Preclinical pharmacology
of milnacipran
by
Briley M, Prost JF, Moret C
Centre de Recherche Pierre Fabre,
Castres, France.
Int Clin Psychopharmacol 1996 Sep;11 Suppl 4:9-14
ABSTRACT
Milnacipran (Ixel) is a new antidepressant which has been developed for its
selective inhibition of both serotonin and noradrenaline reuptake and its lack
of affinity for neurotransmitter receptors. It inhibits virtually equipotently
the reuptake of serotonin and noradrenaline both in vitro and in vivo, as
demonstrated by the antagonism of centrally acting monoamine displacers. It has
no effect on dopamine reuptake. In addition, milnacipran has been shown by
intracerebral microdialysis to increase the extracellular levels of both
serotonin and noradrenaline after acute administration. Milnacipran is devoid of
interactions at any known neurotransmitter receptor or ion channel. In
particular, and unlike tricyclic antidepressants, it does not act at
noradrenergic, muscarinic or histaminergic receptors. Contrary to tricyclic
antidepressants, chronic administration of milnacipran does not modify
beta-adrenoceptor binding or second messenger function. Milnacipran is active on
various animal models of depression such as the forced swimming test in the
mouse, learned helplessness in the rat and the olfactory bulbectomized rat
model. This pharmacological profile, associated with an excellent
bioavailability in man, was predicted to be that required for a powerful and
well-tolerated antidepressant. Subsequent clinical development has shown this
prediction to be well founded.
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Serotonin
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Milnacipran: overview
Milnacipran: structure
Antidepressant mechanisms
Milnacipran versus fluvoxamine
Milnacipran and the dopamine system
Milnacipran for post-stroke depression
Milnacipran for depression after brain injury
Milnacipran (Ixel): dosage and antidepressant response
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