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本文引用的文献

1
Sodium and calcium action potential in pituitary cells.垂体细胞中的钠和钙动作电位。
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2
A quantitative description of membrane current and its application to conduction and excitation in nerve.膜电流的定量描述及其在神经传导和兴奋中的应用。
J Physiol. 1952 Aug;117(4):500-44. doi: 10.1113/jphysiol.1952.sp004764.
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Voltage clamp studies on the effect of internal cesium ion on sodium and potassium currents in the squid giant axon.关于内部铯离子对枪乌贼巨大轴突中钠电流和钾电流影响的电压钳研究。
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Calcium-activated and voltage-dependent potassium conductances in clonal pituitary cells.克隆垂体细胞中的钙激活和电压依赖性钾电导。
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5
Electrical behaviour in a line of anterior pituitary cells (GH cells) and the influence of the hypothalamic peptide, thyrotrophin releasing factor.垂体前叶细胞系(生长激素细胞)中的电活动及下丘脑肽促甲状腺激素释放因子的影响
Neuroscience. 1980;5(2):421-31. doi: 10.1016/0306-4522(80)90117-7.
6
Calcium channels in excitable cell membranes.可兴奋细胞膜上的钙通道。
Annu Rev Physiol. 1983;45:341-58. doi: 10.1146/annurev.ph.45.030183.002013.
7
Sodium and calcium channels in bovine chromaffin cells.牛嗜铬细胞中的钠通道和钙通道。
J Physiol. 1982 Oct;331:599-635. doi: 10.1113/jphysiol.1982.sp014394.
8
A patch-clamp study of bovine chromaffin cells and of their sensitivity to acetylcholine.一项关于牛嗜铬细胞及其对乙酰胆碱敏感性的膜片钳研究。
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9
Studies of calcium channels in rat clonal pituitary cells with patch electrode voltage clamp.采用膜片钳电极电压钳技术对大鼠垂体克隆细胞中的钙通道进行研究。
J Physiol. 1982 Oct;331:231-52. doi: 10.1113/jphysiol.1982.sp014371.
10
Effects of nystatin-mediated intracellular ion substitution on membrane currents in calf purkinje fibres.制霉菌素介导的细胞内离子置换对小牛浦肯野纤维膜电流的影响。
J Physiol. 1982 Aug;329:569-87. doi: 10.1113/jphysiol.1982.sp014320.

垂体前叶细胞转化系中的钠通道和钙通道。

Na and Ca channels in a transformed line of anterior pituitary cells.

作者信息

Matteson D R, Armstrong C M

出版信息

J Gen Physiol. 1984 Mar;83(3):371-94. doi: 10.1085/jgp.83.3.371.

DOI:10.1085/jgp.83.3.371
PMID:6325587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2215643/
Abstract

The ionic conductances of GH3 cells, a transformed line from rat anterior pituitary, have been studied using the whole-cell variant of the patch-clamp technique (Hamill et al., 1981). Pipettes of very low resistance were used, which improved time resolution and made it possible to control the ion content of the cell interior, which equilibrated very rapidly with the pipette contents. Time resolution was further improved by using series resistance compensation and "ballistic charging" of the cell capacitance. We have identified and partially characterized at least three conductances, one carrying only outward current, and the other two normally inward. The outward current is absent when the pipette is filled with Cs+ instead of K+, and has the characteristics of a voltage-dependent potassium conductance. One of the two inward conductances (studied with Cs+ inside) has fast activation, inactivation and deactivation kinetics, is blocked by tetrodotoxin (TTX), and has a reversal potential at the sodium equilibrium potential. The other inward current activates more slowly and deactivates with a quick phase and a very slow phase after a short pulse. Either Ca++ or Ba++ serves as current carrier. During a prolonged pulse, current inactivates fairly completely if there is at least 5 mM Ca++ outside, and the amplitude of the current tails following the pulse diminishes with the time course of inactivation. When Ba++ entirely replaces Ca++ in the external medium, there is no inactivation, but deactivation kinetics of Ca channels vary as pulse duration increases: the slow phase disappears, the fast phase grows in amplitude. Inactivation (Ca++ outside) is unaltered by 50 mM EGTA in the pipette: inactivation cannot be the result of internal accumulation of Ca++.

摘要

利用膜片钳技术的全细胞变体(Hamill等人,1981年),对来自大鼠垂体前叶的转化细胞系GH3细胞的离子电导进行了研究。使用了极低电阻的微电极,这提高了时间分辨率,并使得控制细胞内的离子含量成为可能,细胞内的离子含量能与微电极内的溶液迅速达到平衡。通过使用串联电阻补偿和对细胞电容进行“弹道充电”,时间分辨率得到了进一步提高。我们已经识别并部分表征了至少三种电导,一种仅携带外向电流,另外两种通常为内向电流。当微电极中充满Cs⁺而不是K⁺时,外向电流消失,并且具有电压依赖性钾电导的特征。两种内向电导之一(在细胞内充Cs⁺时进行研究)具有快速激活、失活和去激活动力学,被河豚毒素(TTX)阻断,并且在钠平衡电位处具有反转电位。另一种内向电流激活较慢,在短脉冲后以快速相和非常缓慢的相去激活。Ca²⁺或Ba²⁺均可作为电流载体。在长时间脉冲期间,如果细胞外至少有5 mM Ca²⁺,电流会相当完全地失活,并且脉冲后的电流尾波幅度会随着失活的时间进程而减小。当Ba²⁺完全替代细胞外介质中的Ca²⁺时,没有失活现象,但Ca通道的去激活动力学随脉冲持续时间的增加而变化:缓慢相消失,快速相幅度增大。微电极中50 mM EGTA不会改变(细胞外有Ca²⁺时的)失活现象:失活不可能是细胞内Ca²⁺积累的结果。