Skip to main content
The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 1993 Nov;92(5):2274–2282. doi: 10.1172/JCI116831

Charge selectivity of the glomerular filtration barrier in healthy and nephrotic humans.

A Guasch 1, W M Deen 1, B D Myers 1
PMCID: PMC288408  PMID: 8227342

Abstract

We used dextran sulfate (DS) to evaluate barrier charge selectivity in 11 nonproteinuric subjects and in 11 patients with the nephrotic syndrome due to either membranous nephropathy or minimal change nephropathy. The 3H-DS preparation spanned a molecular radius interval of 10-24 A and exhibited size-dependent protein binding in vitro. Urine and ultrafiltrates of plasma were separated by size into narrow fractions using gel permeation chromatography. The sieving coefficient (theta) for ultrafilterable DS of 15A radius averaged 0.68 +/- 0.03 in nonproteinuric vs. 0.95 +/- 0.05 in nephrotic subjects (P < 0.001). Uncharged dextrans of broad size distribution were used to evaluate barrier size-selectivity in separate groups of nonproteinuric subjects (n = 19) and nephrotic patients with either minimal change (n = 20) or membranous nephropathy (n = 27). The value of theta for an uncharged dextran of similarly small radius (approximately 18 A) was significantly larger than that observed for DS in nonproteinuric subjects, but was similar in nephrotic individuals. Further, impaired barrier size-selectivity, as assessed by the sieving profile for uncharged dextrans (18-60 A radius), failed to account fully for the observed level of albuminuria in almost half of the patients with either minimal change (9/20) or membranous nephropathy (12/27). Together these findings suggest that the human glomerular capillary wall normally provides an electrostatic barrier to filtration of negatively charged macromolecules such as albumin, and that impairment of this electrostatic barrier contributes to the magnitude of albuminuria in the nephrotic syndrome.

