Development of isoform specific sensory neuronal sodium channel blockers

描述（由申请人提供）：电压门控钠通道是神经元兴奋性的关键决定因素。实验和临床证据清楚地表明，钠通道和这些通道的性质变化可以在慢性疼痛和其他神经系统疾病中发挥关键作用。然而，至少六种不同的钠通道亚型在外周感觉神经元中表达，并且由于缺乏亚型特异性神经元钠通道阻断剂，研究特异性电压门控钠通道亚型在感觉神经元的正常和异常电活动中的作用受到阻碍。这项R21拨款提案的目标是开发基于生物肽毒素的选择性钠通道阻滞剂，可用于研究特定钠通道亚型在兴奋性疾病（如疼痛）中的作用。生物毒素在研究离子通道在疾病中的作用方面是非常宝贵的，并且一些靶向离子通道的毒素是重要的治疗剂。我们的初步数据显示，来自虎纹捕鸟蛛（Tarantula Ornithoctonus huwena）的毒液中的毒素抑制TTX敏感性神经元钠通道，但不抑制TTX抗性神经元钠通道、心脏钠通道或骨骼肌钠通道。此外，这些数据表明，该毒素在阻断Nav1.6和Nav1.7 TTX敏感性通道方面比Nav1.1、1.2和1.3 TTX敏感性钠通道更有效。这种毒素是一个很好的候选分子，在此基础上开发亚型特异性感觉神经元钠通道阻滞剂。该项目有两个相关的具体目标：1。确定钠通道对狼蛛毒素敏感性的亚型特异性决定因素。2.开发对特定电压门控钠通道亚型具有增强选择性的毒素类似物。将使用全细胞膜片钳电生理学、重组离子通道的诱变和肽合成来研究毒素通道相互作用。本文提出的实验将确定使用狼蛛毒素作为开发新工具的基础的可行性，以确定特定钠通道在感觉神经元正常和异常生理学中的作用。本研究的长期目标是开发钠通道阻滞剂，其可用作治疗过度兴奋性神经系统疾病（如慢性疼痛）的新型疗法。

DESCRIPTION (provided by applicant): Voltage-gated sodium channels are critical determinants of neuronal excitability. Experimental and clinical evidence clearly demonstrates that sodium channels and changes in the properties of these channels can play crucial roles in chronic pain and other neurological disorders. However, at least six different sodium channel isoforms are expressed in peripheral sensory neurons, and investigating the role of specific voltage- gated sodium channel isoforms in normal and abnormal electrical activity of sensory neurons has been hindered by the lack of isoform specific neuronal sodium channel blockers. The goal of this R21 grant proposal is to develop selective sodium channel blockers based on biological peptide toxins that can be used to investigate the role(s) of specific sodium channel isoforms in disorders of excitability such as pain. Biological toxins have been invaluable in researching the role of ion channels in disease and some toxins that target ion channels are important therapeutics. Our preliminary data show that a toxin in the venom from the tarantula Ornithoctonus huwena inhibits TTX-sensitive neuronal sodium channels but not TTX- resistant neuronal sodium channels, cardiac sodium channels or skeletal muscle sodium channels. Furthermore, these data indicate that this toxin is more potent at blocking Nav1.6 and Nav1.7 TTX-sensitive channels than Nav1.1, 1.2 and 1.3 TTX-sensitive sodium channels. This toxin is an excellent candidate molecule on which to base the development of isoform specific sensory neuronal sodium channel blockers. This project has two related specific aims: 1. Identify the isoform specific determinants of sodium channel sensitivity to tarantula toxins. 2. Develop toxin analogs with enhanced selectivity for specific voltage-gated sodium channel isoforms. Whole-cell patch-clamp electrophysiology, mutagenesis of recombinant ion channels and peptide synthesis will be used to investigate toxin-channel interactions. The experiments proposed here will determine the feasibility of using tarantula toxins as the basis for developing novel tools to determine the roles of specific sodium channels in normal and abnormal physiology of sensory neurons. The long-term goal of this research is to develop sodium channel blockers that are useful as novel therapeutics for the treatment of neurological disorders of hyperexcitability such as chronic pain.