Abstract
The mechanism of action of antidepressant drugs is not well understood. The classical tricyclic antidepressant drugs as well as some newer antidepressants have been developed as inhibitors of the presynaptical re-uptake of the neurotransmitters norepinephrine (NE) (Glowinski and Axelrod, 1964; Iversen, 1965; Carlsson et al., 1966) and 5-hydroxytryptamine (5-HT) (Carlsson et al., 1969; Ross and Renyi, 1969). It has been hypothesized that the therapeutic action of the antidepressant drugs is due to an increased availability of NE and 5-HT at postsynaptic receptors in the brain as the result of the re-uptake blockade (Schildkraut, 1965; Coppen, 1967; van Praag, 1974). However, in recent years some antidepressants (e.g. mianserin and iprindole) have been developed which lack effect or have only very slight effect on the uptake mechanisms.
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Hall, H. (1983). Relationships between receptor affinities of different antidepressants and their clinical profiles. In: Gram, L.F., Usdin, E., Dahl, S.G., Kragh-Sørensen, P., Sjöqvist, F., Morselli, P.L. (eds) Clinical Pharmacology in Psychiatry. Palgrave Macmillan, London. https://doi.org/10.1007/978-1-349-06671-1_23
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