首页> 外文期刊>Biomedical Research on Trace Elements >Suppression by cobalt (II) and enhancement by iron (II) ions of DNA damage induced by 2,2'-azobis (2-amidinopropane) dihydrochloride
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Suppression by cobalt (II) and enhancement by iron (II) ions of DNA damage induced by 2,2'-azobis (2-amidinopropane) dihydrochloride

机译:钴(II)抑制和铁(II)离子增强对2,2'-偶氮双(2-ami基丙烷)二盐酸盐诱导的DNA损伤

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Plasmid DNA damage induced by 2, 2'-azobis (2-amidinopropane) dihydrochloride (AAPH) and the effects of Co(II) and Fe(II) ions on this damage were investigated under aerobic conditions by agarose gel electrophoresis. DNA singlestrand breaks were observed depending on AAPH concentration and treatment time. DNA damage induced by treatment with 10 mM AAPH for 2 hours at 37°C was not inhibited by superoxide dismutase (<200 U), catalase (<200 U), or mannitol (<200 mM), although the damage slightly tended to be decreased by 200 U superoxide dismutase. Damage was inhibited by EDTA or deferoxamine in a concentration-dependent manner. These results suggested the involvement of superoxide anion and metal ions in damage formation. When DNA was incubated with 1mM AAPH, DNA damage was enhanced by 0.001-0.1 mM Fe(II) ion, whereas damage induced by AAPH and Fe(II) ion was totally resolved by 0.1 mM deferoxamine. In contrast, ≥1 mM concentration of Co(II) ion had a suppressive effect on AAPH-induced damage. Co(II) ion in the concentration range of 0.01-0.1 mM suppressed DNA damage induced by both 5 mM AAPH and 0.1 mM Fe(II) ion ; however, a higher concentration (≥5 mM) of Co(II) ion enhanced DNA damage and caused severe DNA breaks, making the DNA bands invisible even in the absence of AAPH. Spectrophotometric analysis suggested the direct interaction of AAPH and Co(II) ion. The above results suggested that Co(II) ion has biphasic effects on DNA damage induced by AAPH depending on its concentration, although Fe(II) ion simply enhances the AAPH-induced DNA damages.
机译:在有氧条件下,通过琼脂糖凝胶电泳研究了2,2'-偶氮双(2-ami基丙烷)二盐酸盐(AAPH)诱导的质粒DNA损伤以及Co(II)和Fe(II)离子对该损伤的影响。根据AAPH浓度和处理时间观察到DNA单链断裂。在37°C下用10 mM AAPH处理2小时诱导的DNA损伤不受超氧化物歧化酶(<200 U),过氧化氢酶(<200 U)或甘露醇(<200 mM)的抑制,尽管这种损伤有轻微的趋势。减少了200 U超氧化物歧化酶。 EDTA或去铁胺以浓度依赖性的方式抑制损伤。这些结果表明超氧化物阴离子和金属离子参与了损伤形成。将DNA与1mM AAPH孵育时,DN​​A损伤会因0.001-0.1 mM Fe(II)离子而增强,而AAPH和Fe(II)离子所引起的损伤会由0.1 mM去铁胺完全消除。相反,浓度≥1 mM的Co(II)离子对AAPH诱导的损伤具有抑制作用。浓度范围为0.01-0.1 mM的Co(II)离子可抑制5 mM AAPH和0.1 mM Fe(II)离子引起的DNA损伤;但是,较高浓度(≥5mM)的Co(II)离子会增强DNA损伤并导致严重的DNA断裂,即使没有AAPH,DNA条带也不可见。分光光度分析表明,AAPH和Co(II)离子直接相互作用。以上结果表明,Co(II)离子根据其浓度对AAPH诱导的DNA损伤具有双相作用,尽管Fe(II)离子简单地增强了AAPH诱导的DNA损伤。

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