Adrenaline facilitates calcium channel currents in osteoblasts

Bull Tokyo Dent Coll. 2014;55(3):163-7. doi: 10.2209/tdcpublication.55.163.

Abstract

Adrenaline (Adr) is known to directly or indirectly modulate bone cell activity under physiological and pathological conditions. Osteoblasts play a major role in bone formation, employing intracellular Ca(2+) as a second messenger to modulate hormonal responses and as a cofactor for mineralization. Voltage-dependent Ca(2+) channels (VDCCs) mediate the influx of Ca(2+) in response to membrane depolarization. The purpose of this study was to investigate the effects of Adr on VDCC currents in osteoblasts using a patch-clamp recording method. Application of 1 mM Adr facilitated VDCC currents in a concentration-dependent manner. Pre-treatment with b receptor antagonist propranolol blocked Adr-induced facilitation of VDCC currents carried by Ba(2+) (IBa). These results indicate that Adr-induced facilitation of IBa was mediated by b receptors in MC3T3-E1 osteoblast-like cells. To our knowledge, the data presented here demonstrate for the first time that Adr facilitates VDCCs in MC3T3-E1 osteoblast-like cells.

MeSH terms

  • 3T3 Cells
  • Adrenergic alpha-1 Receptor Antagonists / pharmacology
  • Adrenergic beta-Agonists / administration & dosage
  • Adrenergic beta-Agonists / pharmacology*
  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Barium / metabolism
  • Calcium Channels / drug effects*
  • Calcium Signaling / drug effects*
  • Dose-Response Relationship, Drug
  • Epinephrine / administration & dosage
  • Epinephrine / pharmacology*
  • Mice
  • Osteoblasts / drug effects*
  • Patch-Clamp Techniques
  • Prazosin / pharmacology
  • Propranolol / pharmacology
  • Signal Transduction / drug effects

Substances

  • Adrenergic alpha-1 Receptor Antagonists
  • Adrenergic beta-Agonists
  • Adrenergic beta-Antagonists
  • Calcium Channels
  • Barium
  • Propranolol
  • Prazosin
  • Epinephrine