Prevalidation of the ex-vivo model PCLS for prediction of respiratory toxicity

被引:29
|
作者
Hess, A. [1 ]
Wang-Lauenstein, L. [2 ,3 ]
Braun, A. [2 ,3 ]
Kolle, S. N. [1 ]
Landsiedel, R. [1 ]
Liebsch, M. [5 ]
Ma-Hock, L. [1 ]
Pirow, R. [5 ]
Schneider, X. [4 ]
Steinfath, M. [5 ]
Vogel, S. [1 ]
Martin, C. [4 ]
Sewald, K. [2 ,3 ]
机构
[1] BASF SE, Expt Toxicol & Ecol, D-67056 Ludwigshafen, Germany
[2] Fraunhofer Inst Toxicol & Expt Med ITEM, Dept Preclin Pharmacol & In Vitro Toxicol, Nikolai Fuchs Str 1, D-30625 Hannover, Germany
[3] German Ctr Lung Res, Biomed Res Endstage & Obstruct Lung Dis Hannover, Hannover, Germany
[4] Rhein Westfal TH Aachen, Fac Med, Inst Pharmacol & Toxicol, Wendlingweg 2, Aachen, Germany
[5] German Fed Inst Risk Assessment BfR, Max Dohrn Str 8-10, D-10589 Berlin, Germany
关键词
Acute inhalation toxicity; Respiratory toxicity; Prevalidation; Reproducibility; Industrial chemicals; Two-group classification model; Precision-cut lung slices; Transferability; Submersed culture conditions; CUT LUNG SLICES; DENDRITIC CELLS; IN-VIVO; CHEMICAL ALLERGEN; EPITHELIAL-CELLS; RAT; VALIDATION; RESPONSES; AIRWAY; CYTOTOXICITY;
D O I
10.1016/j.tiv.2016.01.006
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
In acute inhalation toxicity studies, animals inhale substances at given concentrations. Without additional information, however, appropriate starting concentrations for in-vivo inhalation studies are difficult to estimate. The goal of this project was the prevalidation of precision-cut lung slices (PCLS) as an ex-vivo alternative to reduce the number of animals used in inhalation toxicity studies. According to internationally agreed principles for Prevalidation Studies, the project was conducted in three independent laboratories. The German BfR provided consultancy in validation principles and independent support with biostatistics. In all laboratories, rat PCLS were prepared and exposed to 5 concentrations of 20 industrial chemicals under submerged culture conditions for 1 h. After 23 h post-incubation, toxicity was assessed by measurement of released lactate dehydrogenase and mitochondrial activity. In addition, protein content and pro-inflammatory cytokine IL-1 alpha were measured. For all endpoints IC50 values were calculated if feasible. For each endpoint test acceptance criteria were established. This report provides the final results for all 20 chemicals. More than 900 concentration response curves were analyzed. Log(10)[IC50 (mu M)], obtained for all assay endpoints, showed best infra- and inter-laboratory consistency for the data obtained by WST-1 and BCA assays. While WST-1 and LDH indicated toxic effects for the majority of substances, only some of the substances induced an increase in extracellular IL-1 alpha. Two prediction models (two group classification model, prediction of LC50 by IC50) were developed and showed promising results. (C) 2016 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:347 / 361
页数:15
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