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A novel large-conductance Ca(2+)-activated potassium channel and current in nerve terminals of the rat neurohypophysis.

机译:在大鼠神经垂体神经末梢的新型大电导Ca(2+)激活钾通道和电流。

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摘要

1. Nerve terminals of the rat posterior pituitary were acutely dissociated and identified using a combination of morphological and immunohistochemical techniques. Terminal membrane currents were studied using the 'whole-cell' patch clamp technique and channels were studied using inside-out and outside-out patches. 2. In physiological solutions, but with 7 mM 4-aminopyridine (4-AP), depolarizing voltage clamp steps from different holding potentials (-90 or -50 mV) elicited a fast, inward current followed by a slow, sustained, outward current. This outward current did not appear to show any steady-state inactivation. 3. The threshold for activation of the outward current was -30 mV and the current-voltage relation was 'bell-shaped'. The amplitude increased with increasingly depolarized potential steps. The outward current reversal potential was measured using tail current analysis and was consistent with that of a potassium current. 4. The sustained potassium current was determined to be dependent on the concentration of intracellular calcium. Extracellular Cd2+ (80 microM), a calcium channel blocker, also reversibly abolished the outward current. 5. The current was delayed in onset and was sustained over the length of a 150 ms-duration depolarizing pulse. The outward current reached a peak plateau and then decayed slowly. The decay was fitted by a single exponential with a time constant of 9.0 +/- 2.2 s. The decay constants did not show a dependence on voltage but rather on intracellular Ca2+. The time course of recovery from this decay was complex with full recovery taking > 190 s. 6. 4-AP (7 mM), dendrotoxin (100 nM), apamin (40-80 nM), and charybdotoxin (10-100 nM) had no effect on the sustained outward current. In contrast Ba2+ (200 microM) and tetraethylammonium inhibited the current, the latter in a dose-dependent manner (apparent concentration giving 50% of maximal inhibition (IC50) = 0.51 mM). 7. The neurohypophysial terminal outward current recorded here corresponds most closely to a Ca(2+)-activated K+ current (IK(Ca)) and not to a delayed rectifier or IA-like current. It also has properties different from that of the Ca(2+)-dependent outward current described in the magnocellular neuronal cell bodies of the hypothalamus. 8. A large conductance channel is often observed in isolated rat neurohypophysial nerve terminals. The channel had a unit conductance of 231 pS in symmetrical 150 mM K+.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.结合形态学和免疫组化技术,对大鼠垂体后叶神经末梢进行急性分离。使用“全细胞”膜片钳技术研究末端膜电流,并使用由内而外的膜片通道研究通道。 2.在生理溶液中,但是使用7 mM 4-氨基吡啶(4-AP),来自不同保持电位(-90或-50 mV)的去极化电压钳位步骤会引起快速的内向电流,然后缓慢,持续的外向电流。这种向外的电流似乎没有显示出任何稳态失活。 3.激活向外电流的阈值为-30 mV,电流-电压关系为“钟形”。振幅随着去极化电位阶跃的增加而增加。使用尾电流分析法测量了向外的电流反向电位,该电位与钾电流一致。 4.确定持续的钾电流取决于细胞内钙的浓度。细胞外Cd2 +(80 microM),一种钙通道阻滞剂,也可逆地消除了向外的电流。 5.电流开始延迟,并持续150 ms持续时间的去极化脉冲。向外的电流达到峰值平稳,然后缓慢衰减。衰减由时间常数为9.0 +/- 2.2 s的单个指数拟合。衰减常数与电压无关,而与细胞内Ca2 +有关。从这种衰变中恢复的时间过程很复杂,完全恢复要花费> 190 s。 6. 4-AP(7 mM),树状毒素(100 nM),Apapamin(40-80 nM)和Charybdotoxin(10-100 nM)对持续的外向电流没有影响。相比之下,Ba2 +(200 microM)和四乙铵抑制电流,后者以剂量依赖的方式(表观浓度给出最大抑制作用的50%(IC50)= 0.51 mM)。 7.此处记录的神经垂体末梢向外电流最接近于Ca(2+)激活的K +电流(IK(Ca)),而不是延迟的整流器或IA样电流。它也具有不同于下丘脑的大细胞神经元细胞体中描述的Ca(2+)依赖向外电流的特性。 8.在孤立的大鼠神经垂体神经末梢中经常观察到较大的电导通道。该通道在对称的150 mM K +中具有231 pS的单位电导(抽象截断为400字)

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  • 作者

    Wang, G; Thorn, P; Lemos, J R;

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  • 年度 1992
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  • 正文语种 en
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