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Accelerated Attenuation of Pre-Formed Cholesterol Gallstones by Dietary Tender Cluster Beans (Cyamopsis tetragonoloba) in Mice


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1 Department of Biochemistry and Nutrition, CSIR - Central Food Technological Research Institute, Mysore - 570 020, India
     

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Dietary soluble fibre-rich tender cluster beans (Cyamopsis tetragonoloba) (CB) is previously shown to reduce the susceptibility for cholesterol gallstone (CGS) formation in experimental mice. The present study evaluated if dietary CB could also accelerate dissolution of pre-formed CGS in mice. The possible additive influence of dietary fibre-rich CB and sulfur compounds-rich garlic in dissolving CGS was also evaluated. CGS was induced with a high-cholesterol diet for ten weeks. CB (10%) and garlic (1%) were included individually and in combination in the diet of gallstoneinduced mice for another ten weeks. CB, garlic, and CB+garlic reduced the preestablished CGS by 61, 50, and 72%, respectively, in 10 weeks as compared to 27% regression observed with the control diet. There was a reduction in cholesterol saturation index and ratios of cholesterol: bile acid and cholesterol: phospholipid in the bile, facilitating the desaturation of cholesterol. mRNA expression of CYP7A was up-regulated in CB-fed animals. CB+garlic produced a higher up-regulation of mRNA expression of CYP7A and CYP27. These results corroborate with the observed increase in the bile acid pool as a result of these dietary interventions. Acceleration of the regression of preformed CGS is complimentary to the previously reported CGSpreventive influence of dietary CB.

