Hu Hua, Vervaeke Koen, Storm Johan F
Institute of Physiology, University of Oslo, PB 1103 Blindern, 0317 Oslo, Norway.
J Physiol. 2002 Dec 15;545(3):783-805. doi: 10.1113/jphysiol.2002.029249.
Coherent network oscillations in the brain are correlated with different behavioural states. Intrinsic resonance properties of neurons provide a basis for such oscillations. In the hippocampus, CA1 pyramidal neurons show resonance at theta (theta) frequencies (2-7 Hz). To study the mechanisms underlying theta-resonance, we performed whole-cell recordings from CA1 pyramidal cells (n = 73) in rat hippocampal slices. Oscillating current injections at different frequencies (ZAP protocol), revealed clear resonance with peak impedance at 2-5 Hz at approximately 33 degrees C (increasing to approximately 7 Hz at approximately 38 degrees C). The theta-resonance showed a U-shaped voltage dependence, being strong at subthreshold, depolarized (approximately -60 mV) and hyperpolarized (approximately -80 mV) potentials, but weaker near the resting potential (-72 mV). Voltage clamp experiments revealed three non-inactivating currents operating in the subthreshold voltage range: (1) M-current (I(M)), which activated positive to -65 mV and was blocked by the M/KCNQ channel blocker XE991 (10 microM); (2) h-current (I(h)), which activated negative to -65 mV and was blocked by the h/HCN channel blocker ZD7288 (10 microM); and (3) a persistent Na(+) current (I(NaP)), which activated positive to -65 mV and was blocked by tetrodotoxin (TTX, 1 microM). In current clamp, XE991 or TTX suppressed the resonance at depolarized, but not hyperpolarized membrane potentials, whereas ZD7288 abolished the resonance only at hyperpolarized potentials. We conclude that these cells show two forms of theta-resonance: "M-resonance" generated by the M-current and persistent Na(+) current in depolarized cells, and "H-resonance" generated by the h-current in hyperpolarized cells. Computer simulations supported this interpretation. These results suggest a novel function for M/KCNQ channels in the brain: to facilitate neuronal resonance and network oscillations in cortical neurons, thus providing a basis for an oscillation-based neural code.
大脑中连贯的网络振荡与不同的行为状态相关。神经元的内在共振特性为这种振荡提供了基础。在海马体中,CA1锥体神经元在θ(theta)频率(2 - 7赫兹)处表现出共振。为了研究θ共振背后的机制,我们在大鼠海马切片中对CA1锥体细胞(n = 73)进行了全细胞记录。在不同频率下进行振荡电流注射(ZAP方案),发现在约33摄氏度时,2 - 5赫兹处出现明显共振,峰值阻抗出现(在约38摄氏度时增加到约7赫兹)。θ共振呈现出U形电压依赖性,在阈下、去极化(约 - 60毫伏)和超极化(约 - 80毫伏)电位时较强,但在静息电位(-72毫伏)附近较弱。电压钳实验揭示了在阈下电压范围内起作用的三种非失活电流:(1)M电流(I(M)),在高于 - 65毫伏时激活,被M/KCNQ通道阻滞剂XE991(10微摩尔)阻断;(2)h电流(I(h)),在低于 - 65毫伏时激活,被h/HCN通道阻滞剂ZD7288(10微摩尔)阻断;(3)持续性钠电流(I(NaP)),在高于 - 65毫伏时激活,被河豚毒素(TTX,1微摩尔)阻断。在电流钳实验中,XE991或TTX抑制了去极化膜电位下的共振,但未抑制超极化膜电位下的共振,而ZD7288仅在超极化电位时消除共振。我们得出结论,这些细胞表现出两种形式的θ共振:去极化细胞中由M电流和持续性钠电流产生的“M共振”,以及超极化细胞中由h电流产生的“H共振”。计算机模拟支持了这一解释。这些结果表明大脑中M/KCNQ通道具有一种新功能:促进皮质神经元中的神经元共振和网络振荡,从而为基于振荡的神经编码提供基础。