Interferon- and streptolysin O-induced activation of protein kinases and inhibition of cytochrome P450-dependent monooxygenases in rats

Pharmazie. 1998 Apr;53(4):268-71.

Abstract

Immunostimulants known to initiate cytokine production were found to decrease the activity of hepatic microsomal drug oxidative enzymes but to activate protein kinase C (PKC). The present study investigated the effects of immunostimulating doses of rat interferon-gamma (IFN, 670,000 units i.p.) and streptolysin O (SLO, 100 HU/kg i.v. for 5 days) on hepatic soluble, membrane-bound and nuclear PKC, 7-ethylresorufin-O-deethylase (EROD) and 7-pentylresorufin-O-deethylase (PROD) in male Wistar rats. The SLO- and IFN-mediated decrease of EROD and PROD activity was associated with a characteristic activation of the hepatic and spleenic PKC. In SLO- and IFN-treated animals activities of the cytosolic, membrane-bound and nuclear PKC were significantly higher than in respective controls. Our results suggest that a decrease in hepatic cytochrome P450 content as well as the decrease in the EROD and PROD activities are inversely related to the function of PKC.

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology*
  • Bacterial Proteins
  • Cytochrome P-450 Enzyme Inhibitors*
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology*
  • Interferon-gamma / pharmacology*
  • Isoenzymes / metabolism
  • Liver / drug effects
  • Liver / enzymology
  • Male
  • Membranes / drug effects
  • Membranes / enzymology
  • Mixed Function Oxygenases / antagonists & inhibitors*
  • Organ Size / drug effects
  • Protein Kinase C / metabolism
  • Protein Kinases / metabolism*
  • Rats
  • Rats, Wistar
  • Recombinant Proteins
  • Spleen / drug effects
  • Spleen / enzymology
  • Streptolysins / pharmacology*

Substances

  • Antineoplastic Agents
  • Bacterial Proteins
  • Cytochrome P-450 Enzyme Inhibitors
  • Enzyme Inhibitors
  • Isoenzymes
  • Recombinant Proteins
  • Streptolysins
  • streptolysin O
  • Interferon-gamma
  • Mixed Function Oxygenases
  • Protein Kinases
  • Protein Kinase C