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Mixed function oxidase and UDP-glucuronyltransferase activities in the human Hep G2 hepatoma cell line

  • M H Grant
  • , S J Duthie
  • , A G Gray
  • , M D Burke

Research output: Contribution to journalArticlepeer-review

Abstract

In cultured human hepatoma cells phenolphthalein glucuronidation was increased 3-fold by 2 mM phenobarbitone (PB) in the culture medium but not by 25 microM benz(a)anthracene (BA), while 1-naphthol glucuronidation was not increased by either PB or BA. Ethoxyresorufin O-deethylation (EROD) was increased 15-fold by BA but not by PB, while the O-dealkylations of pentoxyresorufin (PROD) and benzyloxyresorufin (BROD) were increased by either PB or BA. The BROD activity increased by BA was sensitive to inhibition by alpha-naphthoflavone whereas that induced by PB was not. This suggests induction of different cytochrome P-450 isoenzymes. Control Hep G2 cells had similar glucuronide conjugation and cytochrome reductase activities to freshly isolated human adult hepatocytes, but had lower O-dealkylation and elevated microsomal epoxide hydrolase activities.
Original languageEnglish
Pages (from-to)4111-6
Number of pages6
JournalBiochemical Pharmacology
Volume37
Issue number21
Publication statusPublished - 1988

Keywords

  • Carcinoma, Hepatocellular
  • Cytochrome P-450 CYP2B1
  • Epoxide Hydrolases
  • Glucuronosyltransferase
  • Humans
  • Liver
  • Liver Neoplasms
  • Mixed Function Oxygenases
  • Oxazines
  • Oxidation-Reduction
  • Oxidoreductases
  • Tumor Cells, Cultured

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