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Relationship between structure and function of dietary fibre: a comparative study of the effects of three galactomannans on cholesterol metabolism in the rat

Published online by Cambridge University Press:  09 March 2007

A. J. Evans
Affiliation:
CSIRO Division of Food Processing, Food Research Laboratory, PO Box 52, North Ryde, NSW 2113, Australia
R. L. Hood
Affiliation:
CSIRO Division of Food Processing, Food Research Laboratory, PO Box 52, North Ryde, NSW 2113, Australia
D. G. Oakenfull
Affiliation:
CSIRO Division of Food Processing, Food Research Laboratory, PO Box 52, North Ryde, NSW 2113, Australia
G. S. Sidhu
Affiliation:
CSIRO Division of Food Processing, Food Research Laboratory, PO Box 52, North Ryde, NSW 2113, Australia
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Abstract

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Male adult rats were fed on diets containing 80 g/kg galactomannans with different galactose (G): mannose (M) ratios/kg. The galactomannans were compared with purified cellulose (Solkaflok) and the animals were also fed on a basal diet free from fibre. All diets contained cholesterol (10 g/kg) and sodium cholate (2 g/kg). The three galactomannans were fenugreek gum (1G:1M), guar gum (1G:2M) and locust-bean gum (1G:4M). In comparison with the fibre-free and Solkaflok diets, all three galactomannans lowered the concentrations of cholesterol in both liver and blood plasma. The galactomannans also decreased the rate of hepatic synthesis of cholesterol. Dietary galactomannans increased caecal volatile fatty acids, particularly propionic, increased the weight of the caecum and its contents and increased the amount of water in the faeces. The increase in propionic acid production was significantly related to a decrease in caecal pH, but not to changes in plasma cholesterol or hepatic cholesterol synthesis. These effects were significantly influenced by chemical composition and structure of the galactomannan; they were most evident when the proportion of galactose in the galactomannan was highest (i.e. fenugreek gum). The three galactomannans also differed markedly in their effects on the viscosity of the digesta, but the galactomannan which gave the highest viscosity was least effective in lowering plasma cholesterol. A separate experiment with perfused loops of small intestine in vivo showed that the most effective galactomannan, fenugreek gum, had no direct effect on cholesterol absorption.

Type
Effects of Carbohydrates on Lipid Metabolism
Copyright
Copyright © The Nutrition Society 1992

