Saito Mitsuru, Murai Yoshinaka, Sato Hajime, Bae Yong-Chul, Akaike Tadashi, Takada Masahiko, Kang Youngnam
Department of Neuroscience and Oral Physiology, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
J Neurophysiol. 2006 Oct;96(4):1887-901. doi: 10.1152/jn.00176.2006. Epub 2006 Apr 19.
The axon initial segment plays important roles in spike initiation and invasion of axonal spikes into the soma. Among primary sensory neurons, those in the mesencephalic trigeminal nucleus (MTN) are exceptional in their ability to initiate soma spikes (S-spikes) in response to synaptic inputs, consequently displaying two kinds of S-spikes, one caused by invasion of an axonal spike arising from the sensory receptor and the other initiated by somatic inputs. We investigated where spikes are initiated in such MTN neurons and whether there are any differences between the two kinds of S-spikes. Simultaneous patch-clamp recordings from the soma and axon hillock revealed a spike-backpropagation from the spike-initiation site in the stem axon to the soma in response to 1-ms somatic current pulse, which disclosed the delayed emergence of S-spikes after the current-pulse offset. These initiated S-spikes were smaller in amplitude than S-spikes generated by stimulation of the stem axon; however, 4-AP (< or =0.5 mM) eliminated the amplitude difference. Furthermore, 4-AP dramatically shortened the delay in spike initiation without affecting the spike-backpropagation time in the stem axon, whereas it substantially prolonged the refractory period of S-spikes arising from axonal-spike invasion without significantly affecting that of presumed axonal spikes. These observations suggest that 4-AP-sensitive K(+) currents exert two opposing effects on S-spikes depending on their origins: suppression of spike initiation and facilitation of axonal-spike invasion at higher frequencies. Consistent with these findings, strong immunoreactivities for Kv1.1 and Kv1.6, among 4-AP-sensitive and low-voltage-activated Kv1 family examined, were detected in the soma but not in the stem axon of MTN neurons.
轴突起始段在动作电位起始以及轴突动作电位向胞体的传入过程中发挥着重要作用。在初级感觉神经元中,中脑三叉神经核(MTN)的神经元在响应突触输入时引发胞体动作电位(S-动作电位)的能力十分特殊,因此会表现出两种S-动作电位,一种是由感觉受体产生的轴突动作电位传入所致,另一种则由体细胞输入引发。我们研究了此类MTN神经元中动作电位的起始位置,以及这两种S-动作电位之间是否存在差异。对胞体和轴突丘进行同步膜片钳记录发现,响应1毫秒的体细胞电流脉冲时,动作电位会从轴突干的动作电位起始位点向胞体反向传播,这揭示了电流脉冲结束后S-动作电位的延迟出现。这些起始的S-动作电位在幅度上小于刺激轴突干产生的S-动作电位;然而,4-氨基吡啶(≤0.5 mM)消除了幅度差异。此外,4-氨基吡啶显著缩短了动作电位起始的延迟时间,而不影响轴突干中动作电位的反向传播时间,同时它还大幅延长了由轴突动作电位传入引起的S-动作电位的不应期,而对假定的轴突动作电位的不应期没有显著影响。这些观察结果表明,4-氨基吡啶敏感的钾电流根据其起源对S-动作电位产生两种相反的作用:抑制动作电位起始并在较高频率下促进轴突动作电位的传入。与这些发现一致的是,在所检测的对4-氨基吡啶敏感且低电压激活的Kv1家族中,MTN神经元的胞体中检测到了强烈的Kv1.1和Kv1.6免疫反应性,而轴突干中未检测到。