Cell-based assay for screening 11beta-hydroxysteroid dehydrogenase inhibitors using liquid chromatography/tandem mass spectrometry detection

Rapid Commun Mass Spectrom. 2006;20(11):1643-7. doi: 10.1002/rcm.2484.

Abstract

Cortisol is an important glucocorticoid that regulates many physiological pathways by activating various intracellular receptors. The type 1 isozyme of 11beta-hydroxysteroid dehydrogenase (11beta-HSD1) functions in vivo predominantly as a reductase by converting cortisone into cortisol. A high-throughput liquid chromatography/tandem mass spectrometry (LC/MS/MS) method has been developed to screen for inhibitors of 11beta-HSD1 by monitoring cortisol and cortisone simultaneously. The injection cycle time can be as fast as 1 min/sample, making it amenable to the analysis of large numbers of the cell-assay samples in the screening of 11beta-HSD inhibitors. The reductase and dehydrogenase activities of 11beta-HSD1 are assessed separately.

MeSH terms

  • 11-beta-Hydroxysteroid Dehydrogenases / antagonists & inhibitors*
  • 11-beta-Hydroxysteroid Dehydrogenases / genetics
  • Animals
  • Calibration
  • Cells, Cultured
  • Chromatography, High Pressure Liquid
  • Cortisone / analysis*
  • Drug Evaluation, Preclinical
  • Enzyme Inhibitors / pharmacology*
  • HeLa Cells
  • Humans
  • Hydrocortisone / analysis*
  • Mice
  • Rats
  • Tandem Mass Spectrometry

Substances

  • Enzyme Inhibitors
  • 11-beta-Hydroxysteroid Dehydrogenases
  • Cortisone
  • Hydrocortisone