Hostname: page-component-76fb5796d-skm99 Total loading time: 0 Render date: 2024-04-25T16:13:24.780Z Has data issue: false hasContentIssue false

Dietary rhubarb (Rheum rhaponticum) stalk fibre does not lower plasma cholesterol levels in diabetic rats

Published online by Cambridge University Press:  09 March 2007

Sukhinder Kaur Cheema*
Affiliation:
Department of Biochemistry, University of Alberta, Edmonton, Alberta, CanadaT6G 2S2 Department of Biochemistry, Memorial University of Newfoundland, St. John's, Newfoundland, CanadaA1B 3X9
Vinti Goel
Affiliation:
Department of Agricultural, Food and Nutritional Sciences, University of Alberta, Edmonton, Alberta, CanadaT6G 2P5
Tapan K. Basu
Affiliation:
Department of Agricultural, Food and Nutritional Sciences, University of Alberta, Edmonton, Alberta, CanadaT6G 2P5
Luis B. Agellon
Affiliation:
Department of Biochemistry, University of Alberta, Edmonton, Alberta, CanadaT6G 2S2
*
*Corresponding author: Dr Sukhinder Kaur Cheema, fax +1 709 737 2422, email skaur@mun.ca
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.

Rhubarb (Rheum rhapontiam) stalk fibre was previously shown to be hypolipidaemic under clinical and experimental conditions. The present study was undertaken to investigate whether rhubarb stalk fibre has a hypolipidaemic effect under diabetic conditions. Two models of diabetic rats were used: streptozotocin-induced diabetic rats, and diabetes-prone BB (BBdp) rats. The plasma cholesterol and triacylglycerol concentrations were elevated after the onset of diabetes in BBdp rats, but not in sterptozotocin-induced diabetic rats. The rhubarb-fibre diet had no effect on the plasma cholesterol or triacylglycerol concentrations of diabetic rats. The hypolipidaemic effect of rhubarb stalk fibre has been suggested to be due to the bile-acid-binding capacity of rhubarb fibre, which in turn up regulates cholesterol 7α-hydroxylase (cyp7a) activity. cyp7a is the first and the rate-limiting enzyme in the breakdown of cholesterol to bile acids. We measured the cyp7a activity and mRNA levels in control and diabetic rats fed rhubarb- and cellulose-fibre diets. The cyp7a activity and mRNA abundance were increased in both diabetic rat models, indicating that bile acid synthesis is enhanced in diabetes. Feeding a diet enriched with rhubarb fibre caused a slight but significant increase (P<0·05) in cyp7a enzyme activity in BBdp rats, but no change in cyp7a mRNA abundance was detected. These results suggest that although a rhubarb-fibre-enriched diet increased cyp7a activity in BBdp rats, there was no apparent therapeutic benefit in terms of lowering plasma cholesterol concentrations.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2003

