Requirement for, promotion, or inhibition by alpha-tocopherol of radical-induced initiation of plasma lipoprotein lipid peroxidation

被引:220
作者
Neuzil, J [1 ]
Thomas, SR [1 ]
Stocker, R [1 ]
机构
[1] HEART RES INST, BIOCHEM GRP, SYDNEY, NSW 2050, AUSTRALIA
基金
英国医学研究理事会;
关键词
atherosclerosis; free radical; lipid peroxidation; lipoxygenase; low-density lipoprotein; alpha-tocopheroxyl radical; tocopherol-mediated peroxidation; vitamin E;
D O I
10.1016/S0891-5849(96)00224-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
alpha-Tocopherol (alpha-TOH), generally regarded as the most important lipid-soluble, chain-breaking antioxidant in human plasma, can also be a pro-oxidant in isolated low-density lipoprotein (LDL) (Bowry V. W.; Stocker R. J. Am. Chem. Sec. 115:6029-6044; 1993). Here we examined whether this pro-oxidant activity of alpha-TOH is of more general relevance. We compared the oxidizability of lipid hydroperoxide-free, in vivo or in vitro alpha-TOH-depleted LDL and high-density lipoprotein (HDL), as well as plasma reconstituted with alpha-TOH-depleted lipoproteins, with that of the corresponding native and alpha-TOH-supplemented samples, using water- and lipid-soluble peroxyl radicals (ROO .), hydroxyl radicals (. OH), Cu2+, the transition metal-containing Ham's F-10 medium, soybean 15-lipoxygenase, and horseradish peroxidase as oxidants. Lipoprotein and plasma oxidizability was assessed by the loss of cholesteryl esters and alpha-TOH and the accumulation of hydroperoxides of cholesteryl esters and phospholipids. Compared to native LDL, HDL, and plasma, the in vivo and in vitro alpha-TOH-depleted counterparts were highly resistant to peroxidation initiation by all oxidants when used at mild radical flux conditions. Wherever tested, the oxidizability of isolated LDL decreased proportionally with decreasing alpha-TOH content. Initiation of LDL lipid oxidation by lipoxygenase and Cu2+ (even up to Cu2+:LDL ratio of 20:1) had an absolute requirement for alpha-TOH. Oxidation of reconstituted plasma with ROO . showed that in the absence of the vitamin, plasma lipids were largely resistant to oxidation, whereas bilirubin and urate oxidized more rapidly. Replenishing the in vitro depleted LDL with alpha-TOH, but not with alpha-tocopherol acetate, fully restored its original content of vitamin E and its oxidizability. Similarly, dietary supplementation with alpha-TOH restored the vitamin content and oxidizability of the in vivo alpha-TOH-depleted lipoproteins and plasma obtained from a patient with familial isolated vitamin E deficiency. Under high fluxes of ROO . and . OH, the activity of alpha-TOH in LDL switched from pro- to anti-oxidant, with the switching point for OH observed at a lower radical flux than that for ROO .. Together, our results show that alpha-TOH generally makes lipoproteins more reactive towards radical oxidants; this can result in a pro-oxidant activity depending on the specific oxidation conditions. Copyright (C) 1996 Elsevier Science Inc.
引用
收藏
页码:57 / 71
页数:15
相关论文
共 56 条
[21]   OXIDATION RESISTANCE, OXIDATION RATE, AND EXTENT OF OXIDATION OF HUMAN LOW-DENSITY-LIPOPROTEIN DEPEND ON THE RATIO OF OLEIC-ACID CONTENT TO LINOLEIC-ACID CONTENT - STUDIES IN VITAMIN-E-DEFICIENT SUBJECTS [J].
KLEINVELD, HA ;
NABER, AHJ ;
STALENHOEF, AFH ;
DEMACKER, PNM .
FREE RADICAL BIOLOGY AND MEDICINE, 1993, 15 (03) :273-280
[22]   LOW-DENSITY-LIPOPROTEIN OXIDIZABILITY BY COPPER CORRELATES TO ITS INITIAL UBIQUINOL-10 AND POLYUNSATURATED FATTY-ACID CONTENT [J].
KONTUSH, A ;
HUBNER, C ;
FINCKH, B ;
KOHLSCHUTTER, A ;
BEISIEGEL, U .
FEBS LETTERS, 1994, 341 (01) :69-73
[23]   alpha-Tocopherol as a reductant for Cu(II) in human lipoproteins - Triggering role in the initiation of lipoprotein oxidation [J].
Kontush, A ;
Meyer, S ;
Finckh, B ;
Kohlschutter, A ;
Beisiegel, U .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (19) :11106-11112
[24]   A METHOD FOR DEFINING THE STAGES OF LOW-DENSITY-LIPOPROTEIN OXIDATION BY THE SEPARATION OF CHOLESTEROL AND CHOLESTERYL ESTER-OXIDATION PRODUCTS USING HPLC [J].
KRITHARIDES, L ;
JESSUP, W ;
GIFFORD, J ;
DEAN, RT .
ANALYTICAL BIOCHEMISTRY, 1993, 213 (01) :79-89
[25]  
KUHN H, 1994, J LIPID RES, V35, P1749
[26]   INVOLVEMENT OF 15-LIPOXYGENASE IN EARLY STAGES OF ATHEROGENESIS [J].
KUHN, H ;
BELKNER, J ;
ZAISS, S ;
FAHRENKLEMPER, T ;
WOHLFEIL, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (06) :1903-1911
[27]   REDUCTION OF COPPER, BUT NOT IRON, BY HUMAN LOW-DENSITY-LIPOPROTEIN (LDL) - IMPLICATIONS FOR METAL ION-DEPENDENT OXIDATIVE MODIFICATION OF LDL [J].
LYNCH, SM ;
FREI, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (10) :5158-5163
[28]   PROOXIDANT ROLE OF VITAMIN-E IN COPPER-INDUCED LIPID-PEROXIDATION [J].
MAIORINO, M ;
ZAMBURLINI, A ;
ROVERI, A ;
URSINI, F .
FEBS LETTERS, 1993, 330 (02) :174-176
[29]  
NEUZIL J, 1994, J BIOL CHEM, V269, P16712
[30]   OXIDIZED LDL BINDS TO CD36 ON HUMAN MONOCYTE-DERIVED MACROPHAGES AND TRANSFECTED CELL-LINES - EVIDENCE IMPLICATING THE LIPID MOIETY OF THE LIPOPROTEIN AS THE BINDING-SITE [J].
NICHOLSON, AC ;
FRIEDA, S ;
PEARCE, A ;
SILVERSTEIN, RL .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1995, 15 (02) :269-275