Full text

PDF
2274

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ala-Houhala I., Pasternack A. Fractional dextran and protein clearances in glomerulonephritis and in diabetic nephropathy. Clin Sci (Lond) 1987 Mar;72(3):289–296. doi: 10.1042/cs0720289. [DOI] [PubMed] [Google Scholar]
  2. Baldamus C. A., Galaske R., Eisenbach G. M., Krause H. P., Stolte H. Glomerular protein filtration in normal and nephritic rats. A micropuncture study. Contrib Nephrol. 1975;1:37–49. [PubMed] [Google Scholar]
  3. Battilana C., Zhang H. P., Olshen R. A., Wexler L., Myers B. D. PAH extraction and estimation of plasma flow in diseased human kidneys. Am J Physiol. 1991 Oct;261(4 Pt 2):F726–F733. doi: 10.1152/ajprenal.1991.261.4.F726. [DOI] [PubMed] [Google Scholar]
  4. Bennett C. M., Glassock R. J., Chang R. L., Deen W. M., Robertson C. R., Brenner B. M., Troy J. L., ueki I. R., Rasmussen B. Permselectivity of the glomerular capillary wall. Studies of experimental glomerulonephritis in the rat using dextran sulfate. J Clin Invest. 1976 May;57(5):1287–1294. doi: 10.1172/JCI108396. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bertolatus J. A., Hunsicker L. G. Glomerular sieving of anionic and neutral bovine albumins in proteinuric rats. Kidney Int. 1985 Sep;28(3):467–476. doi: 10.1038/ki.1985.153. [DOI] [PubMed] [Google Scholar]
  6. Bohrer M. P., Baylis C., Humes H. D., Glassock R. J., Robertson C. R., Brenner B. M. Permselectivity of the glomerular capillary wall. Facilitated filtration of circulating polycations. J Clin Invest. 1978 Jan;61(1):72–78. doi: 10.1172/JCI108927. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Bohrer M. P., Baylis C., Robertson C. R., Brenner B. M., Troy J. L., Willis W. T. Mechanisms of the puromycin-induced defects in the transglomerular passage of water and macromolecules. J Clin Invest. 1977 Jul;60(1):152–161. doi: 10.1172/JCI108751. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Bohrer M. P., Deen W. M., Robertson C. R., Brenner B. M. Mechanism of angiotensin II-induced proteinuria in the rat. Am J Physiol. 1977 Jul;233(1):F13–F21. doi: 10.1152/ajprenal.1977.233.1.F13. [DOI] [PubMed] [Google Scholar]
  9. Bohrer M. P., Deen W. M., Robertson C. R., Troy J. L., Brenner B. M. Influence of molecular configuration on the passage of macromolecules across the glomerular capillary wall. J Gen Physiol. 1979 Nov;74(5):583–593. doi: 10.1085/jgp.74.5.583. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Boyce N. W., Holdsworth S. R. Glomerular permselectivity in the isolated perfused rat kidney. Am J Physiol. 1985 Nov;249(5 Pt 2):F780–F784. doi: 10.1152/ajprenal.1985.249.5.F780. [DOI] [PubMed] [Google Scholar]
  11. Chagnac A., Kiberd B. A., Fariñas M. C., Strober S., Sibley R. K., Hoppe R., Myers B. D. Outcome of the acute glomerular injury in proliferative lupus nephritis. J Clin Invest. 1989 Sep;84(3):922–930. doi: 10.1172/JCI114254. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Chang R. L., Deen W. M., Robertson C. R., Brenner B. M. Permselectivity of the glomerular capillary wall: III. Restricted transport of polyanions. Kidney Int. 1975 Oct;8(4):212–218. doi: 10.1038/ki.1975.104. [DOI] [PubMed] [Google Scholar]
  13. Chang R. L., Ueki I. F., Troy J. L., Deen W. M., Robertson C. R., Brenner B. M. Permselectivity of the glomerular capillary wall to macromolecules. II. Experimental studies in rats using neutral dextran. Biophys J. 1975 Sep;15(9):887–906. doi: 10.1016/S0006-3495(75)85863-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Chang R. S., Robertson C. R., Deen W. M., Brenner B. M. Permselectivity of the glomerular capillary wall to macromolecules. I. Theoretical considerations. Biophys J. 1975 Sep;15(9):861–886. doi: 10.1016/S0006-3495(75)85862-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Deen W. M., Bridges C. R., Brenner B. M., Myers B. D. Heteroporous model of glomerular size selectivity: application to normal and nephrotic humans. Am J Physiol. 1985 Sep;249(3 Pt 2):F374–F389. doi: 10.1152/ajprenal.1985.249.3.F374. [DOI] [PubMed] [Google Scholar]
  16. Deen W. M., Satvat B., Jamieson J. M. Theoretical model for glomerular filtration of charged solutes. Am J Physiol. 1980 Feb;238(2):F126–F139. doi: 10.1152/ajprenal.1980.238.2.F126. [DOI] [PubMed] [Google Scholar]
