硒化合物对重铬酸钾和过氧化氢的抗基因毒性。

Eduardo Cemeli, Joanna Carder, Diana Anderson, Emma Guillamet, María José Morillas, Amadeu Creus, Ricardo Marcos
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引用次数: 27

摘要

硒是一种普遍存在的环境金属,在世界各地的各种工业活动中都有产生。临床和流行病学研究表明硒具有抗癌和预防作用。硒补充剂可以抑制化学诱导的肿瘤。从遗传毒性的角度来看,硒还没有得到充分的研究,国际癌症研究机构的一项审查得出的结论是,没有足够的数据认为它是一种人类致癌物。相比之下,六价铬被归类为一种已知的呼吸致癌物,通过自由基产生DNA损伤。在本研究中,开展了一项合作研究,以评估硒化合物的遗传毒性及其与重铬酸钾和过氧化氢的可能相互作用。因此,在实验室1(英国),研究了三种硒化合物的遗传毒性作用。用菌株TA102进行Ames试验,用人淋巴细胞进行Comet试验,研究硒酸钠、亚硒酸钠和亚硒酸,并研究它们与重铬酸钾的相互作用。在Ames试验中,重铬酸钾产生了高度的诱变反应,而三种硒化合物则没有。硒酸钠可降低重铬酸钾的遗传毒性,而亚硒酸钠和亚硒酸对遗传毒性没有影响。在彗星试验中,重铬酸钾诱导DNA损伤,但硒化合物也有同样的作用。然而,与重铬酸钾联合使用时,只有硒酸钠降低了其作用,而亚硒酸钠和亚硒酸则加重了DNA损伤。在实验室2(西班牙),在TK6淋巴母细胞样细胞系中,彗星试验显示亚硒酸钠无基因毒性,而重铬酸钾和过氧化氢诱导DNA损伤。亚硒酸钠不降低重铬酸钾和过氧化氢的遗传毒性,无论是前处理还是同时处理,还是重铬酸钾和亚硒酸钠处理的时间不同。因此,在Ames试验和Comet试验中,只有硒酸钠对重铬酸钾表现出抗原性毒性。
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Antigenotoxic properties of selenium compounds on potassium dichromate and hydrogen peroxide.

Selenium is an environmental metal that occurs ubiquitously and is produced throughout the world for various industrial activities. Selenium has been reported to have anticarcinogenic and preventive effects in clinical and epidemiological studies. Selenium supplements can inhibit chemically-induced tumours. From the viewpoint of genotoxicity, selenium has not been adequately studied and an IARC review concluded that there were not sufficient data to consider it a carcinogen for man. In contrast, hexavalent chromium is classified as a known respiratory carcinogen producing DNA damage through free oxygen radicals. In the present study, a collaborative study has been carried out to evaluate the genotoxicity of selenium compounds and their possible interactions with potassium dichromate and hydrogen peroxide. Thus, in laboratory 1 (U.K.), the genotoxic effects of three selenium compounds were examined. Sodium selenate, sodium selenite, and selenous acid were investigated in the Ames test using strain TA102 and in the Comet assay using human lymphocytes, and also investigated for their interaction with potassium dichromate. In the Ames test, it was shown that potassium dichromate produced a highly mutagenic response, whilst the three selenium compounds did not. In combination, sodium selenate reduced the genotoxicity of potassium dichromate, but sodium selenite and selenous acid had no effect. In the Comet assay, potassium dichromate induced DNA damage, but so did the selenium compounds. In combination with potassium dichromate, however, only sodium selenate reduced its effect, whereas sodium selenite and selenous acid exacerbated DNA damage. In laboratory 2 (Spain), in the TK6 lymphoblastoid cell line, the Comet assay showed that sodium selenite was non-genotoxic, while potassium dichromate and hydrogen peroxide induced DNA damage. It was also shown that sodium selenite did not decrease the genotoxicity of potassium dichromate or hydrogen peroxide when administered as a pre-treatment or at the same time, or when potassium dichromate and sodium selenite treatments were for different time periods. Thus, only sodium selenate has shown antigenotoxic properties against potassium dichromate in the Ames test and in human lymphocytes in the Comet assay.

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