Antidepressants Flashcards

1
Q

Identify the likely biological mechanism behind depression.

A

Originally thought that low levels of serotonin was the cause
Now not so clear but likely reduction in serotonin receptors in hippocampus
Would help explain why SSRI takes so long to work
Many studies show people with depression having what is assumed to be normal levels of serotonin

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2
Q

Identify the main classes of antidepressants.

A
  • Mono Amine Oxadase Inhibitors 
MAOI (first class of antidepressants developed, rarely used for depression today)
  • Tricyclic antidepressants
  • SSRIs (most widely prescribed antidepressants)
  • SNRIs
  • Presynaptic alpha₂-adrenoreceptor antagonist (Mirtazapine)

Other drugs with antidepressant properties:

  • Antipsychotics
  • Lithium
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3
Q

Mono Amine Oxadase Inhibitors 
MAOI

  • Mechanism of action
  • Examples
  • Side effects
A

MAOIs

-Inhibit the activity of MAO enzymes, which break down norepinephrine/serotonin and dopamine. Inhibiting MAO thereby increases level of all three transmitters.

-Examples: 
Phenelzine
Selegiline – also used in Parkinsons
Tranylcypromine 
Moclobeminde (REVERSIBLE MAOI) 
-Side effects: 
Weakness
Headache
Weight Gain 
Dizziness
Fatigue
Impotence
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4
Q

Describe the main interactions with MAOIs.

A

1) Should not be used in combination with SSRI/Tricyclic as well as some analgesics such as morphine/Tramadol as they will increase serotonin to potentially dangerous levels causing confusion, hypertension, tremor, coma and possibly death. i.e. neuroleptic malignant syndrome (only way to treat this is to remove cause, give fluids, and possibly diazepam)
Give 14 days washout after stopping MAOI before starting other antidepressants.

2) Foods high in tyramine may also cause a hypertensive crisis (e.g. cheese, venison, alcohol, some grey veggies)

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5
Q

Describe the mechanism of action of Moclobeminde. Describe any differences in interactions with Moclobeminde c.f. othe MAOIs.

A

Reversible MAOI, reported to act by reversible inhibition of MAO type A. Therefore called RIMA (Tyramine has less of an effect)

Short acting so medications can be changed with only one week washout period.

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6
Q

Describe the mechanism of action of tricyclic antidepressants.

A
  • Act by inhibiting re-uptake of norepinephrine and serotonin by blocking the transporters responsible for re-uptake of these neurotransmitters.
  • Increasing concentration of neurotransmitters in the synapses and triggering further neurotransmission.
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7
Q

Identify the main uses of tricyclic antidepressants.

A
  • Depression
  • Anxiety
  • Chronic pain (i.e. fibromyalgia, reflex sympathetic dystrophy syndrome)
  • IBS (reduces peristalsis so slows down gut, so no diarrhea)
  • Neuralgia
  • OCD
  • Nocturnal enuresis
  • PTSD
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8
Q

Identify the main cautions for tricyclic antidepressant use.

A
  • Tricyclics should be used with caution in cardiovascular disease due to risk of arrythmias
  • Tricyclics have antimuscarinic activity that blocks activity of the muscarinic acetylcholine receptor and so reduce intestinal mobility
  • They can induce bradycardia followed by tachycardia, reduce bronchial secretions, urinary retention, dry mouth and confusion
  • Tricyclics are very dangerous in overdose so beware of how much you prescribe for a patient and use with caution in patients at high risk of suicide.
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9
Q

Identify examples of common tricyclics.

A
Amitriptyline
Clomipramine
Imipramine
Lofepramine
Nortriptyline
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10
Q

Identify drugs related to tricyclics. What are the main differences c.f. tricyclics ?

A

Trazodone

This drug is more sedating (used in elderly ppl with dementia, who are agitated and struggle to sleep).

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11
Q

Describe the mechanism of action of SSRIs.

A

Believed to work by increasing levels of neurotransmitter serotonin by limiting its re-absorption and pure SSRI have only a weak affinity for norepinephrine and dopamine transmitters (they are, therefore, cleaner with generally fewer side effects and better tolerated by patients)

5-HT receptors are found in the peripheral and central nervous systems mediating both excitatory and inhibitory neurotransmission. These receptors modulate the release of many neurotransmitters, including GABA, Dopamine, Epinephrine, Norepinephrine, ACh.

