Zebrafish as a Model for Drug Screening in Genetic Kidney Diseases

Genetic disorders account for a wide range of renal diseases emerging during childhood and adolescence. Due to the utilization of modern biochemical and biomedical techniques, the number of identified disease-associated genes is increasing rapidly. Modeling of congenital human disease in animals is...

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Main Authors: Jochen Gehrig (Author), Gunjan Pandey (Author), Jens H. Westhoff (Author)
Format: Book
Published: Frontiers Media S.A., 2018-06-01T00:00:00Z.
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100 1 0 |a Jochen Gehrig  |e author 
700 1 0 |a Gunjan Pandey  |e author 
700 1 0 |a Gunjan Pandey  |e author 
700 1 0 |a Jens H. Westhoff  |e author 
245 0 0 |a Zebrafish as a Model for Drug Screening in Genetic Kidney Diseases 
260 |b Frontiers Media S.A.,   |c 2018-06-01T00:00:00Z. 
500 |a 2296-2360 
500 |a 10.3389/fped.2018.00183 
520 |a Genetic disorders account for a wide range of renal diseases emerging during childhood and adolescence. Due to the utilization of modern biochemical and biomedical techniques, the number of identified disease-associated genes is increasing rapidly. Modeling of congenital human disease in animals is key to our understanding of the biological mechanism underlying pathological processes and thus developing novel potential treatment options. The zebrafish (Danio rerio) has been established as a versatile small vertebrate organism that is widely used for studying human inherited diseases. Genetic accessibility in combination with elegant experimental methods in zebrafish permit modeling of human genetic diseases and dissecting the perturbation of underlying cellular networks and physiological processes. Beyond its utility for genetic analysis and pathophysiological and mechanistic studies, zebrafish embryos, and larvae are amenable for phenotypic screening approaches employing high-content and high-throughput experiments using automated microscopy. This includes large-scale chemical screening experiments using genetic models for searching for disease-modulating compounds. Phenotype-based approaches of drug discovery have been successfully performed in diverse zebrafish-based screening applications with various phenotypic readouts. As a result, these can lead to the identification of candidate substances that are further examined in preclinical and clinical trials. In this review, we discuss zebrafish models for inherited kidney disease as well as requirements and considerations for the technical realization of drug screening experiments in zebrafish. 
546 |a EN 
690 |a zebrafish 
690 |a drug screening 
690 |a compound screening 
690 |a genetic kidney disease 
690 |a high-throughput 
690 |a high-content 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pediatrics, Vol 6 (2018) 
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