Hostname: page-component-586b7cd67f-vdxz6 Total loading time: 0 Render date: 2024-11-22T20:28:09.609Z Has data issue: false hasContentIssue false

Caecal fermentation and energy accumulation in the rat fed on indigestible oligosaccharides

Published online by Cambridge University Press:  09 March 2007

Ei Sakaguchi*
Affiliation:
Laboratory of Animal Nutrition, Faculty of Agriculture, Okayama University, Tsushima-naka 1-1-1, Okayama 700, Japan
Chie Sakoda
Affiliation:
Laboratory of Animal Nutrition, Faculty of Agriculture, Okayama University, Tsushima-naka 1-1-1, Okayama 700, Japan
Yoko Toramaru
Affiliation:
Laboratory of Animal Nutrition, Faculty of Agriculture, Okayama University, Tsushima-naka 1-1-1, Okayama 700, Japan
*
*Corresponding author:Dr Ei Sakaguchi, fax +81 86 251 8388, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The energetic contribution from, and effects on the gastrointestinal tract of, indigestible oligosaccharides in growing rats were compared with those of sucrose (S). S and two types of oligosaccharides, fructo-oligosaccharide (Fru) and 6'-galacto-oligosaccharide (Gal) were added to a basal diet at a level of 100 g/kg. The basal diet was given either ad libitum (group B) or at a level approximately 90% of the ad libitum intakes of the Fru and Gal groups (group BR). During a 50 d feeding period, feed intake, digestibilities of nutrients, and digesta retention times using liquid (Co-EDTA) and particulate (Cr-cell-wall constituents) markers were measured. The carcass and the contents of the stomach and caecum were sampled on the last day of the experimental period. There was no significant difference in feed intake between groups other than BR. Addition of Fru and Gal to the basal diet resulted in increased crude ash digestibility and decreased crude protein and fat digestibilities. Mean retention times of digesta markers were increased by addition of Fru and Gal to the diet, and this was associated with enlargement of the caecum. Concentrations and amounts of total organic acids in the caecum were higher in groups Fru and Gal than the other groups. The amount of energy accumulated in the carcass of rats in the Gal group was significantly (P < 0.05) lower than that of rats fed on S but not Fru. Contributions to energy accumulation tended to be different between Fru and Gal; these were associated with differences in composition of caecal organic acids and of fatty acids in body fat.

