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轮藻动作电位期间的氯离子和钾离子通道电流。膜电压和膜片电流的同步记录。

Cl- and K+ channel currents during the action potential in Chara. Simultaneous recording of membrane voltage and patch currents.

作者信息

Homann U, Thiel G

机构信息

Pflanzenphysiologisches Institut, Universität Göttingen, Germany.

出版信息

J Membr Biol. 1994 Sep;141(3):297-309. doi: 10.1007/BF00235139.

DOI:10.1007/BF00235139
PMID:7807528
Abstract

Patch currents in the cell attached-mode and action potentials (AP) have been recorded simultaneously in internodal cells of Chara corallina. The action potentials are closely correlated with transient patch currents. With pipettes containing either 50 mM CaCl2 or 100 mM KCl plus 1 or 5 mM CaCl2, these transients measured up to 100 to 200 pA per patch at zero mV. Transients had a mean duration (time during which the current was > or = half maximum peak amplitude) of about 1 sec, a maximum slope for current rising of about 400 pA sec-1 and a maximum rate of about 100 pA sec-1 for current decay, with no obvious effect of external Ca2+ on either of these parameters. In well-resolved recordings of current transients triggered by an action potential (AP), activities of two types of Cl--conducting channels (15 and 38 pS) have been identified. Since activity of these channels was only observed during action potentials but not upon positive voltage steps, these channels are not directly voltage gated but point to a cytoplasmic gating factor which accumulates during excitation and propagates from excited areas to the patch. A K(+)-conducting channel (40 pS) could be identified as well during an AP, when 100 mM KCl was in the pipette solution. The activity of this channel relaxed at the end of the APs with a time constant of about 3 sec. Stimulated activity of this channel is understood to cause the repolarization overshoot during the final phase of the action potential, whereas the transient activation of the Cl- channels determines the fast voltage changes of the action potential.

摘要

在珊瑚轮藻的节间细胞中,已同时记录了细胞贴附模式下的膜片电流和动作电位(AP)。动作电位与瞬时膜片电流密切相关。使用含有50 mM氯化钙或100 mM氯化钾加1或5 mM氯化钙的移液管,在零毫伏时,每个膜片的这些瞬变电流测量值高达100至200皮安。瞬变电流的平均持续时间(电流大于或等于最大峰值幅度一半的时间)约为1秒,电流上升的最大斜率约为400皮安/秒,电流衰减的最大速率约为100皮安/秒,外部钙离子对这些参数均无明显影响。在由动作电位触发的电流瞬变的清晰记录中,已识别出两种类型的氯离子传导通道(15和38皮秒)的活动。由于这些通道的活动仅在动作电位期间观察到,而在正向电压阶跃时未观察到,因此这些通道不是直接电压门控的,而是指向一种在兴奋过程中积累并从兴奋区域传播到膜片的细胞质门控因子。当移液管溶液中含有100 mM氯化钾时,在动作电位期间也可以识别出一个钾离子传导通道(40皮秒)。该通道的活动在动作电位结束时以约3秒的时间常数松弛。该通道的刺激活动被认为会导致动作电位最后阶段的复极化过冲,而氯离子通道的瞬时激活则决定了动作电位的快速电压变化。

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