Lipophilic beta-adrenoceptor antagonists stimulate cholesterol biosynthesis in human skin fibroblasts

Biochem Pharmacol. 1987 Jun 15;36(12):1901-6. doi: 10.1016/0006-2952(87)90486-2.

Abstract

The effect of a series of beta-adrenoceptor antagonists on cholesterol biosynthesis was studied in vitro in normal human skin fibroblasts. Some, but not all, of the drugs studied stimulated the incorporation of [2-14C]-acetate into cell sterols in a dose-dependent manner. This effect was unrelated to beta-blocking potency, selectivity for beta 1 or beta 2 adrenoceptors and partial agonistic activity of the drugs, thus ruling out a beta-receptor mediated mechanism. A positive, statistically significant correlation was found, however, between the drug lipophilicity and the stimulation of sterol biosynthesis. Propranolol, the most effective agent in increasing [2-14C]-acetate incorporation into cellular sterols, also enhanced the conversion of 3-hydroxy-3-methylglutaryl CoA (HMGCoA) into mevalonic acid, suggesting an interference of lipophilic beta-adrenoceptor antagonists with HMHCoA-reductase, the feed-back regulated rate limiting step of cholesterol biosynthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology*
  • Cholesterol / biosynthesis*
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Humans
  • Hydroxymethylglutaryl CoA Reductases / metabolism
  • Labetalol / pharmacology
  • Metoprolol / pharmacology
  • Pindolol / pharmacology
  • Propanolamines / pharmacology
  • Propranolol / pharmacology
  • Skin / drug effects
  • Skin / metabolism*
  • Stereoisomerism

Substances

  • Adrenergic beta-Antagonists
  • Propanolamines
  • ICI 118551
  • Cholesterol
  • Propranolol
  • Pindolol
  • Hydroxymethylglutaryl CoA Reductases
  • Metoprolol
  • Labetalol