The Institute for Drug Research (IDR), School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem 9112001, Israel.
Toxins (Basel). 2019 Feb 23;11(2):131. doi: 10.3390/toxins11020131.
Chronic pain is a major medical issue which reduces the quality of life of millions and inflicts a significant burden on health authorities worldwide. Currently, management of chronic pain includes first-line pharmacological therapies that are inadequately effective, as in just a portion of patients pain relief is obtained. Furthermore, most analgesics in use produce severe or intolerable adverse effects that impose dose restrictions and reduce compliance. As the majority of analgesic agents act on the central nervous system (CNS), it is possible that blocking pain at its source by targeting nociceptors would prove more efficient with minimal CNS-related side effects. The development of such analgesics requires the identification of appropriate molecular targets and thorough understanding of their structural and functional features. To this end, plant and animal toxins can be employed as they affect ion channels with high potency and selectivity. Moreover, elucidation of the toxin-bound ion channel structure could generate pharmacophores for rational drug design while favorable safety and analgesic profiles could highlight toxins as leads or even as valuable therapeutic compounds themselves. Here, we discuss the use of plant and animal toxins in the characterization of peripherally expressed ion channels which are implicated in pain.
慢性疼痛是一个主要的医学问题,它降低了数百万人的生活质量,并给全球卫生当局带来了重大负担。目前,慢性疼痛的管理包括一线的药物治疗,但这些治疗效果并不理想,只有一部分患者的疼痛得到缓解。此外,大多数使用的镇痛药会产生严重或无法忍受的副作用,这就需要限制剂量,降低了患者的依从性。由于大多数镇痛药作用于中枢神经系统(CNS),因此通过靶向伤害感受器来阻断疼痛源可能会更有效,同时产生的与 CNS 相关的副作用也最小。这类镇痛药的开发需要确定合适的分子靶点,并深入了解其结构和功能特征。为此,可以使用植物和动物毒素,因为它们可以高效且选择性地作用于离子通道。此外,阐明毒素结合的离子通道结构可以为合理的药物设计生成药效团,而有利的安全性和镇痛特性可以突出毒素作为先导化合物,甚至本身就是有价值的治疗化合物。在这里,我们讨论了植物和动物毒素在鉴定与疼痛有关的外周表达离子通道中的应用。