Cytotoxicity of spin trapping compounds

被引:49
作者
Haseloff, RF [1 ]
Mertsch, K [1 ]
Rohde, E [1 ]
Baeger, I [1 ]
Grigorev, IA [1 ]
Blasig, IE [1 ]
机构
[1] RUSSIAN ACAD SCI,INST ORGAN CHEM,NOVOSIBIRSK 630090,RUSSIA
关键词
cytotoxicity; spin trap; endothelial cell;
D O I
10.1016/S0014-5793(97)01349-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Spin trapping compounds are used frequently to detect free radicals released by cells. Their cytotoxicity has to be considered in order to prevent perturbations of normal cell growth and viability. Eleven spin traps (eight nitrones and three nitroso traps) have been tested for their effects on bovine aortic endothelial cells (toxicity range, 50% survival rate), The lowest cytotoxicity was found for 5,5-dimethylpyrroline-1-oxide and 2,2,4-trimethyl-2H-imidazole-1-oxide whereas nitrosobenzene and 2-methyl-2-nitrosopropane exerted the strongest cytotoxic effects. In addition, three nitronyl nitroxides mere tested, Their cytotoxicity was found to be dependent on substitution, and the toxic concentration of a lipophilic derivative was found to be more than two orders lower as compared to a hydrophilic derivative. The results of this study indicate that most spin traps can be used in cell cultures at customary (i.e. millimolar) concentrations; caution is recommended when nitroso spin traps are applied to cells. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:73 / 75
页数:3
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