Keywords

Cholesterol Gallstones, Cholelithiasic Effect, Cholesterol Saturation Index, Tender Cluster Beans, Garlic.
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  • Berr, F., Holl, J., Jungst, D., Fischer, S., Richter, W.O., et al. Dietary n-3 polyunsaturated fatty acids decrease biliary cholesterol saturation in gallstone disease. Hepatol., 1992, 16, 960-967.
  • Misciagna, G., Centonze, S., Leoci, C., Guerra, V., Cisternino, A.M., Ceo, R. and Trevisan, M. Diet, physical activity and gallstones – a population, case-control study in southern Italy. Am. J. Clin. Nutr., 1999, 69, 120-126.
  • Samarghandian, S., Hadjzadeh, M., Davari, A.S. and Abachi, M. Reduction of serum cholesterol in hypercholesterolemic rats by guar gum. Afr. J. Physiol., 2011, 1, 36-42.
  • James, S.L., Muir, J.G., Curtis, S.L. and Gibson, P.R. Dietary fiber: a roughage guide. Int. Med. J., 2003, 33, 291-296.
  • Tomolin, J., Taylor, J.S. and Read, N.W. The effect of mixed fecal bacteria on a selection of viscous polysaccharide in vitro. Nutr. Rep. Int., 1989, 39, 121-135.
  • Raghavendra, C.K. and Srinivasan, K. Anti-cholelithogenic potential of dietary tender cluster beans (Cyamopsis tetragonoloba) during experimental formation of cholesterol gallstone in mice. Appl. Physiol. Nutr. Metab., 2014, 39, 152-157.
  • Pande, S. and Srinivasan, K. Potentiation of the hypolipidemic influence of dietaty tender cluster bean (Cyamopsis tetragonoloba) by garlic in cholesterol-fed rats. Fd. Chem., 2012, 133, 798-805.
  • Vidyashankar, S., Sambaiah, K. and Srinivasan, K. Regression of pre-established cholesterol gallstones by dietary garlic and onion in experimental mice. Metabol., 2010, 59, 1402-1412.
  • Kannar, D., Wattanapenpaiboon, N., Savige, G.S. and Wahlqvist, M.L. Hypocholesterolemic effect of an enteric-coated garlic supplement. J. Am. Coll. Nutr., 2001, 20, 225-231.
  • Akiyoshi, T., Uchida, K., Takase, H., Nomura, Y. and Takeuchi, N. Cholesterol gallstones in alloxan-diabetic mice. J. Lipid Res., 1986, 27, 915-924.
  • Bligh, E.G. and Dyer, W.J. A rapid method of total lipid extraction and purification, Can. J. Biochem. Physiol., 1959, 37, 911-917.
  • Turley, S.D. and Dietschy, J.M. Re-evaluation of 3α-hydroxysteroid dehydrogenase assay for total bile acids. J. Lipid Res., 1970, 19, 924-928.
  • Folch, J., Lees, M. and Sloane-Stanley, G.H. A simple method for the isolation and purification of total lipids from animal tissue. J. Biol. Chem., 1957, 226, 497-509.
  • Warnick, G.R. and Albers, J.J. A comprehensive evaluation of the heparin-manganese precipitation procedure for estimating high density lipoprotein cholesterol. J. Lipid Res., 1978, 19, 65-76.
  • Searcy, R.L. and Bergquist, L.M. A new colour reaction for the quantification of serum cholesterol. Clin. Chim. Acta, 1960, 5, 192-199.
  • Stewart, J.C.M. Colorimetric estimation of phospholipids with ammonium ferro thiocyanate. Anal. Biochem., 1980, 104, 10-14.
  • Fletcher, M.J. A colorimetric method for estimating serum triglycerides. Clin. Chim. Acta, 1968, 22, 303-307.
  • Ohkawa, H., Ohishi, N. and Yagi, K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal. Biochem., 1979, 95, 351-358.
  • Omaye, S.T., Turnbull, J.D. and Sauberlich, H.E. Selected methods for the determinations of the ascorbic acid in animal cells, tissues and fluids. Methods Enzymol., 1973, 62, 3-11.
  • Warholm, W., Guthenberg, C., Bahr, C.V. and Mannervik, B. Glutathione transferase from human liver. Methods Enzymol., 1985, 113, 499-504.
  • Carlberg, I. and Mannervik, B. Glutathione reductase. Methods Enzymol., 1985, 113, 484-490.
  • Flohe, L. and Gunzler, W.A. Assays of glutathione peroxidase. Methods Enzymol., 1984, 105, 114-121.
  • Aebi, H. Catalase in vitro. Methods Enzymol., 1984, 105, 121-126.
  • Flohe, L. and Otting, F. Superoxide dismutase assays. Methods Enzymol., 1984, 105, 93-104.
  • Bergmeyer, H.U. and Bernt, E. LDH – UV assay with pyruvate and NADH. In: Bergmeyer, H.U. (ed). Methods of Enzymatic Analysis, Vol. 2. Academic Press, New York, 1974, 574-579.
  • Lowry, O.H., Rosebrough, N.J., Farr, A.L. and Randall, R.J. Protein measurement with the Folin phenol reagent. J. Biol. Chem., 1951, 193, 265-275.
  • Petrack, B. and Latario, B.J. Synthesis of 27-hydroxycholesterol in rat liver mitochondria: HPLC assay and marked activation by exogenous cholesterol. J. Lipid Res., 1993, 34, 643-649.
  • Hulcher, F.H. and Oleson, W.H. Simplified spectrophotometric assay for microsomal 3-hydroxy-3-methyl glutaryl CoA reductase by measurement of coenzyme-A. J. Lipid Res., 1973, 14, 625-631.
  • Roslyn, I.T., Binns, G.S. and Mughes, B.F. Open cholecystectomy. A contemporary analysis of 42,474 patients. Ann. Surgery, 1993, 218, 129-137.
  • Bouchier, A.D. New drugs for gallstones. Br. Med. J., 1990, 300, 5927-5931.
  • Frias, A.D. and Sgarbieri, V.C. Guar gum effects on food intake, blood serum lipids and glucose levels of Wistar rats. Plant Fd. Hum. Nutr., 1998, 53, 15-28.
  • Ramirez, M.I., Karaoglu, D., Haro, D., Barillas, T.C., Bashirzadeh, R. and Gil, G. Cholesterol and bile acids regulate cholesterol-7α-hydroxylase expression at the transcriptional level in culture and in transgenic mice. Mol. Cell. Biochem., 1994, 14, 2809-2821.
  • Chen, W.J., Anderson, J.W. and Jennings, D. Propionate may mediate the hypocholesterolemic effects of certain soluble fibre in cholesterol-fed rats. Proc. Soc. Exp. Biol. Med., 1984, 175, 215-218.
  • Chi, M.S., Koh, E.T. and Steward, T.J. Effects of garlic on lipid metabolism in rats fed cholesterol or lard. J. Nutr., 1982, 12, 241-248.
  • Qureshi, A.A., Crenshaw, T.D., Abuirmeileh, N., Peterson, D.M. and Elson, C.E. Influence of minor plant constituents on porcine hepatic lipid metabolism: Impact on serum lipid. Atherosclerosis, 1983, 64, 109-115.
  • Eder, M.I., Miquel, J.F., Jungst, D., Paumgartner, G. and Von Ritter, C. Reactive oxygen metabolites promote cholesterol crystal formation in model bile: role of lipid peroxidation. Free Radic. Biol. Med., 1996, 20, 743-749.
  • Eder, M.I., Jungst, D., Meyer, G., Paumgartner, C. and Von Ritter, C. Lipid peroxidation products are increased in lithogenic human gallbladder bile. Gastroenterol., 1995, 114, 548-552.
  • Holan, K.R., Holzbach, R.T, Hermann, R.E., Cooperman, A.M. and Claffey, W.J. Nucleation time; a key factor in the pathogenesis of cholesterol gallstone disease. Gastroenterol., 1979, 77, 611-617.
  • Gallinger, S., Taylor, R.D., Harvey, P.R., Petrunka, C.N. and Strasberg, S.M. Effect of mucous glycoprotein on nucleation time of human bile. Gastroenterol., 1985, 89, 648-658.
  • Groen, A.K, Stout, J.P., Draper, J.A., Hoek, F.J., Grijm, R. and Tygat, G.N. Effect of cholesterol nucleation. promoting activity on cholesterol solubilisation in model bile. Hepatol, 1988, 8, 347-352.
  • Raghavendra, C.K. and Srinivasan, K. Influence of dietary tender cluster beans (Cyamopsis tetragonoloba) on biliary proteins, bile acid synthesis and cholesterol crystal growth in rat bile. Steroids, 2015, 94, 21-30.

