Comparative effects of cellulose and soluble fibers (pectin, konjac glucomannan, inulin) on fecal water toxicity toward Caco-2 cells, fecal bacteria enzymes, bile acid, and short-chain fatty acids.

The aim of this study was to compare the effects of cellulose and three soluble dietary fibers, pectin, konjac glucomannan (KGM), and inulin, on the cytotoxicity and DNA damage of fecal water-treated Caco-2 cells, a human colon adenocarcinoma cell line, and to investigate the fecal components that potentially modulate the fecal toxicity, that is, bacterial enzymes, bile acids, and short-chain fatty acids. Six-week-old BALB/cJ mice were randomly allocated to consume an AIN-93 diet that contained no dietary fiber (fiber-free) or 5% (w/w) cellulose, pectin, KGM, and inulin for 3 weeks. Feces were collected during days 18-21. Fecal waters were co-incubated with Caco-2 cells to determine the cytotoxicity and DNA damage. In addition, the fecal bacterial enzymes, bile acids, and short-chain fatty acids were determined. Results indicated that all fiber diets similarly increased the survival rate (%) of fecal water-treated Caco-2 cells as compared with the fiber-free diet. The inhibition of fecal water-induced DNA damage in Caco-2 cells was greater for the pectin and inulin diets than for the cellulose and KGM diets. In contrast, cellulose exerted the greatest inhibitory effect on the fecal β-glucuronidase activity. Cellulose and all soluble dietary fibers reduced the secondary bile acid concentrations in the fecal water, but only soluble fibers increased the fecal concentrations of short-chain fatty acids, as compared with no fiber. Therefore, this study suggests that all dietary fibers substantially reduced the fecal water toxicity, which is associated with decreased secondary bile acid levels by all fibers, reduced fecal β-glucuronidase activity by cellulose, and increased short-chain fatty acid levels by soluble dietary fibers.

[1]  S. Yeh,et al.  Partial hydrolysis enhances the inhibitory effects of konjac glucomannan from Amorphophallus konjac C. Koch on DNA damage induced by fecal water in Caco-2 cells. , 2010 .

[2]  M. Glei,et al.  Fermentation products of inulin-type fructans reduce proliferation and induce apoptosis in human colon tumour cells of different stages of carcinogenesis , 2009, British Journal of Nutrition.

[3]  I. Rowland,et al.  Diet, fecal water, and colon cancer--development of a biomarker. , 2009, Nutrition reviews.

[4]  R. Fabiani,et al.  Genotoxic effect of bile acids on human normal and tumour colon cells and protection by dietary antioxidants and butyrate , 2008, European journal of nutrition.

[5]  R. Hughes,et al.  Effect of Colonic Bacterial Metabolites on Caco-2 Cell Paracellular Permeability In Vitro , 2008, Nutrition and cancer.

[6]  A. Klinder,et al.  Prebiotics and Reduction of Risk of Carcinogenesis: Review of Experimental and Human Data , 2008 .

[7]  K. Richter,et al.  Physiological concentrations of butyrate favorably modulate genes of oxidative and metabolic stress in primary human colon cells. , 2007, The Journal of nutritional biochemistry.

[8]  S. Yeh,et al.  Inhibitory Effects of a Soluble Dietary Fiber from Amorphophallus konjac on Cytotoxicity and DNA Damage Induced by Fecal Water in Caco-2 Cells , 2007, Planta medica.

[9]  Wen-Tze Wu,et al.  Konjac acts as a natural laxative by increasing stool bulk and improving colonic ecology in healthy adults. , 2006, Nutrition.

[10]  G. Rechkemmer,et al.  Cloudy apple juice decreases DNA damage, hyperproliferation and aberrant crypt foci development in the distal colon of DMH-initiated rats. , 2005, Carcinogenesis.

[11]  R. Carroll,et al.  Biochemical and Molecular Actions of Nutrients An Increase in Reactive Oxygen Species by Dietary Fish Oil Coupled with the Attenuation of Antioxidant Defenses by Dietary Pectin Enhances Rat Colonocyte Apoptosis , 2004 .

[12]  Young-ho Kim,et al.  Sodium butyrate sensitizes TRAIL-mediated apoptosis by induction of transcription from the DR5 gene promoter through Sp1 sites in colon cancer cells. , 2004, Carcinogenesis.

[13]  I. Rowland,et al.  Antigenotoxicity of probiotics and prebiotics on faecal water-induced DNA damage in human colon adenocarcinoma cells. , 2004, Mutation research.

[14]  L. Yin,et al.  Butyrate suppresses Cox-2 activation in colon cancer cells through HDAC inhibition. , 2004, Biochemical and biophysical research communications.

[15]  W. Sheu,et al.  Konjac Supplement Alleviated Hypercholesterolemia and Hyperglycemia in Type 2 Diabetic Subjects—A Randomized Double-Blind Trial , 2003, Journal of the American College of Nutrition.

[16]  I. Rowland,et al.  Diet and cancer: assessing the risk , 2002, British Journal of Nutrition.

[17]  H. Freeman,et al.  Dietary Fiber Modification of Toxin- or Carcinogen-Induced Effects on Intestinal and Mammary Tissues , 2001 .

[18]  G. Rechkemmer,et al.  A diet high in fat and meat but low in dietary fibre increases the genotoxic potential of 'faecal water'. , 1999, Carcinogenesis.

[19]  C. Rao,et al.  Prevention of colonic aberrant crypt foci and modulation of large bowel microbial activity by dietary coffee fiber, inulin and pectin. , 1998, Carcinogenesis.

[20]  J. Lupton,et al.  Biochemical and Molecular Roles of Nutrients Fish Oil Blocks Azoxymethane-Induced Rat Colon Tumorigenesis by Increasing Cell Differentiation and Apoptosis Rather Than Decreasing Cell Proliferation , 1998 .

[21]  K. Kobashi,et al.  Anticarcinogenic action of apple pectin on fecal enzyme activities and mucosal or portal prostaglandin E2 levels in experimental rat colon carcinogenesis. , 1997, Journal of experimental & clinical cancer research : CR.

[22]  R. van der Meer,et al.  Diet-induced increase of colonic bile acids stimulates lytic activity of fecal water and proliferation of colonic cells. , 1992, Carcinogenesis.

[23]  C. Rémésy,et al.  High propionic acid fermentations and mineral accumulation in the cecum of rats adapted to different levels of inulin. , 1991, The Journal of nutrition.

[24]  F. Czubayko,et al.  A simplified micro-method for quantification of fecal excretion of neutral and acidic sterols for outpatient studies in humans. , 1991, Journal of lipid research.

[25]  B. Flourié,et al.  Effect of chronic ingestion of a fermented dairy product containing Lactobacillus acidophilus and Bifidobacterium bifidum on metabolic activities of the colonic flora in humans. , 1990, The American journal of clinical nutrition.

[26]  A. Roda,et al.  Chemical properties of bile acids. IV. Acidity constants of glycine-conjugated bile acids. , 1987, Journal of lipid research.

[27]  P. Boyle,et al.  Experimental colorectal cancer: The relationship of diet and faecal bile acid concentration to tumour induction , 1986, The British journal of surgery.

[28]  M. Nyman,et al.  Effect of two kinds of pectin and guar gum on 1,2-dimethylhydrazine initiation of colon tumors and on fecal beta-glucuronidase activity in the rat. , 1981, Cancer research.

[29]  H. J. Phillips Dye Exclusion Tests for Cell Viability , 1973 .