The results of early therapeutic trials (1960s and 70s) in mild chroni
c depression (neurotic patients) are difficult to extrapolate to dysth
ymia. Most studies conducted in the early 1980s showed reference drugs
(TCAs and MAOIs) to be poorly effective in chronic mild depression us
ually defined with RDC. The most recent trials using DSM-III-R criteri
a for dysthymic recruitment showed TCAs, new MAOIs (RIMA) and SSRI to
be effective. All these compounds have a rather similar pharmacolo,gic
al mechanism of action. It is therefore of both practical and theoreti
cal interest that amisulpride, a benzamide derivative blocking D-2 and
D-3 pre-synaptic receptors, has been found effective in the treatment
of dysthymia in different placebo and reference controlled trials. Th
is result is in line with the pharmacological data on animal 'anhedoni
c models'.