Kidney tissue somatomedin C and initial renal growth in diabetic and uninephrectomised rats (original) (raw)

Summary

Kidney growth after induction of experimental diabetes in rats was compared to compensatory renal growth in response to unilateral nephrectomy. After 4 days of diabetes, kidney weight had increased from 816±21 mg (SEM) to 940±42 mg (15%). In insulin-treated diabetic rats kidney weight was unchanged at the end of the study, namely 828±15 mg.

In unilaterally nephrectomised rats kidney weight increased from 840±20 mg (SEM) to 1050±60 mg during 4 days (24%). We observed increased kidney content of somatomedin C in both diabetic and uninephrectomised rats. In untreated diabetic rats it was maximal after 48 h, with an increase of 77% (3469±312 ng/g (SEM) versus 1961±173 ng/g). After 4 days the somatomedin C content had returned to initial levels. In insulin-treated rats somatomedin C content did not increase during the observation period. The somatomedin C content of the remaining kidney after unilateral nephrectomy was maximal after 24 h with an increase of 58% (from 1340±203 ng/g (SEM) to 2122±214 ng/g). The somatomedin C content returned to normal at day 4. Serum somatomedin C declined insignificantly in diabetic animals during the experimental period, but a significant decrease (p<0.02) was found in uninephrectomised rats. This study demonstrates that kidney somatomedin C peaks during the first or second day after uninephrectomy or induction of diabetes, respectively, and that insulin treatment sufficient to prevent kidney growth abolishes the increase. These similar rapid initial hypertrophies/hyperplasies may thus be dependent on local somatomedin C formation.

