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Changes in urinary taurine and hypotaurine excretion after two-thirds hepatectomy in the rat

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Summary

This study followed the time course of urinary taurine and hypotaurine excretion after two-thirds hepatectomy in rats. The excretion of both taurine and hypotaurine was elevated during 18th following the hepatectomy, with maximal excretion during the first 6h. Twelve and 24h after partial hepatectomy, the hepatic hypotaurine concentration was increased but liver taurine did not differ significantly from controls. No changes were observed in hypotaurine and taurine concentrations of heart, kidney, lung, muscle tissue and spleen. We postulate that partial hepatectomy induces a rapid increase of hepatic (hypo)taurine synthesis from precursor amino acids. The increased (hypo)taurine concentrations spill over into urine.

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References

  • Akaza K, Nonami T, Kurokawa T, et al (1996) Doxorubicin-induced disturbance of the energy metabolism after hepatectomy. J Surg Res 61: 454–458

    Google Scholar 

  • Brand HS, Meijer AJ, Gustafson LA, et al (1994) Cell-swelling-induced taurine release from isolated perfused rat liver. Biochem Cell Biol 72: 8–11

    Google Scholar 

  • Brand HS, Deutz NEP, Meijer AJ, Jörning GGA, Chamuleau RAFM (1995a) In vivo amino acid fluxes in regenerating liver after two-thirds hepatectomy in the rat. J Hepatol 23: 333–340

    Google Scholar 

  • Brand HS, Meijer AJ, Gustafson LA, Chamuleau RAFM (1995b) Hypoosmotic cell-swelling induced taurine release from rat liver. In: Capocaccia L, Merli M, Riggio O (eds) Advances in hepatic encephalopathy and metabolic nitrogen exchange. CRC Press, Boca Raton, pp 500–506

    Google Scholar 

  • Le Cam A, Rey J-F, Fehlmann M, Kitabgi P, Freychet P (1979) Amino acid transport in isolated hepatocytes after partial hepatectomy in the rat. Am J Physiol 236: E594-E602

    Google Scholar 

  • Chesney RW (1985) Taurine: its biological role and clinical implications. Adv Pediatr 32: 1–42

    Google Scholar 

  • Clawson GA, Madsen KR, Blankenship LJ, Hatem CL (1991) Alterations in nuclear scaffold constituents during carbon tetrachloride-induced liver regeneration. Hepatology 13: 515–522

    Google Scholar 

  • Cockerill MJ, Player TJ, Horton AA (1983) Studies on lipid peroxidation in regenerating rat liver. Biochim Biophys Acta 750: 208–213

    Google Scholar 

  • Dejong CHC, Kampman MT, Deutz NEP, Soeters PB (1992) Altered glutamine metabolism in rat portal drained viscera and hindquarter during hyperammonemia. Gastroenterology 102: 936–948

    Google Scholar 

  • Van Eijk HMH, van der Heijden MAH, van Berlo CLH, Soeters PB (1988) Fully automated liquid-chromatographic determination of amino acids. Clin Chem 34: 2510–2513

    Google Scholar 

  • Ensunsa JL, Hirschberger LL, Stipanuk MH (1993) Catabolism of cystein, cystine, cysteinesulfmate and OTC by isolated perfused rat hindquarter. Am J Physiol 264: E782-E789

    Google Scholar 

  • Fleck C, Zimmermann T, Franke H, Braunlich H, Dargel R (1988) Relation between renal and hepatic excretion of drugs: VII. Hepatic and renal excretion of phenol red in thioacetamide-induced acute and chronic liver damage. Exp Pathol 33: 47–54

    Google Scholar 

  • Fowler FC, Banks RK, Mailliard ME (1992) Characterization of sodium-dependent amino acid transport activity during liver regeneration. Hepatology 16: 1187–1194

    Google Scholar 

  • Garcia RAG, Stipanuk MH (1992) The splanchnic organs, liver and kidney have unique roles in the metabolism of sulfur amino acids and their metabolites in rats. J Nutr 122: 1693–1701

    Google Scholar 

  • Garcia-Marin JJ, Regueiro P, Perez-Antona JC, Villanueva GR, Perez-Barriocanal (1990) Pre-replicative phase-related changes in bile acid-induced chloleresis in the regenerating rat liver. Clin Sci 78: 55–62

    Google Scholar 

  • Gaull GE (1989) Taurine in pediatric nutrition. Review and update. Pediatrics 83: 433–442

    Google Scholar 

  • Grisham JW, Tillman RL, Nägel AEH, Compagno J (1975) Ultrastructure of the proliferating hepatocyte: sinusoidal surfaces and endoplasmic reticulum. In: Lesch R, Reutter W (eds) Liver regeneration after experimental injury. Stratton, New York, pp 6–23

