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来自小脑器官型培养物的大鼠浦肯野细胞体膜中的钠电导和钾电导。

Sodium and potassium conductances in somatic membranes of rat Purkinje cells from organotypic cerebellar cultures.

作者信息

Gähwiler B H, Llano I

机构信息

Brain Research Institute, Zürich, Switzerland.

出版信息

J Physiol. 1989 Oct;417:105-22. doi: 10.1113/jphysiol.1989.sp017793.

Abstract
  1. The somatic voltage-gated conductances of Purkinje cells in organotypic cultures (Gähwiler, 1981) were studied using the outside-out patch recording configuration of the patch-clamp technique (Hamill, Marty, Neher, Sakmann & Sigworth, 1981). 2. When activated by step depolarizations, the tetrodotoxin-sensitive voltage-dependent Na+ current presented two distinct phases: an initial surge of inward current fluctuations which activates rapidly upon pulse onset and decays within 20-40 ms, and a later phase in which discrete bursts of single-channel activity are interspersed with silent periods. 3. Ensemble fluctuation analysis of the current fluctuations during the early phase of the Na+ current and measurements of single channels during both early and late phases indicate that a single type of Na+ channel can account for both phases of the Na+ current. This channel has an elementary current amplitude of -2 pA at -40 mV. This amplitude did not vary significantly between -60 and -20 mV. The mean open time depended on membrane potential, increasing by a factor of three between -60 and -20 mV. 4. The early component of the Na+ current activated at a threshold of -60 mV and reached its maximum amplitude at -20, mid-point for the activation curve being -40 mV. Times-to-peak current decreased with membrane potential, from 3.5 ms at -60 mV to 0.3 ms at 0 mV. The decay phase of the current presented two exponential components, with time constants of 1.5 and 10 ms at -40 mV. The steady-state inactivation curve had a mid-point at -75 mV. 5. The late component of the Na+ current was observed in the voltage range from -60 to -20 mV, with a maximum at -40 mV. Its maximum amplitude corresponded to approximately 1.7% of the peak amplitude of the early component. 6. Macroscopic potassium currents were observed upon step depolarizations above a threshold of -30 mV. The currents activated in a voltage-dependent fashion, times-to-peak decreasing with depolarization, and partially inactivated during 40 ms depolarizing steps. Peak current amplitudes at any given membrane potential were decreased by depolarizing the holding potential. The macroscopic properties of the K+ current varied from patch to patch. 7. Two types of single-channel K+ currents were observed during steady-state depolarizations. The unitary current amplitudes were 2.7 and 10.4 pA at 30 mV, corresponding to chord conductances of 28 and 90 pS respectively.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 使用膜片钳技术的外向膜片记录模式(Hamill、Marty、Neher、Sakmann和Sigworth,1981年),对器官型培养物中浦肯野细胞的体细胞电压门控电导进行了研究(Gähwiler,1981年)。2. 当通过阶跃去极化激活时,河豚毒素敏感的电压依赖性Na⁺电流呈现出两个不同阶段:内向电流波动的初始激增,在脉冲开始时迅速激活,并在20 - 40毫秒内衰减;以及随后的阶段,其中单通道活动的离散爆发与静息期交替出现。3. 对Na⁺电流早期阶段的电流波动进行整体波动分析,并对早期和晚期阶段的单通道进行测量,结果表明单一类型的Na⁺通道可解释Na⁺电流的两个阶段。该通道在-40 mV时的基本电流幅度为-2 pA。在-60 mV至-20 mV之间,该幅度没有显著变化。平均开放时间取决于膜电位,在-60 mV至-20 mV之间增加了两倍。4. Na⁺电流的早期成分在-60 mV的阈值下激活,在-20 mV时达到最大幅度,激活曲线的中点为-40 mV。电流峰值时间随膜电位降低,从-60 mV时的3.5毫秒降至0 mV时的0.3毫秒。电流的衰减阶段呈现出两个指数成分,在-40 mV时的时间常数分别为1.5毫秒和10毫秒。稳态失活曲线的中点为-75 mV。5. 在-60 mV至-20 mV的电压范围内观察到Na⁺电流的晚期成分,在-40 mV时达到最大值。其最大幅度约相当于早期成分峰值幅度的1.7%。6. 在高于-30 mV的阈值进行阶跃去极化时,观察到宏观钾电流。电流以电压依赖性方式激活,峰值时间随去极化而减少,并在40毫秒的去极化步骤中部分失活。在任何给定膜电位下的峰值电流幅度会因钳制电位的去极化而降低。K⁺电流的宏观特性在不同膜片之间有所变化。7. 在稳态去极化期间观察到两种类型的单通道K⁺电流。在30 mV时,单位电流幅度分别为2.7 pA和10.4 pA,分别对应于28 pS和90 pS的弦电导。(摘要截短为400字)
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e54/1189258/61be1ecfff42/jphysiol00479-0121-a.jpg

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