Abstract
The relationship between the therapeutic effects of tricyclic antidepressant drugs (TCAs) and their behavioral and biochemical action in animals is, at present, not well understood. With a few exceptions, most TCAs are characterized by their ability to inhibit the neuronal reuptake of norepinephrine (NE) and/or 5-hydroxytryptamine (5-HT) (Glowinski and Axelrod, 1964; Iversen, 1965; Carlsson et al., 1969a, 1969b; Ross and Renyi, 1969). Therefore, it has generally been believed that the therapeutic action of these drugs is due to an enhancement of NE and/or 5-HT neurotransmission in the brain caused by reuptake inhibition (Schildkraut, 1965; Coppen, 1967; Lapin and Oxenkrug, 1969; U’Prichard et al., 1978). Since the prototype TCAs such as imipramine, amitriptyline and, more recently, clomipramine (Ross and Renyi, 1975) affect both NE and 5-HT reuptake in vivo and thus presumably enhance the functional activity of both amines, the relative role of NE and 5-HT in the therapeutic action of antidepressant drugs has been quite controversial. This is further complicated by their pronounced action on pre- and postsynaptic receptors.
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Georgotas, A., Bush, D., Hapworth, W.E., Kim, M., Gershon, S. (1983). Progress in pharmacotherapy of depression: research implications. In: Usdin, E., Goldstein, M., Friedhoff, A., Georgotas, A. (eds) Frontiers in Neuropsychiatric Research. Palgrave Macmillan, London. https://doi.org/10.1007/978-1-349-06689-6_18
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