Skip to main content
Log in

Effects of weaning on phosphate transport maturation in the rat kidney. Clearance and brush border membrane studies

  • Proceedings of the Fifth International Workshop on Developmental Renal Physiology (Part II) August 26–28, 1992 Tremezzo, Italy
  • Original Article
  • Published:
Pediatric Nephrology Aims and scope Submit manuscript

Abstract

Renal phosphate transport matures via an increase in the carrier affinity for phosphate during the 3rd post-natal week in the rat. This study examines whether weaning, which normally takes place during this period, plays a role in phosphate transport maturation. Early weaning (EW) and prevention of weaning (PW) both increased the fractional excretion of phosphate (EW 26.5±4.9, PW 26.7±2.2, controls 11.3±2.8,P<0.001 andP<0.05,n=6 in each group). EW and PW also decreased the uptake of phosphate into brush border membrane vesicles (BBMV) isolated from the renal cortex of 21-day-old rats. Glucose transport in BBMV was not affected. The kinetics of phosphate uptake, measured in the presence of a sodium gradient, showed lowerV max (4,112±362 pmol/mg protein per 10s) in EW BBMV than in controls (6,030±200,n=5,P<0.001), but the affinity of the carrier for phosphate (1/K m) did not change. The decrease inV max may be due to the enhanced phosphate supply. The affinity of the carrier was lower in PW rats (K m=0.31±0.04 mM) than in controls (0.18±0.04,n=5,P<0.01) but theV max remained unchanged. The low affinity may indicate that normal maturation of tubular transport, in which carrier affinity increases, is altered. The plasma concentrations of corticosterone, parathyroid hormone, insulin and triiodothyronine and their changes during EW and PW are also reported. We conclude that changing the weaning process alters the maturation pattern of phosphate renal transport. Further studies should establish whether this is due to hormonal changes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Lelièvre-Pégorier M, Merlet-Bénichou C, Roinel N, De Rouffignac C (1983) Developmental pattern of water and electrolyte transport in rat superficial nephrons. Am J Physiol 245: F15-F21

    PubMed  Google Scholar 

  2. Lelièvre-Pégorier M, Jean T, Ripoche P, Poujeol P (1983) Transport of phosphate,d-glucose, andl-valine in newborn rat kidney brush border. Am J Physiol 245: F367-F373

    PubMed  Google Scholar 

  3. Horster M (1978) Principles of nephron differentiation. Am J Physiol 235: F387-F393

    PubMed  Google Scholar 

  4. Aperia A, Larsson L, Zetterstrom R (1981) Hormonal induction of Na−K-ATPase in developing proximal tubular cells. Am J Physiol 241: F356-F360

    PubMed  Google Scholar 

  5. Rane S, Aperia A (1985) Ontogeny of Na−K ATPase activity in thick ascending limb and of concentrating capacity. Am J Physiol 249: F723-F728

    PubMed  Google Scholar 

  6. Bolles RC, Woods JP (1964) The ontogeny of behavior in the albino rat. Anim Behav 12: 427–441

    Google Scholar 

  7. Henning SJ, Chang SSP, Gisel EG (1979) Ontogeny of feeding controls in suckling and weanling rats. Am J Physiol 237: R187-R191

    PubMed  Google Scholar 

  8. Henning SJ (1981) Postnatal development: coordination of feeding, digestion, and metabolism. Am J Physiol 241: G199-G214

    PubMed  Google Scholar 

  9. Mahmood A, Patha KRN, Agerwal N (1978) Effect of chronic alloxan diabetes and insulin administration on intestinal brush border enzymes. Experimentis 34: 741–742

    Google Scholar 

  10. Menard D, Malo C (1979) Insulin evoked precocious appearance of intestinal sucrase activity in suckling mice. Dev Biol 69: 661–665