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References

  1. Mogensen CE, Andersen MJF (1973) Increased kidney size and glomerular filtration rate in early juvenile diabetes. Diabetes 22: 706–712
    Google Scholar
  2. Mogensen CE (1971) Glomerular filtration rate and renal plasma flow in short-term and long-term juvenile diabetes mellitus. Scand J Clin Lab Invest 28: 91–100
    Google Scholar
  3. Seyer-Hansen K (1976) Renal hypertrophy in streptozotocin-diabetic rats. Clin Sci 51: 551–555
    Google Scholar
  4. Mogensen CE, Andersen MJR (1975) Increased kidney size and glomerular filtration rate in untreated juvenile diabetes: normalization by insulin treatment. Diabetologia 11: 221–224
    Google Scholar
  5. Seyer-Hansen K (1983) Renal hypertrophy in experimental diabetes mellitus. Kidney Int 23: 643–646
    Google Scholar
  6. Mogensen CE (1982) Diabetes mellitus and the kidney. An introduction. Kidney Int 21: 673–675
    Google Scholar
  7. Clemmons DR, Underwood LE, Van Wyk JJ (1981) Hormonal control of immunoreactive somatomedin production by cultured human fibroblasts. J Clin Invest 67: 10–19
    Google Scholar
  8. Zapf J, Froesch ER, Humbel RE (1981) The IGF of human serum: chemical and biological characterization and aspects of their possible physiological role. Curr Top Cell Regul 19: 257–309
    Google Scholar
  9. Schoenle E, Zaph J, Hombel RE, Froesch ER (1982) Insulin-like growth factor I stimulates growth in hypophysectomized rats. Nature 296: 252–253
    Google Scholar
  10. Salmon WD Jr, Daughaday WH (1957) A hormonally controlled serum factor which stimulates sulfate incorporation by cartilage in vitro. J Lab Clin Med 49: 825–836
    Google Scholar
  11. Daughaday WH, Hall K, Raben MS, Salmon WD Jr, Van den Brande JL, Van Wyk JJ (1972) Somatomedin: proposed designation for sulfation factor. Nature 235: 107
    Google Scholar
  12. D'Ecole AJ, Stilles AD, Underwood LE (1984) Tissue concentration of somatomedin C: further evidence for multiple sites of synthesis and paracrine/autocrine mechanisms of actions. Proc Natl Acad Sci USA 81: 935–939
    Google Scholar
  13. Thorlacius-Ussing O, Flyvbjerg A, Jørgensen K Damm, Ørskov H (1988) Growth hormone restores normal growth in selenium treated rats without increase in circulating SMC. Acta Endocrinol 117: 65–72
    Google Scholar
  14. Thorlacius-Ussing O, Flyvbjerg A, Esmann J (1987) Evidence that selenium induces growth retardation through reduced growth hormone and SMC production. Endocrinology 120: 659–663
    Google Scholar
  15. Munro HN, Fleck A (1966) The determination of nucleic acids. Methods Biochem Anal 14: 113–176
    Google Scholar
  16. Burton K (1956) A study of the conditions and mechanism of the diphenylamine reaction for a colorimetric estimation of deoxyribonucleic acid. Biochem J 62: 315–323
    Google Scholar
  17. Lowry OH, Osebrough NJ, Fara AL, Randall RL (1951) Porcine measurements with the Folin phenol reagents. J Biol Chem 193: 165–175
    Google Scholar
  18. Seyer-Hansen K (1978) Renal hypertrophy in experimental diabetes: a comparison to compensatory hypertrophy. Diabetologia 14: 325–328
    Google Scholar
  19. Preuss HG (1983) Compensatory renal growth symposium. An introduction. Kidney Int 23: 571–574
    Google Scholar
  20. Seyer-Hansen K (1977) Renal hypertrophy in experimental diabetes: relation to severity of diabetes. Diabetologia 13: 141–143
    Google Scholar
  21. Maes M, Ketelslegers JM, Underwood LE (1983) Low plasma SMC in streptozotocin-induced diabetes mellitus. Diabetes 32: 1060–1069
    Google Scholar
  22. Maes M, Underwood LE, Ketelslegers JM (1986) Low serum SMC in insulin-dependent diabetes: evidence for a postreceptor mechanism. Endocrinology 118: 377–382
    Google Scholar
  23. Stiles AD, Sosenko IRS, D'Ercole AJ, Smith BT (1985) Relations of kidney tissue somatomedin-C/insulin-like growth factor I to postnephrectomy renal growth in the rat. Endocrinology 117: 2397–2401
    Google Scholar
  24. Van Buul-Offers S, Ueda I, Van den Brande JL (1986) Biosynthetic somatomedin C (SM-C/IGF I) increases the length and weight of snell dwarf mice. Pediatr Res 20: 825–827
    Google Scholar
  25. D'Ercole AJ, Decedue CJ, Furlanetto RB, Underwood L, Van Wyk JJ (1977) Evidence that SMC is degraded by the kidney and inhibits insulin degradation. Endocrinology 101: 577–586
    Google Scholar
  26. Fleck CH, Bräunlich H (1984) Kidney function after unilateral nephrectomy. Exp Pathol 25: 3–18
    Google Scholar
  27. Michels LD, Davidman M, Keane WF (1981) Determinants of glomerular filtration and plasma flow in experimental diabetic rats. J Lab Clin Med 98: 869–885
    Google Scholar
  28. Seyer-Hansen K (1987) Renal hypertrophy in experimental diabetes: some functional aspects. J Diabetic Complications 1: 7–10
    Google Scholar
  29. Jensen PK, Christiansen JS, Steven K, Parving H-H (1981) Renal function in streptozotocin diabetic rats. Diabetologia 21: 409–414
    Google Scholar
  30. Seyer-Hansen K, Hansen J, Gundersen HJG (1980) Renal hypertrophy in experimental diabetes. A morphometric study. Diabetologia 18: 501–505
    Google Scholar
  31. Rasch R, Rytter-Nörgaard JO (1983) Renal enlargement: comparative autoradiographic studies of 3H-thymidine uptake in diabetic and uninephrectomized rats. Diabetologia 25: 280–287
    Google Scholar
  32. Mogensen CE, Steffes MW, Deckert T, Christiansen JS (1981) Functional and morphological renal manifestations in diabetes mellitus. Diabetologia 21: 89–93
    Google Scholar
  33. Brenner BM, Hostetter TH, Olsen JL, Rennke HG, Venkatachalam MA (1981) The role of glomerular hyperfiltration in the initiation and progression of diabetic nephropathy. Acta Endocrinol (Copenh) 97: [Suppl.] 242: 7–10
    Google Scholar
  34. Ørskov H (1985) Growth hormone hyperproduction inducing some of the vicious circles in diabetes mellitus. Acta Med Scand 217: 343–346
    Google Scholar
  35. Mogensen CE (1986) Early glomerular hyperfiltration in insulin-dependent diabetics and late nephropathy. Scand J Clin Lab Invest 46: 201–206
    Google Scholar

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Authors and Affiliations

  1. Kommunehospitalet, Second University Clinic of Internal Medicine, Denmark
    A. Flyvbjerg
  2. Department Surgery I, County Hospital, Denmark
    O. Thorlacius-Ussing
  3. Institute of Experimental Clinical Research, University of Aarhus, Denmark
    R. Næraa & H. Ørskov
  4. University Department of Clinical Chemistry, Kommunehospitalet, Aarhus C, Denmark
    J. Ingerslev

Authors

  1. A. Flyvbjerg
  2. O. Thorlacius-Ussing
  3. R. Næraa
  4. J. Ingerslev
  5. H. Ørskov

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Flyvbjerg, A., Thorlacius-Ussing, O., Næraa, R. et al. Kidney tissue somatomedin C and initial renal growth in diabetic and uninephrectomised rats.Diabetologia 31, 310–314 (1988). https://doi.org/10.1007/BF00277413

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