Oat Bran, Rye Bran, and Soybean Hull Increase Goblet Cell Volume Density in the Small Intestine of the Golden Hamster a Histochemical and Stereologic Light-Microscopic Study

References

• Neutra M R, Forstner JF. Gastrointestinal mucins: synthesis, secretion and function. Physiology of the gastrointestinal tract.2nd ed., L R Johnson. Raven Press, New York 1987; 975–1009
   Google Scholar
• Cheng H, Leblond CP. Origin, differentiation, and renewal of the four main epithelial cell types in the mouse small intestine. V. Unitarian theory of the origin of the four epithelial cell types. Am J Anat 1974; 141: 537–62
   PubMedGoogle Scholar
• Moe H. On goblet cells, especially of the intestine of some mammalian species. Int Rev Cytol 1955; 4: 299–334
   Google Scholar
• Forstner G G, Forstner JF. Structure and function of gastrointestinal mucus. Molecular and cellular biology of digestion, P Desnuelle, H Sjostrom, O Noren. Elsevier Science Publishers B.V. (Biomedical Division), Amsterdam 1985; Vol. II.
   Google Scholar
• Silberberg A, Meyer FA. Structure and function of mucus. Mucus in health and disease. Vol. II (Adv Exp Med Biol 144), E N Chantler, J B Elder, M Elstein. Plenum Press, New York and London 1982; 53–74
   Google Scholar
• Parsons C L, Stauffer C, Schmidt JD. Impairment of antibacterial effect of bladder surface mucin by protamine sulfate. J Infect Dis 1981; 144: 180
   PubMedGoogle Scholar
• Shora W, Forstner G G, Forstner JF. Stimulation of proteolytic digestion by intestinal goblet cell mucus. Gastroenterology 1975; 68: 470–9
   PubMedGoogle Scholar
• Prizont R, Reed WP. Possible role of colonic content in the mucosal association of pathogenic Shigella. Infect Immun 1980; 29: 1197–9
   PubMedGoogle Scholar
• Smithson K W, Millar D B, Jacobs L R, Gray GM. Intestinal diffusion barrier: unstirred water layer or membrane surface mucus coat. Science 1981; 214: 1241–4
   PubMed Web of Science ®Google Scholar
• Mayer R M, Treadwell C R, Gallo L L, Vahouny GV. Intestinal mucins and cholesterol uptake in vitro. Biochim Biophys Acta 1985; 833: 34–43
   PubMedGoogle Scholar
• Shiau S Y, Chang GW. Effects of dietary fiber on fecal mucinase and β-glucuronidase activity in rats. J Nutr 1983; 113: 138–44
   PubMed Web of Science ®Google Scholar
• Cassidy M M, Lightfoot F G, Grau L, Story J, Kritchevsky D, Vahouny GV. Effect of chronic intake of dietary fibers on the ultrastructural topography of rat jejunum and colon: a scanning electron microscopy study. Am J Clin Nutr 1981; 34: 218–28
   PubMed Web of Science ®Google Scholar
• Cassidy M M, Lightfoot F G, Vahouny GV. Structural-functional modulation of mucin secretory patterns. Structure and function in epithelia, M Dinno. Alan R. Liss, New York 1981; 97–127
   Google Scholar
• Schneeman B O, Richter B D, Jacobs LR. Response to dietary wheat bran in the exocrine pancreas and intestine of rats. J. Nutr 1982; 112: 283–6
   PubMed Web of Science ®Google Scholar
• Vahouny G V, Le T, Ifrim I, Satchithanandam S, Cassidy MM. Stimulation of intestinal cytokinetics and mucin turnover in rats fed wheat bran or cellulose. Am J Clin Nutr 1985; 41: 895–900
   PubMed Web of Science ®Google Scholar
• Asp N G, Johansson C G, Hallmer H, Siljeström M. A rapid enzymatic assay of insoluble and soluble dietary fiber. J Agric Food Chem 1983; 31: 476–482
   PubMed Web of Science ®Google Scholar
• Zhang J X, Lundin E, Reuterving C O, . Effects of rye bran, oat bran and soy bean fibre on lipid and bile metabolism, and gallbladder morphology in male Syrian hamsters. Proceedings of Fibre 90: Chemical and Biological Aspects of Dietary Fibre., D AT Southgate, K Waldron, I T Johnson, G R Fenwick, et al. The Food Chemistry Group of the Royal Society of Chemistry, NorwichEngland 1990; 313–7
   Google Scholar
• Mowry RM. The special value of methods that color both acidic and vicinal hydroxyl groups in the histochemical study of mucins: with revised direction for the colloidal iron stain, the use of alcian blue 8GX and their combinations with the PAS reaction. Ann NY Acad Sci 1963; 106: 402–23
   Web of Science ®Google Scholar
• Spicer SS. Diamine methods for differentiating mucosubstances histochemically. J Histochem Cytochem 1965; 13: 211–34
   PubMed Web of Science ®Google Scholar
• Huang CB. A histochemical stain of mucins in the alimentary tract by the revised high iron diamine method [in Chinese, abstract in English]. Acta Acad Med Zunyi 1986; 9: 25–7
   Google Scholar
• Stenling R, Helander HF. Stereological studies on the small intestinal epithelium of the rat. Cell Tiss Res 1981; 217: 11–21
