We studied the effect of 3 weeks treatment with the selective serotoni
n re-uptake inhibitor (SSRI), paroxetine (30 mg daily), on the neuroen
docrine and hyperthermic responses to the 5-HT2C receptor agonist, m-c
hlorophenylpiperazine (mCPP) (0.05 mg/kg IV), in seven healthy volunte
ers. Following paroxetine treatment, both the prolactin and hypertherm
ic responses to mCPP were significantly attenuated. These data are con
sistent with experimental animal studies indicating that repeated SSRI
treatment leads to a functional desensitisation of 5-HT2C receptors.
This effect may be linked to the anxiolytic properties of SSRIs.