...
首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >Correlation of In Vivo Versus In Vitro Benchmark Doses (BMDs) Derived From Micronucleus Test Data: A Proof of Concept Study
【24h】

Correlation of In Vivo Versus In Vitro Benchmark Doses (BMDs) Derived From Micronucleus Test Data: A Proof of Concept Study

机译:从微核试验数据得出的体内与体外基准剂量(BMD)的相关性:概念研究的证明

获取原文
获取原文并翻译 | 示例

摘要

In this study, we explored the applicability of using in vitro micronucleus (MN) data from human lymphoblastoid TK6 cells to derive in vivo genotoxicity potency information. Nineteen chemicals covering a broad spectrum of genotoxic modes of action were tested in an in vitro MN test using TK6 cells using the same study protocol. Several of these chemicals were considered to need metabolic activation, and these were administered in the presence of S9. The Benchmark dose (BMD) approach was applied using the dose-response modeling program PROAST to estimate the genotoxic potency from the in vitro data. The resulting in vitro BMDs were compared with previously derived BMDs from in vivo MN and carcinogenicity studies. A proportional correlation was observed between the BMDs from the in vitro MN and the BMDs from the in vivo MN assays. Further, a clear correlation was found between the BMDs from in vitro MN and the associated BMDs for malignant tumors. Although these results are based on only 19 compounds, they show that genotoxicity potencies estimated from in vitro tests may result in useful information regarding in vivo genotoxic potency, as well as expected cancer potency. Extension of the number of compounds and further investigation of metabolic activation (S9) and of other toxicokinetic factors would be needed to validate our initial conclusions. However, this initial work suggests that this approach could be used for in vitro to in vivo extrapolations which would support the reduction of animals used in research (3Rs: replacement, reduction, and refinement).
机译:在这项研究中,我们探索了使用来自人类淋巴母细胞TK6细胞的体外微核(MN)数据来得出体内遗传毒性效能信息的适用性。在相同的研究方案下,使用TK6细胞在体外MN测试中测试了涵盖广泛遗传毒性作用模式的19种化学物质。这些化学物质中的几种被认为需要代谢激活,这些化学物质在S9存在的情况下给药。使用剂量响应建模程序PROAST应用了基准剂量(BMD)方法,以从体外数据估算遗传毒性。将所得的体外BMD与先前从体内MN和致癌性研究得出的BMD进行比较。在来自体外MN的BMD与来自体内MN测定的BMD之间观察到成比例的相关性。此外,在来自体外MN的BMD与用于恶性肿瘤的相关BMD之间发现明显的相关性。尽管这些结果仅基于19种化合物,但它们表明,通过体外试验估算出的遗传毒性潜力可能会提供有关体内遗传毒性潜力以及预期的癌症效力的有用信息。为了证实我们的初步结论,需要扩展化合物的数量并进一步研究代谢活化(S9)和其他毒代动力学因子。但是,这项初步工作表明该方法可用于体外到体内外推,这将支持减少研究中使用的动物(3R:替代,减少和改良)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号