Use of a complex approach for assessment of metamizole sodium and acetylsalicylic acid toxicity, genotoxicity and cytotoxicity

被引:16
|
作者
Arkhipchuk, VV
Goncharuk, VV
Chernykh, VP
Maloshtan, LN
Gritsenko, IS
机构
[1] Ukrainian Acad Sci, Inst Colloid Chem & Water Chem, UA-03680 Kiev, Ukraine
[2] Ukrainian Natl Univ Pharm, Kharkov, Ukraine
关键词
drug cytotoxicity; genotoxicity; nucleolar biomarker; micronucleus test; acetylsalicylic acid; metamizole sodium; Carassius auratus gibelio; Ceriodaphnia affinis; Hydra attenuata; Allium cepa;
D O I
10.1002/jat.1027
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
A complex approach based on the use of test organisms belonging to different systematic groups (plants, invertebrates and vertebrates), as well as the nucleolar biomarker and the micronucleus test on their cells, was applied to assess the toxicity, cytotoxicity and genotoxicity of two pharmaceutical substances (metamizole sodium and acetylsalicylic acid) applied at IC50 concentrations for mammalian cells. The compound acetylsalicylic acid was evaluated at a concentration (1.6 X 10(3) mg l(-1)) that was non-toxic for bioassays based on fish (Carassius auratus gibelio) and hydra (Hydra attenuata) and acutely toxic for bioassays with ceriodaphnia (Ceriodaphnia affinis) and onion (Allium cepa). The metamizole sodium solution (6.25%) demonstrated acute toxicity for the whole set of test organisms. Both drugs, after their 30-360 min influence on the test organisms, first changed the nucleolar size in plant and animal cells (i.e. the transcriptional activity of ribosomal genes was affected most significantly). Moreover, the metamizole sodium solution caused nucleolar structural damage in 90% of hydra cells as early as after 30 min of exposure. The acetylsalicylic acid solution inhibited essentially the rate of cell division in the meristem of onion roots (the mitotic index decreased to 9.6parts per thousand, as compared 51.70parts per thousand for the control). The carp incubation and the onion germination in the acetylsalicylic acid solution showed a reproducible increase in the frequency of cells with micronuclei (2 and 5.5 times, respectively) and double nuclei (3 and 1.5 times, respectively). The approach described herein may be applied for obtaining rapid, cost-efficient and useful supplementary data on different types of toxicity for marketed drugs as well as for drugs under development. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:401 / 407
页数:7
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