Hukriede Neil, Vogt Andreas, de Caestecker Mark
Department of Developmental Biology, University of Pittsburgh, Pittsburgh, PA, USA.
Nephron. 2017;137(4):268-272. doi: 10.1159/000476079. Epub 2017 Jun 15.
The cellular responses that occur following acute kidney injury (AKI) are complex and dynamic, involving multiple cells types and molecular pathways. For this reason, early selection of defined molecular targets for therapeutic intervention is unlikely to be effective in complex in vivo models of AKI, let alone Phase 3 clinical trials in patients with even more complex AKI pathobiology. Phenotypic screening using zebrafish provides an attractive alternative that does not require prior knowledge of molecular targets and may identify compounds that modify multiple targets that might be missed in more traditional target-based screens. In this review, we discuss results of an academic drug discovery campaign that used zebrafish as a primary screening tool to discover compounds with favorable absorption, metabolism, and toxicity that enhance repair when given late after injury in multiple models of AKI. We discuss how this screening campaign is being integrated into a more comprehensive, phenotypic, and target-based screen for lead compound optimization.
急性肾损伤(AKI)后发生的细胞反应复杂且动态,涉及多种细胞类型和分子途径。因此,在复杂的AKI体内模型中,早期选择特定的分子靶点进行治疗干预不太可能有效,更不用说在具有更复杂AKI病理生物学的患者中进行的3期临床试验了。使用斑马鱼进行表型筛选提供了一种有吸引力的替代方法,该方法不需要对分子靶点有先验知识,并且可能识别出在更传统的基于靶点的筛选中可能遗漏的可修饰多个靶点的化合物。在这篇综述中,我们讨论了一项学术药物发现活动的结果,该活动使用斑马鱼作为主要筛选工具,以发现具有良好吸收、代谢和毒性的化合物,这些化合物在多种AKI模型中于损伤后期给药时可增强修复。我们还讨论了如何将这一筛选活动整合到一个更全面、基于表型和靶点的筛选中,以优化先导化合物。