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钙离子对兔门静脉平滑肌细胞中去甲肾上腺素诱发的阳离子电流的促进作用。

Facilitatory effect of Ca2+ on the noradrenaline-evoked cation current in rabbit portal vein smooth muscle cells.

作者信息

Helliwell R M, Large W A

机构信息

Department of Pharmacology and Clinical Pharmacology, St George's Hospital Medical School, Cranmer Terrace, London SW17 0RE, UK.

出版信息

J Physiol. 1998 Nov 1;512 ( Pt 3)(Pt 3):731-41. doi: 10.1111/j.1469-7793.1998.731bd.x.

Abstract
  1. The facilitatory effect of external calcium ions (Ca2+o) on the alpha1-adrenoceptor-activated non-selective cation current (Icat) was investigated in rabbit portal vein cells using noise and voltage-jump relaxation analysis of the whole-cell macroscopic current. 2. Micromolar concentrations of Ca2+o potentiated the peak amplitude of Icat at a holding potential (Vh) of -50 mV. The effective [Ca2+]o which produced a 50% potentiation (EC50) was 3 microM. 3. From noise analysis the estimated single channel conductance (gamma) was approximately 23 pS with [Ca2+]o between 3 and 100 microM, whereas in < 10 nM or 1 microM Ca2+o gamma was approximately 10 pS. 4. The spectral density function of Icat at negative potentials could be described by the sum of two Lorentzians in every [Ca2+]o examined. The time constant of the lower frequency Lorentzian component (tau1) was about 11 ms in < 10 nM Ca2+o and was about 45 ms in micromolar concentrations of Ca2+o (1-100 microM). In contrast, the time constant of the higher frequency component (tau2) was similar in < 10 nM Ca2+o and 100 microM Ca2+o (between 1 and 2 ms). 5. The lower frequency Lorentzian component was responsible for about half the total current variance in < 10 nM Ca2+o whereas in micromolar concentrations of Ca2+o it was responsible for most of the measured current variance. 6. In voltage-jump experiments, on stepping the voltage from -50 to +50 mV the instantaneous current was followed by an exponential decline of Icat. Stepping back to -30 mV produced an exponential inward relaxation (Irelax,-30 mV) leading to an increase in the steady-state amplitude of Icat in micromolar concentrations of Ca2+o, but this relaxation was not observed in < 10 nM Ca2+o. The relative amplitude of Irelax,-30 mV increased in an [Ca2+]o-dependent manner (EC50 was 2 microM) although the time constant of this relaxation (taurelax,-30 mV) remained unchanged (about 60 ms between 2 and 100 microM Ca2+o). 7. The data suggest that Ca2+o produces marked changes in the kinetics and single channel conductance of cation channels, which may account for the facilitatory effect of micromolar concentrations of Ca2+o on the peak amplitude of Icat.
摘要
  1. 采用全细胞膜片钳宏观电流的噪声分析和电压阶跃弛豫分析技术,研究了细胞外钙离子(Ca2+o)对兔门静脉细胞中α1 - 肾上腺素能受体激活的非选择性阳离子电流(Icat)的促进作用。2. 微摩尔浓度的Ca2+o在 - 50 mV的钳制电位(Vh)下增强了Icat的峰值幅度。产生50%增强作用的有效[Ca2+]o(EC50)为3 μM。3. 根据噪声分析,在[Ca2+]o为3至100 μM时,估计的单通道电导(γ)约为23 pS,而在<10 nM或1 μM Ca2+o时,γ约为10 pS。4. 在每个检测的[Ca2+]o浓度下,负电位时Icat的功率谱密度函数可用两个洛伦兹函数之和来描述。在<10 nM Ca2+o时,低频洛伦兹分量的时间常数(tau1)约为11 ms,在微摩尔浓度的Ca2+o(1 - 100 μM)时约为45 ms。相比之下,高频分量的时间常数(tau2)在<10 nM Ca2+o和100 μM Ca2+o时相似(在1至2 ms之间)。5. 在<10 nM Ca2+o时,低频洛伦兹分量约占总电流方差的一半,而在微摩尔浓度的Ca2+o时,它占测量电流方差的大部分。6. 在电压阶跃实验中,将电压从 - 50 mV 阶跃到 + 50 mV时,瞬时电流之后是Icat的指数下降。再回到 - 30 mV会产生指数向内弛豫(Irelax,-30 mV),导致微摩尔浓度的Ca2+o时Icat的稳态幅度增加,但在<10 nM Ca2+o时未观察到这种弛豫。Irelax,-30 mV的相对幅度以[Ca2+]o依赖的方式增加(EC50为2 μM),尽管这种弛豫的时间常数(taurelax,-30 mV)保持不变(在2至100 μM Ca2+o之间约为60 ms)。7. 数据表明,Ca2+o会使阳离子通道的动力学和单通道电导发生显著变化,这可能解释了微摩尔浓度的Ca2+o对Icat峰值幅度的促进作用。

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