Department of Neuroscience, Physiology and Pharmacology, University College London London, UK.
Front Mol Neurosci. 2012 May 14;5:63. doi: 10.3389/fnmol.2012.00063. eCollection 2012.
M-channels carry slowly activating potassium currents that regulate excitability in a variety of central and peripheral neurons. Functional M-channels and their Kv7 channel correlates are expressed throughout the somatosensory nervous system where they may play an important role in controlling sensory nerve activity. Here we show that Kv7.2 immunoreactivity is expressed in the peripheral terminals of nociceptive primary afferents. Electrophysiological recordings from single afferents in vitro showed that block of M-channels by 3 μM XE991 sensitized Aδ- but not C-fibers to noxious heat stimulation and induced spontaneous, ongoing activity at 32°C in many Aδ-fibers. These observations were extended in vivo: intraplantar injection of XE991 selectively enhanced the response of deep dorsal horn (DH) neurons to peripheral mid-range mechanical and higher range thermal stimuli, consistent with a selective effect on Aδ-fiber peripheral terminals. These results demonstrate an important physiological role of M-channels in controlling nociceptive Aδ-fiber responses and provide a rationale for the nocifensive behaviors that arise following intraplantar injection of the M-channel blocker XE991.
M 型通道携带缓慢激活的钾电流,调节各种中枢和外周神经元的兴奋性。功能性 M 型通道及其 Kv7 通道相关物在整个躯体感觉神经系统中表达,它们可能在控制感觉神经活动中发挥重要作用。在这里,我们表明 Kv7.2 免疫反应性存在于伤害性初级传入纤维的外周末端。体外对单个传入纤维的电生理记录表明,M 型通道阻断剂 XE991 使 Aδ 纤维而不是 C 纤维对伤害性热刺激敏感,并在许多 Aδ 纤维中在 32°C 时诱导自发持续活动。这些观察结果在体内得到了扩展:XE991 足底内注射选择性增强了深部背角 (DH) 神经元对周围中范围机械和更高范围热刺激的反应,与 Aδ 纤维外周末端的选择性效应一致。这些结果表明 M 型通道在控制伤害性 Aδ 纤维反应中具有重要的生理作用,并为 M 型通道阻断剂 XE991 足底内注射后出现的伤害性行为提供了合理依据。