The omega-3 fatty acids EPA and DHA decrease plasma F2-isoprostanes: Results from two placebo-controlled interventions

被引:77
作者
Mas, Emilie [1 ]
Woodman, Richard J. [1 ]
Burke, Valerie [1 ]
Puddey, Ian B. [1 ]
Beilin, Lawrence J. [1 ]
Durand, Thierry [2 ]
Mori, Trevor A. [1 ]
机构
[1] Univ Western Australia, Sch Med & Pharmacol, Royal Perth Hosp Unit, Perth, WA 6000, Australia
[2] CNRS, IBMM, UMR 5247, UM 1,UM 2, Montpellier, France
关键词
Isoprostanes; fish oil; inflammation; POLYUNSATURATED FATTY-ACIDS; TUMOR-NECROSIS-FACTOR; DOCOSAHEXAENOIC ACID; IN-VIVO; OXIDATIVE STRESS; PROSTANOIDS F2-ISOPROSTANES; LYMPHOCYTE-PROLIFERATION; DIETARY SUPPLEMENTATION; EICOSAPENTAENOIC ACID; CYTOKINE PRODUCTION;
D O I
10.3109/10715762.2010.492830
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
Omega-3 (omega 3) fatty acids, particularly eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), protect against cardiovascular disease. Despite these benefits, concern remains that (omega 3 fatty acids may increase lipid peroxidation. It has previously been shown that urinary F-2-isoprostanes (F-2-IsoPs) were reduced following w3 fatty acid supplementation in humans. It is now determined whether EPA or DHA supplementation affects plasma F-2-IsoPs. In two 6-week placebo-controlled interventions, Study A: overweight, dyslipidaemic men; and Study B: treated-hypertensive Type 2 diabetic, patients were randomized to 4 g daily EPA, DHA. Post-intervention plasma F-2-IsoPs were significantly reduced by EPA (24% in Study A, 19% in Study B) and by DHA (14% in Study A, 23% in Study B) relative to the olive oil group. The fall in plasma F2-lsoPs was not altered in analyses that corrected for changes in plasma arachidonic acid, which was reduced with EPA and DHA supplementation. Neither F-3-nor F-4-IsoPs were observed in plasma in both studies. These results show that in humans, EPA and DHA reduce in vivo oxidant stress as measured in human plasma and urine.
引用
收藏
页码:983 / 990
页数:8
相关论文
共 54 条
[1]   Fish oil supplementation in pregnancy lowers F2-isoprostanes in neonates at high risk of atopy [J].
Barden, AE ;
Mori, TA ;
Dunstan, JA ;
Taylor, AL ;
Thornton, CA ;
Croft, KD ;
Beilin, LJ ;
Prescott, SL .
FREE RADICAL RESEARCH, 2004, 38 (03) :233-239
[2]   Factors regulating isoprostane formation in vivo [J].
Basu, S ;
Helmersson, J .
ANTIOXIDANTS & REDOX SIGNALING, 2005, 7 (1-2) :221-235
[3]   F2-isoprostanes in human health and diseases:: From molecular mechanisms to clinical implications [J].
Basu, Samar .
ANTIOXIDANTS & REDOX SIGNALING, 2008, 10 (08) :1405-1434
[4]  
BURR ML, 1989, LANCET, V2, P757
[5]   n-3 polyunsaturated fatty acids and cytokine production in health and disease [J].
Calder, PC .
ANNALS OF NUTRITION AND METABOLISM, 1997, 41 (04) :203-234
[6]   n-3 polyunsaturated fatty acids and inflammation: From molecular biology to the clinic [J].
Calder, PC .
LIPIDS, 2003, 38 (04) :343-352
[7]   Dietary modification of inflammation with lipids [J].
Calder, PC .
PROCEEDINGS OF THE NUTRITION SOCIETY, 2002, 61 (03) :345-358
[8]   Polyunsaturated fatty acids and inflammatory processes: New twists in an old tale [J].
Calder, Philip C. .
BIOCHIMIE, 2009, 91 (06) :791-795
[9]   The effect on human tumor necrosis factor alpha and interleukin 1 beta production of diets enriched in n-3 fatty acids from vegetable oil or fish oil [J].
Caughey, GE ;
Mantzioris, E ;
Gibson, RA ;
Cleland, LG ;
James, MJ .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1996, 63 (01) :116-122
[10]   In vivo and in vitro lipid peroxidation of arachidonate esters:: The effect of fish oil ω-3 lipids on product distribution [J].
Davis, Todd A. ;
Gao, Ling ;
Yin, Huiyong ;
Morrow, Jason D. ;
Porter, Ned A. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (46) :14897-14904