Noradrenaline inhibits the programmed cell death induced by 1,25-dihydroxyvitamin D3 in glioma

Eur J Pharmacol. 1997 Jan 29;319(2-3):365-8. doi: 10.1016/s0014-2999(96)00942-9.

Abstract

The rat glioma cell line C6.9 has been recently reported to respond to 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) by the induction of a programmed cell death. Since, in vivo, glial cells are thought to be exposed to several neurotransmitters, we investigated the possibility of a neurotransmitter-mediated inhibition of this active cell death process. Noradrenaline and the beta-adrenoceptor agonist isoproterenol showed significant inhibition of the 1,25(OH)2D3-induced programmed cell death. The beta-adrenoceptor antagonist propanolol reversed this inhibition, while the alpha-adrenoceptor antagonist yohimbin was devoid of any effect. This suggests that the efficiency of antiproliferative vitamin D-related therapies could be influenced by endogenous levels of noradrenaline.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Agonists / pharmacology
  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Apoptosis / drug effects*
  • Brain Neoplasms / pathology*
  • Calcitriol / antagonists & inhibitors*
  • Calcitriol / toxicity
  • DNA Fragmentation / drug effects
  • Glioma / pathology*
  • Isoproterenol / pharmacology
  • Neurotransmitter Agents / pharmacology
  • Norepinephrine / pharmacology*
  • Propranolol / pharmacology
  • Rats
  • Tumor Cells, Cultured

Substances

  • Adrenergic beta-Agonists
  • Adrenergic beta-Antagonists
  • Neurotransmitter Agents
  • Propranolol
  • Calcitriol
  • Isoproterenol
  • Norepinephrine