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12
Q

What is the name of Serotonin receptors ?

A

Serotonin receptors are know as 5-hydroxytryptamine (5-HT)

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13
Q

Identify the main uses of SSRIs.

A

They influence aggression, anxiety, cognition, learning memory, mood and sleep

Depression
Anxiety
OCD
Panic disorder
PTSD
Eating disorders
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14
Q

Identify the main side effects of SSRIs.

A

1) Sexual: dysfunction and reduced libido
2) Cardiac: some, especially citalopram, to be used with caution as can cause QT interval prolongation (which can lead to a life threatening arrhythmia known as torsades de pointes) therefore dose dependant with citalopram
3) Bleeding: affects anticoagulants (i.e. warfarin and aspirin) and also increased risk of GI bleeds.
4) Suicide: possible increased risk of suicide especially in children and adolescents (so should not be started in under 18s)
5) Overdose: safer than other antidepressants
Epilepsy: may reduce fit threshold (more likely to have a seizure)
6) Others include:
-Nausea
-Rash
-Muscle aches
-Insomnia
-Sweating

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15
Q

Identify examples of SSRIs, ranking them by order of overdose toxicity.

A
MOST TOXIC
Citalopram (QT interval) 
Escitalopram
Paroxetine

Sertraline
Fluoxetine 
LEAST TOXIC
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16
Q

Identify examples of SNRIs.

A

Duloxetine

Venlafaxine

17
Q

Identify the main uses of Duloxetine (SNRI).

A

Depression
Neuropathic pain (diabetes, fibromyalgia)
Stress urinary incontinence

(reduce dose slowly to prevent withdrawal symptoms)

18
Q

Identify the main side effects of Duloxetine.

A

Nausea
Insomnia
Dizziness

19
Q

Give an example of presynaptic alpha₂-adrenoreceptor antagonist.

A

Mirtazapine (also a noradrenergic and specific serotonergic antidepressant NaSSA)

20
Q

Identify the main uses of Mirtazapine.

A

Depression
Anxiety
PTSD

21
Q

Identify the main side effects of Mirtazapine.

A

Low dose causes drowsiness so best taken at night

Higher dose more stimulant effect (take in the morning)

22
Q

Identify the main uses of Venlafaxine.

A

Major Depressive Disorder
Anxiety
Panic
Social phobia
Metabolized in the body into desvenlafaxine (by cytochrome P206 isoenzyme in the liver)
Often used in treatment of resistant depression

23
Q

Give examples of antipsychotic drugs. What are its main uses ?

A

Risperidone

  • Psychsosis primarily
  • Can also be used for depression.
24
Q

Identify any cautions associated with Risperidone.

A

Should stop after 6 months, because of possible CV effects

25
Q

Identify the main uses of Lithium.

A

Bipolar/mania mood stabilization

26
Q

Identify the main side effects of Lithium.

A

Possible adverse affects on kidney (can reduce kidney function) and thyroid function (can induce hypothyroidisim so watch blood tests)

27
Q

Describe the effect of antidepressants on pain, including mechanism of action.

A

Can be used for nerve damage or abnormal nerve function (neuropathic) and some muscle pains

Direct effect on the mechanisms of the pain, and not through any effect on mood (and also through beneficial effects on sleep)

Tricyclics work by blocking the re-uptake of Noradrenaline and Serotonin (5-HT) into the nerve endings and increasing their levels in the pain control pathways

28
Q

Identify commonly used antidepressants for pain.

A

Amitriptyline
Nortriptyline
Duloxetine (also licensed for diabetic neuropathy)

29
Q

Use of more than one drug that prolongs the QT interval increases the risk of torsades de pointes and ventricular arrhythmia. Identify drugs which prolong QT interval.

A
  • Citalopram (anti-depressant)
  • Erythromycin and Clarithromycin (antibiotic)
  • Methadone
  • Domperidone (anti-emetic)
30
Q

Identify risk factors for QTc prolongation. Why is this clinically important ?

A
  • Major psychiatric disorders
  • Cardiovascular disease
  • The elderly
  • Women

People who have more risk factors for QTc prolongation than the general population are particularly vulnerable to drug-induced LQTS.