    PubMed  Google Scholar 

  11. Moog F (1979) Endocrine influences of the functional differentiation of the small intestine. J Anim Sci 49: 239–249

    PubMed  Google Scholar 

  12. Aurbach GD, Heath DA (1974) Parathyroid hormone and calcitonin regulation of renal function. Kidney Int 6: 331–345

    PubMed  Google Scholar 

  13. Turner ST, Kiebzak GM, Dousa TP (1982) Mechanism of glucocorticoid effect on renal transport of phosphate. Am J Physiol 243: C227-C236

    PubMed  Google Scholar 

  14. Dennis VW, Bello-Reuss E, Robinson RR (1977) Response of phosphate transport to parathyroid hormone in segments of rabbit nephron. Am J Physiol 233: F29-F38

    PubMed  Google Scholar 

  15. Espinosa RE, Keller MJ, Yusufi ANK, Dousa TP (1984) Effect of thyroxine administration on phosphate transport across renal cortical brush border membrane. Am J Physiol 246: F133-F139

    PubMed  Google Scholar 

  16. Webster SK, Haramati A (1985) Developmental changes in the phosphaturic response to parathyroid hormone in the rat. Am J Physiol 249: F251-F255

    PubMed  Google Scholar 

  17. Chen PS, Torribara TY, Warner H (1964) Microdetermination of phosphorus. Anal Chem 28: 1756

    Google Scholar 

  18. Girard J, Cuendet GS, Marliss EB, Kervan A, Rieutort M, Assan R (1973) Fuels, hormones and liver metabolism at term and during the early postnatal period in the rat. J Clin Invest 52: 3190–3200

    PubMed  Google Scholar 

  19. Schmitz J, Preiser H, Maestracci D, Ghosh BK, Cerda JJ, Crane RK (1973) Purification of the human intestinal brush border membrane. Biochim Biophys Acta 323: 98–112

    PubMed  Google Scholar 

  20. Evers C, Haase W, Murer H, Kinne R (1978) Properties of brush border vesicles isolated from rat kidney cortex by calcium precipitation. Membr Biochem 1: 203–219

    PubMed  Google Scholar 

  21. Jean T, Poujeol P, Ripoche P (1981) Interactions between Na+-dependant uptake ofd-glucose, phosphate andl-alanine in renal brush border membrane vesicles. Biochim Biophys Acta 647: 203–210

    PubMed  Google Scholar 

  22. Hopfer U, Nelson K, Perroto J, Isselbacher KJ (1973) Glucose transport in isolated brush border membrane from rat small intestine. J Biol Chem 248: 25–32

    PubMed  Google Scholar 

  23. Dahlquist A (1966) Enzymes of complex saccharide utilization intestinal disaccharidases. Methods Enzymol 8: 584–591

    Google Scholar 

  24. Bergmeyer HU (1970)d-Glucose Bestimmung mit Hexokinase und Glucose-6-Phosphat-Deshydrogenase. In: Methoden der Enzymatischen Analyse. Verlag Chemie, Weinheim, pp 1163–1168

    Google Scholar 

  25. Hübscher G, West GR (1965) Specific assays of some phosphatases in subcellular fractions of small intestinal mucosa. Nature 205: 799–800

    PubMed  Google Scholar 

  26. Quigley JP, Gotterer GS (1969) Distribution of (Na+−K+) stimulated ATPase activity in rat intestinal mucosa. Biochim Biophys Acta 173: 456–468

    PubMed  Google Scholar 

  27. Bradford MM (1976) Rapid and sensitive method for the quantization of microgram quantities of protein utilizing the principle of protein dye binding. Anal Biochem 72: 248–252

    PubMed  Google Scholar 

  28. Johnson V, Spitzer A (1986) Renal reabsorption of Pi during development: whole kidney events. Am J Physiol 251: F251-F256

    PubMed  Google Scholar 

  29. Kaskel F, Kumar AM, Feld LG, Spitzer A (1988) Renal reabsorption of Pi during development: tubular events. Pediatr Nephrol 2: 129–134

    PubMed  Google Scholar 

  30. Caverzasio J, Bonjour JP, Fleisch H (1982) Tubular handling of Pi in young growing and adult rats. Am J Physiol 242: F705-F710

