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小鼠小脑颗粒细胞中失活和非失活的二氢吡啶敏感性Ca2+通道

Inactivating and non-inactivating dihydropyridine-sensitive Ca2+ channels in mouse cerebellar granule cells.

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.

出版信息

J Physiol. 1991 Aug;439:301-23. doi: 10.1113/jphysiol.1991.sp018668.

DOI:10.1113/jphysiol.1991.sp018668
PMID:1654414
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1180110/
Abstract
  1. Granule cells were dissociated from mouse cerebellum and grown in vitro. Currents through single Ca2+ channels were recorded from the cell body with the patch clamp technique. 2. Voltage steps to 0 mV produced brief channel openings with a mean open time of approximately 0.5 ms. The single-channel conductance measured from the amplitude of the single-channel current with 90 mM-Ba2+ in the patch electrode was 22 pS. 3. The probability of Ca2+ channel opening increased with test potentials more positive than -30 mV, with half-activation near 0 mV, and followed the Boltzmann relation for the activation of whole-cell Ca2+ current. 4. Voltage steps to potentials more positive than 0 mV produced more channel activity at the beginning than at the end of the voltage step. The average of the single-channel currents decayed to a non-zero level with a time course similar to that of the whole-cell Ca2+ current. 5. The amplitude as well as the decay of the mean current measured during a test pulse to 0 mV was reduced as the holding potential was made more positive than approximately -90 mV. The change in the open channel probability with holding potential followed the Boltzmann relation which described the inactivation of the whole-cell Ca2+ current. 6. Ca2+ channel activity persisted for over several minutes after excising the patch from the cell body when intracellular cyclic AMP was increased. After patch excision, the number of functional channels decreased to a level where only one channel at a time was active. Ca2+ channel openings appeared as either short bursts at the beginning of the voltage step or long bursts that lasted throughout the pulse. 7. Exposing the cell to the dihydropyridine agonist +(S)-202-791 markedly increased the fraction of sweeps with long openings and produced a non-decaying mean current that was approximately 5 times larger than control. In a fraction of the sweeps, however, long openings occurred more frequently at the beginning than at the end of the voltage step and these produced a decaying mean current. 8. Shifting the holding potential to more positive potentials in the presence of the dihydropyridine agonist preferentially reduced the number of brief openings while sparing the long openings. The amplitude of the mean current was similar to that obtained from the more negative holding potential and there was no change in the fraction of sweeps with long openings that occurred at the beginning of the voltage pulse.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 从小鼠小脑分离出颗粒细胞并在体外培养。采用膜片钳技术从细胞体记录单个Ca2+通道的电流。2. 向0 mV的电压阶跃产生短暂的通道开放,平均开放时间约为0.5毫秒。在膜片电极中使用90 mM - Ba2+,根据单通道电流幅度测得的单通道电导为22 pS。3. Ca2+通道开放的概率随着测试电位比 - 30 mV更正而增加,半激活电位接近0 mV,并遵循全细胞Ca2+电流激活的玻尔兹曼关系。4. 向比0 mV更正的电位进行电压阶跃时,在电压阶跃开始时比结束时产生更多的通道活动。单通道电流的平均值以与全细胞Ca2+电流相似的时间进程衰减到非零水平。5. 当保持电位比约 - 90 mV更正时,在向0 mV的测试脉冲期间测量的平均电流的幅度以及衰减都会降低。开放通道概率随保持电位的变化遵循描述全细胞Ca2+电流失活的玻尔兹曼关系。6. 当细胞内环磷酸腺苷增加时,从细胞体切除膜片后,Ca2+通道活动持续数分钟以上。膜片切除后,功能性通道的数量减少到一次只有一个通道活跃的水平。Ca2+通道开放表现为电压阶跃开始时的短爆发或整个脉冲持续的长爆发。7. 将细胞暴露于二氢吡啶激动剂 +(S)-202-791 显著增加了出现长开放的扫描比例,并产生了一个非衰减的平均电流,该电流比对照大约大5倍。然而,在一部分扫描中,长开放在电压阶跃开始时比结束时更频繁出现,并且这些产生了衰减的平均电流。8. 在存在二氢吡啶激动剂的情况下,将保持电位向更正的电位移动优先减少了短暂开放的数量,同时保留了长开放。平均电流的幅度与从更负的保持电位获得的幅度相似,并且在电压脉冲开始时出现长开放的扫描比例没有变化。(摘要截断于400字)

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Potassium ion current in the squid giant axon: dynamic characteristic.鱿鱼巨轴突中的钾离子电流:动态特性
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