   PubMed Web of Science ®Google Scholar
• Mayhew TM. Geometric model of the rat intestinal mucosa for stereological evaluation of villous amplification factors. J Microsc 1984; 135: 337–46
   PubMed Web of Science ®Google Scholar
• Mayhew T M, Middleton C. Crypts, villi and microvilli in the small intestine of the rat. A stereological study of their variability within and between animals. J Anat 1985; 141: 1–17
   PubMedGoogle Scholar
• Weibel ER. Stereological methods. Vol 1. Practical methods for biological morphometry. Academic Press, London 1979
   Google Scholar
• Snedecor G W, Cochran WG. Statistical methods. 6th ed. Iowa State University Press, Ames, Iowa 1976
   Google Scholar
• Bennett G, Leblond C P, Haddad A. Migration of glycoprotein from the Golgi apparatus to the surface of various cell types as shown by radioautography after labeled fucose injection into rats. J Cell Biol 1974; 60: 258–84
   PubMedGoogle Scholar
• Neutra M R, Phillips T H, Phillips TE. Regulation of intestinal goblet cells in situ, in mucosal explants and in the isolated epithelium. Mucus and mucosa (Ciba Foundation Symposium 109). Pitman, London 1984; 20–9
   Google Scholar
• Goodlad R A, Wright NA. Peptides and epithelial growth regulation. Experientia 1987; 43: 780–4
   PubMedGoogle Scholar
• Johnson I T, Gee J M, Brown JC. Plasma enteroglucagon and small bowel cytokinetics in rats fed soluble nonstarch polysaccharides. Am J Clin Nutr 1988; 47: 1004–9
   PubMedGoogle Scholar
• Musch M, Miller R J, Filed M, Siegal MI. Stimulation of colonic secretion by lipoxygenase metabolites of arachidonic acid. Science 1982; 217: 1255–6
   PubMed Web of Science ®Google Scholar
• Miller H RP, Woodbury R G, Huntley J F, Newlands G. Systemic release of mucosal mast-cell protease in primed rats challenged with Nippostrongylus brasiliensis. Immunology 1983; 49: 471–9
   PubMedGoogle Scholar
• Liener IE. Nutritional significance of lectins in the diet. The lectins: properties, functions and applications in biology and medicine, I E Liener, I Goldstein, N Sharon. Academic Press, New York 1986; 527
   Google Scholar
• Tajiri H, Klein R M, Lebenthal E, Lee P-C. Oral feeding of isolated lectins from red kidney bean stimulates rat small intestinal mucosal DNA synthesis and crypt cell division. Dig Dis Sci 1988; 33: 1364–9
   PubMedGoogle Scholar
• Williamson R CN. Intestinal adaptation. Structural, functional and cytokinetic changes. N Engl J Med 1978; 298: 1393–1402
   PubMedGoogle Scholar
• Dowling RH. Small bowel adaptation and its regulation. Scand J Gastroenterol 1982; 17: 54–74, Suppl 74
   Google Scholar
• Jacobs L R, Bloom S R, Harsoulis P, Dowling RH. Intestinal adaptation in hypothermic hyperphagia. Clin Sci 1975; 48: 13P
   Google Scholar
• Maxton D G, Cynk E U, Thompson R PH. Small intestinal response to ‘elemental’ and ‘complete’ liquid feeds in the rat: effect of dietary bulk. Gut 1987; 28: 688–93
   PubMedGoogle Scholar
• Goodlad R A, Lenton W, Ghatei M A, Bloom S R, Wright NA. Effects of an elemental diet, inert bulk and different types of dietary fibre on the response of the intestinal epithelium to refeeding in the rat and relationship to plasma gastrin, entero-glucagon and PYY levels. Gut 1987; 28: 171–80
   PubMed Web of Science ®Google Scholar
• Jenkins D JA, Jenkins A L, Rao A V, Thompson LU. Starchy foods, type of fibre, and cancer risk. Prev Med 1987; 16: 545–53
   PubMedGoogle Scholar
• Cummings J H, Pomare E W, Branch W J, Naylor C PE, Macfarlane GT. Short chain fatty acids in human large intestine, portal hepatic and venous blood. Gut 1987; 28: 1221–7
   PubMed Web of Science ®Google Scholar
• Sakata T, Yajima T. Influence of short chain fatty acids on the epithelial cell division of digestive tracts. Q J Exp Physiol 1984; 69: 639–48
   PubMed Web of Science ®Google Scholar
• Sakata T. Stimulatory effect of short chain fatty acids on epithelial cell proliferation in the rat small intestine: a possible explanation for trophic effects of fermentable fibre, gut microbes and luminal trophic factors. Br J Nutr 1987; 58: 95–103
   PubMed Web of Science ®Google Scholar
• Jacobs L R, Lupton JR. Effects of dietary fibres on large bowel mucosal growth and cell proliferation. Am J Physiol 1984; 246: G378–85
   PubMedGoogle Scholar
• Goodlad R A, Ratcliffe B R, Lenton W, Wright NA. The effects of dietary fibre on intestinal epithelial cell proliferation in conventional and germ-free rats. Gut 1988; 29: A723
   Google Scholar
• Makita M, Weils WW. Quantitative analysis of fecal bile acids by gas-liquid chromatography. Anal Biochem 1963; 5: 523–30
   PubMedGoogle Scholar