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Is Phosphodiesterase inhibition a new mechanism of antidepressant action?

Authors :
R. von Frenckell
M. Sastre-y-Hernández
H. Wachtel
B. Troisfontaines
M. Breulet
F Guiot-Goffioul
M. A. Gerard-Vandenhove
Daniel P. Bobon
G. Plomteux
M. Schratzer
Source :
European Archives of Psychiatry and Neurological Sciences. 238:2-6
Publication Year :
1988
Publisher :
Springer Science and Business Media LLC, 1988.

Abstract

Unlike conventional antidepressants, rolipram (a new approach in the treatment of depression) stimulates both the presynaptic and the postsynaptic component of monoaminergic transmission. Several double blind trials are under way to assess the clinical efficacy and safety of this compound. The present study was a randomized, 4-week interindividual double blind double-dummy comparison with desipramine in inpatients with major (DSM-III) and/or endogenous (ICD-9) depressions. After a minimum washout period of three days the patients received either 0.50 mg rolipram or 25 mg desipramine orally t.i.d. for the first three days, then 0.75 mg rolipram or 50 mg desipramine t.i.d. until day 28. Rating tests were based principally on the AMDP-system and the HAMD scale. The study showed no differences between the two drugs as regards the efficacy, but a definite trend in favour of rolipram as regards the side effects and, in particular, anticholinergic effects.

Details

ISSN :
14338491 and 0175758X
Volume :
238
Database :
OpenAIRE
Journal :
European Archives of Psychiatry and Neurological Sciences
Accession number :
edsair.doi.dedup.....91b301a2f50de21cc197b4346cef7bfd
Full Text :
https://doi.org/10.1007/bf00381071