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. 1981 Sep;68(3):655–664. doi: 10.1172/JCI110300

Effect of Thyroparathyroidectomy and Parathyroidectomy on Renal Function and the Nephrotic Syndrome in Rat Nephrotoxic Serum Nephritis

Robert C Tomford 1, Malcolm L Karlinsky 1, Bruce Buddington 1, Allen C Alfrey 1
PMCID: PMC370846  PMID: 7276165

Abstract

Dietary phosphorus restriction (PR) prevents uremia in rats with nephrotoxic serum nephritis (NSN). One possible mechanism by which PR could be protective would be through the suppression of parathyroid hormone. To evaluate this possibility two separate protocols were designed. In the first rats were thyroparathyroidectomized (TPTX) before (n = 11) or 5 wk after (n = 7) NSN induction and compared to sham-operated parathyroid intact rats with NSN (n = 12). At the end of the 23-wk study, intact rats were azotemic, plasma creatinine 3.80±0.81 mg/100 ml vs. 0.65±0.07 for TPTX rats (P < 0.001). During the study 75% of intact rats died of uremia in contrast to none of the TPTX rats (P < 0.001). Renal histological damage was greatly diminished and calcification prevented in TPTX rats. The proteinuria of the heterologous phase was unaffected, but the protein excretion and hypertriglyceridemia (HTG) of the autologous phase were markedly decreased in the TPTX rats. The degree of HTG and proteinuria had a high positive correlation (P < 0.001). Late TPTX also produced significant decreases in proteinuria and HTG regardless of the degree of azotemia, and prevented azotemia if the plasma creatinine at the time of TPTX was ≤0.85 mg/100 ml.

In additional studies selective parathyroidectomy (PTX) was performed. The adequacy of this procedure was documented by showing a similar fall in plasma Ca and urinary cyclic AMP in PTX animals as found in TPTX animals. However, selective PTX had no effect on proteinuria, histologic damage, or functional deterioration. These studies further showed that early, histologic damage and functional deterioration preceeded renal parenchymal calcification. Because animals were pair fed and both groups were given 1,25-dihydroxycholecalciferol to normalize serum Ca and P levels these studies exclude alterations in plasma Ca and P levels, dietary intake, urinary P excretion, and vitamin D administration in promoting the protective effect of TPTX on renal function.

We conclude that TPTX is equally effective in preventing functional deterioration and more effective in reducing proteinuria in NSN than PR. The mechanism of this protective effect remains to be elucidated, since it does not primarily involve either the elimination of parathyroid hormone or the prevention of renal parenchymal calcification.

