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Lack of regulation by intracellular Ca2+ of the hyperpolarization-activated cation current in rat thalamic neurones.

机译:大鼠丘脑神经元中细胞内Ca2 +的超极化激活阳离子电流缺乏调控。

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摘要

1. The regulation of the hyperpolarization-activated cation current, Ih, in thalamocortical neurones by intracellular calcium ions has been implemented in a number of mathematical models on the waxing and waning behaviour of synchronized rhythmic activity in thalamocortical circuits. In the present study, the Ca2+ dependence of Ih in thalamocortical neurones was experimentally investigated by combining Ca2+ imaging and patch-clamp techniques in the ventrobasal thalamic complex (VB) in vitro. 2. Properties of Ih were analysed before and during rhythmic stimulation of Ca2+ entry by trains of depolarizing voltage pulses. Despite a significant increase in intracellular Ca2+ concentration ([Ca2+]i) from resting levels of 74 +/- 23 nM to 251 +/- 78 nM upon rhythmic stimulation, significant differences in the voltage dependence of Ih activation did not occur (half-maximal activation at -86.4 +/- 1.3 mV vs. -85.2 +/- 2.9 mV; slope of the activation curve, 11.2 +/- 2.4 mV vs. 12.5 +/- 2.5 mV). Recording of Ih with predefined values of [Ca2+]i (13.2 nM or 10.01 microM in the patch pipette) revealed no significant differences in the activation curve or the fully activated I-V relationship of Ih. 3. In comparison, stimulation of the intracellular cyclic adenosine monophosphate (cAMP) pathway induced a significantly positive shift in Ih voltage dependence of +5.1 +/- 1.9 mV, with no alteration in the fully activated I-V relationship. 4. These data argue against a direct regulation of Ih by intracellular Ca2+, and particularly do not support a primary role of Ca(2+)-dependent modulation of the Ih channels in the waxing and waning of sleep spindle oscillations in thalamocortical neurones.
机译:1.已通过许多数学模型对丘脑皮层回路中同步节律活动的起蜡和减弱行为实施了由细胞内钙离子调节丘脑皮层神经元中超极化激活阳离子电流Ih的调节。在本研究中,通过结合Ca2 +成像和膜片钳技术在体外基底丘脑复合体(VB)中实验研究了Ih在丘脑皮质神经元中的Ca2 +依赖性。 2.通过一系列去极化电压脉冲,有节奏地刺激Ca2 +进入之前和期间,分析了Ih的性质。尽管在有节奏的刺激下,细胞内Ca2 +浓度([Ca2 +] i)从静止水平的74 +/- 23 nM显着增加到251 +/- 78 nM,但Ih激活的电压依赖性并未出现显着差异(一半-86.4 +/- 1.3 mV与-85.2 +/- 2.9 mV时的最大激活;激活曲线的斜率分别为11.2 +/- 2.4 mV和12.5 +/- 2.5 mV)。用[Ca2 +] i的预定值(贴片吸液管中的13.2 nM或10.01 microM)记录Ih时,发现Ih的激活曲线或完全激活的I-V关系没有显着差异。 3.相比之下,细胞内环状单磷酸腺苷(cAMP)通路的刺激引起Ih电压依赖性+5.1 +/- 1.9 mV的显着正移,而完全激活的I-V关系没有改变。 4.这些数据反对细胞内Ca2 +对Ih的直接调节,特别是不支持在丘脑皮层神经元的睡眠纺锤振荡的减弱和减弱过程中,Ih通道的Ca(2+)依赖性调节的主要作用。

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