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A study on lipid metabolism in heart and liver of cholesterol-and pectin-fed rats

Published online by Cambridge University Press:  09 March 2007

Sofie Hexeberg
Affiliation:
Department of Anatomy and Cell Biology, University of Bergen, Årstadveien 19, N-5009 Bergen, Norway
Erik Hexeberg
Affiliation:
Department of Surgery, Division of Biochemistry, University of Bergen, Haukeland Sykehus, N-5021 Bergen, Norway
Nina Willumsen
Affiliation:
Department of Clinical Biology, Division of Biochemistry, University of Bergen, Haukeland Sykehus, N-5021 Bergen, Norway
Rolf K. Berge
Affiliation:
Department of Clinical Biology, Division of Biochemistry, University of Bergen, Haukeland Sykehus, N-5021 Bergen, Norway
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Abstract

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Pectin is known as a cholesterol-reducing dietary fibre, and in the present study we addressed the question whether pectin affected the quantity of lipid in droplets in the myocardial cells and of lipid in the liver cells. Male Wistar rats received either a diet containing cholesterol or a standard diet without cholesterol with 0, 50 or 100 g pectin/kg incorporated for 10 d. The fractional volume of lipid droplets in the myocardial cells decreased as a function of pectin dose in both the standard-fed and the cholesterol-fed rats. Serum cholesterol was significantly reduced in both groups after addition of 100 g pectin/kg diet. The cholesterol diet increased the liver cholesterol level, and 100 g pectin/kg diet resulted in a lower concentration of liver cholesterol in the cholesterol-fed animals, but the influence on standard-fed rats was modest. Hydroxymethylglutaryl-CoA reductase (EC 1.1.1.88; HMG-CoA reductase) activity-increased when pectin was given in the standard diet. Liver triacylglycerol level increased after cholesterol and pectin feeding. Mitochondrial fatty acid oxidation and phosphatidate phosphohydrolase (EC 3.1.3.4) activity tended to decrease, whereas the peroxisomal fatty acid oxidation and acyl-CoA oxidase activity were unchanged. Increased hepatic triacylglycerol content by cholesterol and pectin treatment may be due to inhibited mitochondrial fatty acid oxidation along with increased availability of fatty acid for esterification and triacylglycerol synthesis. The presence of pectin in the diets of cholesterol-fed rats resulted in increased hepatic concentration of triacylglycerols and increased mitochondrial fatty acid oxidation. In this case the hepatic accumulation of triacylglycerol may be mediated by a reduced efflux of triacylglycerols from the liver.

Type
Effects of pectin and cholesterol on lipid metabolism
Copyright
Copyright © The Nutrition Society 1994

