Sundt Danielle, Gamper Nikita, Jaffe David B
Department of Biology, UTSA Neurosciences Institute, University of Texas at San Antonio, San Antonio, Texas;
Department of Pharmacology, Hebei Medical University, Shijiazhuang, People's Republic of China; and Faculty of Biological Sciences, School of Biomedical Sciences, University of Leeds, Leeds, United Kingdom.
J Neurophysiol. 2015 Dec;114(6):3140-53. doi: 10.1152/jn.00226.2015. Epub 2015 Sep 2.
Unmyelinated C-fibers are a major type of sensory neurons conveying pain information. Action potential conduction is regulated by the bifurcation (T-junction) of sensory neuron axons within the dorsal root ganglia (DRG). Understanding how C-fiber signaling is influenced by the morphology of the T-junction and the local expression of ion channels is important for understanding pain signaling. In this study we used biophysical computer modeling to investigate the influence of axon morphology within the DRG and various membrane conductances on the reliability of spike propagation. As expected, calculated input impedance and the amplitude of propagating action potentials were both lowest at the T-junction. Propagation reliability for single spikes was highly sensitive to the diameter of the stem axon and the density of voltage-gated Na(+) channels. A model containing only fast voltage-gated Na(+) and delayed-rectifier K(+) channels conducted trains of spikes up to frequencies of 110 Hz. The addition of slowly activating KCNQ channels (i.e., KV7 or M-channels) to the model reduced the following frequency to 30 Hz. Hyperpolarization produced by addition of a much slower conductance, such as a Ca(2+)-dependent K(+) current, was needed to reduce the following frequency to 6 Hz. Attenuation of driving force due to ion accumulation or hyperpolarization produced by a Na(+)-K(+) pump had no effect on following frequency but could influence the reliability of spike propagation mutually with the voltage shift generated by a Ca(2+)-dependent K(+) current. These simulations suggest how specific ion channels within the DRG may contribute toward therapeutic treatments for chronic pain.
无髓鞘C纤维是传递疼痛信息的主要感觉神经元类型。动作电位传导受背根神经节(DRG)内感觉神经元轴突的分支(T型接头)调节。了解T型接头的形态和离子通道的局部表达如何影响C纤维信号传导对于理解疼痛信号传导很重要。在本研究中,我们使用生物物理计算机建模来研究DRG内轴突形态和各种膜电导对动作电位传播可靠性的影响。正如预期的那样,计算得出的输入阻抗和传播动作电位的幅度在T型接头处均最低。单个动作电位的传播可靠性对主干轴突的直径和电压门控Na(+)通道的密度高度敏感。仅包含快速电压门控Na(+)和延迟整流K(+)通道的模型能够传导频率高达110 Hz的动作电位序列。在模型中添加缓慢激活的KCNQ通道(即KV7或M通道)会将跟随频率降低到30 Hz。要将跟随频率降低到6 Hz,则需要添加更慢的电导(例如Ca(2+)依赖性K(+)电流)产生的超极化。由于离子积累或Na(+)-K(+)泵产生的超极化导致的驱动力衰减对跟随频率没有影响,但可能与Ca(2+)依赖性K(+)电流产生的电压偏移相互影响动作电位传播的可靠性。这些模拟表明DRG内的特定离子通道可能如何有助于慢性疼痛的治疗。