    Google Scholar 

  • Heeneman S, Deutz NEP (1993) Effects of decreased glutamine supply on gut and liver metabolism in vivo in rats. Clin Sci 85: 437–444

    Google Scholar 

  • Higgins GM, Anderson RM (1931) Restoration of the liver of white rat following partial surgical removal. Arch Pathol 12: 186–202

    Google Scholar 

  • Holtta E, Sinervirta R, Janne J (1973) Synthesis and accumulation of polyamines in rat liver regenerating after treatment with carbon tetrachloride. Biochem Biophys Res Comm 54: 350–357

    Google Scholar 

  • Huxtable RJ (1992) Physiological actions of taurine. Physiol Rev 72: 101–163

    Google Scholar 

  • Lorenzi M, De Martino A, Carlucci F, et al (1993) Nitrogen metabolism during liver regeneration. Biochim Biophys Acta 1157: 9–14

    Google Scholar 

  • Luk GD (1986) Essential role of polyamine metabolism in hepatic regeneration. Inhibition of deoxyribonucleic acid and protein synthesis and tissue regeneration by difluoromethylornithine in the rat. Gastroenterology 90: 1261–1267

    Google Scholar 

  • Margeli AP, Theocharis SE, Yannacou NN, Spiliopoulou C (1994) Metallothionein expression during liver regeneration after partial hepatectomy in cadmium-pretreated rats. Arch Toxicol 68: 637–642

    Google Scholar 

  • Martinez-Mas J-V, Ruiz-Montasell B, Felipe A, Casado J, Pastor-Anglada M (1993) Up-regulation of system A activity in the regenerating rat liver. FEBS Lett 329: 189–193

    Google Scholar 

  • Meijer AJ, Lamers WH, Chamuleau RAFM (1990) Nitrogen metabolism and ornithine cycle function. Physiol Rec 70: 701–748

    Google Scholar 

  • Murawaki Y, Ikuta Y, Yamamoto H, Kawasaki H (1992) Serum amino acid levels and hepatic protein synthesis during liver regeneration after partial hepatectomy in rats. Res Comm Chem Pathol Pharmacol 77: 43–54

    Google Scholar 

  • Nakata R, Tsukamoto I, Miyoshi M, Kojo S (1985) Liver regeneration after carbon tetrachloride intoxication in the rat. Biochem Pharmacol 34: 586–588

    Google Scholar 

  • Ogawa M, Mori T, Mori Y, et al (1992) Study on chronic renal injuries induced by carbon tetrachloride: selective inhibition of the nephrotoxicity by irradiation. Nephron 60: 68–73

    Google Scholar 

  • Ohno T, Sabra R, Branch RA (1991) Sodium retention and hepatic function after two-thirds hepatectomy in the rat. Hepatology 14: 511–517

    Google Scholar 

  • Okano K, Tsubouchi T, Yamashita Y, et al (1997) Hepatic protein synthesis in the regenerating rat liver after hepatectopancreatectomy. Surg Today Jpn J Surg 27: 511–517

    Google Scholar 

  • Pasantes-Morales H, Chatagner F, Mandel P (1980) Synthesis of taurine in rat liver and brain in vivo. Neurochem Res 5: 441–451

    Google Scholar 

  • Perez-Barriocanal F, Perez-Antona JC, Regueiro P, Villanueva GR, Marin JJG (1990) Biliary lipid secretion during the pre-replicative phase of rat liver regeneration. J Exp Path 71: 63–68

    Google Scholar 

  • Ryoo HY, Taga M, Sassa T, Oka T, Natori Y (1997) Endocytosis of serum albumin in regenerating liver. Proc Soc Exp Med Biol 215: 179–185

    Google Scholar 

  • Sainz GR, Monte MJ, Barbero ER, Herrera MC, Marin JJG (1997) Bile secretion by the rat liver during synchronized regeneration. Int J Exp Path 78: 109–116

    Google Scholar 

  • Sanins SM, Nicholson JK, Elcombe C, Timbrell JA (1990) Hepatotoxin-induced hypertaurinuria: a proton NMR study. Arch Toxicol 64: 407–411

    Google Scholar 

  • Sasaki Y, Hayashi N, Ito T, Fusamoto H, Sato N, Kamada T (1989) Heterogeneous activation of protein kinase C during rat liver regeneration induced by carbon tetrachloride administration. FEBS Lett 254: 59–65

    Google Scholar 

  • Scornik OA (1974) In vivo rate of translation by ribosomes of normal and regenerating liver. J Biol Chem 249: 3876–3883

