Regulation of serotonin 5-HT2C receptors by chronic ligand exposure

Eur J Pharmacol. 2004 Sep 13;498(1-3):59-69. doi: 10.1016/j.ejphar.2004.07.102.

Abstract

The effect of ligand pretreatment on human 5-hydroxytryptamine2C (5-HT2C) receptors was examined in CHO cells expressing high (CHO-1C7; 67+/-3 pmol/mg) or low (CHO-1C19; 72+/-10 fmol/mg) levels of the receptor. Seventy-two hours pretreatment of CHO-1C7 cells with various ligands did not affect receptor expression. Pretreatment with inverse agonists enhanced 5-HT-mediated inositol phosphate accumulation with no change in constitutive receptor activity. The enhanced agonist responsiveness was inversely correlated with the intrinsic activity of the pretreatment ligand. Seventy-two hours of pretreatment with the weak agonist, 5-methoxygramine, caused an elevation in constitutive activity but no alteration in 5-HT-mediated signaling. In CHO-1C19 cells, 24 but not 72 h of pretreatment with the inverse agonist mianserin enhanced 5-HT-mediated signaling, with no effect on basal signaling; pretreatment with 5-methoxygramine had no significant effect. These findings highlight differences in the pattern of chronic regulation of 5HT2C receptor signaling between high and low receptor expression levels in a common cellular background.

Publication types

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

MeSH terms

  • Algorithms
  • Analysis of Variance
  • Animals
  • Binding, Competitive / drug effects
  • CHO Cells
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Chlorpromazine / pharmacology
  • Cricetinae
  • Cricetulus
  • Dose-Response Relationship, Drug
  • Ergolines / metabolism*
  • Humans
  • Indoles / pharmacology
  • Indophenol / analogs & derivatives*
  • Indophenol / pharmacology
  • Inositol Phosphates / metabolism
  • Kinetics
  • Ligands
  • Lisuride / pharmacology
  • Mianserin / pharmacology
  • Radioligand Assay
  • Receptor, Serotonin, 5-HT2C / genetics
  • Receptor, Serotonin, 5-HT2C / metabolism*
  • Ritanserin / pharmacology
  • Serotonin / pharmacology
  • Serotonin Antagonists / pharmacology
  • Serotonin Receptor Agonists / pharmacology
  • Tritium
  • Tryptamines / pharmacology

Substances

  • Ergolines
  • Indoles
  • Inositol Phosphates
  • Ligands
  • Receptor, Serotonin, 5-HT2C
  • Serotonin Antagonists
  • Serotonin Receptor Agonists
  • Tryptamines
  • dimethoxy-4-indophenyl-2-aminopropane
  • Tritium
  • Ritanserin
  • methoxygramine
  • Mianserin
  • Serotonin
  • Indophenol
  • Lisuride
  • mesulergine
  • Chlorpromazine