Liu Zai-Qun
Department of Organic Chemistry, College of Chemistry, Jilin University, No. 2519 Jiefang Road, Changchun 130021, China.
J Phys Chem A. 2006 May 18;110(19):6372-8. doi: 10.1021/jp053998z.
The objective in this work is to determine the antioxidant capacity and effectiveness of icariin (2-(4'-methoxylphenyl)-3-rhamnosido-5-hydroxyl-7-glucosido-8-(3'-methyl-2-butylenyl)-4-chromanone), the major component in herba epimedii being used widely in traditional Chinese medicine for the treatment of artherosclerosis and neuropathy, in which 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH)-induced peroxidation of linoleic acid (LH) in sodium dodecyl sulfate (SDS) acts as the experimental system. By containing an intramolecular hydrogen bond, icariin protects LH against AAPH-induced peroxidation of LH only in SDS, an anionic micelle. The number of trapping peroxyl radicals (LOO()), n, by icariin is just 0.0167 whereas alpha-tocopherol (TOH) and L-ascorbyl-6-laurate (VC-12) are 2.14 and 1.25, respectively, with reference to the n of 6-hydroxyl-2,5,7,8-tetramethylchroman-2-carboxylic acid (Trolox), 2.00. This is also related to how the intramolecular hydrogen bond enhances the bond dissociation enthalpy (BDE) of O-H in icariin. However, calculation of the inhibition rate constant, k(inh), a kinetic parameter to describe the reaction between the antioxidant and LOO(), results in a k(inh) of icariin at about one magnitude larger than those of Trolox, TOH, and VC-12. This fact reveals that, by the view of kinetics, icariin is an antioxidant with much higher effectiveness. In addition, the antioxidant capacities of icariin used together with other antioxidants have been determined and the results indicate that the n of icariin decreases markedly while the n values of Trolox and TOH increase, even if the n of icariin is a negative value in the presence of VC-12. Furthermore, an analysis of k(inh) in this case reveals that the k(inh)(icariin) increases nearly one magnitude with the decrease of k(inh)(Trolox) and no remarkable change occurs for k(inh)(TOH). The negative value of k(inh)(icariin) in the presence of VC-12 can be regarded as the icariin functions as a prooxidant that can be rectified by VC-12 effectively. These findings implicate that the evaluation of antioxidant activity should not only focus on an n value, a thermodynamic possibility, but k(inh) and the charge property of the micelle should be also taken into account. To some extent, the latter factors are more important than the thermodynamic possibility.
本研究的目的是测定淫羊藿苷(2-(4'-甲氧基苯基)-3-鼠李糖苷-5-羟基-7-葡萄糖苷-8-(3'-甲基-2-丁烯基)-4-色原酮)的抗氧化能力和效果。淫羊藿苷是中药淫羊藿的主要成分,广泛用于治疗动脉粥样硬化和神经病变。以十二烷基硫酸钠(SDS)中2,2'-偶氮二异丁脒盐酸盐(AAPH)诱导的亚油酸(LH)过氧化反应作为实验体系。由于含有分子内氢键,淫羊藿苷仅在阴离子胶束SDS中能保护LH免受AAPH诱导的过氧化反应。相对于6-羟基-2,5,7,8-四甲基色满-2-羧酸(Trolox)的捕获过氧自由基(LOO())数量n为2.00,淫羊藿苷的n值仅为0.0167,而α-生育酚(TOH)和L-抗坏血酸-6-月桂酸酯(VC-12)分别为2.14和1.25。这也与分子内氢键如何提高淫羊藿苷中O-H的键解离焓(BDE)有关。然而,计算抑制速率常数k(inh)(描述抗氧化剂与LOO()反应的动力学参数)时,淫羊藿苷的k(inh)比Trolox、TOH和VC-12大约高一个数量级。这一事实表明,从动力学角度看,淫羊藿苷是一种抗氧化效果更高的抗氧化剂。此外,还测定了淫羊藿苷与其他抗氧化剂共同使用时的抗氧化能力,结果表明,即使在VC-12存在下淫羊藿苷的n值为负值,其n值也会显著降低,而Trolox和TOH的n值会增加。此外,对这种情况下的k(inh)分析表明,随着k(inh)(Trolox)的降低,k(inh)(淫羊藿苷)增加近一个数量级,而k(inh)(TOH)没有明显变化。在VC-12存在下k(inh)(淫羊藿苷)的负值可视为淫羊藿苷起到促氧化剂的作用,但可被VC-12有效纠正。这些发现表明,对抗氧化活性的评估不仅应关注n值(一种热力学可能性),还应考虑k(inh)以及胶束的电荷性质。在某种程度上,后两个因素比热力学可能性更重要。