National Scientific Center of Marine Biology, Far Eastern Branch, Russian Academy of Sciences, Vladivostok 690041, Russia.
School of Biomedicine, Far Eastern Federal University, Vladivostok 690091, Russia.
Mar Drugs. 2018 Sep 26;16(10):352. doi: 10.3390/md16100352.
This review is devoted to the medical application of tetrodotoxin (TTX), a potent non-protein specific blocker of voltage-gated sodium (NaV) channels. The selectivity of action, lack of affinity with the heart muscle NaV channels, and the inability to penetrate the blood⁻brain barrier make this toxin an attractive candidate for anesthetic and analgesic drug design. The efficacy of TTX was shown in neuropathic, acute and inflammatory pain models. The main emphasis of the review is on studies focused on the improvement of TTX efficacy and safety in conjunction with additional substances and drug delivery systems. A significant improvement in the effectiveness of the toxin was demonstrated when used in tandem with vasoconstrictors, local anesthetics and chemical permeation enhancers, with the best results obtained with the encapsulation of TTX in microparticles and liposomes conjugated to gold nanorods.
这篇综述致力于探讨河豚毒素(TTX)在医学上的应用,TTX 是一种强效的非蛋白特异性电压门控钠离子(NaV)通道阻断剂。其作用具有选择性、与心肌 NaV 通道亲和力低且无法穿透血脑屏障,这使得这种毒素成为麻醉和镇痛药物设计的有吸引力的候选物。TTX 在神经性疼痛、急性疼痛和炎症性疼痛模型中均显示出疗效。本综述的主要重点是研究与其他物质和药物输送系统联合使用时提高 TTX 疗效和安全性的相关内容。当与血管收缩剂、局部麻醉剂和化学渗透增强剂联合使用时,毒素的有效性显著提高,而将 TTX 封装在与金纳米棒缀合的微颗粒和脂质体中则可获得最佳效果。