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Vol. 299, Issue 3, 849-857, December 2001
Departments of Pharmacology (J.M.R., D.A.F.), Oncology (M.D.J.,
M.E.L.), and Medicine (M.E.L., D.A.F.), Division of Clinical
Pharmacology, Georgetown University Medical Center, Washington, DC
We used expression microarrays to test the effects of rifampin on the
overall pattern of mRNA expression of multiple metabolic enzymes in
primary human hepatocytes. Two microarrays were utilized, a cDNA-based
array and one that is oligonucleotide-based. The cDNA-based expression
arrays showed that rifampin caused a 7.7 ± 6.6-fold induction in
CYP2A6 and a 4.0 ± 2.0-fold increase in the CYP2C family of
enzymes while having little effect on CYP2E1 or CYP2D6. Many non-P450
enzymes were also induced including FMO-4 and -5, UGT-1A, MAO-B, and
GST-P1. The oligonucleotide-based array made it possible to detect
different levels of induction within the CYP2C family, with rifampin
causing a 6.5-fold increase in expression of CYP2C8 and a 3.7-fold
increase in CYP2C9 while having no effect on the level of CYP2C18 mRNA.
Rifampin also induced other CYP enzymes including CYP2B6 and all three
members of the CYP3A family, with CYP3A4 showing the highest level of
induction at 55.1-fold. RNase protection assays were used to validate
results from the arrays and a comparison of all three methods of mRNA detection showed qualitatively similar results. These data make it
clear that rifampin treatment brings about broad changes in the pattern
of gene expression, rather than increased expression of a small number
of metabolic enzymes. Clinicians and researchers who use and study
rifampin and other drugs that induce drug metabolism should be alert to
the possibility of multiple effects.
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