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Effect of Sargassum polycystum (Phaeophyceae)-sulphated polysaccharide extract against acetaminophen-induced hyperlipidemia during toxic hepatitis in experimental rats

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Abstract

The effect of Sargassum polycystum crude extract on lipid metabolism was examined against acetaminophen-induced (800 mg/kg body wt., intraperitoneally) hyperlipidemia during toxic hepatitis in experimental rats. The animals intoxicated with acetaminophen showed significant elevation in the levels of cholesterol, triglycerides and free fatty acid in both serum and liver tissue. The levels of tissue total lipids and serum LDL-cholesterol were also elevated with depleted levels of serum HDL-cholesterol and tissue phospholipid. The acetaminophen-induced animals showed significant alterations in the activities of lipid metabolizing enzymes serum lecithin cholesterol acyl transferase (LCAT) and hepatic triglyceride lipase (HTGL). The levels of liver tissue fatty acids (saturated, mono and polyunsaturated) such as palmitic acid, stearic acid, oleic acid, linoleic acid, arachidonic acid and linolenic acid monitored by gas chromatography were considerably altered in acetaminophen intoxicated animals when compared with control animals. The prior oral administration of Sargassum polycystum (200 mg/kg body wt./day for a period of 15 days) crude extract showed considerable prevention in the severe disturbances of lipid profile and metabolizing enzymes triggered by acetaminophen during hepatic injury. Liver histology also showed convincing supportive evidence regarding their protective nature against fatty changes induced during acetaminophen intoxication. Thus the present study indicates that the protective nature of Sargassum polycystum extract may be due to the presence of active compounds possessing antilipemic property against acetaminophen challenge. (Mol Cell Biochem 276: 89–96, 2005)

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Abbreviations

LDL:

low-density lipoprotein cholesterol

HDL:

high density lipoprotein cholesterol

LCAT:

lecithin cholesterol acyl transferase

HTGL:

hepatic triglyceride lipase

AAP:

acetaminophen

TG:

triglycerides

FFA:

free fatty acid

VLDL:

Very low-density lipoprotein

References

  1. Chapman VJ, Chapman, DJ: Sea Vegetables (Algae as Food for Man), in Seaweeds and Their Uses, Chapman and Hall, New York, 1980, pp 62–97

    Google Scholar 

  2. Jothi Saraswathi S, Babu B, Rengaswamy R: Seasonal studies on the alginate and its biochemical composition I: Sargassum polycystum (Fucales), phaeophyceae. Phycolol Res 51(4): 240, 2003

    Article  Google Scholar 

  3. Fujihara M, Nagumo T: An influence of the structure of alginate on the chemotactic activity of macrophages and the antitumor activity. Carbohydr Res 243(1): 211–216, 1993

    Article  PubMed  Google Scholar 

  4. Yan X, Nagata T, Fan X: Antioxidant activities in some common seaweeds. Plant Foods Human Nutr 52: 252–262, 1998

    Google Scholar 

  5. Shanmugam M, Mody KH, Oza RM, Ramavat BK: Blood coagulant activity of a green marine algae Codium dwarkense (codiaceae, chlorophyta) in relation to its growth stages. Ind J Mar Sci 30: 49–52, 2001

    Google Scholar 

  6. Ueyama S, Yokokura T: Anti-ulcer effects and biological activities of polysaccharide from marine algae. Biofactors 12(1–4): 267–274, 2000

    PubMed  Google Scholar 

  7. Balaji Raghavendran H, Sathivel A, Devaki T: Efficacy of brown seaweed hot water extract against HCl-ethanol induced gastric mucosal injury in rats. Arch Pharmacol Res 27(4): 449–453, 2004

    Google Scholar 

  8. Kaneda T, Arai S: Studies on the effects of marine products on cholesterol metabolism (IV): fractionation of effective substances from purple laver (1). Bull Jpn Soc Sci Fisheries 31: 152–156, 1965

    Google Scholar 

  9. Skakun NP, Shman’ko VV: Lipid peroxidation and bile formation in a paracetamol lesion of the liver. Farmakol Toksikol Jul–Aug 47(4): 105–108, 1984

    Google Scholar 

  10. Kaneda T, Kamasastri PV, Arai S: Studies on marine products on cholesterol metabolism (I): the effects of edible seaweed. Bull Jpn Soc Sci Fisheries 29: 1020–1023, 1963

    Google Scholar 

  11. Chotigeat W, Tongsupa S, Supamataya K, Phongdara A: Effect of fucoidan on disease resistance of black tiger shrimp. Aquaculture 233: 23–30, 2004

