Antidepressants Flashcards

1
Q

What is the Monoamine Theory

A

Deficits in monoamine neurotransmitters (NA & 5-HT) causes depression
- MAOI increase bio availability of monoamines

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2
Q

2 major forms of MAOI

A

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)
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3
Q

Example of a MAOI

A

Phenelzine

- Non-selective, irreversible

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4
Q

Adverse Effects of MAOIs

A

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

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5
Q

What is “The Cheese Reaction”

A
  • 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

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6
Q

Non-selective TCAs for SERT/NET

A
  • Imipramine
  • Amitriptyline
  • Nortriptyline (2nd gen)
  • Milder SE, Improved compliance
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7
Q

Adverse Effects of TCAs

A

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
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8
Q

Examples of SSRI

A
  • Fluoxetine (1st line)
  • Citalopram

SSRIs have greater 5-HT reuptake selectivity than TCAs

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9
Q

Advantages of SSRI

A

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
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10
Q

Adverse Effects of SSRI

A

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
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11
Q

Example of NARI

A

Reboxetine

Note: NARIs have greater NA reuptake selectivity than TCAs

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12
Q

Advantage of NARIs

A

Fewer SEs than TCA & SSRIs

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13
Q

Adverse Effects of NARI

A
  • Dry mouth, sedation (Anticholinergic effects)
  • Insomnia (Increased NA activity in the CNS)
  • Tachycardia (Increased NA @ sympathetic “fight/flight” synapses)
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14
Q

Examples of SNRIs

A

MOA: Increase synapse levels of both NA & 5-HT

  • Venlafaxine
  • Desvenlafaxine (synthetic metabolite of Venlafaxine)
  • Duloxetine
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15
Q

Advantages of Venlafaxine

A
  • Fewer SE than TCAs
  • Claimed to work FASTER than other antidepressants
  • Claimed to work better in treatment-resistant patients
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16
Q

Adverse Effects of SNRIs

A
  • Nausea
  • Insomnia
  • Sexual dysfunction
  • “Serotonin syndrome” (combined with other serotoninergic drugs)
  • Withdrawal effects may be more common & stronger)
17
Q

Other antidepressants

A

Mirtazapine:
- Norepinephrine & specific serotonin antidepressant

Bupropion:
- Norepinephrine-dopamine reuptake inhibitor

Agomelatine:

  • *Helps in sleep disorders
  • Agonist of melatonin MT1 & MT2 receptors

Ketamine:
- Glutamate NMDA receptor antagonist used as an anaesthetic currently evaluated for rapid-onset antidepressant effect

Vortioxetine:

  • “multimodal serotonergic antidepressant”
  • May be efficacious if resistant to other treatments
  • May have pro-cognitive effects
  • May raise risk of suicidal thoughts/actions in children & teens (Close monitoring required)