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Effects of extracts of high- and low-chromium brewer's yeast on metabolism of glucose by hepatocytes from rats fed on high- or low-Cr diets

Published online by Cambridge University Press:  09 March 2007

E. S. Holdsworth
Affiliation:
Biochemistry Department, University of Tasmania, GPO Box 252C, Hobart, Tasmania 7001, Australia
E. Neville
Affiliation:
Biochemistry Department, University of Tasmania, GPO Box 252C, Hobart, Tasmania 7001, Australia
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Abstract

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Brewer's yeast was grown on a defined medium containing glucose, ammonia, salts and vitamins plus tracer 51Cr without (low-Cr) or with (high-Cr) carrier Cr. The two batches of yeast differed by more than 100-fold in Cr content, containing 80 ng and 10 7mu;g Cr/g dry yeast respectively. Extraction and fractionation procedures were designed to isolate Cr complexes with properties similar to those reported for glucose tolerance factor. After weaning, rats were reared on rat cubes (normal diet) or on a diet containing less than 0.1 μg Cr/kg (low-Cr diet), or on the low-Cr diet supplemented with Cr (1 mg Cr/kg). Hepatocytes from these rats were incubated with [U-14C]glucose and incorporation of 14C into glycogen was measured. Incorporation of glucose-C into glycogen was enhanced by some yeast fractions in the presence of insulin, but had less effect in the absence of insulin. No difference could be detected between the responses to fractions from high- or low-Cr yeast extracts, or between responses by hepatocytes from animals fed on normal or low-Cr diets with or without Cr upplementation. Glycogen synthetase (EC 2.4.1.11) activity (total and percentage in the a form) was similar in hepatocytes isolated from animals on the normal and low-Cr diets. Those yeast fractions which enhanced the response to insulin in the 14C-incorporation experiments also enhanced the percentage of the enzyme in the a form in the presence of insulin, but not in the absence of insulin. The presence in yeast extracts of material which enhances the response to insulin by hepatocytes may help to explain the reported beneficial effects of dietary yeast supplements on glucose tolerance.

Type
Minerals, Nutrition, Metabolism, Bioavailability
Copyright
Copyright © The Nutrition Society 1990

