Evidence for health benefits of plant phenols: local or systemic effects?

被引:240
作者
Hollman, PCH [1 ]
机构
[1] State Inst Qual Control Agr Prod, RIKILT, NL-6708 PD Wageningen, Netherlands
关键词
plant phenols; flavonoids; flavonols; flavones; flavanols; phenolic acids; health effects; systemic effects; epidemiology; cancer; cardiovascular disease; bioavailability; absorption; metabolism;
D O I
10.1002/jsfa.900
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Plant phenols are mostly products of the phenylpropanoid pathway and comprise a large variety of compounds: cinnamic acids, benzoic acids, flavonoids, proanthocyanidins, stilbenes, coumarins, lignans and lignins. They are strong antioxidants and might prevent oxidative damage to biomolecules such as DNA, lipids and proteins which play a role in chronic diseases such as cancer and cardiovascular disease. Plant phenols may interfere with all stages of the cancer process, potentially resulting in a reduction of cancer risk. Only flavonols have been investigated in observational studies. Five out of seven studies showed an inverse association of flavonol intake with subsequent cardiovascular disease (CVD). A protective effect against cancer was only found in one out of four studies. Thus the epidemiological evidence does not yet allow a firm decision on the involvement of flavonols in the aetiology of either CVD or cancer. The epidemiology of flavonols points to a systemic effect. The epidemiology of tea, as a rich source of various phenols, shows inconsistent data for colon cancer, which also does not support a local effect of plant phenols. The absorption and bioavailability of plant phenols have been inadequately studied. Dietary flavonoids were thought to be poorly absorbed because of their presence as P-glycosides (conjugates of sugars). However, conjugation with glucose enhanced human absorption. Flavonoids and other plant phenols are extensively metabolised by colonic bacteria: the ring structure is cleaved, giving a range of phenolic acids which are then absorbed. Human studies showed that only about 1% of a well-absorbed flavonoid was excreted with an intact flavonoid backbone into urine. Major questions to be answered are whether the effective concentrations found in in vitro systems really reflect physiological concentrations. (C) 2001 Society of Chemical Industry.
引用
收藏
页码:842 / 852
页数:11
相关论文
共 123 条
  • [1] Relationship between flavonoid structure and inhibition of phosphatidylinositol 3-kinase: A comparison with tyrosine kinase and protein kinase C inhibition
    Agullo, G
    GametPayrastre, L
    Manenti, S
    Viala, C
    Remesy, C
    Chap, H
    Payrastre, B
    [J]. BIOCHEMICAL PHARMACOLOGY, 1997, 53 (11) : 1649 - 1657
  • [2] The effects of dietary ellagic acid on rat hepatic and esophageal mucosal cytochromes P450 and phase II enzymes
    Ahn, D
    Putt, D
    Kresty, L
    Stoner, GD
    Fromm, D
    Hollenberg, PF
    [J]. CARCINOGENESIS, 1996, 17 (04) : 821 - 828
  • [3] Nitric oxide production and endothelium-dependent vasorelaxation induced by wine polyphenols in rat aorta
    Andriambeloson, E
    Kleschyov, AL
    Muller, B
    Beretz, A
    Stoclet, JC
    Andriantsitohaina, R
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 1997, 120 (06) : 1053 - 1058
  • [4] [Anonymous], 1997, FOOD NUTR PREV CANC
  • [5] Catechin contents of foods commonly consumed in The Netherlands. 1. Fruits, vegetables, staple foods, and processed foods
    Arts, ICW
    van de Putte, B
    Hollman, PCH
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2000, 48 (05) : 1746 - 1751
  • [6] Catechin contents of foods commonly consumed in The Netherlands. 2. Tea, wine, fruit juices, and chocolate milk
    Arts, ICW
    van de Putte, B
    Hollman, PCH
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2000, 48 (05) : 1752 - 1757
  • [7] Absorption and excretion of conjugated flavonols, including quercetin-4′-O-β-glucoside and isorhamnetin-4′-O-β-glucoside by human volunteers after the consumption of onions
    Aziz, AA
    Edwards, CA
    Lean, MEJ
    Crozier, A
    [J]. FREE RADICAL RESEARCH, 1998, 29 (03) : 257 - 269
  • [8] BALANT L, 1979, ARZNEIMITTEL-FORSCH, V29-2, P1758
  • [9] BAMES S, 1995, P SOC EXP BIOL MED, V208, P103
  • [10] Bell JRC, 2000, AM J CLIN NUTR, V71, P103