References

REFERENCES

Anderson, J. W. & Bridges, S. R. (1981). Plant fiber metabolites alter hepatic glucose and lipid metabolism. Diabetes 30, Suppl. 1. 133A.Google Scholar
Behal, K. M., Lee, K. H. & Moser, P. B. (1984). Blood lipids and lipoproteins in adult men fed four refined fibers. American Journal of Clinical Nutrition 39, 209214.Google Scholar
Bligh, E. G., & Dyer, W. J. (1959). A rapid method of total lipid extraction and purification. Canadian Journal of Biochemistry and Physiology 37, 911917.CrossRefGoogle ScholarPubMed
Bourne, M. B. (1982). Food Texture and Rheology: Concept and Measurement. New York: Academic Press.Google Scholar
Chen, W. J. L., Anderson, J. W. & Gould, M. R. (1981). Effects of oat bran, oat gum and pectin on lipid metabolism of cholesterol-fed rats. Nutrition Reports International 24, 10931098.Google Scholar
Cheng, B. Q., Trimble, R. P., Illman, R. J., Stone, B. A. & Topping, D. L. (1987). Comparative effects of dietary wheat bran and its morphological components (aleurone and pericarp-seed coat) on volatile fatty acid concentrations in the rat. British Journal of Nutrition 57, 6981.CrossRefGoogle ScholarPubMed
Dea, I. C. M. & Morrison, A. (1975). Chemistry and interactions of seed galactomannans. Advances in Carbohydrate Chemistry and Biochemistry 31, 241312.CrossRefGoogle Scholar
Eastwood, M. A. & Hamilton, D. (1968). Studies on the adsorption of bile salts to non-absorbed components of diet. Biochimica et Biophysica Acta 152, 165173.CrossRefGoogle ScholarPubMed
Gee, J. M., Blackburn, N. A. & Johnson, I. T. (1983). The influence of guar gum on intestinal cholesterol transport in the rat. British Journal of Nutrition 50, 215224.CrossRefGoogle ScholarPubMed
Heaton, K. W. (1972). Bile Salts in Health and Disease. Edinburgh: Churchill-Livingstone.Google Scholar
Hood, R. L. (1987). A note on the cholesterol content of beef rib steaks. CSIRO Food Research Quarterly 47, 4446.Google Scholar
Hood, R. L. (1990). Effect of diet and substrate on the in vitro measurement of cholesterol and fatty acid synthesis in hepatic tissue of Japanese quail (Coturnix coturnix japonica). Poultry Science 69, 647652.CrossRefGoogle Scholar
Ide, T., Okamastu, H. & Sugano, M. (1978). Regulation of dietary fats of 3-hydroxy-3-methylglutaryl-coenzyme A reductase in rat liver. Journal of Nutrition 108, 601607.CrossRefGoogle Scholar
Illman, R. J. & Topping, D. L. (1985). Effects of dietary oat bran on faecal steroid excretion, plasma volatile fatty acids and lipid synthesis in rats. Nutrition Research 5, 839846.CrossRefGoogle Scholar
Illman, R. J., Topping, D. L., Mclntosh, G. H., Trimble, R. P., Storer, G. B., Taylor, M. N. & Cheng, B. Q. (1988). Hypocholesterolaemic effects of dietary propionate studies in whole animals and perfused rat liver. Annals of Nutrition and Metabolism 32, 97106.CrossRefGoogle ScholarPubMed
Jenkins, D. J. A., Leeds, A. R., Newton, C. & Cummings, J. H. (1975). The effect of pectin, guar gum and wheat fibre on serum cholesterol. Lancet i, 11161117.CrossRefGoogle Scholar
Johnson, I. T. & Gee, J. M. (1986). Gastrointestinal adaptation in response to soluble non-available polysaccharides in the rat. British Journal of Nutrition 55, 497505.CrossRefGoogle ScholarPubMed
Judd, P. A. & Truswell, A. S. (1982). Comparison of effects of high- and low-mcthoxyl pectins on blood and faecal lipids in man. British Journal of Nutrition 48, 451458.CrossRefGoogle ScholarPubMed
Judd, P. A. & Truswell, A. S. (1985). The hypocholesterolaemic effects of pectins in rats. British Journal of Nutrition 53, 409425.CrossRefGoogle ScholarPubMed
Kay, R. M. & Truswell, A. S. (1977). Effect of citrus pectin on blood lipids and faecal sterol excretion in man. American Journal of Clinical Nutrition 30, 171176.CrossRefGoogle ScholarPubMed
Kirby, R. W., Anderson, J. W. & Sieling, B. (1981). Oat-bran intake selectively lowers serum low-density lipoprotein cholesterol concentrations of hypercholesterolemic men. American Journal of Clinical Nutrition 34, 824829.CrossRefGoogle ScholarPubMed
Kritchevsky, D. & Story, J. A. (1974). Binding of bile salts in vitro by non-nutritive fiber. Journal of Nutrition 104, 458462.CrossRefGoogle Scholar
Morgan, L. M., Goulder, T. J., Tsioladis, D., Marks, V. A. & Alberti, K. G. M. M. (1979). The effect of unabsorbable carbohydrate on gut hormones. Modification of postprandial GIP secretion by guar. Diabetologia 17, 8589.CrossRefGoogle ScholarPubMed
Oakenfull, D. G. (1988). Oat bran – Does oat bran lower plasma cholesterol…and if so, how? CSIRO Food Research Quarterly 48, 3739.Google Scholar
Osilesi, O., Trout, D. L., Glover, E. E., Harper, S. M., Koh, E. T., Behal, K. M., O'Dorisio, T. M. & Tartt, J. (1985). Use of xanthan gum in dietary management of diabetes mellitus. American Journal of Clinical Nutrition 42, 597603.CrossRefGoogle ScholarPubMed
Rudel, L. L. & Morris, M. D. (1973). Determination of cholesterol using o-phthalaldehyde. Journal of Lipid Research 14, 364366.CrossRefGoogle ScholarPubMed
Sharma, R. D. (1985). Hypocholesterolemic effect of gum acacia in men. Nutrition Research 5, 13211326.CrossRefGoogle Scholar
Sharma, R. D. (1986). Effect of fenugreek seeds and leaves on blood glucose and serum insulin response in human subjects. Nutrition Research 6, 13531364.CrossRefGoogle Scholar
Sherman, P. (1970). Industrial Rheology. London: Academic Press.Google Scholar
Simons, L. A., Gayst, S., Balasubramaniam, S. & Ruys, J. (1982). Long-term treatment of hypercholesterolaemia by a new palatable formulation of guar gum. Atherosclerosis 45, 101109.CrossRefGoogle ScholarPubMed
Smith, C. J. & Bryant, M. P. (1979) Introduction of metabolic activities of intestinal bacteria. American Journal of Clinical Nutrition 32, 149163.CrossRefGoogle ScholarPubMed
Snedecor, G. W. & Cochran, W. G. (1989). Statistical Methods, 8th ed., p. 177. Ames: Iowa State University Press.Google Scholar
Stanley, J. C. & Newsholme, E. A. (1985). The effects of dietary guar gum on the activities of some key enzymes of carbohydrate and lipid metabolism in mouse liver. British Journal of Nutrition 53, 215222.CrossRefGoogle ScholarPubMed
Topping, D. L., Oakenfull, D., Trimble, R. P. & Illman, R. J. (1988). A viscous fibre (methyl cellulose) lowers blood glucose and plasma triacylglycerols and increases liver glycogen independently of volatile fatty acid production in the rat. British Journal of Nutrition 59, 2130.CrossRefGoogle ScholarPubMed
Zavoral, J. H., Hannon, P., Fields, D. J., Hanson, M. N., Frantz, I. D., Kuba, K., Elmer, P. & Jacobs, D. R. (1983). The hypolipidemic effect of locust bean gum in familial hypercholesterolemic adults and children. American Journal of Clinical Nutrition 38, 285294.CrossRefGoogle ScholarPubMed