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Selected References

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  1. Allain C. C., Poon L. S., Chan C. S., Richmond W., Fu P. C. Enzymatic determination of total serum cholesterol. Clin Chem. 1974 Apr;20(4):470–475. [PubMed] [Google Scholar]
  2. BAKER R., SISON F. Demonstration of altered tissue mucopolysaccharides in renal calculus disease by selective staining techniques. J Urol. 1954 Dec;72(6):1032–1045. doi: 10.1016/S0022-5347(17)67712-7. [DOI] [PubMed] [Google Scholar]
  3. Bhan A. K., Schneeberger E. E., Collins A. B., McCluskey R. T. Evidence for a pathogenic role of a cell-mediated immune mechanism in experimental glomerulonephritis. J Exp Med. 1978 Jul 1;148(1):246–260. doi: 10.1084/jem.148.1.246. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cantin M. Kidney, parathyroid, and lipemia. Lab Invest. 1965 Sep;14(9):1691–1698. [PubMed] [Google Scholar]
  5. Contiguglia S. R., Alfrey A. C., Miller N. L., Runnells D. E., Le Geros R. Z. Nature of soft tissue calcification in uremia. Kidney Int. 1973 Sep;4(3):229–235. doi: 10.1038/ki.1973.104. [DOI] [PubMed] [Google Scholar]
  6. Craddock P. R., Yawata Y., VanSanten L., Gilberstadt S., Silvis S., Jacob H. S. Acquired phagocyte dysfunction. A complication of the hypophosphatemia of parenteral hyperalimentation. N Engl J Med. 1974 Jun 20;290(25):1403–1407. doi: 10.1056/NEJM197406202902504. [DOI] [PubMed] [Google Scholar]
  7. Dousa T. P., Barnes L. D., Ong S. H., Steiner A. L. Immunohistochemical localization of 3':5'-cyclic AMP and 3':5'-cyclic GMP in rat renal cortex: effect of parathyroid hormone. Proc Natl Acad Sci U S A. 1977 Aug;74(8):3569–3573. doi: 10.1073/pnas.74.8.3569. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Farber E. ATP and cell integrity. Fed Proc. 1973 Apr;32(4):1534–1539. [PubMed] [Google Scholar]
  9. Fletcher M. J. A colorimetric method for estimating serum triglycerides. Clin Chim Acta. 1968 Nov;22(3):393–397. doi: 10.1016/0009-8981(68)90041-7. [DOI] [PubMed] [Google Scholar]
  10. HEYMANN W., NASH G., GILKEY C., LEWIS M. Studies on the causal role of hypoalbuminemia in experimental nephrotic hyperlipemia. J Clin Invest. 1958 Jun;37(6):808–812. doi: 10.1172/JCI103668. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Haut L. L., Alfrey A. C., Guggenheim S., Buddington B., Schrier N. Renal toxicity of phosphate in rats. Kidney Int. 1980 Jun;17(6):722–731. doi: 10.1038/ki.1980.85. [DOI] [PubMed] [Google Scholar]
  12. Ibels L. S., Alfrey A. C., Haut L., Huffer W. E. Preservation of function in experimental renal disease by dietary restriction of phosphate. N Engl J Med. 1978 Jan 19;298(3):122–126. doi: 10.1056/NEJM197801192980302. [DOI] [PubMed] [Google Scholar]
  13. Ichikawa I., Humes H. D., Dousa T. P., Brenner B. M. Influence of parathyroid hormone on glomerular ultrafiltration in the rat. Am J Physiol. 1978 May;234(5):F393–F401. doi: 10.1152/ajprenal.1978.234.5.F393. [DOI] [PubMed] [Google Scholar]
  14. Ismail-Beigi F., Edelman I. S. The mechanism of the calorigenic action of thyroid hormone. Stimulation of Na plus + K plus-activated adenosinetriphosphatase activity. J Gen Physiol. 1971 Jun;57(6):710–722. doi: 10.1085/jgp.57.6.710. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. KRAKOWER C. A., GREENSPON S. A. Localization of the nephrotoxic antigen within the isolated renal glomerulus. AMA Arch Pathol. 1951 Jun;51(6):629–639. [PubMed] [Google Scholar]
  16. Karlinsky M. L., Haut L., Buddington B., Schrier N. A., Alfrey A. C. Preservation of renal function in experimental glomerulonephritis. Kidney Int. 1980 Mar;17(3):293–302. doi: 10.1038/ki.1980.35. [DOI] [PubMed] [Google Scholar]
  17. Kather H., Heuck C. C., Tschöpe W., Ritz E., Simon B. Unchanged hormone sensitivity of rat fat cell adenylate cyclase in uremia. Clin Nephrol. 1977 Jul;8(1):324–327. [PubMed] [Google Scholar]
