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

被引:12
作者
Tsai, JY
Chou, CJ
Chen, CF
Chiou, WF
机构
[1] Natl Res Inst Chinese Med, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Sch Life Sci, Inst Pharmacol, Taipei 112, Taiwan
关键词
Piper kadsura (Choisy) Ohwi; Piperaceae; piperlactam S; low-density lipoprotein; TBARS; endothelial cells; free radicals; cytotoxicity;
D O I
10.1055/s-2003-37040
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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 muM) 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.
引用
收藏
页码:3 / 8
页数:6
相关论文
共 20 条
[1]  
AREIAS FM, 2000, BIOCHEM PHARMACOL, V62, P111
[2]   Andrographolide suppresses the expression of inducible nitric oxide synthase in macrophage and restores the vasoconstriction in rat aorta treated with lipopolysaccharide [J].
Chiou, WF ;
Lin, JJ ;
Chen, CF .
BRITISH JOURNAL OF PHARMACOLOGY, 1998, 125 (02) :327-334
[3]   INHIBITION OF OXIDATION OF HUMAN LOW-DENSITY-LIPOPROTEIN BY PHENOLIC SUBSTANCES IN RED WINE [J].
FRANKEL, EN ;
KANNER, J ;
GERMAN, JB ;
PARKS, E ;
KINSELLA, JE .
LANCET, 1993, 341 (8843) :454-457
[4]  
HAN G-Q, 1990, Planta Medica, V56, P583, DOI 10.1055/s-2006-961189
[5]   ALPHA-TOCOPHEROL CONSUMPTION DURING LOW-DENSITY-LIPOPROTEIN OXIDATION [J].
JESSUP, W ;
RANKIN, SM ;
DEWHALLEY, CV ;
HOULT, JRS ;
SCOTT, J ;
LEAKE, DS .
BIOCHEMICAL JOURNAL, 1990, 265 (02) :399-405
[6]   Effect of para-substituents of phenolic antioxidants [J].
Kajiyama, T ;
Ohkatsu, Y .
POLYMER DEGRADATION AND STABILITY, 2001, 71 (03) :445-452
[7]   Regulation of cell proliferation, gene expression, production of cytokines, and cell cycle progression in primary human T lymphocytes by piperlactam S isolated from Piper kadsura [J].
Kuo, YC ;
Yang, NS ;
Chou, CJ ;
Lin, LC ;
Tsai, WJ .
MOLECULAR PHARMACOLOGY, 2000, 58 (05) :1057-1066
[8]   Reduction of Cu(II) by lipid hydroperoxides: Implications for the copper-dependent oxidation of low-density lipoprotein [J].
Patel, RP ;
Svistunenko, D ;
Wilson, MT ;
DarleyUsmar, VM .
BIOCHEMICAL JOURNAL, 1997, 322 :425-433
[9]   OXYGEN FREE-RADICALS AND HYPERCHOLESTEROLEMIC ATHEROSCLEROSIS - EFFECT OF VITAMIN-E [J].
PRASAD, K ;
KALRA, J .
AMERICAN HEART JOURNAL, 1993, 125 (04) :958-973
[10]   EFFECTS OF DIMETHYLTHIOUREA ON THE CARDIAC-FUNCTION AND OXYRADICAL STATUS IN ISCHEMIA-REPERFUSION INJURY [J].
PRASAD, K ;
DEBNATH, D ;
KALRA, J ;
LEE, P .
CELLULAR, BIOCHEMICAL, AND MOLECULAR ASPECTS OF REPERFUSION INJURY, 1994, 723 :375-379