斑马鱼
达尼奥
药物发现
计算生物学
生物
模式生物
背景(考古学)
有机体
鉴定(生物学)
功能(生物学)
生物信息学
基因
细胞生物学
遗传学
生态学
古生物学
作者
Margrit Kamel,Nikolay Ninov
标识
DOI:10.1016/j.coph.2017.08.007
摘要
Traditionally, the development of novel therapeutics for metabolic diseases has relied mainly on high-throughput screening using biochemical or cell-based assays. While this approach represents a driving force in drug discovery, there is also a need to perform large-scale screens without disrupting inter-organ communication and tissue architecture, essential components for understanding the complexity of metabolic regulation and the identification of small molecules with appropriate biological activities in vivo. Hence, the zebrafish Danio rerio is gaining popularity in metabolic research and drug discovery, as this animal model allows screening of small molecules in the context of the whole-organism. Moreover, the zebrafish exhibits conserved function of the pancreas, liver and adipose tissue, which can be leveraged to identify novel targets in metabolic regulation, as well as to study the role of conserved genes associated with the risk of metabolic diseases in humans. Here we highlight recent advances in the identification of targets in metabolic regulation using the zebrafish as a model.
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