Subscribe to RSS
DOI: 10.1055/s-0030-1250664
© Georg Thieme Verlag KG Stuttgart · New York
Dose-dependent Effects of Polyphenolic Extracts from Green Tea, Blue-Berried Honeysuckle, and Chokeberry on Rat Caecal Fermentation Processes
Publication History
received Sept. 10, 2009
revised Nov. 16, 2010
accepted Dec. 5, 2010
Publication Date:
14 January 2011 (online)
Abstract
The physiological status of the colon or ceacum is known to be very important for the host organism. Therefore, the aim of this study was to estimate the influence of high doses of polyphenolic extracts from chokeberry (CH), blue-berried honeysuckle (H), and green tea (GT) on fermentation processes in the caecum and caecal parameters of rats fed casein diets. In a 4-week experiment, 35-day-old rats were fed diets containing 0.4, 0.8, and 1.2 % of pure polyphenols. The greatest weight of digesta was recorded in rats fed 1.2 % of GT extract, and these animals were also characterised by having the lowest content of dry matter. Supplementation of diets with the extracts of interest caused a reduction in pH values and ammonia concentrations in caecal digesta in comparison to control animals. The results of a two-way analysis of variance indicated dose-dependent (except for 0.4 % supplementation) inhibition of enzymatic activity compared to control animals. Introduction of CH and H extracts significantly reduced the activity of β-glucuronidase compared to rats fed tea diets. Two-way analysis of variance showed a significant decrease in volatile fatty acids concentration in rats fed diets supplemented with H and CH extracts in comparison to control and tea-fed rats. The obtained results showed that the extracts tested can distinctly influence caecal parameters and metabolism.
Key words
polyphenols - extract - caecum - fermentation - rat
References
- 1 Kuroda Y, Hara Y. Antimutagenic and anticarcinogenic activity of tea polyphenols. Mutat Res. 1999; 436 69-97
- 2 Hollman P C H. Evidence for health benefits of plant phenols: local or systemic effects?. J Food Agric Sci. 2001; 81 842-852
- 3 Facino M R, Carini M, Aldini G, Berti F, Rossoni G, Bombardelli G, Morazzoni P. Diet enriched with procyanidins enhances antioxidant activity and reduces myocardial post-ischaemic damage in rats. Life Sci. 1999; 64 627-642
- 4 Mei Y, Wei D, Liu J. Modulation effect of tea polyphenol toward N-methyl-N-nitro-N-nitrosoguanidine-induced precancerous gastric lesions in rats. J Nutr Biochem. 2005; 16 172-177
- 5 Yamakoshi J, Saito M, Kataoka S, Tokutake S. Procyanidin-rich extract from grape seeds prevents catarct formation in hereditary catarctous (ICR/f) rats. J Agric Food Chem. 2002; 50 4983-4988
- 6 Wiseman S A, Balentine D A, Frei B. Antioxidants in tea. Crit Rev Food Nutr. 1997; 37 705-718
- 7 Wang H, Provan G P, Helliwell K. Tea flavanoids: their functions, utilization and analysis. Trends Food Sci Technol. 2000; 11 152-160
- 8 Slimestad R, Torstengerpoll K, Natel H S, Johanessen T, Giske N H. Flavanoids from chokeberries, Aronia melanocarpa. J Food Comp Anal. 2005; 18 61-68
- 9 Frejnagel S. Comparison of polyphenolic composition of extracts from honeysuckle, chokeberries and green tea – a short report. Pol J Food Nutr Sci. 2007; 57 83-86
- 10 Spencer J P E. Metabolism of tea flavanoids in the gastrointestinal tract. J Nutr. 2003; 133 3255S-3261S
- 11 Gonthier M-P, Verny M-A, Besson C, Remesey C. Chlorogenic acid bioavailability largely depends on its metabolism by the gut microflora in rats. J Nutr. 2003; 133 1853-1859
- 12 Simons A L, Renouf M, Hendrich S, Murphy P A. Human gut microbial degradation of flavanoids: structure-function relationships. J Agric Food Chem. 2005; 53 4258-4263
- 13 Selma M V, Espin J C, Tomas-Barberan F A. Interaction between phenolics and gut microbiota: role in human health. J Agric Food Chem. 2009; 57 6485-6501
- 14 Rechner A R, Smith M A, Kuhnle G, Gibson G R, Debnam E S, Srai S K S, Moore K P, Rice-Evans C A. Colonic metabolism of dietary polyphenols: influence of structure on microbial fermentation products. Free Radic Biol Med. 2004; 36 212-225
- 15 Goñi I, Martin N, Saura-Calixto F. In vitro digestibility and intestinal fermentation of grape seed and peel. Food Chem. 2005; 90 281-286
- 16 Aprikian O, Duclos V, Guyot S, Besson C, Manach C, Bernalier A, Morand C, Remesey C, Demigne C. Apple pectin and a polyphenol-rich apple concentrate are more effective together than separately on cecal fermentation and plasma lipids in rats. J Nutr. 2003; 133 1860-1865