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  • Accelerated Attenuation of Pre-Formed Cholesterol Gallstones by Dietary Tender Cluster Beans (Cyamopsis tetragonoloba) in Mice

Abstract Views: 357  |  PDF Views: 2

Authors

Chikkanna K. Raghavendra
Department of Biochemistry and Nutrition, CSIR - Central Food Technological Research Institute, Mysore - 570 020, India
Krishnapura Srinivasan
Department of Biochemistry and Nutrition, CSIR - Central Food Technological Research Institute, Mysore - 570 020, India

Abstract


Dietary soluble fibre-rich tender cluster beans (Cyamopsis tetragonoloba) (CB) is previously shown to reduce the susceptibility for cholesterol gallstone (CGS) formation in experimental mice. The present study evaluated if dietary CB could also accelerate dissolution of pre-formed CGS in mice. The possible additive influence of dietary fibre-rich CB and sulfur compounds-rich garlic in dissolving CGS was also evaluated. CGS was induced with a high-cholesterol diet for ten weeks. CB (10%) and garlic (1%) were included individually and in combination in the diet of gallstoneinduced mice for another ten weeks. CB, garlic, and CB+garlic reduced the preestablished CGS by 61, 50, and 72%, respectively, in 10 weeks as compared to 27% regression observed with the control diet. There was a reduction in cholesterol saturation index and ratios of cholesterol: bile acid and cholesterol: phospholipid in the bile, facilitating the desaturation of cholesterol. mRNA expression of CYP7A was up-regulated in CB-fed animals. CB+garlic produced a higher up-regulation of mRNA expression of CYP7A and CYP27. These results corroborate with the observed increase in the bile acid pool as a result of these dietary interventions. Acceleration of the regression of preformed CGS is complimentary to the previously reported CGSpreventive influence of dietary CB.

Keywords


Cholesterol Gallstones, Cholelithiasic Effect, Cholesterol Saturation Index, Tender Cluster Beans, Garlic.

References