    PubMed  Google Scholar 

  31. Haramati A, Mulroney SE, Webster SK (1988) Development changes in the tubular capacity for phosphate reabsorption in the rat. Am J Physiol 255: F287-F291

    PubMed  Google Scholar 

  32. Kiebzak G, Sacktor B (1986) Effect of age on renal conservation of phosphate in the rat. Am J Physiol 251: F399-F407

    PubMed  Google Scholar 

  33. Spitzer A (1985) The developing kidney and the process of growth. In: Seldin DW, Giebisch G (eds) The kidney: physiology and pathophysiology: Raven, New-York, pp 1979–2015

    Google Scholar 

  34. Hoffmann N, Thees M, Kinne R (1975) Phosphate transport by isolated renal brush border vesicles. Pflugers Arch 362: 147–156

    Google Scholar 

  35. Kinne R, Murer H, Kinne-Safran E, Thees M, Sachs G (1975) Sugar transport by renal plasma membrane vesicles. J Membr Biol 21: 375–395

    Google Scholar 

  36. Cheng L, Liang CT, Sacktor B (1983) Pi uptake by renal membrane vesicles of rabbit adapted to high and low phosphorus diet. Am J Physiol 245: F175-F180

    PubMed  Google Scholar 

  37. Gmaj P, Murer H (1986) Cellular mechanisms of inorganic phosphate transport in kidney. Physiol Rev 66: 36–70

    PubMed  Google Scholar 

  38. Mulroney SE, Haramati A (1990) Renal adaptation to change in dietary phosphate during development. Am J Physiol 258: F1650-F1656

    PubMed  Google Scholar 

  39. Neiberger RE, Barac-Nieto M, Spitzer A (1989) Renal reabsorption of phosphate during development: transport kinetics in BBMV. Am J Physiol 257: F268-F274

    PubMed  Google Scholar 

  40. Luckey TD, Mende TJ, Pleasants J (1954) The physical and chemical characterization of rat's milk. J Nutr 54: 345–350

    PubMed  Google Scholar 

  41. Keen CL, Lonnerdal BO, Clegg M, Hurley LS (1981) Developmental changes in composition of rate milk: trace elements, minerals, protein, carbohydrate and fat. J Nutr 111: 226–230

    PubMed  Google Scholar 

  42. Lelièvre-Pégorier M, Leroy B, Moreau E, Herpe-Patsouris L, Merlet-Benichou C (1992) Effects of an early weaning on phosphate transport maturation in the rat kidney: influence of the phosphate content of the diet. Pediatr Res 32: 704–709

    PubMed  Google Scholar 

  43. Rane S, Aperia A, Eneroth P, Lundin S (1985) Development of urinary concentrating capacity in weaning rats. Pediatr Res 19: 472–475

    PubMed  Google Scholar 

  44. Kempson SA (1985) Effects of fasting compared to low phosphorus diet on the kinetics of phosphate transport by renal brush border membranes. Biochim Biophys Acta 815: 85–90

    PubMed  Google Scholar 

  45. Daniels VG, Hardy RN, Malinowska KW, Nathanielsz PW (1973) The influence of exogenous steroids on macromolecule uptake by the small intestine of the new-born rat. J Physiol 229: 681–695

    PubMed  Google Scholar 

  46. Girard J, Férré P, Kervran A, Pégorier JP, Assan A (1977) Influence of insulin/glucagon ratio in the changes of hepatic metabolism during development of the rat. In: Foa PP, Bajaj JS, Foa NL (eds) Glucagon: its role in physiology and clinical medecine. Proc. Intern. Verlag, New York, pp 563–581

    Google Scholar 

  47. Decaux FJ, Férré P, Girard J (1986) Effect of weaning on different diets on hepatic glucogenesis in the rat. Biol Neonate 50: 331–336

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lelièvre-Pégorier, M., Merlet-Bénichou, C. Effects of weaning on phosphate transport maturation in the rat kidney. Clearance and brush border membrane studies. Pediatr Nephrol 7, 807–814 (1993). https://doi.org/10.1007/BF01213365

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01213365

Key words

Navigation