Antidepressants Flashcards
What is the Monoamine Theory
Deficits in monoamine neurotransmitters (NA & 5-HT) causes depression
- MAOI increase bio availability of monoamines
2 major forms of MAOI
1) MAO-A
2) MAO-B
- 5-HT broken down mainly by MAO-A
- Both forms acts on NA & dopamine
(eg. MAO-B selective inhibitors used in Parkinson’s disease)
Example of a MAOI
Phenelzine
- Non-selective, irreversible
Adverse Effects of MAOIs
Postural hypotension
- Sympathetic block produced by accumulation of dopamine in cervical (neck) ganglia, which acts as inhibitory transmitter
Restlessness & insomnia
- CNS stimulation due to too much NA
Note: Should not be combined with other serotoninergic drugs (eg. pethidine)
–> Hyperexcitability, increased muscular tone, myoclonus, loss of consciousness
What is “The Cheese Reaction”
- Tyramines in food are broken down by MAO
- MAOIs lead to accumulation of tyramine & a sympathomimetic effect
- Tyramine is taken up into adrenergic terminals (Competes with NA for the vesicular compartment) -> Increase release of NA into synapses
Effects: Acute hypert/s, severe throbbing headache, occasionally intracranial haemorrhage
Non-selective TCAs for SERT/NET
- Imipramine
- Amitriptyline
- Nortriptyline (2nd gen)
- Milder SE, Improved compliance
Adverse Effects of TCAs
Sedation
- H1 histamine receptor antagonism
Postural hypotension
- Alpha-adrenoreceptor sympathetic block
Dry mouth, blurred vision, constipation
- Muscarinic receptor antagonism
DDI
- Plasma protein bound
- Hepatic metabolism
Examples of SSRI
- Fluoxetine (1st line)
- Citalopram
SSRIs have greater 5-HT reuptake selectivity than TCAs
Advantages of SSRI
1) Fewer adverse effects than TCAs
- Low affinity for alpha-adrenoceptors -> Lack of CVS effects, safer in overdose
- Lack of effect at histamine receptors -> Reduced sedation (note: Citaprolam still has some histamine receptor antagonism leading to sedation)
- Low affinity for muscarinic cholinergic receptors -> Minimal anticholinergic SEs
2) Safer in overdose
3) Better compliance (bc of less side effects)
4) Prescription of more adequate doses (bc well tolerated)
TLDR: Efficacy, Safety, Tolerability! 1st line therapy but... - Only 2/3 get remission - Adverse effects especially at start - Discontinuation can be a problem in some
Adverse Effects of SSRI
Nausea & Insomnia (usually only at the start, will go away)
Sexual dysfunction
- Due to increased stimulation of 5HT2 receptors
- Management: Cyproheptadine (H-HT2 blocker)
Serotonin syndrome (DDI when used with other drugs that increase serotoninergic activity) - Tremor, hyperthermia, CVS collapse
Example of NARI
Reboxetine
Note: NARIs have greater NA reuptake selectivity than TCAs
Advantage of NARIs
Fewer SEs than TCA & SSRIs
Adverse Effects of NARI
- Dry mouth, sedation (Anticholinergic effects)
- Insomnia (Increased NA activity in the CNS)
- Tachycardia (Increased NA @ sympathetic “fight/flight” synapses)
Examples of SNRIs
MOA: Increase synapse levels of both NA & 5-HT
- Venlafaxine
- Desvenlafaxine (synthetic metabolite of Venlafaxine)
- Duloxetine
Advantages of Venlafaxine
- Fewer SE than TCAs
- Claimed to work FASTER than other antidepressants
- Claimed to work better in treatment-resistant patients