Electrophysiological characterization of the effect of long-term duloxetine
administration on the rat serotonergic and noradrenergic systems
by
Rueter LE, De Montigny C, Blier P
Department of Psychiatry,
McGill University, Montreal, Quebec, Canada.
J Pharmacol Exp Ther 1998 May;285(2):404-12
ABSTRACT
Duloxetine is a dual serotonin (5-HT)/norepinephrine (NE) re-uptake blocker
with antidepressant potential. In the present in vivo electrophysiological
study, the changes in the function of the rat 5-HT and NE systems after 2- and
21-day administration of duloxetine (20 mg/kg/day) were assessed in the dorsal
hippocampus and the dorsal raphe nucleus (DRN). The firing rate of DRN neurons
was decreased after 2 days of duloxetine, but returned to the control level
after 21-day administration. This recovery of firing rate was presumably due to
the desensitization of the DRN somatodendritic 5-HT1A autoreceptors found after
long-term duloxetine administration. Overall serotonergic tone was assessed by
examining the ability of the 5-HT1A antagonist WAY 100635 to alter hippocampal
firing. WAY 100635 increased hippocampal firing rates in 21-day treated rats to
a greater extent than in 2-day treated or control rats, suggesting that
long-term administration induced an increase in endogenous levels of 5-HT in
postsynaptic regions. This increase in 5-HT levels was accompanied by selective
changes in the 5-HT and NE systems induced by long-term duloxetine
administration, i.e., the desensitization of the alpha-2 adrenergic
heteroreceptor on 5-HT terminals and the continued blockade of the 5-HT
transporters. In contrast, the sensitivity of the alpha-2 adrenergic and
terminal 5-HT1B autoreceptors, as well as that of the postsynaptic 5-HT1A
receptor after 21-day treatment was unchanged. Therefore, this study
demonstrates that duloxetine increases serotonergic tone in a limbic forebrain
structure and may therefore be effective in the treatment of depression.
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