References

Abbey, M, Triantafilidis, C & Topping, DL (1993) Dietary nonstarch polysaccharides interact with cholesterol and fish oil in their effects on plasma lipids and hepatic lipoprotein receptor activity in rats. Journal of Nutrition 123, 900908.CrossRefGoogle ScholarPubMed
Agellon, LB (1997) Partial transfection of liver with a synthetic cholesterol 7α-hydroxylase transgene is sufficient to stimulate the reduction of cholesterol in the plasma of hypercholesterolemic mice. Biochemistry and Cell Biology 75, 255262.CrossRefGoogle ScholarPubMed
Agellon, LB & Torchia, EC (2000) Intracellular transport of bile acids. Biochimica et Biophysica Acta 1486, 198209.CrossRefGoogle ScholarPubMed
Basu, TK, Ooraikul, B & Garg, M (1993) The lipid lowering effects of rhubarb stalk fibre: a new source of dietary fibre. Nutrition Research 13, 10171024.CrossRefGoogle Scholar
Bennion, LJ & Grundy, SM (1977) Effects of diabetes mellitus on cholesterol metabolism in man. New England Journal of Medicine 296, 13651371.CrossRefGoogle ScholarPubMed
Brown, WV (1994) Lipoprotein disorders in diabetes mellitus. Medical Clinics of North America 78, 143161.CrossRefGoogle ScholarPubMed
Cheema, SK, Cikaluk, D & Agellon, LB (1997) Dietary fats modulate the regulatory potential of dietary cholesterol on cholesterol 7α-hydroxylase gene expression. Journal of Lipid Research 38, 315323.CrossRefGoogle Scholar
Chomczynski, P & Sacchi, N (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate–phenol–chloroform extraction. Analytical Biochemistry 162, 156158.CrossRefGoogle ScholarPubMed
Feingold, KR, Wilson, DE, Wood, LC, Kwong, LK, Moser, AH & Grunfeld, C (1994) Diabetes increases hepatic hydroxymethyl glutaryl coenzyme A reductase protein and mRNA levels in the small intestine. Metabolism 43, 450454.CrossRefGoogle ScholarPubMed
Fernandez, ML (1995) Distinct mechanisms of plasma LDL lowering by dietary fibre in the guinea pig: specific effects of pectin, guar gum and psyllium. Journal of Lipid Research 36, 23942404.CrossRefGoogle ScholarPubMed
Fernandez, ML, Lin, EC, Trejo, A & McNamara, DJ (1992) Prickly pear (Opuntia sp.) pectin reverses low density lipoprotein receptor suppression induced by a hypercholesterolemic diet in guinea pigs. Journal of Nutrition 122, 23302340.CrossRefGoogle ScholarPubMed
Gallaher, DD, Hassel, CA, Lee, KJ & Gallaher, CM (1993) Viscosity and fermentability as attributes of dietary fibre responsible for hypocholesterolemic effect in hamsters. Journal of Nutrition 123, 244252.Google ScholarPubMed
Goel, V, Cheema, SK, Agellon, LB, Ooraikul, B & Basu, TK (1999) Dietary rhubarb (Rheum rhaponticum) stalk fibre stimulates cholesterol 7α-hydroxylase gene expression and bile acid excretion in cholesterol-fed C57BL/6J mice. British Journal of Nutrition 81, 6571.CrossRefGoogle ScholarPubMed
Goel, V, Cheema, SK, Agellon, LB, Ooraikul, B, McBurney, MI & Basu, TK (1998) In vitro binding of bile salt to rhubarb stalk powder. Nutrition Research 18, 893903.CrossRefGoogle Scholar
Goel, V, Ooraikul, B & Basu, TK (1997) Cholesterol lowering effects of rhubarb fibre in hypercholesterolemic men. Journal of American College of Nutrition 16, 600604.Google ScholarPubMed
Gonzalez, J & Fevery, J (1992) Spontaneously diabetic biobreeding rats and impairment of bile acid-independent bile flow and increased biliary bilirubin, calcium and lipid secretion. Hepatology 16, 426432.CrossRefGoogle ScholarPubMed
Hansson, R (1989) Effect of diabetes, starvation, ethanol and isoniazid on rat liver microsomal 12α-hydroxylase activity involved in bile acid biosynthesis. Biochemical Pharmacology 38, 33863389.CrossRefGoogle Scholar
Horton, JD, Cuthbert, JA & Spady, DK (1994) Regulation of hepatic 7α-hydroxylase expression by dietary psyllium in the hamster. Journal of Clinical Investigation 93, 20842092.CrossRefGoogle Scholar
Kessler, II (1971) Mortality experience of diabetic patients: a twenty-six year follow-up study. American Journal of Medicine 51, 715724.CrossRefGoogle ScholarPubMed
Kimura, K, Ogura, Y & Ogura, M (1988) Increased rate of cholic acid formation from 3 alpha, 7 alpha-dihydroxy-5 beta-cholestane in perfused livers from diabetic rats. Biochimica et Biophysica Acta 963, 329332.CrossRefGoogle ScholarPubMed
Kimura, K, Ogura, Y & Ogura, M (1992) Biosynthesis of cholic acid accelerated by diabetes: its mechanism and effect of vanadate administration. Biochimica et Biophysica Acta 1123, 303308.CrossRefGoogle ScholarPubMed
Nakayama, H & Nakagawa, S (1977) Influence of streptozotocin diabetes on intestinal 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in the rat. Diabetes 26, 439444.CrossRefGoogle ScholarPubMed
National Research Council (1995) Nutrient requirements of laboratory animals, 4th revised ed., pp. 1179. Washington, DC: The National Academic Press.Google Scholar
Nervi, FO, Severin, CH & Valdivieso, VD (1978) Bile acid pool changes and regulation of cholate synthesis in experimental diabetes. Biochimica et Biophysica Acta 529, 212223.CrossRefGoogle ScholarPubMed
Steel, RGD & Torrie, JH (1980) Principles and Procedures of Statistics: A Biometrical Approach, pp. 67119. New York: McGraw-Hill.Google Scholar
Subbiah, MTR & Yunker, RL (1984) Cholesterol 7α-hydroxylase of rat liver: an insulin sensitive enzyme. Biochemical and Biophysical Research Communications 124, 896902.CrossRefGoogle ScholarPubMed
Torchia, EC, Cheema, SK & Agellon, LB (1996) Coordinate regulation of bile acid biosynthetic and recovery pathways. Biochemical and Biophysical Research Communications 255, 128133.CrossRefGoogle Scholar
Turrill, EL, McCarron, MM & Mikkelson, WP (1961) Gallstone and diabetes, ominous association. American Journal of Surgery 102, 184190.CrossRefGoogle ScholarPubMed
Twisk, J, Hoekman, FM, Lehman, EM, Meijer, P, Mager, WH & Princen, HMG (1995) Insulin suppresses bile acid synthesis in cultured hepatocytes by down regulation of cholesterol 7α-hydroxylase and sterol 27-hydroxylase gene transcription. Hepatology 21, 501510.Google ScholarPubMed
Uchida, K, Takase, H, Kadowaki, M, Nomura, Y, Matsubara, T & Takeuchi, N (1979) Altered bile acid metabolism in alloxan diabetic rats. Japanese Journal of Pharmacology 29, 553562.CrossRefGoogle ScholarPubMed
Yokode, M, Hammer, RE, Ishibashi, S, Brown, MS & Goldstein, JL (1990) Diet induced hypercholesterolemia in mice: prevention by overexpression of LDL receptors. Science 250, 12731275.CrossRefGoogle ScholarPubMed
Young, NL, Saudek, CD & Crawford, SA (1982) Total hydroxy-methylglutaryl CoA reductase activity in the small intestine and liver of insulin-deficient rats. Journal of Lipid Research 23, 266275.CrossRefGoogle Scholar