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成年大鼠交感神经元中的双脉冲钙通道电流易化

Double-pulse calcium channel current facilitation in adult rat sympathetic neurones.

作者信息

Ikeda S R

机构信息

Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta 30912-2300.

出版信息

J Physiol. 1991 Aug;439:181-214. doi: 10.1113/jphysiol.1991.sp018663.

Abstract
  1. Double-pulse facilitation of Ca2+ channel currents in enzymatically dispersed adult rat superior cervical ganglion neurones was investigated using the whole-cell variant of the patch-clamp technique. Voltage-clamp recordings were performed at room temperature (21-24 degrees C) in solutions designed to isolate Ca2+ channel currents. 2. Ba2+ currents, elicited by a 0 mV test pulse, were increased in amplitude when preceded by a 40 ms pulse to voltages greater than 0 mV. The magnitude of facilitation was dependent on pre-pulse voltage and reached a maximum of 50% (i.e. 1.5 x the current amplitude elicited without a pre-pulse) at a pre-pulse voltage of +80 mV. Half-maximal facilitation occurred at about +25 mV. A small decrease (-6%) in test pulse amplitude was present at pre-pulse voltages between -40 and 0 mV. The magnitude of facilitation was also dependent on test pulse voltage. Facilitation was greatest between test pulse voltages of -10 and 0 mV. 3. Facilitation slowly decreased during prolonged (1 h) dialysis of the neurone even though the Ba2+ current amplitude was well maintained. 4. Increasing the pre-pulse duration over the range 0-120 ms produced an exponential increase in facilitation with a time constant of 17.3 ms. Conversely, lengthening the interpulse duration over the range 5-915 ms, while maintaining a constant pre-pulse amplitude and duration, resulted in an exponential decrease in facilitation with a time constant of 197 ms. 5. At a test potential of 0 mV, the decay of the facilitated Ba2+ current component was fitted to a double exponential function with time constants of about 25 and 150 ms. The time constants had little pre-pulse voltage dependence between +30 to +80 mV. 6. The initial rising phase of both the control and facilitated Ba2+ current were reasonably well described by a single exponential (tau rise) after a delay of 300 microseconds. The tau rise versus test pulse potential relationship was 'bell shaped' over the test pulse voltage of -20 to +30 mV reaching a maximum near -5 mV. tau rise was similar for control and facilitated currents except at potentials greater than +10 mV where the rise of the facilitated current was accelerated. 7. Control and facilitated activation curves, as derived from tail current amplitudes, were described by the sum of two Boltzmann functions. A facilitating pre-pulse produced an increase in the proportion of the current contributed by the component activated at more hyperpolarized test potentials.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 运用膜片钳技术的全细胞变体,研究了酶解分散的成年大鼠颈上神经节神经元中Ca2+通道电流的双脉冲易化现象。在室温(21 - 24摄氏度)下,于旨在分离Ca2+通道电流的溶液中进行电压钳记录。2. 由0 mV测试脉冲引发的Ba2+电流,在由一个40 ms脉冲将电压提升至大于0 mV的电压之前施加时,其幅度会增大。易化程度取决于预脉冲电压,在预脉冲电压为 +80 mV时达到最大值50%(即无预脉冲时引发的电流幅度乘以1.5)。半最大易化发生在约 +25 mV。在预脉冲电压为 -40至0 mV之间时,测试脉冲幅度有小幅下降(-6%)。易化程度还取决于测试脉冲电压。在测试脉冲电压为 -10至0 mV之间时易化作用最大。3. 即使Ba2+电流幅度保持良好,在对神经元进行长时间(1小时)透析期间,易化作用仍会缓慢降低。4. 将预脉冲持续时间在0 - 120 ms范围内增加,会使易化作用呈指数增加,时间常数为17.3 ms。相反,在保持预脉冲幅度和持续时间不变的情况下,将脉冲间隔持续时间在5 - 915 ms范围内延长,会导致易化作用呈指数降低,时间常数为197 ms。5. 在测试电位为0 mV时,易化的Ba2+电流成分的衰减拟合为双指数函数,时间常数约为25和150 ms。在 +30至 +80 mV之间,时间常数对预脉冲电压的依赖性较小。6. 在延迟300微秒后,对照和易化的Ba2+电流的初始上升阶段都能较好地用单个指数(tau上升)来描述。在 -20至 +30 mV的测试脉冲电压范围内,tau上升与测试脉冲电位的关系呈“钟形”,在接近 -5 mV处达到最大值。对照和易化电流的tau上升相似,除了在大于 +10 mV的电位处,易化电流的上升加速。7. 由尾电流幅度得出的对照和易化激活曲线由两个玻尔兹曼函数之和来描述。一个易化预脉冲使在更超极化测试电位下激活的电流成分所占比例增加。(摘要截断于400字)
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2c/1180105/5bd0a618f8b0/jphysiol00443-0214-a.jpg

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