Lopes G K, Schulman H M, Hermes-Lima M
Departamento de Biologia Celular, Universidade de Brasília, Brazil.
Biochim Biophys Acta. 1999 Oct 18;1472(1-2):142-52. doi: 10.1016/s0304-4165(99)00117-8.
Tannic acid (TA), a plant polyphenol, has been described as having antimutagenic, anticarcinogenic and antioxidant activities. Since it is a potent chelator of iron ions, we decided to examine if the antioxidant activity of TA is related to its ability to chelate iron ions. The degradation of 2-deoxyribose induced by 6 microM Fe(II) plus 100 microM H2O2 was inhibited by TA, with an I50 value of 13 microM. Tannic acid was over three orders of magnitude more efficient in protecting against 2-deoxyribose degradation than classical *OH scavengers. The antioxidant potency of TA was inversely proportional to Fe(II) concentration, demonstrating a competition between H2O2 and AT for reaction with Fe(II). On the other hand, the efficiency of TA was nearly unchanged with increasing concentrations of the *OH detector molecule, 2-deoxyribose. These results indicate that the antioxidant activity of TA is mainly due to iron chelation rather than *OH scavenging. TA also inhibited 2-deoxyribose degradation mediated by Fe(III)-EDTA (iron = 50 microM) plus ascorbate. The protective action of TA was significantly higher with 50 microM EDTA than with 500 microM EDTA, suggesting that TA removes Fe(III) from EDTA and forms a complex with iron that cannot induce *OH formation. We also provided evidence that TA forms a stable complex with Fe(II), since excess ferrozine (14 mM) recovered 95-96% of the Fe(II) from 10 microM TA even after a 30-min exposure to 100-500 microM H2O2. Addition of Fe(III) to samples containing TA caused the formation of Fe(II)n-TA, complexes, as determined by ferrozine assays, indicating that TA is also capable of reducing Fe(III) ions. We propose that when Fe(II) is complexed to TA, it is unable to participate in Fenton reactions and mediate *OH formation. The antimutagenic and anticarcinogenic activity of TA, described elsewhere, may be explained (at least in part) by its capacity to prevent Fenton reactions.
单宁酸(TA)是一种植物多酚,具有抗诱变、抗癌和抗氧化活性。由于它是铁离子的有效螯合剂,我们决定研究TA的抗氧化活性是否与其螯合铁离子的能力有关。TA抑制了由6 microM Fe(II)加100 microM H2O2诱导的2-脱氧核糖降解,I50值为13 microM。单宁酸在防止2-脱氧核糖降解方面比经典的OH清除剂效率高三个数量级以上。TA的抗氧化能力与Fe(II)浓度成反比,表明H2O2和TA在与Fe(II)反应方面存在竞争。另一方面,随着OH检测分子2-脱氧核糖浓度的增加,TA的效率几乎不变。这些结果表明,TA的抗氧化活性主要是由于铁螯合而不是OH清除。TA还抑制了由Fe(III)-EDTA(铁 = 50 microM)加抗坏血酸介导的2-脱氧核糖降解。50 microM EDTA时TA的保护作用明显高于500 microM EDTA,这表明TA从EDTA中去除Fe(III)并与铁形成一种不能诱导OH形成的复合物。我们还提供了证据表明TA与Fe(II)形成稳定的复合物,因为即使在100 - 500 microM H2O2中暴露30分钟后,过量的亚铁嗪(14 mM)仍能从10 microM TA中回收95 - 96%的Fe(II)。向含有TA的样品中添加Fe(III)会导致形成Fe(II)n-TA复合物,通过亚铁嗪测定法确定,这表明TA也能够还原Fe(III)离子。我们提出,当Fe(II)与TA络合时,它无法参与芬顿反应并介导*OH的形成。TA在其他地方描述的抗诱变和抗癌活性,可能(至少部分)由其预防芬顿反应的能力来解释。