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

机译:氯丙嗪的体外生物学和二聚醇蛋白在重复暴露后聚集大鼠脑细胞培养物

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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.
机译:化合物的神经毒性效应可以使用细胞系统在体外进行体外测试。一个例子是聚集大鼠脑细胞培养物。对于对体外数据的外推到体内情况,重要的是考虑测试化合物的生物机。此外,体内暴露通常是较长的一段时间;因此,将其掺入体外测定中至关重要。在该研究中,通过重复的暴露将聚集大鼠脑细胞培养物暴露于氯丙嗪(CPZ)和DiazePam(DZP)中的12天。在第一个和最后一次暴露日的特定时间点,从股票,试验介质,细胞培养基和细胞中取出样品。通过HPLC-UV分析这些样品。培养基中的CPZ的量随时间减少,而细胞中的量显示出增加。在12天重复的暴露中看到细胞中CPZ的积累。培养基中的DZP的量随着时间的推移仍然稳定,并且在细胞中仅发现了高达2%的DZP。发现CPZ和DZP的不同生物动态行为。可能的解释是摄取到细胞或从细胞中排出的差异。在培养基中的CPZ降低与稳定量的DZP导致暴露浓度随时间的差异,这在解释体外效应数据时应考虑。 (c)2014年elestvier有限公司保留所有权利。

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