References

REFERENCES

Aas, M. & Daae, L. N. W. (1971). Fatty acid activation and acyl transfer in organs from rats in different nutritional states. Biochimica et Biophysica Acta 239, 208216.CrossRefGoogle ScholarPubMed
Alberts, A. W., Chen, J., Kuron, G., Hunt, V., Huff, J., Hoffman, C., Rothrock, J., Lopez, M., Joshua, H., Harris, E., Patchett, A., Monaghan, R., Currie, S., Stapley, E., Alberts-Schonberg, G., Hensens, O., Hirshfield, J., Hoogsteen, K., Liesch, J. & Springer, J. (1980). Mevinolin: A highly potent competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase and a cholesterol-lowering agent. Proceedings of the National Academy of Sciences USA 77, 39573961.CrossRefGoogle Scholar
Anderson, W. A. (1986). Fiber and health: An Overview. American Journal of Gastroenterology 81, 892897.Google ScholarPubMed
Berge, R. & Farstad, M. (1979). Dual localization of long-chain acyl-CoA hydrolase in rat liver: One in the microsomes and one in the mitochondrial matrix. European Journal of Biochemistry 95, 8997.CrossRefGoogle ScholarPubMed
Berge, R. K., Flatmark, T. & Christiansen, E. N. (1987). Effect of a high-fat diet with partially hydrogenated fish oil on long-chain fatty acid metabolizing enzymes in subcellular fractions of rat liver. Archives of Biochemistry and Biophysics 252, 269276.Google Scholar
Berge, R. K., Flatmark, T. & Osmundsen, H. (1984). Enhancement of long-chain acyl-CoA hydrolase activity in peroxisomes and mitochondria of rat liver by peroxisomal proliferators. European Journal of Biochemistry 141, 637644.CrossRefGoogle ScholarPubMed
Björkhem, I. (1985). Mechanism of bile acid biosynthesis in mammalian liver. In New Comprehensive Biochemistry. pp. 231278 [Danielsson, H. & Sjövall, J., editors]. Amsterdam: Elsevier Scientific Publishing Co.Google Scholar
Brindley, D. N. & Sturton, R. G. (1982). Phosphatidate metabolism and its relation to triacylglycerol biosynthesis. In Phospholipids - New. Comprehensive Biochemistry, vol. 4, pp, 179213 [Hawthorne, J. N. & Ansell, G. B., editors]. Amsterdam: Elsevier Scientific Publishing Co.Google Scholar
Brown, M. S., Goldstein, J. L. & Dietschy, J. M. (1979). Active and inactive forms of 3-hydroxy-3-methylglutaryl coenzyme A reductase in the liver of the rat. Journal of Biological Chemistry 254, 51445149.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
Edwards, P. A. & Gould, R. G. (1974). Dependence of the circadian rhythm of hepatic β-hydroxy-β-methylglutaryl Coenzyme A ribonucleic acid synthesis. Journal of Biological Chemistry 249, 28912896.CrossRefGoogle ScholarPubMed
Fuster, V., Badiman, J. J. & Badiman, L. (1992). Clinical-pathological correlations of coronary disease progression and regression. Circulation 86, Suppl. III, III.Google Scholar
Harry, D. S., Dini, M. & McIntyre, N. (1973). Effect of cholesterol feeding and biliary obstruction on hepatic cholesterol biosynthesis in the rat. Biochimica et Biophysica Acta 296, 209220.CrossRefGoogle ScholarPubMed
Hexeberg, S., Willumsen, N., Rotevatn, S., Hexeberg, E. & Berge, R. K. (1993). Cholesterol induced lipid accumulation in myocardial cells of rats. Cardiovascular Research 27, 442446.CrossRefGoogle ScholarPubMed
Judd, P. A. & Truswell, A. S. (1985). Dietary fibre and blood lipids in man. In Dietary Fibre; Perspectives, Reviews and Bibliography, pp. 2339 [Leeds, A. R., editor]. London: Libbey.Google Scholar
Kelly, M. J., Thomas, J. N. & Story, J. A. (1992). Changes in cholesterol accumulation and steroid excretion in response to cellulose, alfalfa or oats in cholesterol-fed rats. Nutrition Research 12, 509518.Google Scholar
Kritchevsky, D. (1988). Dietary fiber. Annual Review of Nutrition 8, 301328.Google Scholar
Kritchevsky, D., Tepper, S. A., Satchithanandam, S., Cassidy, M. M. & Vahouny, G. V. (1988). Dietary fiber supplements: Effects on serum and liver lipids and on liver phospholipid composition in rats. Lipids 2324, 318321.CrossRefGoogle ScholarPubMed
Madar, Z. & Thorne, R. (1987). Dietary fiber. Progress in Food and Nutrition Science 11, 153174.Google ScholarPubMed
Martin-Sanz, P., Hopewell, R. & Brindley, D. N. (1984). Long-chain fatty acids and their acyl-CoA esters cause the translocation of phosphatidate phosphohydrolase from the cytosolic to the microsomal fraction of rat liver. FEBS Letters 175, 284288.CrossRefGoogle Scholar
Mavis, R. D., Finkelstein, J. N. & Hall, B. P. (1978). Pulmonary surfactmt synthesis. A highly active microsomal phosphatidate phosphohydrolase in the lung. Journal of Lipid Research 19, 467477.Google Scholar
Morgan, B., Heald, M., Atkin, S. D. & Green, J. (1974). Dietary fibre and sterol metabolism in the rat. British Journal of Nutrition 32, 441455.CrossRefGoogle ScholarPubMed
Nervi, F. O. & Dietschy, J. M. (1975). Ability of six different lipoprotein fractions to regulate the rate of hepatic cholesterogenesis in vivo. Journal of Biological Chemistry 250, 87048711.CrossRefGoogle ScholarPubMed
Nishina, P. M. & Freedland, R. A. (1990). The effects of dietary fiber feeding on cholesterol metabolism in rats. Journal of Nutrition 120, 800805.CrossRefGoogle ScholarPubMed
Nishina, P. M., Schneeman, B. O. & Freedland, R. A. (1991). Effects of dietary fibers on nonfastiiig plasma lipoprotein and apolipoprotein levels in rats. Journal of Nutrition 121, 431437.CrossRefGoogle ScholarPubMed
Orekhov, A. N., Tertov, V. V., Novikov, I. D., Krushisky, A. V., Andrew, E. R., Lankin, V. Z. & Smirnov, V. N. (1985). Lipids in cells of atherosclerotic and uninvolved human aorta. Experimental and Molecular Pathology 42, 117137.CrossRefGoogle ScholarPubMed
Orekhov, A. N., Tertov, V. T., Mukhin, D. N., Koteliansky, V. E., Glukhova, M. A., Khashimov, K. A. & Smirna, V. N. (1987). Association of low-density lipoprotein with particulate connective tissue matrix components enhances cholesterol accumulation in cultured subendothelial cells of human aorta. Biochimica et Biophysica Acta 928, 251258.CrossRefGoogle ScholarPubMed
Rolandelli, R. H., Koruda, M. J., Settle, R. G., Leskiw, M. J., Stein, T. P. & Rombeau, J. L. (1989). The effect of pectin on hepatic lipogenesis in the enterally-fed rat. Journal of Nutrition 119, 8993.Google Scholar
Skorve, J., Asiedu, D., Rustan, A. C., Drevon, C. A., Al-Shurbaji, A. & Berge, R. K. (1990). Regulation of fatty acid oxidation and triglyceride and phospholipid metabolism by hypolipidemic sulfur-substituted fatty acid analogues. Journal of Lipid Research 31, 16271635.CrossRefGoogle ScholarPubMed
Small, G. M., Burdett, K. & Connock, M. J. (1985). A sensitive spectrophotometric assay for peroxisomal acyl-CoA oxidase. Biochemical Journal 227, 205210.CrossRefGoogle ScholarPubMed
Tertov, V. V., Orekhov, A. N., Sobenin, I. A., Gabbasov, Z. A., Papov, E. G., Yaroslavov, A. A. & Smirnov, V. N. (1992). Three types of naturally occurring modified lipoproteins induce intracellular lipid accumulation due to lipoprotein aggregation. Circulation Research 71, 218228.CrossRefGoogle ScholarPubMed
Vigne, J. L., Lairon, D., Borel, P., Portugal, H., Pauli, A. M., Hauton, J. C. & Lafont, H. (1987). Effect of pectin, wheat bran and cellulose on serum lipids and lipoproteins in rats fed on a low- or high-fat diet. British Journal of Nutrition 58, 405413.Google Scholar