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从小鼠小脑培养的颗粒细胞中钙电流的失活。

Inactivation of calcium currents in granule cells cultured from mouse cerebellum.

作者信息

Slesinger P A, Lansman J B

机构信息

Graduate Program in Neuroscience, School of Medicine, University of California, San Francisco 94143-0450.

出版信息

J Physiol. 1991 Apr;435:101-21. doi: 10.1113/jphysiol.1991.sp018500.

Abstract
  1. Cells dissociated from mouse cerebellum were grown in vitro. Ca2+ channel currents were recorded from granule cells with the patch-clamp technique under conditions which suppressed currents through Na+ and K+ channels and minimized run-down of current through Ca2+ channels. 2. A strong depolarizing voltage step from a hyperpolarized holding potential produced inward Ca2+ channel current that decayed exponentially to a non-zero level. Inward current decayed to approximately 40% of its peak amplitude (range 20-90%). 3. The inward current increased in amplitude when Ca2+ was replaced with Ba2+ or after raising the concentration of extracellular Ba2+, but the rate of decay of current was unaffected. 4. The current-voltage (I-V) relation showed that peak or sustained current increased with voltage pulses more positive than approximately -30 mV, reached a maximum amplitude near +20 mV and became progressively smaller with larger depolarizations. 5. The tail currents produced after rapidly repolarizing the membrane potential to -70 mV from a positive test pulse decayed along a single exponential time course with a time constant of approximately 0.5 ms. The amplitude of tail current measured at a fixed repolarization potential increased as the pre-pulse was made more positive and reached a maximum with pre-pulses more positive than +40 mV. A plot of normalized amplitude of the tail current as a function of the pre-pulse potential was fitted with a Boltzmann relation with V1/2 = approximately + 8 mV and steepness k = 14 mV. 6. Shifting the holding potential to more positive potentials reduced the amplitude of the Ca2+ channel current elicited by the fixed voltage step and abolished the decay of the inward current. The peak current was normalized to the maximum peak current elicited from a very negative holding potential and plotted as a function of holding potential. The points were fitted with a Boltzmann relation for inactivation with V1/2 = approximately -57 mV and steepness k = 14 mV. 7. The onset of inactivation was studied in two-pulse experiments in which the duration of conditioning pre-pulse was varied. Increasing the duration of a pre-pulse to a fixed potential reduced the peak inward current evoked by the second test pulse. Plotting normalized current as a function of pre-pulse duration showed that inactivation developed along a double exponential time course. Both fast and slow time constants decreased as the pre-pulse potential was made more positive.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 从小鼠小脑分离出的细胞在体外培养。采用膜片钳技术在抑制钠通道和钾通道电流并使钙通道电流衰减最小化的条件下,记录颗粒细胞的钙通道电流。2. 从超极化的钳制电位施加一个强去极化电压阶跃,产生内向钙通道电流,该电流呈指数衰减至非零水平。内向电流衰减至其峰值幅度的约40%(范围为20 - 90%)。3. 当用钡离子替代钙离子或提高细胞外钡离子浓度时,内向电流幅度增加,但电流衰减速率不受影响。4. 电流 - 电压(I - V)关系表明,峰值或持续电流在电压脉冲大于约 - 30 mV时随电压增加,在 + 20 mV附近达到最大幅度,且随着更大的去极化逐渐减小。5. 在从正向测试脉冲将膜电位快速复极化至 - 70 mV后产生的尾电流,沿单一指数时间进程衰减,时间常数约为0.5 ms。在固定复极化电位下测量的尾电流幅度随着预脉冲电位更正而增加,在预脉冲电位大于 + 40 mV时达到最大。将尾电流归一化幅度作为预脉冲电位的函数作图,拟合得到玻尔兹曼关系,V1/2约为 + 8 mV,斜率k为14 mV。6. 将钳制电位向更正电位移动,可降低由固定电压阶跃诱发的钙通道电流幅度,并消除内向电流的衰减。将峰值电流归一化至从非常负的钳制电位诱发的最大峰值电流,并作为钳制电位的函数作图。这些点拟合得到失活的玻尔兹曼关系,V1/2约为 - 57 mV,斜率k为14 mV。7. 在双脉冲实验中研究失活的起始,其中条件预脉冲的持续时间可变。将预脉冲到固定电位的持续时间增加,会降低第二个测试脉冲诱发的内向峰值电流。将归一化电流作为预脉冲持续时间的函数作图表明,失活沿双指数时间进程发展。随着预脉冲电位更正,快速和慢速时间常数均减小。(摘要截断于400字)

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