    Article  Google Scholar 

  12. Balaji Raghavendran H, Sathivel A, Devaki T: Hepatoprotective nature of seaweed alcoholic extract on acetaminophen induced hepatic oxidative stress. J Health Sci 50(1): 1–5, 2004

    Article  Google Scholar 

  13. Krishnamurthy KV: Methods in Plant Histochemistry; S. Viswanathan Pvt. Ltd., Madras, 1988, pp 14–15

    Google Scholar 

  14. Dubois M, Gilles KA, Hamilton JK, Rebers PA, Smith F: Colorimetric method for determination of sugars and related substances. Anal Chem 28: 350–356, 1956

    Article  Google Scholar 

  15. Belcher R, Godhert AL: Semi-Micro Quantitative Organic Analysis, 2nd edn. Longmans, Green and Co., London, 1954, pp 102–107

    Google Scholar 

  16. Dodgson KS, Price RG: A note on the determination of ester sulphate content of sulphated polysaccharide. Biochem J 84: 106–110, 1962

    PubMed  Google Scholar 

  17. Knutson CA, Jeans A: A new modification of the carbazole analysis. Application to heteropolysaccharides. Anal Biochem 24: 470–481, 1968

    Article  PubMed  Google Scholar 

  18. Doner LW, Whistler RL: Fucoidan industrial gums polysaccharide and their derivatives. Academic press, New York, 1973, pp 115–120

    Google Scholar 

  19. Parekh AC, Jung DH: Cholesterol determination with ferric acetate-uranyl acetate and sulphuric acid-ferrous sulphate reagents. Anal Chem 42: 1423–1427, 1970

    Article  Google Scholar 

  20. Rice EW: Triglycerides in serum. In: P. Roedrick, R.P. McDonald (eds), Standard Methods in Clinical Chemistry, Academic Press, New York, 1970, p 215

    Google Scholar 

  21. Hron WT, Menahan LA: Asensitive method for the determination of free fatty acids in plasma. J Lipid Res 122: 377–381, 1981

    Google Scholar 

  22. Hitz J, Steinmetz J, Siest G: Plasma lecithin: cholesterol acyl tranferase- reference values and effects of xenobiotics. Clin Chem Acta 133: 85–86, 1983

    Article  Google Scholar 

  23. Burstein M, Scholnick HR: Precipitation of chylomicron and very low-density lipoprotein from human serum with sodium lauryl sulphate. Life Sci 11: 177–184, 1972

    Article  Google Scholar 

  24. Floch J, Lees M, Stanley GHS: A simple method for the isolation and purification of total lipids from animal tissues. J Biol Chem 226: 497–509, 1957

    PubMed  Google Scholar 

  25. Schmidt FH, Strike H, Dahl K: In: H.V. Bergmeyer (ed), Methods in Enzymatic Analysis, Vol 2. Academic Press, New York, 1974, p 819

    Google Scholar 

  26. Fiske CH, Subbarow Y: The colorimetric determination of phosphorous. J Biol Chem 66: 375–400, 1925

    Google Scholar 

  27. Morrison WR, Smith LM: Preparations of fatty acid methyl esters and dimethylacetals from lipids with boron fluoride methanol. J Lipid Res 5: 600–607, 1964

    Google Scholar 

  28. Owen JS: Extra hepatic cell membrane lipid abnormalities and cellular dysfunction in liver disease. Drugs 40, 73–83, 1990

    Google Scholar 

  29. McIntyre N: Plasma lipids and lipoproteins in liver disease. Gut 19: 526–530, 1978

    PubMed  Google Scholar 

  30. Glickman RM, Sebesin SM: Lipid metabolism. In: I.M. Arias, D. Schachter, H. Popper, D.A. Shafritz (eds), The Liver Biology and Pathobiology. Raven Press, New York, 1982, pp 123–142

    Google Scholar 

  31. Tsuji K, Tsuji E, Suzuki S: Effect of polysaccharides on cholesterol metabolism. VII. Effects of various polysaccharide derivatives, lignin and synthetic polymers on serum and liver cholesterol levels in rats. Eiyogaku Zasshi 35: 227–234, 1977

    Google Scholar 

  32. Watanabe K, Iwata K, Tandai et al.: Effects of soluble sodium alginates on the excretion of cholesterol, Trp-P-1 and aflatoxin B1 in rats. Eisei Kagaku [in Japanese] 38: 258–262, 1992

