Effects of taurine on plasma and liver lipids, erythrocyte ouabain sensitive Na efflux and platelet aggregation in Sprague Dawley rats

  • Park, In-Sun (Department of Foods & Nutrition, Cheju National University) ;
  • Kang, Young-Hee (Division of life Sciences and Institute of Environment and Life Science, Hallym University) ;
  • Kang, Jung-Sook (Department of Foods & Nutrition, Cheju National University)
  • Published : 2007.09.20

Abstract

The effects of taurine on plasma and liver cholesterol, erythrocyte ouabain sensitive Na efflux and platelet aggregation were examined in Sprague Dawley rats fed control or 0.5% cholesterol with 0.2% cholate diet. Plasma and liver levels of total cholesterol were increased significantly (p<0.05) in rats fed cholesterol diet compared to the control, and taurine significantly decreased the elevated plasma level of cholesterol in rats fed cholesterol diet (p<0.05). HDL-cholesterol was decreased in groups fed the cholesterol diet regardless of taurine supplementation and the difference between groups with and without cholesterol was significant (p<0.01). Plasma triglyceride was decreased and liver triglyceride was increased both significantly (p<0.05) in rats fed cholesterol compared to the control. Plasma and liver triglyceride in rats fed taurine was decreased significantly compared to the control (p<0.05). Intracellular Na tended to be lower in rats fed cholesterol or taurine and higher in rats fed cholesterol plus taurine compared to the control. Na efflux through Na-K ATPase and the passive leak of Na was somewhat reduced in rats fed cholesterol or taurine and was augmented in rats fed cholesterol plus taurine compared to the control, which showed a similar trend to the intracellular Na. Taurine supplementation caused a suppression of Na efflux in groups fed control diet and restored the suppressed Na efflux in groups fed cholesterol. Platelet aggregation was significantly decreased in the group fed taurine compared to the control (p<0.05) and the group fed cholesterol plus taurine was also a little lower in aggregation than the group fed cholesterol. Microscopic examination showed that taurine prevented fatty liver in rats fed cholesterol diet. Taurine known for stimulating Na-K ATPase in some cell types rather decreased erythrocyte ouabain sensitive Na-K ATPase in the present study. Taurine had hypolipidemic and hypocholesterolemic effects and inhibited platelet aggregation which may be favorable for prevention of cardiovascular diseases.

