Long-term citalopram maintenance in mice: selective reduction of alcohol-heightened aggression.

Academic Article

Abstract

  • BACKGROUND: Selective serotonin reuptake inhibitors (SSRIs) alleviate many affective disturbances in human clinical populations and are used in animal models to study the influence of serotonin (5-HT) on aggressive behavior and impulsivity. OBJECTIVE: We hypothesized that long-term SSRI treatment may reduce aggressive behavior escalated by alcohol consumption in mice. Therefore, aggression was tested in male CFW mice to determine whether repeated citalopram (CIT) administration reduces alcohol-heightened aggression. MATERIALS AND METHODS: Resident male mice self-administered alcohol by performing an operant response on a panel placed in their home cage that delivered a 6% alcohol solution. Mice repeatedly confronted an intruder 15 min after self-administration of either 1 g/kg alcohol (EtOH) or water (H(2)O). Aggressive behaviors were higher in most mice when tests occurred after EtOH intake relative to H(2)O. Once baseline aggression was established, animals were injected (i.p.) twice daily with 10 mg/kg CIT or saline (SAL) for 32 days. Every 4 days throughout the CIT treatment period, aggressive encounters occurred 6 h after CIT injections, with testing conditions alternating between EtOH and H(2)O intake. RESULTS: Aggression was only modestly affected by CIT in the first 2 weeks of treatment. However, by day 17 of CIT treatment, alcohol-heightened aggressive behavior was abolished, while baseline aggression remained stable. These data lend support for the role of the 5-HT transporter in the control of alcohol-related aggressive behavior, and the time course of effects suggests that a change in density of 5HT(1A) autoreceptors is necessary before antidepressant drugs produce beneficial outcomes.
  • Authors

  • Caldwell, Elizabeth
  • Miczek, Klaus A
  • Status

    Publication Date

  • February 2008
  • Published In

  • Psychopharmacology  Journal
  • Keywords

  • Aggression
  • Animals
  • Behavior, Animal
  • Central Nervous System Depressants
  • Citalopram
  • Conditioning, Operant
  • Disease Models, Animal
  • Ethanol
  • Injections, Intraperitoneal
  • Male
  • Mice
  • Receptor, Serotonin, 5-HT1A
  • Serotonin Plasma Membrane Transport Proteins
  • Serotonin Uptake Inhibitors
  • Time Factors
  • Digital Object Identifier (doi)

    Pubmed Id

  • 17952412
  • Start Page

  • 407
  • End Page

  • 416
  • Volume

  • 196
  • Issue

  • 3