The opposing effects of n-3 and n-6 fatty acids

被引:899
作者
Schmitz, Gerd [1 ]
Ecker, Josef [1 ]
机构
[1] Univ Regensburg, Inst Clin Chem, D-93042 Regensburg, Germany
关键词
arachidonic acid; docosahexaenoic acid; eicosanoids; eicosapentaenoic acid; gene expression; inflammation; lipid metabolism; n-3; n-6;
D O I
10.1016/j.plipres.2007.12.004
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
Polyunsaturated fatty acids (PUFAs) can be classified in n-3 fatty acids and n-6 fatty acids, and in westernized diet the predominant dietary PUFAs are n-6 fatty acids. Both types of fatty acids are precursors of signaling molecules with opposing effects, that modulate membrane microdomain composition, receptor signaling and gene expression. The predominant n-6 fatty acid is arachidonic acid, which is converted to prostaglandins, leukotrienes and other lipoxygenase or cyclooxygenase products. These products are important regulators of cellular functions with inflammatory, atherogenic and prothrombotic effects. Typical n-3 fatty acids are docosahexaenoic acid and eicosapentaenoic acid, which are competitive substrates for the enzymes and products of arachidonic acid metabolism. Docosahexaenoic acid- and eicosapentaenoic acid-derived eicosanoids antagonize the pro-inflammatory effects of n-6 fatty acids. n-3 and n-6 fatty acids are ligands/modulators for the nuclear receptors NF kappa B, PPAR and SREBP-1c, which control various genes of inflammatory signaling and lipid metabolism. n-3 Fatty acids down-regulate inflammatory genes and lipid synthesis, and stimulate fatty acid degradation. In addition, the n-3/n-6 PUFA content of cell and organelle membranes, as well as membrane microdomains strongly influences membrane function and numerous cellular processes such as cell death and survival. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:147 / 155
页数:9
相关论文
共 92 条
[81]   Prostaglandin E2 production and T cell function after fish-oil supplementation:: response to antioxidant cosupplementation [J].
Trebble, TM ;
Wootton, SA ;
Miles, EA ;
Mullee, M ;
Arden, NK ;
Ballinger, AB ;
Stroud, MA ;
Burdge, GC ;
Calder, PC .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2003, 78 (03) :376-382
[82]   Endogenous anti-inflammatory mediators from arachidonate in human neutrophils [J].
Vachier, I ;
Chanez, P ;
Bonnans, C ;
Godard, P ;
Bousquet, J ;
Chavis, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 290 (01) :219-224
[83]  
VONSCHACKY C, 1993, J LAB CLIN MED, V121, P302
[84]   Bile acids lower triglyceride levels via a pathway involving FXR, SHP, and SREBP-1c [J].
Watanabe, M ;
Houten, SM ;
Wang, L ;
Moschetta, A ;
Mangelsdorf, DJ ;
Heyman, RA ;
Moore, DD ;
Auwerx, J .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (10) :1408-1418
[85]   THE CONVERSION OF DIETARY EICOSAPENTAENOIC ACID TO PROSTANOIDS AND LEUKOTRIENES IN MAN [J].
WEBER, PC ;
FISCHER, S ;
VONSCHACKY, C ;
LORENZ, R ;
STRASSER, T .
PROGRESS IN LIPID RESEARCH, 1986, 25 :273-276
[86]   Docosahexaenoic acid induces an anti-inflammatory profile in lipopolysaccharide-stimulated human THP-1 macrophages more effectively than eicosapentaenoic acid [J].
Weldon, Sinead M. ;
Mullen, Anne C. ;
Loscher, Christine E. ;
Hurley, Lisa A. ;
Roche, Helen M. .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2007, 18 (04) :250-258
[87]   Polyunsaturated fatty acids decrease expression of promoters with sterol regulatory elements by decreasing levels of mature sterol regulatory element-binding protein [J].
Worgall, TS ;
Sturley, SL ;
Seo, T ;
Osborne, TF ;
Deckelbaum, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (40) :25537-25540
[88]   Sterol regulatory element binding protein-1 expression is suppressed by dietary polyunsaturated fatty acids - A mechanism for the coordinate suppression of lipogenic genes by polyunsaturated fats [J].
Xu, J ;
Nakamura, MT ;
Cho, HP ;
Clarke, SD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (33) :23577-23583
[89]   Polyunsaturated fatty acids suppress hepatic sterol regulatory element-binding protein-1 expression by accelerating transcript decay [J].
Xu, J ;
Teran-Garcia, M ;
Park, JHY ;
Nakamura, MT ;
Clarke, SD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (13) :9800-9807
[90]   Cross-talk between peroxisome proliferator-activated receptor (PPAR) α and liver X receptor (LXR) in nutritional regulation of fatty acid metabolism.: I.: PPARs suppress sterol regulatory element binding protein-1c promoter through inhibition of LXR signaling [J].
Yoshikawa, T ;
Ide, T ;
Shimano, H ;
Yahagi, N ;
Amemiya-Kudo, M ;
Matsuzaka, T ;
Yatoh, S ;
Kitamine, T ;
Okazaki, H ;
Tamura, Y ;
Sekiya, M ;
Takahashi, A ;
Hasty, AH ;
Sato, R ;
Sone, H ;
Osuga, JI ;
Ishibashi, S ;
Yamada, N .
MOLECULAR ENDOCRINOLOGY, 2003, 17 (07) :1240-1254