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大鼠垂体神经末梢中一种缓慢激活的电压依赖性钾电流。

A slowly activating voltage-dependent K+ current in rat pituitary nerve terminals.

作者信息

Kilic G, Stolpe A, Lindau M

机构信息

Department of Molecular Cell Research, Max-Planck Institute for Medical Research, Heidelberg, Germany.

出版信息

J Physiol. 1996 Dec 15;497 ( Pt 3)(Pt 3):711-25. doi: 10.1113/jphysiol.1996.sp021802.

Abstract
  1. A novel slowly activating voltage-dependent K+ current was observed in isolated nerve terminals from rat neurohypophysis using the whole-cell configuration of the patch-clamp technique. 2. The activation kinetics of the slow current could be fitted assuming Hodgkin--Huxley-type kinetics, an exponential, n, of 1.3 and activation time constants decreasing from 4 s at -50 mV to 0.7s at +40 mV. 3. A positive shift of reversal potential was observed when [K+] was increased in the bath solution. The current is carried mainly but not exclusively by K+ ions. 4. When intracellular free [Mg2+] was low (approximately 60 microM), average current density was 74 pA pF-1 at membrane potentials around 0 mV. In 83% of nerve terminals current amplitude was > 10 pA pF-1. 5. The slow current was never observed when the pipette contained 4.6 mM free Mg2+. At a physiological level of free Mg2+ (0.5 mM) the average current density was 16 pA pF-1. 6. When nerve terminals were analysed after patch-clamp experiments for vasopressin content by immunodetection, no difference in current amplitude was found between the terminals containing vasopressin and all analysed terminals. 7. The voltage dependence of activation was fitted by a Boltzmann equation giving a half-activation potential of -37 mV and a slope factor of about 9 mV. 8. Tail current deactivation kinetics was biexponential with time constants of 0.12 and 1.5s. Kinetics was dependent on the duration of the activating pulse. 9. Noise analysis of the slow current indicated a single-channel current of 0.33 pA at +6 mV, corresponding to a single-channel conductance of 4.3 pS. 10. This is the first demonstration of a current similar to the slow K+ current, IKs, in a neurone, suggesting that a protein similar to the IKs-inducing channel protein IsK (minK) may be present in peptidergic nerve terminals. 11. The activation properties are consistent with a role of the slow current in inhibition of excitability, at least at the level of the nerve terminal.
摘要
  1. 运用膜片钳技术的全细胞模式,在大鼠神经垂体分离出的神经末梢中观察到一种新型的缓慢激活的电压依赖性钾电流。2. 假设霍奇金-赫胥黎型动力学,缓慢电流的激活动力学可以得到拟合,指数n为1.3,激活时间常数从-50mV时的4秒降至+40mV时的0.7秒。3. 当浴液中[K⁺]增加时,观察到反转电位正向移动。该电流主要但并非完全由K⁺离子携带。4. 当细胞内游离[Mg²⁺]较低(约60微摩尔)时,在膜电位约为0mV时平均电流密度为74皮安皮法⁻¹。在83%的神经末梢中电流幅度>10皮安皮法⁻¹。5. 当移液管中含有4.6毫摩尔游离Mg²⁺时,从未观察到缓慢电流。在生理水平的游离Mg²⁺(0.5毫摩尔)下,平均电流密度为16皮安皮法⁻¹。6. 在膜片钳实验后,通过免疫检测分析神经末梢中的加压素含量,发现含有加压素的末梢与所有分析的末梢之间在电流幅度上没有差异。7. 激活的电压依赖性通过玻尔兹曼方程拟合,给出半激活电位为-37mV,斜率因子约为9mV。8. 尾电流失活动力学是双指数的,时间常数分别为0.12和1.5秒。动力学取决于激活脉冲的持续时间。9. 对缓慢电流的噪声分析表明,在+6mV时单通道电流为0.33皮安,对应单通道电导为4.3皮西门子。10. 这是首次在神经元中证明存在类似于缓慢钾电流IKs的电流,表明在肽能神经末梢中可能存在类似于诱导IKs的通道蛋白IsK(minK)的蛋白质。11. 其激活特性与缓慢电流在抑制兴奋性方面的作用一致,至少在神经末梢水平是如此。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ad/1160967/a2dec84be54e/jphysiol00387-0136-a.jpg

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