The in vivo systemic effect of human recombinant interleukin-1 beta on fibronectin in rats

Clin Physiol Biochem. 1992;9(2):55-61.

Abstract

The in vivo systemic effect of interleukin (IL)-1 beta on plasma and cartilage fibronectin was studied in arthritic rats, as well as alpha 1-acid glycoprotein and albumin. Plasma fibronectin showed a 27% increase in the arthritic group, while alpha 1-acid glycoprotein increased 22-fold and albumin decreased by 46%. IL-1 effect depended on the administered dose. 2 micrograms injection significantly increased plasma fibronectin and alpha 1-acid glycoprotein. In cartilage, fibronectin was significantly modified in arthritic animals but increased in a dose-related manner after IL-1 treatment. As IL-1 increases fibronectin-degrading enzyme production and as some of these fragments can develop properties that do not possess the intact molecule, one can postulate a vicious circle in matrix degradation in the inflammatory process of the joint.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arthritis, Experimental / metabolism*
  • Cartilage / drug effects
  • Cartilage / metabolism*
  • Disease Models, Animal
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Fibronectins / blood
  • Fibronectins / metabolism*
  • Humans
  • Interleukin-1 / pharmacology*
  • Orosomucoid / metabolism
  • Random Allocation
  • Rats
  • Rats, Inbred WF
  • Recombinant Proteins / pharmacology
  • Serum Albumin / analysis

Substances

  • Fibronectins
  • Interleukin-1
  • Orosomucoid
  • Recombinant Proteins
  • Serum Albumin