Molecular targets of dietary polyphenols with anti-inflammatory properties

被引:270
作者
Yoon, JH
Baek, SJ
机构
[1] Univ Tennessee, Coll Vet Med, Dept Pathobiol, Knoxville, TN 37996 USA
[2] Yonsei Univ, Coll Med, Dept Otorhinolaryngol, Seoul 120749, South Korea
[3] Yonsei Univ, Coll Med, Airway Mucus Inst, Seoul 120749, South Korea
关键词
polypbenol; anti-inflammation; COX; LOX; NAG-1; NSAID;
D O I
10.3349/ymj.2005.46.5.585
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There is persuasive epidemiological and experimental evidence that dietary polyphenols have anti-inflammatory activity. Aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) have long been used to combat inflammation. Recently, cyclooxygenase (COX) inhibitors have been developed and recommended for treatment of rheumatoid arthritis (RA) and osteoarthritis (OA). However, two COX inhibitors have been withdrawn from the market due to unexpected side effects. Because conventional therapeutic and surgical approaches have not been able to fully control the incidence and outcome of many inflammatory diseases, there is an urgent need to find safer compounds and to develop mechanism-based approaches for the management of these diseases. Polyphenols are found in many dietary plant products, including fruits, vegetables, beverages, herbs, and spices. Several of these compounds have been found to inhibit the inflammation process as well as tumorigenesis in experimental animals; they can also exhibit potent biological properties. In addition, epidemiological studies have indicated that populations who consume foods rich in specific polyphenols have lower incidences of inflammatory disease. This paper provides an overview of the research approaches that can be used to unravel the biology and health effects of polyphenols. Polyphenols have diverse biological effects, however, this review will focus on some of the pivotal molecular targets that directly affect the inflammation process.
引用
收藏
页码:585 / 596
页数:12
相关论文
共 85 条
[1]   Cyclooxygenase inhibitors induce the expression of the tumor suppressor gene EGR-1, which results in the up-regulation of NAG-1, an antitumorigenic protein [J].
Baek, SJ ;
Kim, JS ;
Moore, SM ;
Lee, SH ;
Martinez, J ;
Eling, TE .
MOLECULAR PHARMACOLOGY, 2005, 67 (02) :356-364
[2]   Epicatechin gallate-induced expression of NAG-1 is associated with growth inhibition and apoptosis in colon cancer cells [J].
Baek, SJ ;
Kim, JS ;
Jackson, FR ;
Eling, TE ;
McEntee, MF ;
Lee, SH .
CARCINOGENESIS, 2004, 25 (12) :2425-2432
[3]   Dual function of nonsteroidal anti-inflammatory drugs (NSAIDs): Inhibition of cyclooxygenase and induction of NSAID-activated gene [J].
Baek, SJ ;
Wilson, LC ;
Lee, CH ;
Eling, TE .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 301 (03) :1126-1131
[4]   Resveratrol enhances the expression of non-steroidal anti-inflammatory drug-activated gene (NAG-1) by increasing the expression of p53 [J].
Baek, SJ ;
Wilson, LC ;
Eling, TE .
CARCINOGENESIS, 2002, 23 (03) :425-434
[5]   Cyclooxygenase inhibitors regulate the expression of a TGF-β superfamily member that has proapoptotic and antitumorigenic activities [J].
Baek, SJ ;
Kim, KS ;
Nixon, JB ;
Wilson, LC ;
Eling, TE .
MOLECULAR PHARMACOLOGY, 2001, 59 (04) :901-908
[6]   Inhibition of TNFα-induced cyclooxygenase-2 expression by amentoflavone through suppression of NF-κB activation in A549 cells [J].
Banerjee, T ;
Valacchi, G ;
Ziboh, VA ;
van der Vliet, A .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2002, 238 (1-2) :105-110
[7]   FLAVONOIDS AND RELATED-COMPOUNDS AS INHIBITORS OF ARACHIDONIC-ACID PEROXIDATION [J].
BAUMANN, J ;
BRUCHHAUSEN, FV ;
WURM, G .
PROSTAGLANDINS, 1980, 20 (04) :627-639
[8]   Resveratrol, an extract of red wine, inhibits lipopolysaccharide induced airway neutrophilia and inflammatory mediators through an NF-κB-independent mechanism [J].
Birrell, MA ;
McCluskie, K ;
Wong, SS ;
Donnelly, LE ;
Barnes, PJ ;
Belvisi, MG .
FASEB JOURNAL, 2005, 19 (02) :840-+
[9]   MIC-1, a novel macrophage inhibitory cytokine, is a divergent member of the TGF-beta superfamily [J].
Bootcov, MR ;
Bauskin, AR ;
Valenzuela, SM ;
Moore, AG ;
Bansal, M ;
He, XY ;
Zhang, HP ;
Donnellan, M ;
Mahler, S ;
Pryor, K ;
Walsh, BJ ;
Nicholson, RC ;
Fairlie, WD ;
Por, SB ;
Robbins, JM ;
Breit, SN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11514-11519
[10]   Characterization of the rat, mouse, and human genes of growth/differentiation factor-15/macrophage inhibiting cytokine-1 (GDF-15/MIC-1) [J].
Böttner, M ;
Laaff, M ;
Schechinger, B ;
Rappold, G ;
Unsicker, K ;
Suter-Crazzolara, C .
GENE, 1999, 237 (01) :105-111