References

REFERENCES

Anderson, R. A., Brantner, J. H. & Polansky, M. M. (1978). An improved assay for biologically active chromium. Journal of Agricultural and Food Chemistry 26, 12191221.CrossRefGoogle ScholarPubMed
Bergmeyer, H. V. (1974). Methods of Enzymatic Analysis, 2nd ed. London & New York: Academic Press.Google Scholar
Davidson, M. B. (1981). Autoregulation by glucose of hepatic glucose balance: permissive effect of insulin. Metabolism 30, 279284.CrossRefGoogle ScholarPubMed
Davies, D. M., Holdsworth, E. S. & Sherriff, J. L. (1985). The isolation of glucose tolerance factors from brewer's yeast and their relationship to chromium. Biochemical Medicine 33, 297311.CrossRefGoogle ScholarPubMed
Donaldson, D. L., Lee, D. M., Smith, C. C. & Rennert, O. M. (1985). Glucose tolerance and plasma lipid distributions in rats fed a high-sucrose, high-cholesterol, low-chromium diet. Metabolism 34, 10861093.CrossRefGoogle ScholarPubMed
Holdsworth, E. S. & Appleby, G. J. (1984). Assays of glucose tolerance factor and its mode of action, studied with brewer's yeast. Journal of Inorganic Biochemistry 21, 3144.CrossRefGoogle ScholarPubMed
Holdsworth, E. S. & Neville, E. (1988). Extracts of brewer's yeast contain GABA which enhances activation of glycogen synthetase by insulin in isolated rat hepatocytes. Biochemistry International 17, 11071116.Google ScholarPubMed
Hwang, D. L., Lev-Ran, A., Papoian, T. & Beech, W. K. (1987). Insulin-like activity of chromium-binding fractions from brewer's yeast. Journal of Inorganic Biochemistry 30, 219225.CrossRefGoogle ScholarPubMed
Jain, R., Verch, R. L., Wallach, S. & Peabody, R. A. (1981). Tissue chromium exchange in the rat. American Journal of Clinical Nutrition 34, 21992204.CrossRefGoogle ScholarPubMed
Katz, J., Golden, S. & Wals, P. A. (1976). Stimulation of hepatic glycogen synthesis by amino acids. Proceedings of the National Academy of Sciences, USA 13, 34333437.CrossRefGoogle Scholar
Krebs, H. A., Cornell, N. W., Lund, P. & Hems, R. (1974). Isolated liver cells as experimental material. In Alfred Benzon Symposium, vol. 6, pp. 726750 [Lindquist, F. and Tygstrup, N., editors]. Copenhagen: Munksgaard.Google Scholar
Lee, E. Y. C. & Whelan, W. J. (1966). Enzymic methods for the micro-determination of glycogen and amylopectin, and their unit chain lengths. Archives of Biochemistry and Biophysics 116, 162167.CrossRefGoogle Scholar
Mertz, W. (1976). Chromium and its relation to carbohydrate metabolism. Medical Clinics of North America 60, 739744.CrossRefGoogle ScholarPubMed
Mertz, W., Toepfer, E. W., Roginski, E. E. & Polansky, M. M. (1974). Present knowledge of the role of chromium. Federation Proceedings 33, 22752280.Google ScholarPubMed
Mokrasch, L. C. (1967). Use of 2,4,6-trinitrobenzene-sulfonic acid for the coestimation of amines, amino acids and proteins in mixtures. Analytical Biochemistry 18, 6471.CrossRefGoogle Scholar
Offenbacher, E. G.& Pi-Sunyer, F. X. (1988). Chromium in human nutrition. Annual Review of Nutrition 8, 543563.CrossRefGoogle ScholarPubMed
Schwarz, K. (1951). Production of dietary necrotic liver degeneration using American Torula yeast. Proceedings of the Society for Experimental Biology and Medicine 11, 818823.CrossRefGoogle Scholar
Schwarz, K. & Mertz, W. (1959). Chromium (III) and the glucose tolerance factor. Archives of Biochemistry and Biophysics 85, 292295.CrossRefGoogle ScholarPubMed
Schroeder, H. A. (1966). Chromium deficiency in rats: a syndrome simulating diabetes mellitus with retarded growth. Journal of Nutrition 88, 439445.CrossRefGoogle ScholarPubMed
Shah, J. H., Wongsurawat, N., Aran, P. P., Motto, G. S. & Bowser, E. N. (1977). A method for studying acute insulin secretion and glucose tolerance in unanaesthetised and unrestrained rats: the effect of mild stress on carbohydrate metabolism. Diabetes 26, 16.CrossRefGoogle Scholar
Sherriff, J. L. (1983). GTF activity in adipocytes. MSc Thesis, University of Tasmania.Google Scholar
Thomas, J. A., Schlender, K. K. & Larner, J. (1968). A rapid filter paper assay for UDPglucose-glycogen glucosyl transferase, including an improved biosynthesis of UDP-14C-glucose. Analytical Biochemistry 25, 486499.CrossRefGoogle Scholar
Toepfer, E. W., Mertz, W., Polansky, M. M., Roginski, E. E. & Wolf, W. R. (1977). Preparation of chromium-containing material of glucose tolerance factor activity from brewer's yeast and by synthesis. Journal of Agricultural and Food Chemistry 25, 162166.CrossRefGoogle Scholar
Tokuda, M., Kashiwagi, A., Wakamiya, E., Oguni, T., Mino, M. & Kagamiyama, H (1987). Glucose tolerance factor stimulates 3-O-methylglucose transport into isolated adipocytes. Biochemical and Biophysical Research Communications 144 1237–122.CrossRefGoogle Scholar
Vinson, J. A. & Bose, P. (1984). The effect of a high-chromium yeast on the blood glucose control and blood lipids of normal and diabetic human subjects. Nutrition Reports International 30, 911918.Google Scholar
Vinson, J. A. & Hsaio, K.-H. (1985). Comparative effect of various forms of chromium on serum glucose: an assay for biologically active chromium. Nutrition Reports International 32, 17.Google Scholar
Wallach, S. (1985). Clinical and biochemical aspects of chromium deficiency. Journal of the American College of Nutrition 4, 107120.CrossRefGoogle ScholarPubMed
Wooliscroft, J. & Barbosa, J. (1977). Analysis of chromium induced carbohydrate intolerance in the rat. Journal of Nutrition 107, 17021706.CrossRefGoogle Scholar