- 17 Tebib K, Besancon P, Rouanet J-M. Effects of dietary grape seed tannins on rat cecal fermentation and colonic bacterial enzymes. Nutr Res. 1996; 16 105-110
- 18 Levrat M A, Texier O, Regerat F, Demigne C, Remesey C. Comparison of the effects of condensed tannin and pectin on cecal fermentations and lipid metabolism in the rat. Nutr Res. 1993; 13 427-433
- 19 Johnson I T. Anticarcinogenic effects of diet-related apoptosis in the colorectal mucosa. Food Chem Toxicol. 2002; 40 1171-1178
- 20 Goldin B R, Gorbach S L. The relationship between diet and rat fecal bacterial enzymes in colon cancer. J Natl Cancer Inst. 1976; 57 371-375
- 21 Reddy B S, Engle A, Simi B, Goldman M. Effect of dietary fiber on colonic bacterial enzymes and bile acids in relation to colon cancer. Gastroenterology. 1992; 102 1475-1482
- 22 Frei B, Higdon J V. Antioxidant activity of tea polyphenols in vivo: evidence from animal studies. J Nutr. 2003; 133 3275S-3284S
- 23 Reeves P. AIN-93 purified diets for laboratory rodents: final report of the American Institute of Nutrition ad hoc writing committee on the reformation of the AIN-76A rodent diet. J Nutr. 1997; 123 1939-1951
- 24 Hofirek B, Haas D. Comparative studies of ruminal fluid collected by oral tube or by puncture of the caudorental ruminal sac. Acta Vet Brno. 2001; 70 27-33
- 25 Djouzi Z, Andrieux C. Compared effect of three oligosaccharides on metabolism of intestinal microflora on rats inoculated with a human faecal flora. Br J Nutr. 1997; 78 313-324
- 26 Griffiths L A, Barrow A. Metabolism of flavonoid compounds in germ-free rats. Biochem J. 1972; 130 1161-1172
- 27 Kuhnle G, Spencer J P E, Schroeter H, Shenoy B, Debnam E S, Srai S K, Rice-Evans C, Hahn U. Epicatechin and catechin are O-methylated and glucuronidated in the small intestine. Biochem Biophys Res Commun. 2000; 277 507-512
- 28 Keppler K, Humpf H-U. Metabolism of anthocyanins and their phenolic degradation products by the intestinal microflora. Bioorg Med Chem. 2005; 13 5195-5205
- 29 Jansman A J M, Verstegen M W A, Huisman J. Effects of dietary inclusion of hulls of faba beans (Vicia faba L.) with a low and high content of condensed tannins on digestion and some physiological parameters in piglets. Anim Feed Sci Technol. 1993; 43 239-257
- 30 Meselhy M R, Nakamura N, Hattori M. Biotransformation of (−)-epicatechin-O-gallate by human intestinal bacteria. Chem Pharm Bull. 1997; 45 888-893
- 31 Bazzocco S, Mattila I, Guyot S, Renard C M, Aura A M. Factors affecting the conversion of apple polyphenols to phenolic acids and fruit matrix to short-chain fatty acids by human faecal microbiota in vitro. Eur J Nutr. 2008; 47 442-452
- 32 Deprez S, Brezillon C, Rabot S, Philippe C, Mila I, Lapierre C, Scalbert A. Polymeric proanthocyanidins are catabolized by human colonic microflora into low-molecular-weight phenolic acids. J Nutr. 2000; 130 2733-2738
- 33 Vitaglione P, Donnarumma G, Napolitano A, Galvano F, Gallo A, Scalfi L, Fogliano V. Protocatechuic acid is the major human metabolite of cyaniding-glucosides. J Nutr. 2007; 137 2043-2048
- 34 Bravo L, Abia R, Eastwood M A, Saura-Calixto F. Degradation of polyphenols (catechin and tannic acid) in the rat intestinal tract. Effect on colonic fermentation and faecal output. Br J Nutr. 1994; 71 933-946
- 35 Guarner F, Malagelada J R. Gut microflora in health and disease. Lancet. 2003; 361 512-519
- 36 Kim D-H, Jung E-A, Sohng I-S, Han J-A, Kim T-H, Han M J. Intestinal bacterial metabolism of flavonoids and its relation to some biological activities. Arch Pharm Res. 1998; 21 17-23
- 37 Juskiewicz J, Wroblewska M, Zhaki K, Zdunczyk Z, Hussein L. Biological activity of faba beans proanthocyanidins. Acta Alim. 2001; 30 63-69
- 38 Mai V, Katki H A, Harmsen H, Gallaher D, Schatzkin A, Baer D J, Clevidence B. Effects of a controlled diet and black tea drinking on the fecal microflora composition and the fecal bile acid profile of human volunteers in a double-blinded randomized feeding study. J Nutr. 2004; 134 473-478
Slawomir Frejnagel
Department of Biological Functions of Food
Institute of Animal Reproduction and Food Research
Polish Academy of Sciences
Tuwima Str. 10
10-747 Olsztyn
Poland
Phone: +48 8 95 23 46 01
Fax: +48 8 95 24 01 24
Email: s.frejnagel@pan.olsztyn.pl