Berghmans Stéphane, Butler Paul, Goldsmith Paul, Waldron Gareth, Gardner Iain, Golder Zoe, Richards Frances M, Kimber Gillian, Roach Alan, Alderton Wendy, Fleming Angeleen
Summit (Cambridge) Ltd., Cambridge, United Kingdom.
J Pharmacol Toxicol Methods. 2008 Jul-Aug;58(1):59-68. doi: 10.1016/j.vascn.2008.05.130. Epub 2008 Jun 8.
Safety pharmacology is integral to the non-clinical safety assessment of new chemical entities prior to first administration to humans. The zebrafish is a well established model organism that has been shown to be relevant to the study of human diseases. The potential role of zebrafish in safety pharmacology was evaluated using reference compounds in three models assessing cardiac, visual and intestinal function.
Compound toxicity was first established in zebrafish to determine the non toxic concentration of a blinded set of 16 compounds. In the cardiac assay, zebrafish larvae at 3 days post fertilisation (d.p.f.) were exposed to compounds for 3 h before measurement of the atrial and ventricular rates. To investigate visual function, the optomotor response was assessed in 8 d.p.f. larvae following a 5 day compound exposure. In the intestinal function assay, the number of gut contractions was measured in 7 d.p.f. larvae after a 1 h compound exposure. Finally, compound uptake was determined for 9 of the 16 compounds to measure the concentration of compound absorbed by the zebrafish larvae.
Seven compounds out of nine produced an expected effect that was statistically significant in the cardiac and visual functions assays. In the gut contraction assay, six out of ten compounds showed a statistically significant effect that was also the expected result whilst two displayed anticipated but non-significant effects. The compound uptake method was used to determine larval tissue concentrations and allowed the identification of false negatives when compound was poorly absorbed into the zebrafish.
Overall, results generated in three zebrafish larvae assays demonstrated a good correlation between the effects of compounds in zebrafish and the data available from other in vivo models or known clinical adverse effects. These results suggest that for the cardiac, intestinal and visual function, zebrafish assays have the potential to predict adverse drug effects and supports their possible role in early safety assessment of novel compounds.
安全药理学是新化学实体在首次人体给药前非临床安全性评价的重要组成部分。斑马鱼是一种成熟的模式生物,已被证明与人类疾病研究相关。使用参考化合物在评估心脏、视觉和肠道功能的三个模型中评估了斑马鱼在安全药理学中的潜在作用。
首先在斑马鱼中确定化合物毒性,以确定一组16种化合物的无毒浓度。在心脏试验中,受精后3天(d.p.f.)的斑马鱼幼虫在测量心房和心室率之前暴露于化合物3小时。为了研究视觉功能,在暴露于化合物5天后,对8 d.p.f.的幼虫评估视动反应。在肠道功能试验中,在暴露于化合物1小时后,测量7 d.p.f.幼虫的肠道收缩次数。最后,测定了16种化合物中的9种的化合物摄取量,以测量斑马鱼幼虫吸收的化合物浓度。
9种化合物中有7种产生了预期效果,在心脏和视觉功能试验中具有统计学意义。在肠道收缩试验中,10种化合物中有6种显示出具有统计学意义的效果,这也是预期结果,而2种显示出预期但无统计学意义的效果。化合物摄取方法用于确定幼虫组织浓度,并在化合物吸收到斑马鱼体内较差时识别假阴性。
总体而言,在三个斑马鱼幼虫试验中产生的结果表明,化合物在斑马鱼中的作用与其他体内模型获得的数据或已知的临床不良反应之间具有良好的相关性。这些结果表明,对于心脏、肠道和视觉功能,斑马鱼试验有可能预测药物不良反应,并支持它们在新型化合物早期安全性评价中的可能作用。