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胡椒酰胺S的抗氧化活性:预防铜诱导的低密度脂蛋白过氧化并改善自由基诱导的内皮细胞氧化应激。

Antioxidant activity of piperlactam S: prevention of copper-induced LDL peroxidation and amelioration of free radical-induced oxidative stress of endothelial cells.

作者信息

Tsai Jeng-Yan, Chou Cheng-Jeng, Chen Chieh-Fu, Chiou Wen-Fei

机构信息

Institute of Pharmacology, School of Life Sciences, National Yang-Ming University, Taipei, ROC.

出版信息

Planta Med. 2003 Jan;69(1):3-8. doi: 10.1055/s-2003-37040.

Abstract

The protective effects of piperlactam S, an alkaloid isolated from Piper kadsura (Choisy) Ohwi, on lipid peroxidation and free radical-mediated cell injuries were investigated. Piperlactam S (1 to 20 microM) concentration-dependently prevented the copper-catalyzed oxidative modification of human low-density lipoproteins (LDL) measured through (i) the lag period, (ii) the slope of the propagation phase, (iii) the total amount of conjugated dienes formed, and (iv) the electrophoretic mobility of LDL. Fe2+-induced oxidative modification of cell membrane was also significantly attenuated by piperlactam S as measured by thiobarbituric acid-reactive substances (TBARS). Furthermore, piperlactam S effectively minimized the loss of cell viability induced by Fenton's reagent (H2O2/FeSO4) in cultured endothelial cells and significantly reversed H2O2/FeSO4-induced impairment of endothelium-dependent relaxation to acetylcholine in rat aorta. Since the oxidative modification of LDL plays an important role in the genesis of atherosclerosis, piperlactam S may help to reduce the risk of atherosclerosis, not only by protecting LDL and membrane lipids from oxidative modification but also by reducing free radical-induced endothelial injury and/or dysfunction.

摘要

研究了从海风藤中分离得到的生物碱胡椒内酰胺S对脂质过氧化和自由基介导的细胞损伤的保护作用。胡椒内酰胺S(1至20微摩尔)呈浓度依赖性地抑制铜催化的人低密度脂蛋白(LDL)氧化修饰,通过以下指标进行测定:(i)延滞期;(ii)增殖期斜率;(iii)共轭二烯形成的总量;(iv)LDL的电泳迁移率。用硫代巴比妥酸反应性物质(TBARS)测定,胡椒内酰胺S也能显著减轻Fe2 +诱导的细胞膜氧化修饰。此外,胡椒内酰胺S有效减少了培养的内皮细胞中由芬顿试剂(H2O2/FeSO4)诱导的细胞活力丧失,并显著逆转了H2O2/FeSO4诱导的大鼠主动脉内皮依赖性舒张功能对乙酰胆碱的损害。由于LDL的氧化修饰在动脉粥样硬化的发生中起重要作用,胡椒内酰胺S可能有助于降低动脉粥样硬化风险,不仅通过保护LDL和膜脂质免受氧化修饰,还通过减少自由基诱导的内皮损伤和/或功能障碍。

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