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1. The influence of anti-rheumatic drugs on hepatic mRNA levels of acute-phase proteins in rats with adjuvant arthritis

Author

B. Jagher, Irmgard Wiesenberg, Tscherry Bj, T Geiger, and Werner Pignat

Subjects
Male, medicine.medical_specialty, Cyclophosphamide, medicine.medical_treatment, Prednisolone, Immunology, Indomethacin, Down-Regulation, Pharmacology, Toxicology, Fibrinogen, Internal medicine, medicine, Animals, Pharmacology (medical), RNA, Messenger, biology, business.industry, Albumin, Acute-phase protein, Arthritis, Experimental, Rheumatology, Rats, Endocrinology, Cytokine, Liver, Rats, Inbred Lew, biology.protein, Cyclosporine, Cyclooxygenase, business, medicine.drug, Acute-Phase Proteins
Abstract

Using specific cDNA probes, we have investigated drug-induced changes in hepatic mRNA levels of the major acute-phase proteins (APP) fibrinogen, alpha 2-macroglobulin (alpha 2-MG), albumin and alpha 1-acid glycoprotein (alpha 1-AGP) in male Lewis rats with adjuvant arthritis. Test compounds were given orally from day 0 to 20 and hepatic mRNA analysis was performed at day 21. Prednisolone (1, 3, 10 mg/kg), Cyclosporine A (1, 3, 10 mg/kg) and cyclophosphamide (3 mg/kg) dose-dependently normalized hepatic mRNA levels of all four APP. Equipotent anti-inflammatory doses of indomethacin (0.3, 1 mg/kg) significantly downregulated alpha 2-MG mRNA levels but were much less effective in influencing albumin and alpha 1-AGP mRNA levels and even slightly increased hepatic fibrinogen mRNA levels. These results suggest that cytokine over-production, which is thought to be responsible for the acute-phase response in rats with adjuvant arthritis, can be effectively downregulated by immunosuppressive drugs, but is distinctly less affected by the cyclooxygenase inhibitor indomethacin.

Published
1993

2. Changes in hepatic mRNA levels of acute phase proteins during rat adjuvant arthritis.

Author

Geiger T, Fischer M, Jagher B, Pignat W, Tscherry BJ, and Wiesenberg I

Subjects
Acute-Phase Proteins analysis, Acute-Phase Proteins metabolism, Albumins genetics, Animals, Arthritis, Experimental metabolism, Blotting, Northern, DNA Probes, Fibrinogen genetics, Interleukin-1 metabolism, Interleukin-6 metabolism, Liver metabolism, Male, Orosomucoid genetics, RNA, Messenger genetics, Rats, Rats, Inbred Lew, Tumor Necrosis Factor-alpha metabolism, alpha-Macroglobulins genetics, Acute-Phase Proteins genetics, Arthritis, Experimental genetics, Liver chemistry, RNA, Messenger analysis
Abstract

Using specific cDNA probes, we have investigated changes in hepatic mRNA concentrations of the major acute phase proteins fibrinogen, alpha 2-macroglobulin (alpha 2-MG), albumin and alpha 1-acid glycoprotein (alpha 1-AGP) during developing adjuvant arthritis in Lewis rats. Continuously increasing levels in the mRNA of the positive reactants beta-fibrinogen, alpha 2-MG and alpha 1-AGP were found during developing disease with peak levels from day 15 to 21, whereas mRNA concentrations of the negative reactant albumin decreased, reaching their lowest levels on day 11 to 15. As early as 4 days after arthritis induction, the hepatic mRNA levels of beta-fibrinogen, alpha 1-AGP and albumin were distinctly different from control values. The most dramatic changes in the hepatic mRNA levels and plasma concentrations of acute phase reactants were seen between days 11 and 21. These results indicate that overproduction of the major inflammatory cytokines IL-1, TNF-alpha and IL-6, which are now felt to be largely responsible for the acute phase response in the rat, is an early event during adjuvant arthritis and that the highest amounts are produced during the inflammatory phase of the disease. mRNA changes in the acute phase proteins alpha 1-AGP and albumin, which are mainly regulated by IL-1/TNF alpha, were more pronounced than those of alpha 2-MG and beta-fibrinogen, which are predominantly controlled by IL-6.(ABSTRACT TRUNCATED AT 250 WORDS)

Published
1992

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