Effect of valproic acid on serotonin-2A receptor signaling in C6 glioma cells

J Neurochem. 2004 Sep;90(5):1269-75. doi: 10.1111/j.1471-4159.2004.02690.x.

Abstract

Valproic acid (VPA), which has demonstrated efficacy in the treatment of bipolar disorder, has been shown to alter components of the phosphoinositide (PI) signaling cascade and to increase gene expression mediated by the transcription factor activator protein 1 (AP-1). Central serotonin-2A (5-HT2A) receptors, which have been implicated in the pathophysiology of manic-depressive illness, are coupled to PI hydrolysis. The promoter region of the 5-HT2A receptor gene contains AP-1 binding sites. We examined in C6 glioma cells the effect of VPA on 5-HT2A receptor signaling. Treatment of cells with VPA (100 microg/mL) for 20 h, but not 1.5 h, resulted in an enhancement of 5-HT2A receptor-stimulated PI hydrolysis. This effect of 20-h VPA exposure appeared not to be at the level of G protein or effector (i.e. phospholipase C: PLC) as inositol phosphate accumulation stimulated by aluminum fluoride or the PLC activator 2,4,6-trimethyl-N-(m-3-trifluromethylphenyl) benzenesulfonamide was not increased. The number of 5-HT2A receptors, as determined in saturation binding experiments using [3H]ketanserin, was increased by 20-h VPA treatment, with no change in affinity (KD). Taken together, our data suggest that the increase in 5-HT2A receptor-mediated PI hydrolysis following 20-h VPA exposure is not due to a general effect of VPA on this signaling cascade, but due to the up-regulation of 5-HT2A receptor number.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Anticonvulsants / pharmacology
  • Binding Sites / drug effects
  • Cell Line
  • Dose-Response Relationship, Drug
  • Glioma / pathology
  • Ketanserin / pharmacokinetics
  • Mice
  • Phosphatidylinositols / metabolism
  • Quipazine / pharmacology
  • Receptor, Serotonin, 5-HT2A / physiology*
  • Signal Transduction / drug effects*
  • Signal Transduction / physiology
  • Time Factors
  • Tritium / pharmacokinetics
  • Valproic Acid / pharmacology*

Substances

  • Anticonvulsants
  • Phosphatidylinositols
  • Receptor, Serotonin, 5-HT2A
  • Tritium
  • Quipazine
  • Valproic Acid
  • Ketanserin