Dietary supplementation with β-carotene, but not with lycopene, inhibits endothelial cell-mediated oxidation of low-density lipoprotein

被引:66
作者
Dugas, TR
Morel, DW
Harrison, EH
机构
[1] Univ Sci Philadelphia, Dept Pharmaceut Sci, Philadelphia, PA 19104 USA
[2] MCP Hahnemann Sch Med, Dept Biochem, Philadelphia, PA USA
[3] USDA, Human Nutr Res Ctr, Beltsville, MD USA
关键词
carotenoids; antioxidants; LDL oxidation; free radicals; atherosclerosis; lipid peroxidation; beta-carotene; lycopene;
D O I
10.1016/S0891-5849(98)00321-9
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
Carotenoids may protect low-density lipoprotein from oxidation, a process implicated in the development of atherosclerosis. Our previous studies showed that in vitro enrichment of low-density lipoprotein (LDL) with beta-carotene protected it from cell-mediated oxidation. However, in vitro enrichment with either lutein or lycopene actually enhanced oxidation of the LDL. In the present studies we have examined the impact of LDL carotenoid content on its oxidation by human aortic endothelial cells (EaHy-1) in culture, comparing the effects of in vivo supplementation with in vitro enrichments. The beta-carotene content in human LDL was increased three- to sixfold by daily supplementation with 15 mg beta-carotene for 3 weeks, and the lycopene content of LDL in other individuals was increased two- to threefold by ingestion of one glass (12 ounce) of tomato juice daily for 3 weeks. LDL isolated from these healthy, normolipidemic donors not taking supplemental carotenoid was incubated at 0.25 mg protein/ml with EaHy-1 cells in Ham's F-10 medium for up to 48 h. Following dietary beta-carotene supplementation, LDL oxidation (as assessed by formation of lipid hydroperoxides) was markedly inhibited, to an even greater extent than was observed for LDL enriched in vitro with beta-carotene (that resulted in an 11- to 12-fold increase in LDL beta-carotene). No effect on cell-mediated oxidation was observed, however, for LDL enriched in vivo with lycopene. Thus, beta-carotene appears to function as an antioxidant in protecting LDL from cell-mediated oxidation although lycopene does not. The fact that the three- to sixfold enrichments of LDL with beta-carotene achieved by dietary supplementation were more effective in inhibiting oxidation than the 11- to 12-fold enrichments achieved by an in vitro method suggests that dietary supplementation is a more appropriate procedure for studies involving the enrichment of lipoprotein with carotenoids. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:1238 / 1244
页数:7
相关论文
共 38 条
[1]  
Alpha-Tocopherol Beta Carotene Cancer Prevention Study Group, 1994, N Engl J Med, V330, P1029, DOI 10.1056/NEJM199404143301501
[2]  
BARUA AB, 1992, METHOD ENZYMOL, V213, P273
[3]  
BARUA AB, 1989, J MICRONUTR ANAL, V5, P291
[4]   The role of oxidized lipoproteins in atherogenesis [J].
Berliner, JA ;
Heinecke, JW .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (05) :707-727
[5]  
BJORNSON LK, 1976, J LIPID RES, V17, P343
[6]   NUTRITION INTERVENTION TRIALS IN LINXIAN, CHINA - SUPPLEMENTATION WITH SPECIFIC VITAMIN MINERAL COMBINATIONS, CANCER INCIDENCE, AND DISEASE-SPECIFIC MORTALITY IN THE GENERAL-POPULATION [J].
BLOT, WJ ;
LI, JY ;
TAYLOR, PR ;
GUO, WD ;
DAWSEY, S ;
WANG, GQ ;
YANG, CS ;
ZHENG, SF ;
GAIL, M ;
LI, GY ;
YU, Y ;
LIU, BQ ;
TANGREA, J ;
SUN, YH ;
LIU, FS ;
FRAUMENI, JF ;
ZHANG, YH ;
LI, B .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (18) :1483-1492
[7]  
Clinton SK, 1996, CANCER EPIDEM BIOMAR, V5, P823
[8]   Mechanisms of disease - Antioxidants and atherosclerotic heart disease [J].
Diaz, MN ;
Frei, B ;
Vita, JA ;
Keaney, JF .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (06) :408-416
[9]  
Dugas TR, 1998, J LIPID RES, V39, P999
[10]   Carotenoid and tocopherol concentrations in plasma, peripheral blood mononuclear cells, and red blood cells after long-term beta-carotene supplementation in men [J].
Fotouhi, N ;
Meydani, M ;
Santos, MS ;
Meydani, SN ;
Hennekens, CH ;
Gaziano, JM .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1996, 63 (04) :553-558