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藜芦碱诱导牛嗜铬细胞胞质钙和膜电位的振荡。

Veratridine-induced oscillations of cytosolic calcium and membrane potential in bovine chromaffin cells.

作者信息

López M G, Artalejo A R, García A G, Neher E, García-Sancho J

机构信息

Departamento de Bioquímica y Biología Molecular y Fisiología, Facultad de Medicina, Universidad de Valladolid, Spain.

出版信息

J Physiol. 1995 Jan 1;482 ( Pt 1)(Pt 1):15-27. doi: 10.1113/jphysiol.1995.sp020496.

Abstract
  1. Veratridine (VTD) induced large oscillations of the cytosolic Ca2+ concentration ([Ca2+]i) and the membrane potential (Vm) in otherwise silent bovine chromaffin cells loaded with fura-2. 2. Depletion of the intracellular Ca2+ stores by thapsigargin or ryanodine did not affect these oscillations. Caffeine had a complex effect, decreasing them in cells with high activity but increasing them in cells with low activity. 3. The [Ca2+]i oscillations required extracellular Ca2+ and Na+ and were blocked by Ni2+ or tetrodotoxin. They were antagonized by high external concentrations of Mg2+ and/or Ca2+. 4. The oscillations of Vm had three phases: (i) slow depolarization (20 mV in 10-40 s); (ii) further fast depolarization (30 mV in 1 s); and (iii) rapid (5 s) repolarization. [Ca2+]i decreased during (i), increased quickly during (ii) with a 1 s delay with regard to the peak depolarization, and decreased during (iii). 5. Slight depolarizations increased the frequency of the oscillations whereas large depolarizations decreased it. 6. The Ca(2+)-dependent K+ channel blocker apamin increased the duration and decreased the frequency of the oscillations. 7. We propose the following mechanism for the oscillations: (i) the membrane depolarizes slowly by a decrease of potassium conductance (gK), perhaps due to a gradual decrease of [Ca2+]i; (ii) the threshold for activation of Na+ channels (decreased by VTD) is reached, producing further depolarization and recruiting Ca2+ channels, and inactivation of both Ca2+ and VTD-poisoned Na+ channels is slow; and (iii) gK increases, aided by activation of Ca(2+)-dependent K+ channels by the increased [Ca2+]i, and the membrane repolarizes. The contribution of the Na+ channels seems essential for the generation of the oscillations. 8. Bovine chromaffin cells have the machinery required for [Ca2+]i oscillations even though the more physiological stimulus tested here (high K+, field electrical stimulation, nicotinic or muscarinic agonists) produced mainly non-oscillatory responses.
摘要
  1. 藜芦定(VTD)可使负载fura - 2的原本静息的牛嗜铬细胞的胞质Ca2 +浓度([Ca2 +]i)和膜电位(Vm)产生大幅振荡。2. 毒胡萝卜素或ryanodine耗尽细胞内Ca2 +储备并不影响这些振荡。咖啡因有复杂的作用,在高活性细胞中使其降低,而在低活性细胞中使其增加。3. [Ca2 +]i振荡需要细胞外Ca2 +和Na +,并被Ni2 +或河豚毒素阻断。它们被高浓度的细胞外Mg2 +和/或Ca2 +拮抗。4. Vm的振荡有三个阶段:(i)缓慢去极化(10 - 40秒内20 mV);(ii)进一步快速去极化(1秒内30 mV);以及(iii)快速(5秒)复极化。[Ca2 +]i在(i)期间降低,在(ii)期间迅速增加,相对于去极化峰值延迟1秒,在(iii)期间降低。5. 轻微去极化增加振荡频率,而大的去极化降低振荡频率。6. Ca(2 +)依赖性K +通道阻滞剂蜂毒明肽增加振荡持续时间并降低振荡频率。7. 我们提出以下振荡机制:(i)膜通过钾电导(gK)降低而缓慢去极化,这可能是由于[Ca2 +]i逐渐降低;(ii)达到Na +通道激活阈值(被VTD降低),产生进一步去极化并募集Ca2 +通道,并且Ca2 +和被VTD毒害的Na +通道的失活缓慢;以及(iii)gK增加,这得益于增加的[Ca2 +]i激活Ca(2 +)依赖性K +通道,膜复极化。Na +通道的作用似乎对振荡的产生至关重要。8. 牛嗜铬细胞具备产生[Ca2 +]i振荡所需的机制,尽管此处测试的更生理性刺激(高K +、场电刺激、烟碱或毒蕈碱激动剂)主要产生非振荡性反应。

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