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黄酮类化合物与铁离子和铜离子的相互作用:其抗氧化活性的一种机制

Interactions of flavonoids with iron and copper ions: a mechanism for their antioxidant activity.

作者信息

Mira Lurdes, Fernandez M Tereza, Santos Marta, Rocha Rui, Florêncio M Helena, Jennings Keith R

机构信息

Departamento de Química e Bioquímica, Faculdade de Ciências de Universidade de Lisboa, Edificio C8, Campo Grande, 1749-016 Lisboa, Portugal.

出版信息

Free Radic Res. 2002 Nov;36(11):1199-208. doi: 10.1080/1071576021000016463.

Abstract

The metal chelating properties of flavonoids suggest that they may play a role in metal-overload diseases and in all oxidative stress conditions involving a transition metal ion. A detailed study has been made of the ability of flavonoids to chelate iron (including Fe3+) and copper ions and its dependence of structure and pH. The acid medium may be important in some pathological conditions. In addition, the ability of flavonoids to reduce iron and copper ions and their activity-structure relationships were also investigated. To fulfill these objectives, flavones (apigenin, luteolin, kaempferol, quercetin, myricetin and rutin), isoflavones (daidzein and genistein), flavanones (taxifolin, naringenin and naringin) and a flavanol (catechin) were investigated. All flavonoids studied show higher reducing capacity for copper ions than for iron ions. The flavonoids with better Fe3+ reducing activity are those with a 2,3-double bond and possessing both the catechol group in the B-ring and the 3-hydroxyl group. The copper reducing activity seems to depend largely on the number of hydroxyl groups. The chelation studies were carried out by means of ultraviolet spectroscopy and electrospray ionisation mass spectrometry. Only flavones and the flavanol catechin interact with metal ions. At pH 7.4 and pH 5.5 all flavones studied appear to chelate Cu2+ at the same site, probably between the 5-hydroxyl and the 4-oxo groups. Myricetin and quercetin, however, at pH 7.4, appear to chelate Cu2+ additionally at the ortho-catechol group, the chelating site for catechin with Cu2+ at pH 7.4. Chelation studies of Fe3+ to flavonoids were investigated only at pH 5.5. Only myricetin and quercetin interact strongly with Fe3+, complexation probably occurring again between the 5-hydroxyl and the 4-oxo groups. Their behaviour can be explained by their ability to reduce Fe3+ at pH 5.5, suggesting that flavonoids reduce Fe3+ to Fe2+ before association.

摘要

类黄酮的金属螯合特性表明,它们可能在金属过载疾病以及所有涉及过渡金属离子的氧化应激条件中发挥作用。已经对类黄酮螯合铁(包括Fe3+)和铜离子的能力及其对结构和pH的依赖性进行了详细研究。酸性介质在某些病理条件下可能很重要。此外,还研究了类黄酮还原铁和铜离子的能力及其活性-结构关系。为了实现这些目标,对黄酮类(芹菜素、木犀草素、山奈酚、槲皮素、杨梅素和芦丁)、异黄酮类(大豆苷元和染料木黄酮)、黄烷酮类(紫杉叶素、柚皮素和柚皮苷)以及一种黄烷醇(儿茶素)进行了研究。所有研究的类黄酮对铜离子的还原能力均高于对铁离子的还原能力。具有较好Fe3+还原活性的类黄酮是那些具有2,3-双键且在B环中同时具有邻苯二酚基团和3-羟基的类黄酮。铜还原活性似乎很大程度上取决于羟基的数量。螯合研究通过紫外光谱和电喷雾电离质谱进行。只有黄酮类和黄烷醇儿茶素与金属离子相互作用。在pH 7.4和pH 5.5时,所有研究的黄酮类似乎都在同一位置螯合Cu2+,可能在5-羟基和4-氧代基团之间。然而,杨梅素和槲皮素在pH 7.4时,似乎还在邻苯二酚基团处螯合Cu2+,这是儿茶素在pH 7.4时与Cu2+的螯合位点。仅在pH 5.5时研究了Fe3+与类黄酮的螯合。只有杨梅素和槲皮素与Fe3+强烈相互作用,络合可能再次发生在5-羟基和4-氧代基团之间。它们的行为可以通过它们在pH 5.5时还原Fe3+的能力来解释,这表明类黄酮在缔合之前将Fe3+还原为Fe2+。

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