Genotoxic and cytotoxic effects of the drug dipyrone sodium in African green monkey kidney (Vero) cell line exposed in vitro

被引:7
|
作者
Gomes, Lorena M. [1 ]
Moyses, Daniele A. [1 ]
Nascimento, Henrique F. S. [1 ]
Mota, Tatiane C. [1 ]
Bonfim, Lais T. [1 ]
Cardoso, Plinio C. S. [1 ]
Burbano, Rommel M. R. [1 ]
Bahia, Marcelo O. [1 ]
机构
[1] Fed Univ Para UFPA, Inst Biol Sci, Lab Human Cytogenet, Av Augusto Correa 01, BR-66075110 Belem, Para, Brazil
关键词
Dipyrone; Genotoxicity; Cytotoxicity; Reactive oxygen species; N-NITROSODIMETHYLAMINE; DNA-DAMAGE; INHIBITION; METAMIZOLE; CYCLOOXYGENASES; MUTAGENICITY; SALMONELLA; MECHANISMS; HUMANS; GROWTH;
D O I
10.1007/s00210-021-02078-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dipyrone or metamizole is one of the most used analgesics, mainly due to its low financial cost. However, in some countries, the sale of dipyrone is prohibited due to reported severe cases of agranulocytosis as a result of its use. Despite its high use, studies showing genotoxic and cytotoxic effects of dipyrone in mammalian cells are scarce. Therefore, in the present study, we assessed cell viability, genotoxic effects, cytotoxic effects (by apoptosis and necrosis induction), and the induction of reactive oxygen species (ROS) in Vero cells (a cell line obtained from the red kidney of green monkey) exposed to dipyrone. Our results showed a significant reduction in viability of cells exposed to dipyrone by the MTT assay. A significant increase in damage index evaluated by a comet assay was also observed, which indicates its genotoxic effects. In which concerns the cytotoxic effects of dipyrone, we observed a significant increase in the number of apoptotic cells using fluorescent dyes after 24 h and 48 h of treatment with the drug. Our results also showed that there was no significant difference in the induction of ROS generation after treatment of the cells with the drug assessed by the DCFH-DA assay. Thus, our work showed that dipyrone is both a genotoxic and cytotoxic drug to Vero cells in the assessed conditions.
引用
收藏
页码:1529 / 1535
页数:7
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