Keywords

References

  1. Burdakov D, Liss B & Ashcroft FM (2003). Orexin excites GABAergic neuron of the arcuate nucleus by activating the sodiumcalcium exchanger. J Neurosci 25:4951-4957
  2. Chen W, Matuda K, Nishimura N & Yokogoshi H (2004). The effect of taurine on cholesterol degradation in mice fed a high-cholesterol diet. Life Sci 27; 74:1889-1898
  3. Elisaf M, Karabina SA, Bairaktari E, Goudevenos JA, Siamopoulos KC & Tselepis AD (1999). Increased platelet reactivity to the aggregatory effect of platelet activating factor, in vitro, in patients with heterozygous familial hypercholesterolaemia. Platelets 10: 124-131 https://doi.org/10.1080/09537109976185
  4. Folch J, Lees M & Sloane stanley GH (1957). A simple method for the isolation and rification of total lipids from animal tissues. J Biol chem 226:497-509
  5. Friedrich B, Matskevich I & Lang F (2006). Cell volume regulatory mechanisms. Contrib Nephrol 152:1-8
  6. Hakam AC & Hussain T (2006). Angiotensin type 2 receptor agonist directly inhibits proximal tubule sodium pump activity in obese but not in lean Zuker rats. Hypertension 47:1117-1124 https://doi.org/10.1161/01.HYP.0000220112.91724.fc
  7. Hall JA, Kirk J, Potts JR, Rae C & Kirk K (1996). Anion channel blockers inhibit swelling-activated anion, cation and nonelectrolyte transport in HeLa cells. Am J Physiol 271:579-588 https://doi.org/10.1152/ajpcell.1996.271.2.C579
  8. Handa RK & Stranhoy JW (2003). Platelet activating factor (PAF) and solute transport process in the kidney. Am J Physiol Renal Physiol 284:274-281 https://doi.org/10.1152/ajprenal.00117.2002
  9. Huxtable RJ (1992). Physiological actions of taurine. Physiological Rev 72:454-516 https://doi.org/10.1152/physrev.1992.72.1.101
  10. Igisu H, Izumi K, Goto I & Kina K (1976). Effects of taurine on the ATPase activity in the human erythrocyte membrane. Pharmacology 14:362-366 https://doi.org/10.1159/000136616
  11. Kang JS, Cregor MD & Smith JB (1990). Effect of calcium on blood pressure, platelet aggregation and erythrocyte sodium transport in Dahl salt-sensitive rats. J Hypertens 8:245-250
  12. Kontro P & Oja SS (1987). Taurine and GABA release from mouse cerebral cotex slice: effects of structural analogues and drugs. Neurochem Res 12:475-482 https://doi.org/10.1007/BF00972301
  13. Kurup RK & Kurup PA (2003). Hypothalamic digoxin, hemispheric chemical dominance, and Alzheimer's disease. Int J Neurosci 113:361-381 https://doi.org/10.1080/00207450390162146
  14. Lijnen P & Petrov V (1995). Cholesterol modulation of transmembrane cation transport systems in human erythrocytes. Biochem Mol Med 56:52-62 https://doi.org/10.1006/bmme.1995.1056
  15. Liu CH, Huang MT & Huang PC (1995). Source of triglyceride accumulation in liver of rats fed a cholesterol supplemented diet. Lipids 30:527-531 https://doi.org/10.1007/BF02537027
  16. Mayol V, Duran MJ, Gerbi A, Levy S, Sampol J & Maixent JM (1999). Cholesterol and omega 3 fatty acids inhibit Na-K ATPase activity in human endothelial cells. Atherosclerosis 142:327-333 https://doi.org/10.1016/S0021-9150(98)00253-6
  17. McCarty MF (2004). Sub-optimal taurine status may promote platelet hyperaggregability in vegetarians. Med Hypotheses 63: 426-433 https://doi.org/10.1016/j.mehy.2002.11.007
  18. Mochizuki H, Takido J, Oda H & Yokogoshi H (1999). Improving effect of dietary taurine on marked hypercholesterolemia induced by a high cholesterol diet in streptozotocin induced diabetic rats. Biosci Biotechnol Biochem 63:1984-1987 https://doi.org/10.1271/bbb.63.1984
  19. Mrsny RJ & Meizel S (1985). Inhibition of hamster sperm Na+, K+-ATPase activity by taurine and hypotaurine. Life Sci 36:271-275 https://doi.org/10.1016/0024-3205(85)90069-4
  20. Murakami S, Kondo Y, Toda Y, Kitajima H, Kameo K, Sakono M & Fukuda N (2002). Effect of taurine on cholesterol metabolism in hamsters: up-regulation of low density lipoprotein (LDL) receptor by taurine. Life Science 70:2355-2366 https://doi.org/10.1016/S0024-3205(02)01507-2
  21. Oh IS, Kang JA & Kang JS (2002). Gender difference in the effects of gonadectomy and hypercholesterol diet on plasma and liver cholesterol and TG levels, platelet aggregation and liver tissue in Sprague Dawley rats. Nutritional Sciences 35:15-23
  22. Qi B, Yamagami T, Naruse Y, Sokejima S & Kagamimori S (1995). Effect of taurine on depletion of erythrocyte membrane Na-K ATPase activity due to ozone exposure or cholesterol enrichment. J Nutr Sci Vitaminol 41:627-634 https://doi.org/10.3177/jnsv.41.627
  23. Rabini RA, Staffolani R, Martarelli D, Fumelli P, Ravaglia F, Dousset N, Curatola G & Mazzanti L (1999). Influence of low density lipoprotein from insulin-dependent diabetic patients on platelet functions. J Clin Endocrinol Metab 84:3770-3774 https://doi.org/10.1210/jc.84.10.3770
  24. Shefer S, Nguyen LB, Salen G, Ness GC, Chowdhary IR, Lerner S, Batta AK & Tint GS (1992). Differing effects of cholesterol and taurocholate on steady state hepatic HMG-CoA reductase and cholesterol 7 alpha-hydroxylase activities and mRNA levels in the rat. J Lipid Res 33:1193-2000
  25. Smith JB, Ash KO, Sprowell WL, Hentchel WM & Williams RR (1984). An improved non-radioisotopic method for increasing ouabain sensitive Na efflux from erythrocytes. Clin Chim Acta 143:295-299 https://doi.org/10.1016/0009-8981(84)90081-0
  26. Sobolová L, Skottová N, Vecera R & Urbánek K (2006). Effect of silymarin and its polyphenolic fraction on cholesterol absorption in rats. Pharmacol Res 53:104-112 https://doi.org/10.1016/j.phrs.2005.09.004
  27. Sorci-Thomas M, Prack MM, Dashti N, Johnson F, Rudel LL & Williams DL (1989). Differential effects of dietary fat on the tissue specific expression of apo A-1 gene; relationship to plasma concentration of high density lipoproteins. J Lipid Res 30:1397-1403
  28. Thut PD, Hruska RE, Huxtable RJ & Bressler R (1976). Effect of taurine on eating and drinking behavior. In:Taurine, edited by RJ Huxtable and A Barbeau, p.357-364. New York Raven. USA
  29. Tranquilli AL, Cester N, Nanetti L & Mazzanti L (2004). Plasma lipids and physicochemical properties of the erythrocyte plasma membrane throughout pregnancy. Acta Obstet Gynecol Scand 83:443-448 https://doi.org/10.1111/j.0001-6349.2004.00341.x
  30. Tufft LS & Jensen LS (1992). Influence of dietary taurine on performance and fat retention in broilers and turkey poults fed varying levels of fat. Poult Sci 71:880-885 https://doi.org/10.3382/ps.0710880
  31. Winocour PD, Vickers JD, Kinlough-Rathbone RL, Packham MA & Mustard JF (1990). Thrombin-induced inositol phosphate production by platelets from rats with diet induced or genetically determined hypercholesterolemia. J Lab Clin Med 115:241-248
  32. Yamamoto K, Yoshitama A, Sakono M, Nasu T, Murakami S & Fukuda N (2000). Dietary taurine decreases hepatic secretion of cholesterol ester in rats fed a high-cholesterol diet. Pharmacology 60:27-33 https://doi.org/10.1159/000028343
  33. Yoshimura H, Nariai Y, Terashima M, Mitani T & Tanigawq Y (2005). Taurine suppresses platelet derived growth factor (PDGF) BB-induced PDGF-beta receptor phosphorylation by protein tyrosine phosphatase-mediated dephosphorylation in vascular smooth muscle cells. Biochim Biophys Acta 1745:350-360 https://doi.org/10.1016/j.bbamcr.2005.07.005
  34. Zicha J, Negrin CD, Dobesova Z, Kunes J & Dominiczak AF (2001). Altered Na+-K+ pump activity and plasma lipids in salthypertensive Dahl rats: relationship to Atp1a1 gene. Physiol Genomics 6:99-104 https://doi.org/10.1152/physiolgenomics.2001.6.2.99