  18. Katz A. I., Hampers C. L., Merrill J. P. Secondary hyperparathyroidism and renal osteodystrophy in chronic renal failure. Analysis of 195 patients, with observations on the effects of chronic dialysis, kidney transplantation and subtotal parathyroidectomy. Medicine (Baltimore) 1969 Sep;48(5):333–374. [PubMed] [Google Scholar]
  19. Katz A. I., Hampers C. L., Wilson R. E., Bernstein D. S., Wachman A., Merrill J. P. The place of subtotal parathyroidectomy in the management of patients with chronic renal failure. Trans Am Soc Artif Intern Organs. 1968;14:376–384. [PubMed] [Google Scholar]
  20. Kuzela D. C., Huffer W. E., Conger J. D., Winter S. D., Hammond W. S. Soft tissue calcification in chronic dialysis patients. Am J Pathol. 1977 Feb;86(2):403–424. [PMC free article] [PubMed] [Google Scholar]
  21. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  22. Miyada D. S., Baysinger V., Notrica S., Nakamura R. M. Albumin quantitation by dye binding and salt fractionation techniques. Clin Chem. 1972 Jan;18(1):52–56. [PubMed] [Google Scholar]
  23. POLLAK V. E., SCHNEIDER A. F., FREUND G., KARK R. M. Chronic renal disease with secondary hyperparathyroidism. AMA Arch Intern Med. 1959 Feb;103(2):200–218. doi: 10.1001/archinte.1959.00270020028004. [DOI] [PubMed] [Google Scholar]
  24. SCHNEIDER A. F., REAVEN E. P., REAVEN G. A comparison of renal calcification produced by parathyroid extract or calcium gluconate. Endocrinology. 1960 Dec;67:733–743. doi: 10.1210/endo-67-6-733. [DOI] [PubMed] [Google Scholar]
  25. Schreiner G. F., Cotran R. S., Pardo V., Unanue E. R. A mononuclear cell component in experimental immunological glomerulonephritis. J Exp Med. 1978 Feb 1;147(2):369–384. doi: 10.1084/jem.147.2.369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Sraer J., Sraer J. D., Chansel D., Jueppner H., Hesch R. D., Ardaillou R. Evidence for glomerular receptors for parathyroid hormone. Am J Physiol. 1978 Aug;235(2):F96–103. doi: 10.1152/ajprenal.1978.235.2.F96. [DOI] [PubMed] [Google Scholar]
  27. Staprans I., Felts J. M. The effect of alpha1-acid glycoprotein (orosomucoid) on triglyceride metabolism in the nephrotic syndrome. Biochem Biophys Res Commun. 1977 Dec 21;79(4):1272–1278. doi: 10.1016/0006-291x(77)91143-3. [DOI] [PubMed] [Google Scholar]
  28. Steiner A. L., Kipnis D. M., Utiger R., Parker C. Radioimmunoassay for the measurement of adenosine 3',5'-cyclic phosphate. Proc Natl Acad Sci U S A. 1969 Sep;64(1):367–373. doi: 10.1073/pnas.64.1.367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Tata J. R. Membrane phospholipid synthesis and the action of hormones. Nature. 1967 Feb 11;213(5076):566–569. doi: 10.1038/213566a0. [DOI] [PubMed] [Google Scholar]
  30. UNANUE E. R., DIXON F. J. EXPERIMENTAL GLOMERULONEPHRITIS. V. STUDIES ON THE INTERACTION OF NEPHROTOXIC ANTIBODIES WITH TISSUE OF THE RAT. J Exp Med. 1965 May 1;121:697–714. doi: 10.1084/jem.121.5.697. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Walser M., Mitch W. E., Collier V. U. The effect of nutritional therapy on the course of chronic renal failure. Clin Nephrol. 1979 Feb;11(2):66–70. [PubMed] [Google Scholar]
  32. Werner S., Löw H. Stimulation of lipolysis and calcium accumulation by parathyroid hormone in rat adipose tissue in vitro after adrenalectomy and administration of high doses of cortisone acetate. Horm Metab Res. 1973 Jul;5(4):292–296. doi: 10.1055/s-0028-1093931. [DOI] [PubMed] [Google Scholar]
  33. de Mendoza S. G., Kashyap M. L., Chen C. Y., Lutmer R. F. High density lipoproteinuria in nephrotic syndrome. Metabolism. 1976 Oct;25(10):1143–1149. doi: 10.1016/0026-0495(76)90022-6. [DOI] [PubMed] [Google Scholar]

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