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Studies on renal adaptation to altered dietary amino acid intake: reduced renal cortex taurine content increases the Vmax of taurine uptake by brush border membrane vesicles

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Abstract

Rats were placed on a normal taurine diet (NTD), low taurine diet (LTD) or a high taurine diet (HTD) for 14 days. β-Alanine was fed to half of the animals in each group and resulted in a lowered renal cortex taurine content. Brush border membrane vesicle (BBMV) uptake of taurine was higher after β-alanine feeding and was associated with an increase in Vmax of uptake. β-Alanine feeding to HTD animals also altered the Km of uptake, possibly since the load of sulfur amino acids (6% of diet) was high. As a control, glycine (3%) feeding for 8 days along with each diet did not alter the plasma or renal cortex content; BBMV uptake as well as Km and Vmax of taurine accumulation were minimally altered. Accordingly, ingestion of a non-sulfur-containing α-amino acid did not change β-amino acid transport. This study provides evidence that whole body taurine homeostasis is maintained in the presence of a taurine-depleting agent (β-alanine feeding) by an increase in the number of Na+-taurine uptake sites.

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References

  1. Friedman AL, Albright PW, Chesney RW (1981) Dietary adaptation of taurine transport by rat renal epithelium. Life Sci 29: 2415–2419

    Google Scholar 

  2. Friedman AL, Albright PW, Gusowski N, Padilla M, Chesney RW (1983) Renal adaptation to alteration in dietary amino acid intake. Am J Physiol 245: F159-F166

    Google Scholar 

  3. Rozen R, Scriver CR (1982) Renal transport of taurine adapts to perturbed taurine homeostasis. Proc Natl Acad Sci USA 79: 2101–2105

    Google Scholar 

  4. Chesney RW, Friedman PW, Albright PW, Gusowski N (1982) Fasting reverses the renal adaptation to altered dietary amino acid intake. Proc Soc Exp Biol Med 170: 493–501

    Google Scholar 

  5. Chesney RW, Gusowski N, Friedman AL (1983) Renal adaptation to altered dietary sulfur amino acid intake occurs at luminal brush border membrane. Kidney Int 24: 588–594

    Google Scholar 

  6. Shaffer JE, Kocsis JJ (1981) Taurine mobilizing effects of β-alanine and other inhibitors of taurine transport. Life Sci 28: 2727–2736

    Google Scholar 

  7. Sturman JA, Hayes KC (1980) The biology of taurine in nutrition and development: In: Draper HH (ed) (ed) Advances in nutrition research, vol 3. Plenum Publishing Corp, New York, pp 231–299

    Google Scholar 

  8. Chesney RW (1985) Taurine: Its biological role and clinical implications. In: Barness LA (ed) Advances in pediatrics, vol 32. Chicago Year Book Medical Publishers, Chicago, pp. 1–42

    Google Scholar 

  9. Chesney RW, Gusowski N, Dabbagh S (1985) Renal cortex taurine content regulates renal adaptive response to altered dietary intake of sulfur amino acids. J Clin Invest 76: 2213–2221

    Google Scholar 

  10. Chesney RW, Jax DK (1979) Developmental aspects of renal β-amino acid transport: I. Ontogeny of taurine reabsorption and accumulation in renal rat cortex. Pediatr Res 13: 854–860

    Google Scholar 

  11. Booth AG, Kenny AJ (1974) A rapid method for the preparation of microvilli from rabbit kidney. Biochem J 142: 575–581

    Google Scholar 

  12. Glossman H, Neville DM, Jr (1972) γ-glutamyl transferase in kidney brush border membranes. FEBS Lett 19: 340–344

    Google Scholar 

  13. Dixon TF, Purdom M (1954) Serum 5-nucleotidase. J Clin Pathol 7: 341–343

    Google Scholar 

  14. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the folin phenol reagent. J Biol Chem 193: 265–275

    Google Scholar 

  15. Chesney RW, Sacktor B, Rowen RR (1973) The binding of D-glucose to the isolated rabbit renal brush border. J Biol Chem 218: 2182–2191

    Google Scholar 

  16. Neal JL (1972) Analysis of Michaelis kinetics for two independent saturable membrane transport functions. J Theor Biol 35: 113–118

    Google Scholar 

  17. Hayes KC, Carey RE, Schmidt SY (1975) Retinal degeneration associated with taurine deficiency in the cat. Science 189: 949–951

    Google Scholar 

  18. Sturman JA, Wen GY, Wisniewski HM, Neuringer MD (1984) Retinal degeneration in primates raised on a synthetic human infant formula. Int J Dev Neurosci 2: 121–129

    Google Scholar 

  19. Rigo J, Senterre J (1977) Is taurine essential for the neonate? Biol Neonate 32: 73–76

    Google Scholar 

  20. Gaull GE, Rassin DK, Räihä NC, Heinonen K (1977) Milk protein quantity and quality in low-birthweight infants III. Effects on sulfur amino acids in plasma and urine. J Pediatr 90: 348–355

    Google Scholar 

  21. Geggel HS, Ament ME, Heckelively JR, Martin DA, Kopple JD (1985) Nutritional requirement for taurine in patients receiving long-term parenteral nutrition. N Engl J Med 312: 142–146

    Google Scholar 

  22. Zeukovic I, Chesney RW: Interpersonal communication

  23. Cooper A, Betts JM, Pereira GR, Ziegler MM (1984) Taurine deficiency in the severe hepatic dysfunction complicating total parenteral nutrition. J Pediatr Surg 19: 462–466

