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乙酰胆碱受体通道及其在培养的牛嗜铬细胞中被可乐定阻断的情况。

Acetylcholine receptor channels and their block by clonidine in cultured bovine chromaffin cells.

作者信息

Cull-Candy S G, Mathie A, Powis D A

机构信息

Department of Pharmacology, University College, London.

出版信息

J Physiol. 1988 Aug;402:255-78. doi: 10.1113/jphysiol.1988.sp017203.

Abstract
  1. Acetylcholine (10-50 microM) applied to bovine chromaffin cells under whole-cell voltage clamp produced an inward current and an increase in the noise level of the current trace. At concentrations greater than or equal to 20 microM the ACh current desensitized with time. Spectral analysis of the ACh-induced increase in current noise showed that it could be fitted by a single Lorentzian component with a time constant, tau noise = 11 +/- 0.9 ms (Vm = -80 mV). 2. Clonidine (2-30 microM) markedly reduced the size of the ACh-induced whole-cell current, and altered the shape of the noise spectrum. In the presence of clonidine, ACh noise spectra were fitted by two Lorentzian components with time constants which varied with clonidine concentration. The single-channel conductance from noise (gamma = 24 pS) was unaltered by clonidine. 3. The reduction in the size of the whole-cell ACh current, produced by clonidine, was not mimicked by adrenaline (at concentrations up to 60 microM). GABA-induced whole-cell currents and spectra of GABA noise were also unchanged suggesting that the effect of clonidine was specific for the ACh receptor channel. 4. When applied intracellularly (from the patch pipette) clonidine had no apparent influence on the whole-cell ACh current. Furthermore, when clonidine was perfused over the cell surface at a concentration sufficient to block the whole-cell ACh response, single ACh channels could still be recorded under the patch-pipette tip (i.e. in cell-attached patches, not exposed to clonidine). 5. Clonidine block showed little voltage dependence; the peak ACh current remained linearly dependent on clamp potential. In addition, the fast and slow time constants derived from ACh noise spectra in the presence of clonidine did not show the sort of dependence on antagonist concentration expected for simple channel block; this suggests that clonidine has a complex blocking action. 6. Single ACh channels recorded in outside-out patches had a conductance of gamma = 39 +/- 0.7 pS, although a subpopulation of smaller and larger events also occurred in some patches. The mean single-channel conductance in outside-out patches was unaltered by clonidine. 7. Under normal conditions the kinetics of single ACh channels were more complex than suggested from noise analysis. Burst length distributions could be described by two exponential components with fast and slow time constants of tau f = 0.69 +/- 0.17 and tau s = 9.51 +/- 0.84 ms.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在全细胞电压钳制下,将乙酰胆碱(10 - 50微摩尔)施加于牛嗜铬细胞,可产生内向电流,并使电流记录的噪声水平增加。当浓度大于或等于20微摩尔时,乙酰胆碱电流随时间脱敏。对乙酰胆碱诱导的电流噪声增加进行频谱分析表明,它可以用一个单一的洛伦兹分量拟合,时间常数τnoise = 11 ± 0.9毫秒(膜电位Vm = -80毫伏)。2. 可乐定(2 - 30微摩尔)显著减小了乙酰胆碱诱导的全细胞电流大小,并改变了噪声频谱的形状。在可乐定存在的情况下,乙酰胆碱噪声频谱由两个洛伦兹分量拟合,其时间常数随可乐定浓度而变化。由噪声得出的单通道电导(γ = 24皮安)不受可乐定影响。3. 可乐定导致的全细胞乙酰胆碱电流大小的减小,肾上腺素(浓度高达60微摩尔)无法模拟。γ-氨基丁酸诱导的全细胞电流和γ-氨基丁酸噪声频谱也未改变,这表明可乐定的作用对乙酰胆碱受体通道具有特异性。4. 当从膜片吸管内向细胞内施加可乐定时,对全细胞乙酰胆碱电流没有明显影响。此外,当以足以阻断全细胞乙酰胆碱反应的浓度将可乐定灌注到细胞表面时,仍可在膜片吸管尖端下方记录到单个乙酰胆碱通道(即,在细胞贴附式膜片中,未暴露于可乐定)。5. 可乐定阻断几乎没有电压依赖性;乙酰胆碱电流峰值仍与钳制电位呈线性相关。此外,在可乐定存在的情况下,从乙酰胆碱噪声频谱得出的快速和慢速时间常数并未表现出简单通道阻断预期的那种对拮抗剂浓度的依赖性;这表明可乐定具有复杂的阻断作用。6. 在外侧向外式膜片中记录的单个乙酰胆碱通道电导为γ = 39 ± 0.7皮安,尽管在一些膜片中也出现了较小和较大事件的亚群。外侧向外式膜片中的平均单通道电导不受可乐定影响。7. 在正常条件下,单个乙酰胆碱通道的动力学比噪声分析所显示的更为复杂。爆发长度分布可用两个指数分量描述,快速和慢速时间常数分别为τf = 0.69 ± 0.17毫秒和τs = 9.51 ± 0.84毫秒。(摘要截断于400字)

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