Induction and inhibition of cytochromes P450 by the St. John's wort constituent hyperforin in human hepatocyte cultures

Drug Metab Dispos. 2004 May;32(5):512-8. doi: 10.1124/dmd.32.5.512.


St. John's wort extract (SJW) (Hypericum perforatum L.) is among the most commonly used herbal medications in the United States. The predominance of clinical reports indicates that SJW increases the activity of cytochrome P450 3A4 (CYP3A4) enzyme and reduces plasma concentrations of certain drugs. Although the inductive effect of SJW on CYP3A4 is clear, other reports indicate that SJW constituents may have, to a small degree, some enzyme inhibitory effects. Therefore, we sought to study the induction and inhibition effects of the constituents of SJW on CYP3A4 in the human hepatocyte model. Moreover, most research has focused on the induction of CYP3A4 by SJW with little attention paid to other prominent drug-metabolizing enzymes such as CYP1A2, CYP2C9, and CYP2D6. To examine the effects of SJW on CYP1A2, CYP2C9, CYP2D6, as well as CYP3A4, hepatocytes were exposed to hyperforin and hypericin, the primary constituents of SJW extract. Hepatocytes treated with hypericin or hyperforin were exposed to probe substrates to determine enzyme activity and protein and RNA harvested. Hyperforin treatment resulted in significant increases in mRNA, protein, and activity of CYP3A4 and CYP2C9, but had no effect on CYP1A2 or CYP2D6. Acute administration of hyperforin at 5 and 10 microM 1 h before and along with probe substrate inhibited CYP3A4 activity. Hypericin had no effect on any of the enzymes tested. These results demonstrate that with chronic exposure, the inductive effect of SJW on drug-metabolizing enzymes predominates, and human hepatocyte cultures are a versatile in vitro tool for screening the effect of herbal products on cytochrome P450 enzymes.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Bridged Bicyclo Compounds / pharmacology*
  • Cells, Cultured
  • Cytochrome P-450 Enzyme Inhibitors*
  • Cytochrome P-450 Enzyme System / biosynthesis*
  • Dose-Response Relationship, Drug
  • Enzyme Induction / drug effects
  • Enzyme Induction / physiology
  • Enzyme Inhibitors / pharmacology
  • Hepatocytes / drug effects*
  • Hepatocytes / enzymology*
  • Humans
  • Hypericum*
  • Phloroglucinol / analogs & derivatives*
  • Phloroglucinol / pharmacology*
  • RNA, Messenger / biosynthesis
  • Terpenes / pharmacology*


  • Bridged Bicyclo Compounds
  • Cytochrome P-450 Enzyme Inhibitors
  • Enzyme Inhibitors
  • RNA, Messenger
  • Terpenes
  • Cytochrome P-450 Enzyme System
  • Phloroglucinol
  • hyperforin