Using your textbooks, draw up a classification of the drugs that are used as antidepressants.
Tricyclic antidepressants
Imipramine
Mono amine oxidase inhibitors
Phenelzine
Tranylcypromine
Selegiline
Serotonin noradrenaline reuptake inhibitors
Duloxetine
Venlafaxine
Levomilnacipran
Serotonin Modulators
Nefazodone
Trazodone
Vortioxetine
Noradrenalin receptor inhibitors
Reboxetine
Tetracyclic and unicyclic antidepressants
Bupropion
Amoxapine
Maprotiline
Mirtazapine
Mianserin
Cascadic rhythm regulators
Agomelatine
Selective serotonin reuptake inhibitors
Fluoxetine
Citalopram
Escitalopram
Paroxetine
Sentraline
What do the existing drugs all have in common regarding their mechanisms of action?
All drugs that treat depression has an effect on the neurotrophic and endocrine factors within the brain.
How long does it take for the anti-depressive effects of these drugs to appear? What is the reason for this?
14-21 days or even longer because it takes up to two weeks or more for neurotrophic factors to be synthesised
How do the TADs and the selective serotonin reuptake inhibitors (SSRI’s) differ in respect of:
TAD’s has an high affinity for the serotonin and noradrenaline re-uptake transport receptor because of their structure while SSRis only has an affinity for blocking the re uptake of serotonin.
They have a large amount of side effects anticholinergic side effects such as sedation, weight gain , alpha receptor blockage, arrythmia and seizures if high doses is administered while SSRI causes sexual dysfunction and increases risk for serotonin syndrome if co administered with monoamine oxidase inhibitors
It as a long half life and causes convulsions at high doses while SSRI’s as the risk for serotonin syndrome is used with other drugs. SSRI’s is first line treatment thus its is relatively safe at recommended dosage.
Block alpha 2 receptors and both Noradrenaline(autoreceptors) and serotonin release (heteroreceptors) which stimulates serotonin 1A indirectly and serotonin 2 an 3 blockage
Block both Serotonin and Noradrenaline re uptake
Is a agonist of both melatonin 1 and 2 receptors and serotonin 2 C antagonist