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地塞米松对促肾上腺皮质激素细胞系中A型钾电流的选择性增强作用。

Selective enhancement of an A type potassium current by dexamethasone in a corticotroph cell line.

作者信息

Pennington A J, Kelly J S, Antoni F A

机构信息

Department of Pharmacology, University of Edinburgh, UK.

出版信息

J Neuroendocrinol. 1994 Jun;6(3):305-15. doi: 10.1111/j.1365-2826.1994.tb00587.x.

Abstract

Perforated patch recording was used to examine the effect of the synthetic steroid dexamethasone on the whole cell potassium (K+) current, in the mouse corticotroph tumour cell line AtT20/D16-16. In 15 out of 52 control cells (29%) there was a rapidly-activating, rapidly-inactivating K+ current of the A type, the amplitude of which was strongly dependent on the holding potential in use prior to its activation by depolarising voltage pulses, and which was blocked by 1 mM 4-aminopyridine (4-AP, n = 5). The effect of dexamethasone (100 nM, 2 h, 37 degrees C) was that the A current increased in prevalence (24 out of 31 cells, 77%), lost its dependence on holding potential (over the range studied), and as a result became significantly larger than in controls, for certain voltage steps (peak A current density was 18.5 +/- 2.4 pA/pF (n = 12) for control cells and 26.3 +/- 3.9 pA/pF (n = 18) for dexamethasone treated cells, for a step to +30 mV from -60 mV, values are mean +/- SEM). All cells exhibited a slowly-activating, sustained K+ current, which was unaffected by changes in the holding potential, unaffected by 4-AP and consisted of at least 3 components: one blocked by 30 mM tetraethylammonium(TEA) or 100 nM charybdotoxin (CTX); a second blocked by 100 nM apamin; and a third not blocked by TEA, CTX, apamin, clofilium (100 nM) or niflumic acid (0.1 mM). Dexamethasone produced no change in the slowly-activating, sustained current nor in any of its individual components. The effect of dexamethasone on the A current was completely blocked by 0.1 mM puromycin, a protein synthesis blocker, while puromycin alone did not affect the size or frequency of the A current, nor alter the slowly-activating, sustained current. Secretion studies using 4-AP confirmed that the A current has a role in stimulated adrenocorticotrophic hormone (ACTH) secretion. In summary, AtT20 cells contain at least four types of K+ current: an A current and 3 currents contributing to the slowly-activating current. Selective enhancement of the A current by dexamethasone, shown here to require synthesis of new protein, is one of the mechanisms whereby glucocorticoids exert inhibitory control on ACTH secretion.

摘要

采用穿孔膜片钳记录技术,研究合成类固醇地塞米松对小鼠促肾上腺皮质激素瘤细胞系AtT20/D16-16全细胞钾(K+)电流的影响。在52个对照细胞中,有15个(29%)存在快速激活、快速失活的A型K+电流,其幅度强烈依赖于去极化电压脉冲激活前所用的钳制电位,且被1 mM 4-氨基吡啶(4-AP,n = 5)阻断。地塞米松(100 nM,2小时,37℃)的作用是,A型电流的发生率增加(31个细胞中有24个,77%),失去了对钳制电位的依赖性(在所研究的范围内),结果在某些电压阶跃时,其幅度显著大于对照细胞(从-60 mV阶跃到+30 mV时,对照细胞的A型电流峰值密度为18.5±2.4 pA/pF(n = 12),地塞米松处理细胞为26.3±3.9 pA/pF(n = 18),数值为平均值±标准误)。所有细胞均表现出缓慢激活、持续的K+电流,该电流不受钳制电位变化的影响,不受4-AP影响,至少由3个成分组成:一个被30 mM四乙铵(TEA)或100 nM蝎毒素(CTX)阻断;第二个被100 nM蜂毒明肽阻断;第三个不受TEA、CTX、蜂毒明肽、氯非铵(100 nM)或氟尼酸(0.1 mM)阻断。地塞米松对缓慢激活、持续电流及其任何单个成分均无影响。地塞米松对A型电流的作用被0.1 mM嘌呤霉素(一种蛋白质合成阻断剂)完全阻断,而单独的嘌呤霉素不影响A型电流的大小或频率,也不改变缓慢激活、持续电流。使用4-AP的分泌研究证实,A型电流在刺激促肾上腺皮质激素(ACTH)分泌中起作用。总之,AtT20细胞至少含有四种类型的K+电流:一种A型电流和三种构成缓慢激活电流的电流。地塞米松对A型电流的选择性增强(此处显示需要合成新蛋白质)是糖皮质激素对ACTH分泌施加抑制性控制的机制之一。

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