Schaumlöffel N, Gebel T
Medical Institute of General Hygiene and Environmental Health, University of Göttingen, Germany.
Mutagenesis. 1998 May;13(3):281-6. doi: 10.1093/mutage/13.3.281.
Data on the mechanism of antimony genotoxicity is scarce. Arsenic and antimony are proposed to share some toxicological features. Thus comparative and combined experiments with As(III) and Sb(III) were performed to gain a deeper knowledge of the mechanism of antimony genotoxicity. Trivalent arsenic proved to be five times more cytotoxic and one order of magnitude more potent in induction of micronuclei in human lymphocytes in vitro than was antimony. Significantly increased micronucleus frequencies were achieved with As(III) at a dose of 0.5 microM and with Sb(III) at a dose of 5 microM. Neither the number of micronuclei induced by As(III) nor by Sb(III) could be suppressed by co-incubation with superoxide dismutase or catalase. This suggests that induction of oxidative stress may not be a crucial step in the mechanism of DNA damage induction by arsenic and antimony. The combined genotoxicity in micronucleus test co-incubation experiments with arsenic and antimony seemed best described by simple additivity. In the single cell gel test with human lymphocytes a significant induction of DNA damage was observed with 0.01 microM As(III) and 5 microM Sb(III). In contrast to Sb(III), As(III) proved to be a very potent inducer of DNA-protein crosslinks. It may be that Sb(III) as well as As(III) causes DNA damage by inhibition of enzymes involved in DNA repair. Further investigations will have to identify the relevant sites of action.
关于锑的遗传毒性机制的数据很少。砷和锑被认为具有一些共同的毒理学特征。因此,进行了砷(III)和锑(III)的比较及联合实验,以更深入地了解锑的遗传毒性机制。三价砷在体外对人淋巴细胞的细胞毒性比锑高五倍,诱导微核的能力强一个数量级。砷(III)在0.5微摩尔剂量下和锑(III)在5微摩尔剂量下均可使微核频率显著增加。与超氧化物歧化酶或过氧化氢酶共同孵育,既不能抑制砷(III)也不能抑制锑(III)诱导的微核数量。这表明氧化应激的诱导可能不是砷和锑诱导DNA损伤机制中的关键步骤。在微核试验联合孵育实验中,砷和锑的联合遗传毒性似乎最能通过简单相加来描述。在人淋巴细胞单细胞凝胶试验中,0.01微摩尔砷(III)和5微摩尔锑(III)可显著诱导DNA损伤。与锑(III)不同,砷(III)被证明是DNA - 蛋白质交联的强力诱导剂。可能是锑(III)以及砷(III)通过抑制参与DNA修复的酶来导致DNA损伤。进一步的研究将必须确定相关的作用位点。