  17. Flexner C., Barditch-Crovo P. A., Kornhauser D. M., Farzadegan H., Nerhood L. J., Chaisson R. E., Bell K. M., Lorentsen K. J., Hendrix C. W., Petty B. G. Pharmacokinetics, toxicity, and activity of intravenous dextran sulfate in human immunodeficiency virus infection. Antimicrob Agents Chemother. 1991 Dec;35(12):2544–2550. doi: 10.1128/aac.35.12.2544. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Guasch A., Hashimoto H., Sibley R. K., Deen W. M., Myers B. D. Glomerular dysfunction in nephrotic humans with minimal changes or focal glomerulosclerosis. Am J Physiol. 1991 May;260(5 Pt 2):F728–F737. doi: 10.1152/ajprenal.1991.260.5.F728. [DOI] [PubMed] [Google Scholar]
  19. Hourani M. R., Mayor G. H., Greenbaum D. S., Hugget D. O., Patterson M. J. Hepatitis B surface antigen in urine of hemodialysis patients. Kidney Int. 1978 Apr;13(4):324–328. doi: 10.1038/ki.1978.46. [DOI] [PubMed] [Google Scholar]
  20. Knisel W., Müller M., Besenthal I., di Nicuolo A., Rebstock M., Risler T., Eggstein M. Application of a new LDL apheresis system using two dextran sulfate cellulose columns in combination with an automatic column-regenerating unit and a blood cell separator. J Clin Apher. 1991;6(1):11–15. doi: 10.1002/jca.2920060103. [DOI] [PubMed] [Google Scholar]
  21. Mayer G., Lafayette R. A., Oliver J., Deen W. M., Myers B. D., Meyer T. W. Effects of angiotensin II receptor blockade on remnant glomerular permselectivity. Kidney Int. 1993 Feb;43(2):346–353. doi: 10.1038/ki.1993.52. [DOI] [PubMed] [Google Scholar]
  22. Mernissi G. E., Doucet A. Stimulation of Na-K-ATPase in the rat collecting tubule by two diuretics: furosemide and amiloride. Am J Physiol. 1984 Sep;247(3 Pt 2):F485–F490. doi: 10.1152/ajprenal.1984.247.3.F485. [DOI] [PubMed] [Google Scholar]
  23. Mogensen C. E., Sølling Studies on renal tubular protein reabsorption: partial and near complete inhibition by certain amino acids. Scand J Clin Lab Invest. 1977 Oct;37(6):477–486. doi: 10.3109/00365517709101835. [DOI] [PubMed] [Google Scholar]
  24. Myers B. D. Pathophysiology of proteinuria in diabetic glomerular disease. J Hypertens Suppl. 1990 Mar;8(1):S41–S46. doi: 10.1097/00004872-199003001-00009. [DOI] [PubMed] [Google Scholar]
  25. Oken D. E., Kirschbaum B. B., Landwehr D. M. Micropuncture studies of the mechanisms of normal and pathologic albuminuria. Contrib Nephrol. 1981;24:1–7. doi: 10.1159/000395223. [DOI] [PubMed] [Google Scholar]
  26. Oliver J. D., 3rd, Anderson S., Troy J. L., Brenner B. M., Deen W. H. Determination of glomerular size-selectivity in the normal rat with Ficoll. J Am Soc Nephrol. 1992 Aug;3(2):214–228. doi: 10.1681/ASN.V32214. [DOI] [PubMed] [Google Scholar]
  27. Olson J. L., Hostetter T. H., Rennke H. G., Brenner B. M., Venkatachalam M. A. Altered glomerular permselectivity and progressive sclerosis following extreme ablation of renal mass. Kidney Int. 1982 Aug;22(2):112–126. doi: 10.1038/ki.1982.143. [DOI] [PubMed] [Google Scholar]
  28. Olson J. L., Rennke H. G., Venkatachalam M. A. Alterations in the charge and size selectivity barrier of the glomerular filter in aminonucleoside nephrosis in rats. Lab Invest. 1981 Mar;44(3):271–279. [PubMed] [Google Scholar]
  29. Remuzzi A., Perticucci E., Ruggenenti P., Mosconi L., Limonta M., Remuzzi G. Angiotensin converting enzyme inhibition improves glomerular size-selectivity in IgA nephropathy. Kidney Int. 1991 Jun;39(6):1267–1273. doi: 10.1038/ki.1991.160. [DOI] [PubMed] [Google Scholar]
  30. Scandling J. D., Black V. M., Deen W. M., Myers B. D. Glomerular permselectivity in healthy and nephrotic humans. Adv Nephrol Necker Hosp. 1992;21:159–176. [PubMed] [Google Scholar]
  31. Shemesh O., Ross J. C., Deen W. M., Grant G. W., Myers B. D. Nature of the glomerular capillary injury in human membranous glomerulopathy. J Clin Invest. 1986 Mar;77(3):868–877. doi: 10.1172/JCI112384. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Vanrenterghem Y., Vanholder R., Lammens-Verslijpe M., Lambert P. P. Sieving studies in 'urea-induced nephropathy' in the dog. Clin Sci (Lond) 1980 Jan;58(1):65–75. doi: 10.1042/cs0580065. [DOI] [PubMed] [Google Scholar]
  33. Weening J. J., Rennke H. G. Glomerular permeability and polyanion in adriamycin nephrosis in the rat. Kidney Int. 1983 Aug;24(2):152–159. doi: 10.1038/ki.1983.139. [DOI] [PubMed] [Google Scholar]
  34. Weening J. J., van der Wal A. Effect of decreased perfusion pressure on glomerular permeability in the rat. Lab Invest. 1987 Aug;57(2):144–149. [PubMed] [Google Scholar]

Articles from Journal of Clinical Investigation are provided here courtesy of American Society for Clinical Investigation

RESOURCES