O. Rilke et al., Behavioral and neurochemical effects of anpirtoline and citalopram in isolated and group housed mice, PROG NEUR-P, 25(5), 2001, pp. 1125-1144
Citations number
46
Categorie Soggetti
Neurosciences & Behavoir
Journal title
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
1. Acute effects of serotonergic drugs acting via different mechanisms were
investigated by a social interaction test and subsequent determination of
serotonin and dopamine metabolisms in mice housed in groups or isolated for
G weeks.
2. A resident / intruder test was performed with anpirtoline (5-HT1B recept
or agonist in rodents; 1 mg/kg), citalopram (SSRI; 0.5 mg/kg) and saline tr
eatment before animals were decapitated and different brain regions were fr
ozen for subsequent HPLC-analyses.
3. Behavioral investigations indicated a strong increase of aggressive beha
vior after 6 weeks of isolation housing. Acute citalopram treatment did not
influence behavioral parameters of isolated and group housed mice. In cont
rast, anpirtoline antagonized isolation induced aggressive behavioral compo
nents in a specific manner.
4. Analysis of dopamine and serotonin metabolism revealed that citalopram t
reatment did not affect dopamine metabolism, but reduced serotonin metaboli
sm in the striatum, hippocampus, cortex and midbrain independent of housing
conditions.
5. In contrast, anpirtoline treatment increased dopamine metabolism in cort
ex, striatum and midbrain as well as influenced serotonin metabolism in a s
tructure- and state-specific manner. Whereas anpirtoline decreased serotoni
n metabolism in the cortex, the midbrain and the hippocampus independent of
housing conditions, in the striatum anpirtoline abolished the isolation in
duced decrease of serotonin metabolism.
6. These results indicate that anpirtoline might induce antiaggressive effe
cts via postsynaptic receptor- and structure- specific activation of seroto
nergic but also dopaminergic processes, whereas structure independent incre
ase of synaptic serotonin via citalopram was ineffective to reverse aggress
ivity in isolated mice.