The in vitro biokinetics of chlorpromazine and diazepam in aggregating rat brain cell cultures after repeated exposure

被引:5
作者
Broeders, Jessica J. W. [1 ]
Hermens, Joop L. M. [1 ]
Blaauboer, Bas J. [1 ]
Zurich, Marie-Gabrielle [2 ]
机构
[1] Univ Utrecht, Inst Risk Assessment Sci, NL-3508 TD Utrecht, Netherlands
[2] Univ Lausanne, Dept Physiol, Lausanne, Switzerland
关键词
Biokinetics; In vitro; Aggregating rat brain cell cultures; Chlorpromazine; Diazepam; Repeated exposure; P-GLYCOPROTEIN; PROTEIN-BINDING; NEUROTOXICITY; DRUGS; PHOSPHOLIPIDOSIS; PERMEABILITY; TOXICITY; ASSAY; RELEVANCE; TRANSPORT;
D O I
10.1016/j.tiv.2014.07.015
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Neurotoxic effects of compounds can be tested in vitro using cell systems. One example is aggregating rat brain cell cultures. For the extrapolation of in vitro data to the in vivo situation, it is important to take the biokinetics of the test compound into account. In addition, the exposure in vivo is often for a longer period of time; therefore, it is crucial to incorporate this into in vitro assays as well. In this study, aggregating rat brain cell cultures were exposed to chlorpromazine (CPZ) and diazepam (DZP) for 12-days with repeated exposure. Samples were taken from the stocks, test media, cell culture media and cells at specific time points on the first and last exposure day. These samples were analysed by HPLC-UV. The amount of CPZ in the medium decreased over time, whereas the amount in the cells showed an increase. Accumulation of CPZ in the cells was seen over the 12-day repeated exposure. The amount of DZP in the medium remained stable over time and only up to 2% of DZP added was found in the cells. Different biokinetic behaviour was found for CPZ and DZP. Possible explanations are differences in uptake into the cells or efflux out of the cells. The decrease of CPZ in the medium versus the stable amount of DZP results in differences in exposure concentrations over time, which should be taken into account when interpreting in vitro effect data. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:185 / 191
页数:7
相关论文
共 40 条
[1]   Comparative studies on in vitro methods for evaluating in vivo function of MDR1 P-glycoprotein [J].
Adachi, Y ;
Suzuki, H ;
Sugiyama, Y .
PHARMACEUTICAL RESEARCH, 2001, 18 (12) :1660-1668
[2]   Drug-induced phospholipidosis [J].
Anderson, Nora ;
Borlak, Juergen .
FEBS LETTERS, 2006, 580 (23) :5533-5540
[3]  
[Anonymous], 2020, Bacterial Reverse Mutation Test
[4]  
[Anonymous], 2007, DERMATOTOXICOLOGY, DOI DOI 10.1201/9781420009774.CH33
[5]   GUIDELINES FOR THE RATIONAL USE OF BENZODIAZEPINES - WHEN AND WHAT TO USE [J].
ASHTON, H .
DRUGS, 1994, 48 (01) :25-40
[6]   Relevance of in vitro neurotoxicity testing for regulatory requirements: Challenges to be considered [J].
Bal-Price, Anna K. ;
Hogberg, Helena T. ;
Buzanska, Leonora ;
Coecke, Sandra .
NEUROTOXICOLOGY AND TERATOLOGY, 2010, 32 (01) :36-41
[7]  
Ban Thomas A, 2007, Neuropsychiatr Dis Treat, V3, P495
[8]   The Use of Biomarkers of Toxicity for Integrating In Vitro Hazard Estimates Into Risk Assessment for Humans [J].
Blaauboer, Bas J. ;
Boekelheide, Kim ;
Clewell, Harvey J. ;
Daneshian, Mardas ;
Dingemans, Milou M. L. ;
Goldberg, Alan M. ;
Heneweer, Marjoke ;
Jaworska, Joanna ;
Kramer, Nynke I. ;
Leist, Marcel ;
Seibert, Hasso ;
Testai, Emanuela ;
Vandebriel, Rob J. ;
Yager, James D. ;
Zurlo, Joanne .
ALTEX-ALTERNATIVES TO ANIMAL EXPERIMENTATION, 2012, 29 (04) :411-425
[9]   Biokinetics of chlorpromazine in primary rat and human hepatocytes and human HepaRG cells after repeated exposure [J].
Broeders, Jessica J. W. ;
Parmentier, Celine ;
Truisi, Germaine L. ;
Josse, Rozenn ;
Alexandre, Eliane ;
Savary, Camille C. ;
Hewitt, Philip G. ;
Mueller, Stefan O. ;
Guillouzo, Andre ;
Richert, Lysiane ;
van Eijkeren, Jan C. H. ;
Hermens, Joop L. M. ;
Blaauboer, Bas J. .
TOXICOLOGY IN VITRO, 2015, 30 (01) :52-61
[10]   Transport of Chlorpromazine in the Caco-2 Cell Permeability Assay: A Kinetic Study [J].
Broeders, Jessica J. W. ;
van Eijkeren, Jan C. H. ;
Blaauboer, Bas J. ;
Hermens, Joop L. M. .
CHEMICAL RESEARCH IN TOXICOLOGY, 2012, 25 (07) :1442-1451