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6 Cards in this Set

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Tricyclic Antidepressants
The acute effect of tricyclic drugs is to inhibit the reuptake mechanisms (transporters) responsible for the termination of the synaptic actions of both NE and 5-HT in the brain. This presumably results in potentiation of their neurotransmitter actions at postsynaptic receptors.
Selective Serotonin Reuptake Inhibitors
The acute effect of SSRIs is a highly selective action on the serotonin transporter (SERT). SSRIs allosterically inhibit the transporter, binding at a site other than that of serotonin
Serotonin-norepinephrine reuptake inhibitors (SNRIs)
SNRIs bind to transporters for both serotonin and NE, presumably enhancing the actions of both neurotransmitters
The SNRIs differ from the TCAs in lacking significant blocking effects on peripheral receptors including histamine H1, muscarinic, or -adrenergic receptors.
Serotonin 5-HT2 Receptor Antagonists
The major antidepressant actions of nefazodone and trazodone appear to result from block of the 5-HT 2A receptor, a G-protein–coupled receptor located in several CNS regions including the neocortex
MAOIs
Drugs inhibiting monoamine oxidases that metabolize norepinephrine and serotonin MAO type A) and dopamine (MAO type B)
Mirtazapine
Mirtazapine has a unique action to increase amine release from nerve endings by antagonism of presynaptic 2 adrenoceptors involved in feedback inhibition. The drug is also an antagonist at serotonin 5-HT 2 receptors