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1
Disease modeling in genetic kidney diseases: zebrafish.遗传性肾脏疾病的疾病建模:斑马鱼
Cell Tissue Res. 2017 Jul;369(1):127-141. doi: 10.1007/s00441-017-2593-0. Epub 2017 Mar 22.
2
Drug Discovery in Fish, Flies, and Worms.鱼类、果蝇和线虫中的药物发现
ILAR J. 2016 Dec;57(2):133-143. doi: 10.1093/ilar/ilw034.
3
Zebrafish small molecule screens: Taking the phenotypic plunge.斑马鱼小分子筛选:投身表型研究
Comput Struct Biotechnol J. 2016 Sep 18;14:350-356. doi: 10.1016/j.csbj.2016.09.001. eCollection 2016.
4
Bridging translation for acute kidney injury with better preclinical modeling of human disease.通过更好地对人类疾病进行临床前建模来实现急性肾损伤的桥接翻译。
Am J Physiol Renal Physiol. 2016 May 15;310(10):F972-84. doi: 10.1152/ajprenal.00552.2015. Epub 2016 Mar 9.
5
Delayed treatment with PTBA analogs reduces postinjury renal fibrosis after kidney injury.使用PTBA类似物进行延迟治疗可减轻肾损伤后的损伤后肾纤维化。
Am J Physiol Renal Physiol. 2016 Apr 15;310(8):F705-F716. doi: 10.1152/ajprenal.00503.2015. Epub 2015 Dec 9.
6
Targeting Endogenous Repair Pathways after AKI.急性肾损伤后靶向内源性修复途径。
J Am Soc Nephrol. 2016 Apr;27(4):990-8. doi: 10.1681/ASN.2015030286. Epub 2015 Nov 18.
7
Therapeutic Targets of Human AKI: Harmonizing Human and Animal AKI.人类急性肾损伤的治疗靶点:协调人类与动物急性肾损伤研究
J Am Soc Nephrol. 2016 Jan;27(1):44-8. doi: 10.1681/ASN.2015030233. Epub 2015 Oct 30.
8
Nephron organoids derived from human pluripotent stem cells model kidney development and injury.源自人类多能干细胞的肾单位类器官可模拟肾脏发育和损伤。
Nat Biotechnol. 2015 Nov;33(11):1193-200. doi: 10.1038/nbt.3392.
9
Zebrafish as tools for drug discovery.斑马鱼作为药物发现的工具。
Nat Rev Drug Discov. 2015 Oct;14(10):721-31. doi: 10.1038/nrd4627. Epub 2015 Sep 11.
10
A PTBA small molecule enhances recovery and reduces postinjury fibrosis after aristolochic acid-induced kidney injury.一种 PTBA 小分子可增强马兜铃酸诱导的肾损伤后的恢复并减少损伤后纤维化。
Am J Physiol Renal Physiol. 2014 Mar 1;306(5):F496-504. doi: 10.1152/ajprenal.00534.2013. Epub 2013 Dec 26.

药物研发以阻止急性肾损伤进展为慢性肾病:急性肾损伤中表型药物研发的实例

Drug Discovery to Halt the Progression of Acute Kidney Injury to Chronic Kidney Disease: A Case for Phenotypic Drug Discovery in Acute Kidney Injury.

作者信息

Hukriede Neil, Vogt Andreas, de Caestecker Mark

机构信息

Department of Developmental Biology, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Nephron. 2017;137(4):268-272. doi: 10.1159/000476079. Epub 2017 Jun 15.

DOI:10.1159/000476079
PMID:28614822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7197487/
Abstract

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.

摘要

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。