3,4-N-methlenedioxymethamphetamine-induced hypophagia is maintained in 5-HT1B receptor knockout mice, but suppressed by the 5-HT2C receptor antagonist RS102221

Neuropsychopharmacology. 2005 Jun;30(6):1056-63. doi: 10.1038/sj.npp.1300662.

Abstract

3,4-Methylenedioxy-N-methamphetamine (MDMA or 'ecstasy') is a psychoactive substance, first described as an appetite suppressant in humans, inducing side effects and even death. MDMA increases serotonin (5-HT) levels, and 5-HT inhibits food intake, but the 5-HT receptors involved in MDMA-induced changes in feeding behavior are unknown. We examined whether a systemic MDMA injection would reduce the physiological drive to eat in starved mice and tested if the inactivation of 5-HT1B or 5-HT2C receptors could restore this response. Our results indicate that in starved mice, MDMA (10 mg/kg) provoked an initial hypophagia for 1 h (-77%) followed by a period of hyperphagia (studied between 1 and 3 h). This biphasic feeding behavior due to MDMA treatment was maintained in 5-HT1B receptor-null mice or in animals treated with the 5-HT1B/1D receptor antagonist GR127935 (3 or 10 mg/kg). In contrast, MDMA-induced hypophagia (for the first 1 h period) was suppressed when combined with the 5-HT2C receptor antagonist RS102221 (2 mg/kg). However, RS102221 did not alter MDMA-induced hyperphagia (for the 1-3 h period) but did exert a stimulant effect, when administered alone, during that period. We have previously shown that MDMA or 5-HT1A/1B receptor agonist RU24969 fails to stimulate locomotor activity in 5-HT1B receptor-null mice. Our present data indicate that the 5-HT2C receptor antagonist RS102221 suppresses MDMA-induced hyperlocomotion. These findings provide the first evidence that the inactivation of 5-HT2C receptors may reduce hypophagia and motor response to MDMA, while a genetic deficit or pharmacological inactivation of 5-HT1B receptors was insufficient to alter the feeding response to MDMA.

MeSH terms

  • Animals
  • Body Weight / drug effects
  • Eating / drug effects
  • Hallucinogens / antagonists & inhibitors
  • Hallucinogens / pharmacology*
  • Kinetics
  • Male
  • Mice
  • Mice, Knockout
  • N-Methyl-3,4-methylenedioxyamphetamine / antagonists & inhibitors
  • N-Methyl-3,4-methylenedioxyamphetamine / pharmacology*
  • Oxadiazoles / pharmacology
  • Piperazines / pharmacology
  • Receptor, Serotonin, 5-HT1B / genetics
  • Receptor, Serotonin, 5-HT1B / physiology*
  • Receptor, Serotonin, 5-HT2C / drug effects*
  • Serotonin Antagonists / pharmacology*
  • Spiro Compounds / pharmacology*
  • Starvation / psychology
  • Sulfonamides / pharmacology*

Substances

  • 8-(5-(5-amino-2,4-dimethoxyphenyl)-5-oxopentyl)-1,3,8-triazaspiro(4.5)decane-2,4-dione
  • Hallucinogens
  • Oxadiazoles
  • Piperazines
  • Receptor, Serotonin, 5-HT1B
  • Receptor, Serotonin, 5-HT2C
  • Serotonin Antagonists
  • Spiro Compounds
  • Sulfonamides
  • GR 127935
  • N-Methyl-3,4-methylenedioxyamphetamine