Effect of interleukin 6 on the hepatic metabolism of itraconazole and its metabolite hydroxyitraconazole using primary human hepatocytes

Paul O. Gubbins, Russell B. Melchert, Scott A. McConnell, Amy M. Franks, Scott R. Penzak, Bill J. Gurley

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

A potential cytokine-drug interaction between interleukin 6 (IL-6) and itraconazole (ITZ) was studied using human hepatocytes in primary culture. Cultures from 5 adult males (mean age 42 ± 15 years) who had not received any medicines known to interact with CYP3A4 were studied. Cultures were exposed to ITZ 500 ng/ml, and the effects of 120 μg/ml cimetidine, 50 ng/ml human IL-6, or IL-6 plus IL-6 receptor antagonist were analyzed for 2, 4, 8, and 12 h. Intracellular ITZ and hydroxyitraconazole concentrations were measured using HPLC and normalized to total cellular protein. Mean intracellular concentrations between groups were compared using one-way Anova (f test; p<0.10) and corresponding Bonferroni versus control test for multiple comparisons (p<0.02). Mean intracellular ITZ concentrations between the groups were similar at all time points. Human hepatocytes in primary culture can metabolize ITZ. However, IL-6 did not inhibit hydroxyitraconazole formation, but it may inhibit its subsequent metabolism.

Original languageEnglish
Pages (from-to)195-201
Number of pages7
JournalPharmacology
Volume67
Issue number4
DOIs
StatePublished - 2003

Keywords

  • Drug metabolism
  • Interleukin 6
  • Itraconazole

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