Rat strain differences in the early stage of porcine-serum-induced hepatic fibrosis

Exp Toxicol Pathol. 2004 Mar;55(5):325-30. doi: 10.1078/0940-2993-00336.

Abstract

Rat strain differences in the early development of porcine serum (PS)-induced hepatic fibrosis were histologically and immunohistochemically examined using Brown Norway (BN), Sprague Dawley (SD) and Wistar rats. They were injected i.p. with 0.5 ml sterile PS twice a week for 4 and 8 weeks. In addition, rats treated with physiological saline in the same way served as controls. At 4 weeks, hepatic fibrosis accompanying fibrous septa mainly composed of type III collagens developed in BN and SD rats but not in Wistar rats. In addition, the numbers of eosinophils, CD3-positive cells and ED-1-positive cells significantly increased in BN and SD rats, that of CD45RA-positive cells in BN rats, and that of alpha-smooth muscle actin (SMA)-positive cells in SD rats, respectively. Such differences in the number of inflammatory cells may be related with the absence of hepatic fibrosis in Wistar rats at 4 weeks. At 8 weeks, hepatic fibrosis with formation of many small-sized pseudolobules was observed in all strains at almost similar degree, and the numbers of infiltrating cells increased in all strains of rats with some exception. In addition, the main location of inflammatory cells was different, suggesting a different role of each inflammatory cell in the process of hepatic fibrosis.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Collagen Type III / metabolism
  • Disease Models, Animal
  • Ectodysplasins
  • Eosinophils / pathology
  • Immunohistochemistry
  • Liver / metabolism
  • Liver / pathology
  • Liver Cirrhosis, Experimental / immunology
  • Liver Cirrhosis, Experimental / metabolism
  • Liver Cirrhosis, Experimental / pathology*
  • Male
  • Mast Cells / pathology
  • Membrane Proteins / metabolism
  • Organ Size
  • Rats
  • Rats, Inbred Strains*
  • Species Specificity
  • Spleen / pathology
  • Swine* / blood
  • Swine* / immunology

Substances

  • Collagen Type III
  • Ectodysplasins
  • Membrane Proteins