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豚鼠培养心内神经元电生理特性的细胞内研究。

Intracellular studies of the electrophysiological properties of cultured intracardiac neurones of the guinea-pig.

作者信息

Allen T G, Burnstock G

机构信息

Department of Anatomy and Embryology, University College, London.

出版信息

J Physiol. 1987 Jul;388:349-66. doi: 10.1113/jphysiol.1987.sp016618.

Abstract
  1. The electrophysiological properties of intracardiac neurones cultured from ganglia within the atria and interatrial septum of the new-born guinea-pig heart were studied using intracellular micro-electrodes. 2. Three types of neurones with resting membrane potentials in the range -45 to -76 mV were detected. The first type, AHs cells, had high (15-28 mV) firing thresholds, pronounced slow post-spike after-hyperpolarizations and fired only once to prolonged intrasomal current injection. The second type, AHm cells, were similar to AHs cells, except that they could fire short bursts of spikes (100-400 ms) at the onset of current injection. The third type, M cells, had low firing thresholds (10-15 mV), no slow after-hyperpolarizations and produced non-adapting trains of action potentials in response to depolarizing current injection. 3. The generation of action potentials in M cells was prevented by tetrodotoxin (TTX; 0.3 microM), whereas in AHs and AHm cells action potentials displayed a channel blockade using solutions containing the divalent cations cadmium, cobalt or manganese (0.02-1 mM). 4. The post-spike after-hyperpolarization in AHs and AHm cells was abolished by the removal of extracellular calcium, shortened in solutions containing the calcium entry blockers CdCl2, MnSO4 and CoCl2 (0.02-1 mM) and prolonged by the addition of calcium (5.0 mM), tetraethylammonium (1-3 mM), 4-aminopyridine (1-3 mM), cyanide (10 microM) or caffeine (100 microM) to the perfusate. 5. The reversal potential of the post-spike after-hyperpolarization was -89.1 mV. This value changed by 62.9 mV for a 10-fold increase in extracellular potassium concentration. 6. The peak conductance change during the post-spike after-hyperpolarization (gK,Ca), was largely independent of membrane potential between -50 and -110 mV. The peak increase in gK,Ca and the duration of the after-hyperpolarization increased with the number of spikes preceding it. 7. It is concluded that calcium entry during the action potential is responsible for the activation of an outward potassium current in the two types of AH cells; the roles played by intracellular calcium extrusion as well as sequestration mechanisms in the generation of the response are discussed.
摘要
  1. 使用细胞内微电极研究了从新生豚鼠心脏心房和房间隔内神经节培养的心脏内神经元的电生理特性。2. 检测到三种静息膜电位在 -45 至 -76 mV 范围内的神经元。第一种类型,AHs 细胞,具有高(15 - 28 mV)的放电阈值,明显的慢的锋后超极化,并且仅在长时间的胞内电流注入时发放一次冲动。第二种类型,AHm 细胞,与 AHs 细胞相似,只是它们在电流注入开始时能够发放短串的冲动(100 - 400 ms)。第三种类型,M 细胞,具有低放电阈值(10 - 15 mV),没有慢的超极化,并且在去极化电流注入时产生非适应性的动作电位序列。3. 河豚毒素(TTX;0.3 μM)可阻止 M 细胞动作电位的产生,而在 AHs 和 AHm 细胞中,使用含有二价阳离子镉、钴或锰(0.02 - 1 mM)的溶液时动作电位显示出通道阻断。4. 去除细胞外钙可消除 AHs 和 AHm 细胞的锋后超极化,在含有钙通道阻滞剂 CdCl2、MnSO4 和 CoCl2(0.02 - 1 mM)的溶液中超极化缩短,而通过向灌流液中添加钙(5.0 mM)、四乙铵(1 - 3 mM)、4 - 氨基吡啶(1 - 3 mM)、氰化物(10 μM)或咖啡因(100 μM)可使其延长。5. 锋后超极化的反转电位为 -89.1 mV。细胞外钾浓度增加 10 倍时,该值变化 62.9 mV。6. 锋后超极化期间的峰值电导变化(gK,Ca)在很大程度上与 -50 至 -110 mV 之间的膜电位无关。gK,Ca 的峰值增加和超极化的持续时间随其之前的冲动数量增加而增加。7. 得出的结论是,动作电位期间的钙内流负责两种类型的 AH 细胞中外向钾电流的激活;讨论了细胞内钙外流以及螯合机制在该反应产生中所起的作用。

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