    Google Scholar 

  24. Cooke RJ, Whitington PF, Kelts D (1984) Effect of taurine supplementation on hepatic function during shortterm parenteral nutrition in the premature infant. J Pediatr Gastroenterol Nutr 3: 224–238

    Google Scholar 

  25. Sturman JA, Hayes KC (1980) The biology of taurine in nutrition and development. Adv Nutr Res 3: 231–299

    Google Scholar 

  26. Lombardini JB (1985) Opposite effects of α-amino ethanesulfonic acid (taurine) and aminomethanesulfonic acid on calcium ion uptake in rat retinal preparations. Eur J Pharmacol 110: 385–387

    Google Scholar 

  27. Lombardini JB (1985) Taurine effects the transition temperature in Arrhenius plots of ATP-dependent calcium ion uptake in rat retinal membrane preparations. Biochem Pharmacol 34: 3741–3745

    Google Scholar 

  28. Weiss SJ, Klein R, Slivka A, Wei M (1982) Chlorination of taurine by human neutrophils: Evidence for hypochlorous acid generation. J Clin Invest 70: 598–607

    Google Scholar 

  29. Test ST, Lampert MB, Ossanna PJ, Thoene JB, Weiss SF (1984) Generation of nitrogen-chlorine oxidants by human phagocytes. J Clin Invest 74: 1341–1349

    Google Scholar 

  30. Persantes-Morales H, Cruz CJ (1984) Protective effect of taurine and zinc on peroxidation-induced damage in photoreceptor outer segments. J Neurosci Res 11: 303–311

    Google Scholar 

  31. Pasantes-Morales H, Wright CE, Gaull GE (1984) Protective effects of taurine, zinc, and tocopherol on retinol-induced damage in human lymphoblastoid cells. J Nutr 114: 2256–2261

    Google Scholar 

  32. Kerwin RW, Pycock CJ (1979) Role of taurine as a possible transmitter in the thermoregulatory pathways of the rat. J Pharm Pharmacol 31: 466–470

    Google Scholar 

  33. Garcia de Yebenes Prous J, Carlsson A, Mena Gomez MA (1978) The effect of taurine on motor behavior, body temperature and monoamine metabolism in rat brain. Naunyn-Schmiedeberg's Arch Pharmacol 304: 95–99

    Google Scholar 

  34. Scheibel J, Elsasser T, Brown B, Dom R, Ondo JG (1984) The stimulation of prolactin secretion by taurine: studies on the site of action. Brain Res Bull 13: 49–52

    Google Scholar 

  35. Hanretta AT, Lombardini JB (1985) Effects of intrahypothalamic kainic acid injection on taurine levels, binding and uptake. Brain Res 338: 351–354

    Google Scholar 

  36. Schrock J, Forster RP, Goldstein L (1982) Renal handling of taurine in marine fish. Am J Physiol 242: FR64-FR71

    Google Scholar 

  37. Thurston JH, Haubart RE, Dugo JA (1980) Taurine, a role in osmotic regulation of mammalian brain and possible clinical significance. Life Sci 26: 1561–1565

    Google Scholar 

  38. Forster RP, Goldstein L (1979) Amino acids and cell volume regulation. Yale J Biol Med 52: 497–519

    Google Scholar 

  39. Chesney RW, Lippincott SE, Gusowski N, Padilla M, Zelikovic I (1986) Studies on renal adaptation to altered dietary amino acid intake: tissue taurine responses in nursing and adult animals. J Nutr (in press)

  40. Mitch WE, Chesney RW (1983) Amino acid metabolism by the kidney. Miner Electrolyte Metab 9: 190–202

    Google Scholar 

  41. Scriver CR, Chesney RW, McInnes RR (1976) Genetic aspects of renal tubular transport: diversity and topology of carriers. Kidney Int 9: 149–171

    Google Scholar 

  42. Silbernagl S, Foulkes EC, Deetjen P (1975) Renal transport of amino acids. In: Reviews of physiology, biochemistry and pharmacology, vol 74. Springer, Berlin Heidelberg New York, pp 105–167

    Google Scholar 

  43. Segal S, Their SO (1973) Renal handling of amino acids. In: Handbook of physiology, American Physiological Society. Williams & Wilkins, Washington, pp 653–676

    Google Scholar 

  44. Young JA, Freedman BS (1971) Renal tubular transport of amino acids. Clin Chem 17: 245–266

    Google Scholar 

  45. Grosvenor MB, Zeman FJ (1983) In vitro amino acid transport by renal tubules of prenatally protein-deprived fetal rats. J Nutr 113: 1513–1520

    Google Scholar 

  46. Coates ME, O'Donoghue DN, Doyne PR, Ward RJ (eds) (1969) Dietary standards for laboratory rats and mice; In: Laboratory animal handbook No. 2. Laboratory Ltd, London

    Google Scholar 

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Supported in part by grants from NIH RO1 AM 31682-02, AM 37223-01 and the Medical School and Graduate School Research Committees of The University of Wisconsin. Dr. Dabbagh is supported by the Pearl M. Stetler Foundation. Dr. Chesney was the recipient of a Research Career Development Award KO4 AM 00421.

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Chesney, R.W., Gusowski, N. & Dabbagh, S. Studies on renal adaptation to altered dietary amino acid intake: reduced renal cortex taurine content increases the Vmax of taurine uptake by brush border membrane vesicles. Pediatr Nephrol 1, 9–15 (1987). https://doi.org/10.1007/BF00866878

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  • DOI: https://doi.org/10.1007/BF00866878

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