Kari G, Rodeck U, Dicker A P
Department of Radiation Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Clin Pharmacol Ther. 2007 Jul;82(1):70-80. doi: 10.1038/sj.clpt.6100223. Epub 2007 May 9.
In vivo studies represent an essential step in drug development and currently rely largely on mice, yet limitations of mammalian models motivated the search for complementary vertebrate model systems. This review focuses on zebrafish, Danio rerio, as a facile model system to study human disease and drug responses. Zebrafish are particularly suited for this purpose because they represent a vertebrate species, their genome is sequenced, and a large number of synchronously developing, transparent embryos can be produced. Zebrafish embryos are permeable to drugs and can easily be manipulated using well-established genetic and molecular approaches. Here, we summarize recent work on drug discovery and toxicity in zebrafish embryos. In addition, we provide a synopsis of current efforts to establish disease models in zebrafish focusing on neoplasia. The results of these studies highlight the potential of zebrafish as a viable addition to established animal models by offering medium and, potentially, high throughput capabilities.
体内研究是药物研发过程中的关键环节,目前主要依赖小鼠模型,但哺乳动物模型存在的局限性促使人们寻找互补的脊椎动物模型系统。本综述聚焦于斑马鱼(Danio rerio),它是一种用于研究人类疾病和药物反应的简易模型系统。斑马鱼特别适合用于此目的,因为它们属于脊椎动物物种,其基因组已测序,并且能够产生大量同步发育的透明胚胎。斑马鱼胚胎对药物具有通透性,并且可以使用成熟的遗传和分子方法轻松进行操作。在此,我们总结了斑马鱼胚胎在药物发现和毒性方面的最新研究成果。此外,我们还概述了目前利用斑马鱼建立疾病模型的工作,重点是肿瘤形成。这些研究结果凸显了斑马鱼作为现有动物模型的可行补充的潜力,因为它具备中等通量乃至可能的高通量能力。