependent upon the potassium, but not the calcium, gradient. Sub levels of conductance of about two-thirds and, less commonly, one-third of the fully conducting channel state were sometimes seen.4. Membrane patches were studied which showed one to about twelve levels of outward current which were presumed to result from the opening of up to twelve channels having the same characteristics. The probability of channel open state varied with membrane potential, increasing in the potential range -40 to +40 mV. Channel openings were rare negative to -40 mV. No inward currents through these potassium channels were observed as openings were not seen at membrane potentials negative to EK.5. When the probability of channel opening was low, channel openings occurred in bursts which could be separated by several seconds. Analysis of the openings of a single channel revealed that open times and short closed times were exponentially distributed with mean durations of 15-45 ms and about 6 ms at zero potential. In some patches regular cyclical openings of several channels occurred. In other patches openings of individual channels appeared to be independent events as they were reasonably fitted by a binomial distribution.6. Following a step change from negative potentials, where channels were closed, to more positive potentials, channel openings increased during a period of 10 s to reach a steady state. No evidence of inactivation was observed.7. These results suggest the existence of a population of potential-sensitive potassium-selective ion channels in the smooth muscle cell membrane which are closed at the resting membrane potential and which open upon depolarization with slow (seconds) kinetics; these may be involved in the slow potential (wave) activity of this muscle.
机译:1.膜片钳技术用于研究胶原酶处理分散的兔空肠纵向平滑肌细胞膜片中的单通道电流。从细胞贴片和分离贴片上进行记录。2。观察到的主要单位电流以与钾平衡电位(EK)正的膜电位向外流出,并被四乙铵(TEA)快速且可逆地阻断。它们的大小随EK的变化而变化,但不受ENa,EC1或ECa的变化的明显影响;在无钙的EGTA溶液中变化很小。因此,这些电流显然主要地(如果不是排他性的话)是由钾离子通过对钙离子浓度不敏感的通道的运动引起的。本研究描述了这些钾通道的性质。3。在大多数实验中,单位电导随电位的变化略有不同。零电位附近约为50 pS。电导率取决于钾的梯度,而不取决于钙的梯度。有时会看到电导水平低于全导电沟道状态的三分之二,而很少见的是三分之一。4。对膜片进行了研究,该膜片显示出一到大约十二个水平的外向电流,推测是由于打开多达十二个具有相同特性的通道而导致的。通道打开状态的概率随膜电位而变化,在-40至+40 mV的电位范围内增加。通道开口很少会出现负值,即-40 mV。没有观察到通过这些钾通道的内向电流,因为在膜电势为EK.5时未见开口。当通道打开的可能性很低时,通道打开会突然爆发,可能会间隔几秒钟。对单个通道的打开进行分析后发现,打开时间和短关闭时间呈指数分布,平均持续时间为15-45 ms,零电势时约为6 ms。在某些补丁中,发生了几个通道的定期周期性打开。在其他斑块中,单个通道的开口似乎是独立的事件,因为它们通过二项分布合理地拟合。6。从通道关闭的负电位逐步变为更多正电位之后,通道开口在10 s的时间内增加,达到稳态。没有观察到灭活的证据。7。这些结果表明,在平滑肌细胞膜中存在电位敏感的钾选择性离子通道,这些通道在静止膜电位处关闭,并且在去极化时以慢速(秒)动力学打开。这些可能与该肌肉的缓慢潜伏(波)活动有关。

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