Contribution of hepatic reticuloendothelial system to glomerular IgA deposition in rat liver injury

Am J Pathol. 1988 Jun;131(3):411-7.

Abstract

Liver damage was induced in rats by a single dose of dimethylnitrosamine or D-galactosamine. In the dimethylnitrosamine model, marked glomerular IgA deposition occurred between Days 4 and 28, with its peak at Day 14. Serum IgA levels were significantly increased at Days 2 and 4, then gradually decreased, and normalized at Day 14. In the D-galactosamine model, however, no such deposition was observed, though serum IgA levels similarly increased on Days 2 and 4. IgA content in high molecular weight fraction from serum increased at Day 3 in both models. This increment remained at Day 7 only in the dimethylnitrosamine model, in which carbon clearance from the circulation was significantly decreased at Day 3. These data suggest that dysfunction of the hepatic reticuloendothelial system is a factor contributing to glomerular IgA deposition occurring in liver injury.

MeSH terms

  • Alanine Transaminase / metabolism
  • Animals
  • Carbon / blood
  • Chemical Fractionation
  • Chemical and Drug Induced Liver Injury
  • Dimethylnitrosamine / pharmacology
  • Galactosamine / pharmacology
  • Immunoglobulin A / analysis
  • Immunoglobulin A / metabolism*
  • Kidney Glomerulus / metabolism*
  • Liver / physiopathology*
  • Liver Diseases / metabolism
  • Liver Diseases / physiopathology*
  • Male
  • Molecular Weight
  • Mononuclear Phagocyte System / physiopathology*
  • Rats
  • Rats, Inbred Strains

Substances

  • Immunoglobulin A
  • Carbon
  • Galactosamine
  • Alanine Transaminase
  • Dimethylnitrosamine