TechnoPhage, SA, Av. Prof. Egas Moniz, 1649-028, Lisboa, Portugal.
Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, 1649-028, Lisboa, Portugal.
Sci Rep. 2019 Jul 19;9(1):10475. doi: 10.1038/s41598-019-47006-w.
Spinal cord injury (SCI) is a complex condition, with limited therapeutic options, that results in sensory and motor disabilities. To boost discovery of novel therapeutics, we designed a simple and efficient drug screening platform. This innovative approach allows to determine locomotor rescue properties of small molecules in a zebrafish (Danio rerio) larval spinal cord transection model. We validated our screening platform by showing that Riluzole and Minocycline, two molecules that are in clinical trials for SCI, promote rescue of the locomotor function of the transected larvae. Further validation of the platform was obtained through the blind identification of D-Cycloserine, a molecule scheduled to enter phase IV clinical trials for SCI. Importantly, we identified Tranexamic acid and further showed that this molecule maintains its locomotor recovery properties in a rodent female contusion model. Our screening platform, combined with drug repurposing, promises to propel the rapid translation of novel therapeutics to improve SCI recovery in humans.
脊髓损伤 (SCI) 是一种复杂的病症,治疗选择有限,会导致感觉和运动功能障碍。为了促进新型疗法的发现,我们设计了一种简单高效的药物筛选平台。这种创新方法可以在斑马鱼(Danio rerio)幼体脊髓横切模型中确定小分子的运动恢复特性。我们通过证明两种正在进行 SCI 临床试验的分子——利鲁唑和米诺环素——促进横切幼体运动功能的恢复,验证了我们的筛选平台。通过盲法鉴定 D-环丝氨酸进一步验证了该平台的有效性,该分子计划进入 SCI 的第四阶段临床试验。重要的是,我们鉴定出氨甲环酸,并进一步表明该分子在雌性啮齿动物挫伤模型中保持其运动恢复特性。我们的筛选平台与药物再利用相结合,有望加速新型疗法的快速转化,以改善人类 SCI 的恢复。