Literature DB >> 6162382

Minimal change nephropathy: an electrochemical disorder of the glomerular membrane.

B J Carrie, W R Salyer, B D Myers.   

Abstract

To investigate the mechanism of proteinuria in minimal change nephropathy, the renal handling of dextrans was studied in seven nephrotic patients with this disorder. Although the urinary excretion of albumin was greatly increased, the urinary excretion and fractional clearance of dextrans (Einstein-Stokes radius (ESR), range 20 to 48 A) were depressed relative to those in nonproteinuric healthy volunteers. This suggests that mean glomerular pore size or pore density was reduced. Uptake of colloidal iron by glomeruli obtained from these patients by needle biopsy was diminished, suggesting loss of glomerular polyanion. Since the fractional clearance of dextrans similar in size to albumin was depressed, not increased, it is proposed that the lack of electrostatic interaction between the glomerular capillaries and polyanionic plasma albumin (ESR = 36 A) accounts for the selective albuminuria which characterizes minimal change nephropathy.

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Year:  1981        PMID: 6162382     DOI: 10.1016/0002-9343(81)90760-9

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  16 in total

1.  Distribution of endogenous albumin in the glomerular wall of proteinuric patients.

Authors:  P A Russo; M Bendayan
Journal:  Am J Pathol       Date:  1990-12       Impact factor: 4.307

2.  Glycosaminoglycan excretion in children with nephrotic syndrome.

Authors:  Nurcan Cengiz; Aysun K Bayazit; Aytul Noyan; Ruksan Anarat; Ali Anarat
Journal:  Pediatr Nephrol       Date:  2005-02-16       Impact factor: 3.714

3.  Superior sagittal sinus thrombosis in a child with nephrotic syndrome.

Authors:  A A Divekar; U S Ali; M D Ronghe; A R Singh; R B Dalvi
Journal:  Pediatr Nephrol       Date:  1996-04       Impact factor: 3.714

Review 4.  [Minimal change disease and focal segmental glomerulosclerosis].

Authors:  J Müller-Deile; H Schenk; M Schiffer
Journal:  Internist (Berl)       Date:  2019-05       Impact factor: 0.743

Review 5.  Pathogenesis of proteinuria in idiopathic minimal change disease: molecular mechanisms.

Authors:  Gabriel Cara-Fuentes; William L Clapp; Richard J Johnson; Eduardo H Garin
Journal:  Pediatr Nephrol       Date:  2016-07-06       Impact factor: 3.714

6.  Glomerular and urinary heparan sulphate in congenital nephrotic syndrome.

Authors:  C Vermylen; M Levin; J Mossman; T M Barratt
Journal:  Pediatr Nephrol       Date:  1989-04       Impact factor: 3.714

7.  An ultrastructural study of the effect of the steroid in puromycin aminonucleoside nephrosis rats.

Authors:  Y Fujiwara
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1984

8.  Disruption of glomerular basement membrane charge through podocyte-specific mutation of agrin does not alter glomerular permselectivity.

Authors:  Scott J Harvey; George Jarad; Jeanette Cunningham; Angelique L Rops; Johan van der Vlag; Jo H Berden; Marcus J Moeller; Lawrence B Holzman; Robert W Burgess; Jeffrey H Miner
Journal:  Am J Pathol       Date:  2007-07       Impact factor: 4.307

9.  Urinary protein excretion patterns in reactive (secondary) systemic amyloidosis.

Authors:  A M Teppo; C P Maury
Journal:  Rheumatol Int       Date:  1988       Impact factor: 2.631

10.  Mechanisms of proteinuria in human glomerulonephritis.

Authors:  B D Myers; T B Okarma; S Friedman; C Bridges; J Ross; S Asseff; W M Deen
Journal:  J Clin Invest       Date:  1982-10       Impact factor: 14.808

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