Ye Pin, Jiao Yunlu, Li Zhenwei, Hua Liming, Fu Jin, Jiang Feng, Liu Tong, Ji Yonghua
Laboratory of Neuropharmacology and Neurotoxicology, Shanghai University, Shanghai, 200436, China.
Protein Cell. 2015 Jun;6(6):443-52. doi: 10.1007/s13238-015-0154-4. Epub 2015 Apr 24.
Voltage-gated sodium channels (VGSCs) in primary sensory neurons play a key role in transmitting pain signals to the central nervous system. BmK I, a site-3 sodium channel-specific toxin from scorpion Buthus martensi Karsch, induces pain behaviors in rats. However, the subtypes of VGSCs targeted by BmK I were not entirely clear. We therefore investigated the effects of BmK I on the current amplitude, gating and kinetic properties of Nav1.8, which is associated with neuronal hyperexcitability in DRG neurons. It was found that BmK I dose-dependently increased Nav1.8 current in small-sized (<25 μm) acutely dissociated DRG neurons, which correlated with its inhibition on both fast and slow inactivation. Moreover, voltage-dependent activation and steady-state inactivation curves of Nav1.8 were shifted in a hyperpolarized direction. Thus, BmK I reduced the threshold of neuronal excitability and increased action potential firing in DRG neurons. In conclusion, our data clearly demonstrated that BmK I modulated Nav1.8 remarkably, suggesting BmK I as a valuable probe for studying Nav1.8. And Nav1.8 is an important target related to BmK I-evoked pain.
初级感觉神经元中的电压门控钠通道(VGSCs)在将疼痛信号传递至中枢神经系统的过程中发挥着关键作用。BmK I是一种来自东亚钳蝎的3型钠通道特异性毒素,可在大鼠中诱发疼痛行为。然而,BmK I所靶向的VGSCs亚型尚不完全清楚。因此,我们研究了BmK I对背根神经节(DRG)神经元中与神经元兴奋性过高相关的Nav1.8电流幅度、门控和动力学特性的影响。研究发现,BmK I可剂量依赖性地增加急性分离的小尺寸(<25μm)DRG神经元中的Nav1.8电流,这与其对快速和慢速失活的抑制作用相关。此外,Nav1.8的电压依赖性激活和稳态失活曲线向超极化方向移动。因此,BmK I降低了DRG神经元的兴奋性阈值并增加了动作电位发放。总之,我们的数据清楚地表明BmK I对Nav1.8有显著调节作用,提示BmK I是研究Nav1.8的一种有价值的探针。并且Nav1.8是与BmK I诱发疼痛相关的一个重要靶点。