The effects of CGS 16949A, an aromatase inhibitor on adrenal mineralocorticoid biosynthesis

J Clin Endocrinol Metab. 1990 Apr;70(4):1162-6.

Abstract

The family of cytochrome P450 enzymes that mediates steroid hydroxylations are distinct but structurally related proteins. Inhibitors of these steroidogenic steps generally exhibit only relative and dose-related specificity. We evaluated an imidazole, cytochrome P450-related inhibitor, CGS 16949A, in postmenopausal patients with metastatic breast cancer. While a relatively specific aromatase inhibitor at daily dosages of 1-2 mg, CGS 16949A significantly blunted cortisol responses to ACTH at a dose of 16 mg daily. To further evaluate other inhibitory effects of this drug, we determined blood levels of aldosterone (ALDO) and 18-hydroxycorticosterone and their respective urinary metabolites, tetrahydroaldosterone and tetrahydro-18-hydroxy-11-dehydrocorticosterone in 16 postmenopausal women receiving CGS 16949A. At a dose of 16 mg/day, CGS 16949A produced significant (P less than 0.001) suppression of both basal and ACTH-stimulated ALDO production. This was accompanied by a significant rise in the blood 18-hydroxycorticosterone/ALDO ratio (11.4 +/- 0.19; normal, less than 2; P less than 0.001), consistent with a corticosterone methyloxidase type II inhibition. A similar significant elevation (7.5 +/- 1.2; normal, less than 5; P less than 0.001) in the urinary tetrahydro-18-hydroxy-11-dehydrocorticosterone/tetrahydroaldosterone ratio was also observed. These results suggest that CGS 16949A is a potent inhibitor of the corticosterone methyloxidase type II enzyme at a dose of 16 mg daily. At doses of 1-2 mg daily, CGS 16949A blocks aromatase without altering basal aldosterone production and, thus, exhibits dose-related specificity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 18-Hydroxycorticosterone / analysis
  • Adrenal Cortex / drug effects*
  • Adrenal Cortex / metabolism
  • Adrenocorticotropic Hormone
  • Aged
  • Aldosterone / analogs & derivatives
  • Aldosterone / analysis
  • Aldosterone / biosynthesis*
  • Aromatase Inhibitors*
  • Binding Sites / drug effects
  • Breast Neoplasms / analysis
  • Breast Neoplasms / enzymology
  • Breast Neoplasms / secondary
  • Chemical Phenomena
  • Chemistry
  • Cytochrome P-450 CYP11B2*
  • Cytochrome P-450 Enzyme Inhibitors
  • Electrolytes / blood
  • Electrolytes / urine
  • Fadrozole
  • Female
  • Humans
  • Hydrocortisone / analysis
  • Imidazoles / pharmacology*
  • In Vitro Techniques
  • Mineralocorticoids / biosynthesis*
  • Mineralocorticoids / blood
  • Mineralocorticoids / urine
  • Mixed Function Oxygenases / antagonists & inhibitors
  • Nitriles / pharmacology*

Substances

  • Aromatase Inhibitors
  • Cytochrome P-450 Enzyme Inhibitors
  • Electrolytes
  • Imidazoles
  • Mineralocorticoids
  • Nitriles
  • tetrahydroaldosterone
  • Aldosterone
  • 18-Hydroxycorticosterone
  • Adrenocorticotropic Hormone
  • Mixed Function Oxygenases
  • Cytochrome P-450 CYP11B2
  • corticosterone methyl oxidase II
  • Fadrozole
  • Hydrocortisone