    Google Scholar 

  • Sharma R, Kodavanti UP, Smith LL, Mehendale HM (1995) The uptake and metabolism of cytamine and taurine by isolated perfused rat and rabbit lungs. Int J Biochem Cell Biol 27: 655–664

    Google Scholar 

  • Sturman JA (1980) Formation and accumulation of hypotaurine in rat liver after partial hepatectomy. Life Sci 26: 267–272

    Google Scholar 

  • Sturman JA, Fellman JH (1982) Taurine metabolism in the rat: effect of partial hepatectomy. Int J Biochem 14: 1055–1060

    Google Scholar 

  • Sturman JA, Fellman JH (1983) Methionine metabolism in the rat: accumulation of hypotaurine after partial hepatectomy. Progr Clin Biol Res 125: 435–447

    Google Scholar 

  • Tamura J, Ohkuma S, Ida S, Zuo PP, Kuriyama K (1984) Cysteine uptake and taurine biosynthesis in freshly isolated and primary cultured rat hepatocytes. Cell Biochem Funct 2: 195–200

    Google Scholar 

  • Teshigawara M, Matsumoto S, Tsuboi S, Ohmori S (1995) Changes in levels of glutathione and related compunds and activities of glutathione-related enzymes during rat liver regeneration. Res Exp Med 195: 55–60

    Google Scholar 

  • Timbrell JA, Waterfield CJ (1996) Changes in taurine as an indicator of hepatic dysfunction and biochemical perturbations. Adv Exp Med Biol 403: 125–134

    Google Scholar 

  • Timbrell JA, Waterfield CJ, Draper RP (1995) Use of urinary taurine and creatine as biomarkers of organ dysfunction and metabolic perturbations. Comp Haematol Int 5: 112–119

    Google Scholar 

  • Tohyama C, Suzuki JS, Hemelraad J, Nishimura N, Nishimura H (1993) Induction of metallothionein and its localization in the nucleus of rat hepatocytes after partial hepatectomy. Hepatology 18: 1193–1201

    Google Scholar 

  • Tsuboi S, Miyazaki M, Kondo Y, et al (1992) Increase of S-(1,2-dicarboxyethyl)glutathione in regenerating rat liver. Res Exp Med 192: 281–286

    Google Scholar 

  • Tsujikawa K, Suzuki N, Sagawa K, et al (1994) Induction and subcellular localization of metallothionein in regenerating rat liver. Eur J Cell Biol 63: 240–246

    Google Scholar 

  • Waterfield CJ, Turton JA, Scales MDC, Timbrell JA (1991) Taurine, a possible urinary marker of liver damage: a study of taurien excretion in carbon tetrachloride-treated rats. Arch Toxicol 65: 548–555

    Google Scholar 

  • Waterfield CJ, Turton JA, Scales MDC, Timbrell JA (1993a) Investigations into the effects of various hepatotoxic compounds on urinary and liver taurine levels in rats. Arch Toxicol 67: 244–254

    Google Scholar 

  • Waterfield CJ, Turton JA, Scales MD, Timbrell JA (1993b) Effect of various non-hepatotoxic compounds on urinary and liver taurine levels in rats. Arch Toxicol 67: 538–546

    Google Scholar 

  • Waterfield CJ, Turton JA, Scales MDC, Timbrell JA (1993c) Reduction of liver taurine in rats by β-alanine treatmment increases carbon tetrachloride toxicity. Toxicology 77: 7–20

    Google Scholar 

  • Waterfield CJ, Asker DS, Timbrell JA (1996) Does urinary taurine reflect changes in protein metabolism? a study with cycloheximide in rats. Biomarkers 1: 107–114

    Google Scholar 

  • Wollenberger A, Ristau O, Schoffa G (1960) Eine einfache Technik der extrem schnellen Abkählung grösserer Gewebestücke. Pflügers Arch 270: 399–412

    Google Scholar 

  • Wright CE, Tallan HH, Lin YY, Gaul GE (1986) Taurine — biological update. Annu Rev Biochem 55: 427–453

    Google Scholar 

  • Zimmermann SW, Norback DH, Powers K (1983) Carbon tetrachloride nephrotoxicity in rats with reduced renal mass. Arch Pathol Lab Med 107: 264–269

    Google Scholar 

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Brand, H.S., Jörning, G.G.A. & Chamuleau, R.A.F.M. Changes in urinary taurine and hypotaurine excretion after two-thirds hepatectomy in the rat. Amino Acids 15, 373–383 (1998). https://doi.org/10.1007/BF01320901

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