Inhibitory action of L-type Ca2+ current by paeoniflorin, a major constituent of peony root, in NG108-15 neuronal cells

Eur J Pharmacol. 2005 Oct 31;523(1-3):16-24. doi: 10.1016/j.ejphar.2005.08.042. Epub 2005 Oct 21.

Abstract

The effects of paeoniflorin, a glycoside isolated from the root of Paeonia lactiflora, on ion currents in a mouse neuroblastoma and rat glioma hybrid cell line, NG108-15 were investigated. Paeoniflorin (1-300 microM) reversibly produced an inhibition of L-type voltage-dependent Ca2+ current (I(Ca,L)) in a concentration-dependent manner. Paeoniflorin caused no change in the overall shape of the current-voltage relationship of I(Ca,L). The IC50 value of paeoniflorin-induced inhibition of I(Ca,L) was 14 microM. However, neither adenosine deaminase (1 U/ml) nor 8-cyclopentyl-1, 3-dipropylxanthine (10 microM) could reverse the inhibition by paeoniflorin of I(Ca,L). Paeoniflorin (30 microM) shifted the steady-state inactivation curve of I(Ca,L) to more negative membrane potentials by approximately -10 mV. It also prolonged the recovery of I(Ca,L). The inhibitory effect of paeoniflorin on I(Ca,L) exhibited tonic and use-dependent characteristics. Paeoniflorin could effectively suppress I(Ca,L) evoked by action potential waveforms. Paeoniflorin at a concentration of 30 microM produce a slight inhibition of voltage-dependent Na+ current and delayed rectifier K+ current. Under current-clamp configuration, unlike adenosine, this compound decreased the firing of action potentials. Taken together, this study indicates that paeoniflorin can block L-type Ca2+ channels in NG108-15 cells in a mechanism unlinked to the binding to adenosine receptors. The effects of paeoniflorin on ion currents may partly, if not entirely, contribute to the underlying mechanisms through which it affects neuronal or neuroendocrine function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / drug effects
  • Animals
  • Benzoates / isolation & purification
  • Benzoates / pharmacology*
  • Bridged-Ring Compounds / isolation & purification
  • Bridged-Ring Compounds / pharmacology*
  • Calcium Channel Blockers / isolation & purification
  • Calcium Channel Blockers / pharmacology*
  • Calcium Channels, L-Type / drug effects*
  • Calcium Channels, L-Type / metabolism
  • Calcium Signaling / drug effects*
  • Delayed Rectifier Potassium Channels / drug effects
  • Delayed Rectifier Potassium Channels / metabolism
  • Dose-Response Relationship, Drug
  • Glucosides / isolation & purification
  • Glucosides / pharmacology*
  • Mice
  • Monoterpenes
  • Neurons / drug effects
  • Neurons / metabolism
  • Paeonia / chemistry*
  • Plant Roots
  • Potassium / metabolism
  • Rats
  • Sodium / metabolism
  • Sodium Channels / drug effects
  • Sodium Channels / metabolism
  • Time Factors
  • Tumor Cells, Cultured

Substances

  • Benzoates
  • Bridged-Ring Compounds
  • Calcium Channel Blockers
  • Calcium Channels, L-Type
  • Delayed Rectifier Potassium Channels
  • Glucosides
  • Monoterpenes
  • Sodium Channels
  • peoniflorin
  • Sodium
  • Potassium