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Toxicol In Vitro. 2015 Dec 25;30(1 Pt A):138-65. doi: 10.1016/j.tiv.2015.05.016. Epub 2015 May 27.

Evaluation of drug-induced neurotoxicity based on metabolomics, proteomics and electrical activity measurements in complementary CNS in vitro models.

Author information

1
Department of Animal Physiology, Institute of Biological Sciences, University of Rostock, D-18051 Rostock, Germany.
2
Department of Physiology, Faculty of Biology and Medicine, University of Lausanne, Lausanne, Switzerland.
3
Laboratoire de la barrière hémato-encéphalique (LBHE) - EA2465, Université d'Artois, Faculté Jean Perrin, 62307 Lens, France.
4
Department of Toxicology, University of Wuerzburg, D-97078 Wuerzburg, Germany.
5
Department of Molecular Biology, Paris-Lodron University, Salzburg, Austria.
6
Department of Mathematics and Computer Science, Freie Universitaet Berlin, D-14195 Berlin, Germany.
7
NeuroProof GmbH, D-18119 Rostock, Germany.
8
Department of Animal Physiology, Institute of Biological Sciences, University of Rostock, D-18051 Rostock, Germany; NeuroProof GmbH, D-18119 Rostock, Germany.
9
European Commission Joint Research Centre, Institute for Health and Consumer Protection, I-21027 Ispra, VA, Italy. Electronic address: anna.price@jrc.ec.europa.eu.

Abstract

The present study was performed in an attempt to develop an in vitro integrated testing strategy (ITS) to evaluate drug-induced neurotoxicity. A number of endpoints were analyzed using two complementary brain cell culture models and an in vitro blood-brain barrier (BBB) model after single and repeated exposure treatments with selected drugs that covered the major biological, pharmacological and neuro-toxicological responses. Furthermore, four drugs (diazepam, cyclosporine A, chlorpromazine and amiodarone) were tested more in depth as representatives of different classes of neurotoxicants, inducing toxicity through different pathways of toxicity. The developed in vitro BBB model allowed detection of toxic effects at the level of BBB and evaluation of drug transport through the barrier for predicting free brain concentrations of the studied drugs. The measurement of neuronal electrical activity was found to be a sensitive tool to predict the neuroactivity and neurotoxicity of drugs after acute exposure. The histotypic 3D re-aggregating brain cell cultures, containing all brain cell types, were found to be well suited for OMICs analyses after both acute and long term treatment. The obtained data suggest that an in vitro ITS based on the information obtained from BBB studies and combined with metabolomics, proteomics and neuronal electrical activity measurements performed in stable in vitro neuronal cell culture systems, has high potential to improve current in vitro drug-induced neurotoxicity evaluation.

KEYWORDS:

3D brain culture; Drug development; In vitro blood brain barrier; MEA; Neuronal network culture; OMICs

PMID:
26026931
DOI:
10.1016/j.tiv.2015.05.016
[Indexed for MEDLINE]
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