    Google Scholar 

  33. Satorres J, Perez-Mateo M, Mayol MJ, Esteban A, Graells ML: Protective effect of diltiazem against acetaminophen hepatotoxicity in mice. Liver 15(1): 16–19, 1995

    PubMed  Google Scholar 

  34. Kass GEN, Nictera P, Orrenius S: In: N. Grunnet, B. Quistorff (eds), Regulation of Hepatic Function, Munksgaard, Copenhagen, 1991, pp 344–354

    Google Scholar 

  35. Ray SD, Sorge CL, Raucy JL, Corcoran GB: Early loss of large genomic DNA in vivo with accumulation of Ca2+ in the nucleus during acetaminophen-induced liver injury. Toxicol Appl Pharmacol 106: 346–351, 1990

    Article  PubMed  Google Scholar 

  36. Koster R, Anderson M, De Beer EJ: Acetic acid for analgesic screening. Fed Proc 18: 412–416, 1959

    Google Scholar 

  37. Gross AJ, Sizer IW: The oxidation of tyramine, tyrosine, and related compounds by peroxidase. J Biol Chem 1611–1614, 1959

  38. Anggadiredja J, Hasanudin Sidiq A, Pratomo S, Rudyansyah A: Screening of marine algae from Warambadi seashore of Sumba island of Indonesia for antibacterial activity. Phytomed Suppl I: 37, 1996

    Google Scholar 

  39. Daugherty A, Zweifel BS, Schonfeld G: The effects of probucol on the progression of atherosclerosis in mature watanabe heritable hyperlipidemic rabbits. Br J Pharmacol 103: 1013–1018, 1991

    PubMed  Google Scholar 

  40. Younes MC, Sause CP, Siegers lemoine R: Effect of deferrioxamine and diethydithiocarbamate on paracetamol-induced hepato- and nephrotoxicity. The role of lipid peroxidation. J Appl Toxicol 8: 261–265, 1988

    PubMed  Google Scholar 

  41. Chander R, Kapoor NK: High-density lipoprotein is a scavenger of superoxide anions. Biochem Pharmacol 40: 1663–1665, 1990

    Article  PubMed  Google Scholar 

  42. Hall ED: Free radical scavengers and antioxidants. Acute Ther Intervent 8: 195–206, 1997

    Google Scholar 

  43. Richter C: Biophysical consequences of lipid peroxidation in membranes. Chem Phys Lipids 44: 175–189, 1987

    Article  PubMed  Google Scholar 

  44. Fromenty B, Pessayre D: Inhibition of mitochondrial beta-oxidation as a mechanism of hepatotoxicity. Pharmacol Ther 67: 101–154, 1995

    Article  PubMed  Google Scholar 

  45. Pinto HC, Baptista A, Camilo ME, Bruno de Costa E, Valente A, Carneiro de Moura M: Tamoxifen-associated steatohepatitis – report of three cases. J Hepatol 23: 95–97, 1995

    Article  PubMed  Google Scholar 

  46. Ide T, Ontko JA: Increased secretion of very low density lipoprotein triglyceride following inhibition of long chain fatty acid oxidation in isolated rat liver. J Biol Chem 256: 10247–10255, 1981

    PubMed  Google Scholar 

  47. Corkey BE, Hale DE, Glennon MC, Kelley RI, Coates PM, Kilpatrick et al.: Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndrome. J Clin Invest 82: 782–788, 1988

    PubMed  Google Scholar 

  48. Xu SH, Ding LS, Wang MK, Peng SL, Liao X: Studies on the Chemical Constituents of the Algae Sargassum polycystum. Youji Huaxue. Chinese J Org Chem 22: 138–140, 2002

    Google Scholar 

  49. Kulkarni AP, Byczkowski JZ: Hepatotoxicity. In: E. Hodgson, P.E. Levi (eds), Introduction to Biochemical Toxicology, 2nd edn. Appleton & Lange, Norwalk, Connecticut, 1994, pp 495–490

    Google Scholar 

  50. Seal CJ, Mathers JC: Comparative gastrointestinal and plasma cholesterol responses of rats fed on cholesterol-free diets supplemented with guar gum and sodium alginate. Br J Nutr 85: 317–324, 2001

    PubMed  Google Scholar 

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Correspondence to Thiruvengadam Devaki.

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Raghavendran, H.R.B., Sathivel, A. & Devaki, T. Effect of Sargassum polycystum (Phaeophyceae)-sulphated polysaccharide extract against acetaminophen-induced hyperlipidemia during toxic hepatitis in experimental rats. Mol Cell Biochem 276, 89–96 (2005). https://doi.org/10.1007/s11010-005-3194-x

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