Department of Pharmacology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.
Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.
J Neuroimmunol. 2019 Jul 15;332:198-211. doi: 10.1016/j.jneuroim.2019.05.002. Epub 2019 May 4.
Excitation of dorsal root ganglion (DRG) neurons by interleukin 1β (IL-1β) is implicated in the onset of neuropathic pain. To understand its mechanism of action, isolectin B4 positive (IB) DRG neurons were exposed to 100pM IL-1β for 5-6d. A reversible increase in action potential (AP) amplitude reflected increased TTX-sensitive sodium current (TTX-S I). An irreversible increase in AP duration reflected decreased Ca- sensitive K conductance (BK(Ca) channels). Different processes thus underlie regulation of the two channel types. Since changes in AP shape facilitated Ca influx, this explains how IL-1β facilitates synaptic transmission in the dorsal horn; thereby provoking pain.
白细胞介素 1β (IL-1β) 激活背根神经节 (DRG) 神经元与神经性疼痛的发作有关。为了了解其作用机制,将 isolectin B4 阳性 (IB) DRG 神经元暴露于 100pM 的 IL-1β 中 5-6 天。动作电位 (AP) 幅度的可逆增加反映了增加的 TTX 敏感钠电流 (TTX-S I)。AP 持续时间的不可逆增加反映了钙敏感钾电导 (BK(Ca) 通道) 的减少。因此,两种通道类型的调节有不同的过程。由于 AP 形状的变化促进了 Ca 内流,这解释了 IL-1β 如何促进背角中的突触传递,从而引发疼痛。