Polyphenolic compounds: Interactions with the gut and implications for human health

被引:93
作者
Gee, JM [1 ]
Johnson, IT [1 ]
机构
[1] Food Res Inst, Norwich Lab, Norwich NR4 7UA, Norfolk, England
关键词
D O I
10.2174/0929867013372256
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
Polyphenolic compounds are abundant throughout the plant kingdom and are found in a wide variety of human foods. The flavonoids, which are the best defined group of polyphenols in the human diet, themselves comprise a large and complex group, all of which contain a three-ring structure with two aromatic centres and a central oxygenated heterocycle. Recent evidence suggests that significant quantities of quercetin and possibly myricetin and kaempferol are absorbed in the gut. A larger fraction probably remains in the lumen, and thus a substantial proportion of the gastrointestinal mucosa is exposed to biologically significant concentrations of these compounds. A substantial body of experimental work has established that flavonoids can suppress carcinogenesis in animal models and there is considerable interest in the biological effects of these compounds at the cellular level. Flavonoids interact with cellular signal pathways controlling the cell cycle, differentiation and apoptosis. Their potentially antineoplastic effects include antioxidant activity, induction of Phase II enzyme activity, inhibition of protein kinases and interactions with Type II estrogen binding sites. Naturally occuring polyphenolic compounds may play a role in the protective effects of fruits and vegetables against cancers in general, and they appear to have considerable potential for pharmaceutical uses as chemopreventive agents against neoplastic changes in the alimentary tract. Future research should therefore focus on the biological effects of flavonoids in the human body, using biomarkers to define their effects at each stage in the onset of neoplasia.
引用
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页码:1245 / 1255
页数:11
相关论文
共 149 条
[21]   QUERCETIN AND RUTIN AS INHIBITORS OF AZOXYMETHANOL-INDUCED COLONIC NEOPLASIA [J].
DESCHNER, EE ;
RUPERTO, J ;
WONG, G ;
NEWMARK, HL .
CARCINOGENESIS, 1991, 12 (07) :1193-1196
[22]   Effect of dietary chlorogenic acid on multiple immune functions and formation of aberrant crypt foci in rats [J].
Exon, JH ;
Magnuson, BA ;
South, EH ;
Hendrix, K .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, 1998, 53 (05) :375-384
[23]  
Ferrandina G, 1998, INT J CANCER, V77, P747, DOI 10.1002/(SICI)1097-0215(19980831)77:5<747::AID-IJC14>3.0.CO
[24]  
2-Z
[25]   Review of the biology of quercetin and related bioflavonoids [J].
Formica, JV ;
Regelson, W .
FOOD AND CHEMICAL TOXICOLOGY, 1995, 33 (12) :1061-1080
[26]   CONSUMPTION OF RED WINE WITH MEALS REDUCES THE SUSCEPTIBILITY OF HUMAN PLASMA AND LOW-DENSITY-LIPOPROTEIN TO LIPID-PEROXIDATION [J].
FUHRMAN, B ;
LAVY, A ;
AVIRAM, M .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1995, 61 (03) :549-554
[27]  
Fujiki H, 2000, CANCER DETECT PREV, V24, P91
[28]   ANTICARCINOGENIC EFFECTS OF (-)-EPIGALLOCATECHIN GALLATE [J].
FUJIKI, H ;
YOSHIZAWA, S ;
HORIUCHI, T ;
SUGANUMA, M ;
YATSUNAMI, J ;
NISHIWAKI, S ;
OKABE, S ;
NISHIWAKIMATSUSHIMA, R ;
OKUDA, T ;
SUGIMURA, T .
PREVENTIVE MEDICINE, 1992, 21 (04) :503-509
[29]  
GALI HU, 1991, CANCER RES, V51, P2820
[30]  
Gee Jennifer Margaret, 2000, Gastroenterology, V118, pA547