Literature DB >> 3820937

Effect of chronic administration of different Bence Jones proteins on rat kidney.

P Smolens, J L Barnes, J H Stein.   

Abstract

The role of Bence Jones proteins (BJPs) in the genesis of the renal dysfunction that develops in patients with multiple myeloma is not clearly defined. We previously evaluated renal function and morphology in a unique strain of rats (LOU/m) bearing tumors which synthesized BJPs with isoelectric points of 5.2, 4.3 and 6.7. Myeloma cast nephropathy developed in one tumor bearing group (pI 5.2), tubular necrosis was observed in another (pI 4.3), and renal function and histology remained normal in a third group (pI 6.7). To see if these renal outcomes were a function of the BJP being excreted or other factors which could be present in the tumor bearing animals, we have examined the effect of chronic intravenous administration of these three BJPs on renal function and histology in non-tumor-bearing LOU/m rats. Urine containing the BJP was collected from tumor bearing rats, sterilized by passage through a 0.2 mu millipore filter, concentrated to 50 mg/ml, and dialyzed extensively so as to remove material with a molecular weight less than 3500. Chronic indwelling-venous catheters were placed in non-tumor-bearing LOU/m rats and these rats were given 100 mg/day for five days of one of the three BJPs. Polyfructosan clearance (Cin) was measured prior to and following the five days of BJP administration. Renal histology was examined at the completion of the second Cin. In the pI 5.2 group (N = 6), a severe distal nephron cast nephropathy occurred and Cin fell from 2.88 +/- 0.24 to 0.90 +/- 0.17 ml/min (P less than 0.002).(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1986        PMID: 3820937     DOI: 10.1038/ki.1986.267

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  8 in total

Review 1.  Acute renal failure. Lessons from pathophysiology.

Authors:  J H Stein
Journal:  West J Med       Date:  1992-02

2.  Differential nephrotoxicity of low molecular weight proteins including Bence Jones proteins in the perfused rat nephron in vivo.

Authors:  P W Sanders; G A Herrera; A Chen; B B Booker; J H Galla
Journal:  J Clin Invest       Date:  1988-12       Impact factor: 14.808

3.  Mapping the binding domain of immunoglobulin light chains for Tamm-Horsfall protein.

Authors:  W Z Ying; P W Sanders
Journal:  Am J Pathol       Date:  2001-05       Impact factor: 4.307

4.  Electrophoretic study of the physico-chemical characteristics of Bence-Jones proteinuria and its association with kidney damage.

Authors:  M C Diemert; L Musset; O Gaillard; S Escolano; A Baumelou; F Rousselet; J Galli
Journal:  J Clin Pathol       Date:  1994-12       Impact factor: 3.411

5.  Pathogenic potential of human monoclonal immunoglobulin light chains: relationship of in vitro aggregation to in vivo organ deposition.

Authors:  E A Myatt; F A Westholm; D T Weiss; A Solomon; M Schiffer; F J Stevens
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-12       Impact factor: 11.205

6.  Bence Jones proteins bind to a common peptide segment of Tamm-Horsfall glycoprotein to promote heterotypic aggregation.

Authors:  Z Q Huang; K A Kirk; K G Connelly; P W Sanders
Journal:  J Clin Invest       Date:  1993-12       Impact factor: 14.808

7.  Protracted remission of proteinuria after combined therapy with plasmapheresis and anti-CD20 antibodies/cyclophosphamide in a child with oligoclonal IgM and glomerulosclerosis.

Authors:  Gian Marco Ghiggeri; Luca Musante; Giovanni Candiano; Maurizio Bruschi; Laura Santucci; Giancarlo Barbano; Antonella Trivelli; Lucia Rivabella; Rosanna Gusmano; Francesco Perfumo
Journal:  Pediatr Nephrol       Date:  2007-07-28       Impact factor: 3.714

Review 8.  Acute renal failure: the glomerular and tubular connection.

Authors:  J E Bird; R C Blantz
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

  8 in total

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