Type
Research Article
Copyright
Copyright © The Nutrition Society 1998

References

Association of Official Analytical Chemists (1975) Official Methods of Analysis of the Association of Official Analytical Chemists, 12th ed. Washington, DC: Association of Official Analytical Chemists.Google Scholar
Brandt, CS & Thacker, EJ (1958) A concept of rate of food passage through the gastrointestinal tract. Journal of Animal Science 17, 218223.CrossRefGoogle Scholar
Buchanan, CA, Fry, SC & Eastwood, MA (1994 a) Metabolism and fate of dietary (U-14C)-labelled spinach cell walls in the rat. Journal of the Science of Food and Agriculture 64, 135140.CrossRefGoogle Scholar
Buchanan, CA, Fry, SC & Eastwood, MA (1994 b) The metabolism and fate of [methyl-14C] and [uronate-6-14C]pectin-labelled dietary plant cell wall in the rat. Journal of the Science of Food and Agriculture 66, 163173.CrossRefGoogle Scholar
Chen, W-JL, Anderson, JW & Jennings, D (1984) Propionate may mediate the hypocholesterolemic effects of certain soluble plant fibers in cholesterol fed rats. Proceedings of the Society for Experimental Biology and Medicine 175, 215218.CrossRefGoogle ScholarPubMed
Coombe, JB & Kay, RNB (1965) Passage of digesta through the large intestines of the sheep: retention times in the small and large intestine. British Journal of Nutrition 19, 325338.CrossRefGoogle Scholar
Demigné, C, Yacoub, C, Rémésy, C & Fafournoux, P (1986) Effects of absorption of large amounts of volatile fatty acids on rat liver metabolism. Journal of Nutrition 116, 7786.CrossRefGoogle ScholarPubMed
Duncan, DB (1955) Multiple range and multiple F tests. Biometrics 11, 142.CrossRefGoogle Scholar
Hagen, P & Robinson, KW (1953) The production and absorption of volatile fatty acids in the intestine of the guinea-pig. Australian Journal of Experimental Biology and Medical Science 31, 99104.CrossRefGoogle ScholarPubMed
Henning, SJ & Hird, FJR (1972) Ketogenesis from butyrate and acetate by the caecum and the colon of rabbits. Biochemical Journal 130, 785790.CrossRefGoogle ScholarPubMed
Hoshi, S, Sakata, T, Mikuni, K, Hashimoto, H & Kimura, S (1994) Galactosylsucrose and xylosylfructoside alter digestive tract size and concentrations of cecal organic acids in rats fed diets containing cholesterol and cholic acid. Journal of Nutrition 124, 5260.CrossRefGoogle ScholarPubMed
Hosoya, N, Dhorranintra, B & Hidaka, H (1988) Utilization of [U-14C]fructooligosaccharides in man as energy resources. Journal of Clinical Biochemistry and Nutrition 5, 6774.CrossRefGoogle Scholar
Ikegami, S, Tsuchihashi, F, Harada, H, Tsuchihashi, N, Nishide, E & Innami, S (1990) Effect of viscous indigestible polysaccharides on pancreatic-biliary secretion and digestive organs in rats. Journal of Nutrition 120, 353360.CrossRefGoogle ScholarPubMed
Illman, RJ, Topping, DL, McIntosh, GH, Trimble, RP, Storer, GB, Taylor, MN & Cheng, B-Q (1988) Hypocholesterolemic effects of dietary propionate: studies in whole animals and perfused rat liver. Annals of Nutrition and Metabolism 32, 97107.CrossRefGoogle Scholar
Imaizumi, K, Nakatsu, Y, Sato, M, Sedarnawati, Y & Sugano, M (1991) Effects of xylooligosaccharides on blood glucose, serum and liver lipids and cecum short-chain fatty acids in diabetic rats. Agricultural and Biological Chemistry 55, 199205.Google Scholar
Kikuchi, H & Yajima, T (1992) Correlation between water-holding capacity of different types of cellulose in vitro and gastrointestinal retention time in vivo of rats. Journal of the Science of Food and Agriculture 60, 139146.CrossRefGoogle Scholar
Matsumoto, K, Kobayashi, Y, Ueyama, S, Watanabe, T, Tanaka, R, Kan, T, Kuroda, A & Sumihara, Y (1993) Galactooligosacchar-ides. In Japanese Technology Reviews, Vol. 3, no. 2. Oligosac-charides: Production, Properties, and Applications, pp. 90106 [Nakakuki, T, editor]. Switzerland: Gordon and Breach Science Publishers.Google Scholar
Ohta, A, Ohtsuki, M, Baba, S, Adachi, T, Sakata, T & Sakaguchi, E (1995) Calcium and magnesium absorption from the colon and rectum are increased in rats fed fructooligosaccharides. Journal of Nutrition 125, 24172424.CrossRefGoogle ScholarPubMed
Ohta, A, Osakabe, N, Yamada, K, Saito, Y & Hidaka, H (1993) Effects of fructooligosaccharides on Ca, Mg and P absorption in rats. Journal of the Japanese Society of Nutrition and Food Science 46, 123129.CrossRefGoogle Scholar
Pond, WG, Church, DC & Pond, KR (1995) Basic Animal Nutrition and Feeding, 4th ed., p. 151. New York, NY: John Wiley & Sons.Google Scholar
Rémésy, C, Levrat, MA, Gamet, I & Demigné, C (1993) Cecal fermentations in rats fed oligosaccharides (inulin) are modulated by dietary calcium level. American Journal of Physiology 264, G855G862.Google ScholarPubMed
Roberfroid, M, Gibson, GR & Delzenne, N (1993) The biochemistry of oligofructose, a nondigestible fiber: an approach to calculate its caloric value. Nutrition Reviews 51, 137146.CrossRefGoogle ScholarPubMed
Roediger, WEW (1980) Role of anaerobic bacteria in the metabolic welfare of the colonic mucosa in man. Gut 21, 793798.CrossRefGoogle ScholarPubMed
Schulz, AGM, Amelsvoort, JMM & Beynen, AC (1993) Dietary native resistant starch but not retrograded resistant starch raises magnesium and calcium absorption in rats. Journal of Nutrition 123, 17241731.CrossRefGoogle Scholar
Schumann, WC, Magnusson, I, Chandramouli, V, Rumaran, K, Wahren, J & Randan, BR (1991) Metabolism of [2-14C]acetate and its use in assessing hepatic Krebs cycle activity and gluconeogenesis. Journal of Biological Chemistry 266, 69856990.CrossRefGoogle ScholarPubMed
Thacker, PA, Salomons, MO, Aherne, FX, Milligan, LP & Bowland, JP (1981) Influence of propionic acid on the cholesterol metabolism of pigs fed hypercholesterolemic diets. Canadian Journal of Animal Science 61, 969975.CrossRefGoogle Scholar
Tokunaga, T, Oku, T & Hosoya, N (1986) Influence of chronic intake of new sweetener fructooligosaccharide (Neosugar) on growth and gastrointestinal function of the rat. Journal of Nutritional Science and Vitaminology 32, 111121.CrossRefGoogle ScholarPubMed
Tokunaga, T, Oku, T & Hosoya, N (1989) Utilization and excretion of a new sweetener, fructooligosaccharide (neosugar), in rats. Journal of Nutrition 119, 553559.CrossRefGoogle ScholarPubMed
Udén, P, Colucci, PE & Van Soest, PJ (1980) Investigation of chromium, cerium and cobalt as markers in digesta rate of passage studies. Journal of the Science of Food and Agriculture 31, 625632.CrossRefGoogle ScholarPubMed
Van Soest, PJ (1963) The use of detergents in the analysis of fibrous feeds. II. A rapid method for the determination of fiber and lignin. Journal of the Association of Official Analytical Chemists 46, 829835.Google Scholar
Van Soest, PJ & Wine, RH (1967) Use of detergents in the analysis of fibrous feeds. IV. Determination of plant cell-wall constituents. Journal of the Association of Official Analytical Chemists 50, 5055.Google Scholar
Williams, CH, David, DJ & Iismaa, O (1962) The determination of chromic oxide in faeces samples by atomic absorption spectro-photometry. Journal of Agricultural Science, Cambridge 59, 381385.CrossRefGoogle Scholar
Yoneyama, M, Mandai, T, Aga, H, Fujii, K, Sakai, S, Shintani, T, Mou, K & Katayama (Sugawa), Y (1992) Effect of lactosucrose feeding on cecal pH, short-chain fatty acid concentration and microflora in rats. Nippon Eiyo Shokuryou Gakkaishi 45, 109115.CrossRefGoogle Scholar