Department of Clinical Biochemistry and Immunohematology, University of Talca, Talca, Chile.
Molecules. 2009 Sep 30;14(10):3906-13. doi: 10.3390/molecules14103906.
This study assessed the inhibitory effect of three C-glycosylflavonoids from Cymbopogon citratus leaves--isoorientin (1), swertiajaponin (2) and isoorientin 2"-Orhamnoside (3)--on human LDL oxidation. Isolated LDL was incubated with compounds 1-3 and the kinetics of lipid peroxidation were assessed by conjugated diene and malondialdehyde-thiobarbituric acid reactive substances (MDA-TBARS) formation after addition of copper ions. Significant differences (p < 0.05) between the lag time phase of the control and the lag time phase in the presence of the compounds 1 (0.25 microM) and 2 (0.50 microM) were observed. After five hours of incubation all three compounds showed a significant inhibitory effect on MDA-TBARS formation with respect to the control. After six hours of incubation only compound 1 kept a remarkable antioxidant effect. This study demonstrates that isoorientin (1) is an effective inhibitor of in vitro LDL oxidation. As oxidative damage to LDL is a key event in the formation of atherosclerotic lesions, the use of this natural antioxidant may be beneficial to prevent or attenuate atherosclerosis.
本研究评估了来自香茅叶片中的三种 C-糖苷黄酮——异荭草素(1)、荭草苷(2)和异荭草素 2”-O-鼠李糖苷(3)——对人 LDL 氧化的抑制作用。分离的 LDL 与化合物 1-3 孵育,并在加入铜离子后通过共轭二烯和丙二醛-硫代巴比妥酸反应物质(MDA-TBARS)形成来评估脂质过氧化的动力学。在化合物 1(0.25 μM)和 2(0.50 μM)存在下,与对照的滞后时间相比,观察到明显的差异(p < 0.05)。孵育五小时后,所有三种化合物与对照相比均对 MDA-TBARS 形成表现出显著的抑制作用。孵育六小时后,只有化合物 1 保持显著的抗氧化作用。本研究表明,异荭草素(1)是体外 LDL 氧化的有效抑制剂。由于 LDL 的氧化损伤是动脉粥样硬化病变形成的关键事件,因此使用这种天然抗氧化剂可能有助于预防或减轻动脉粥样硬化。