PR3136 > Antipsychotics > Flashcards

Antipsychotics Flashcards

(44 cards)

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1
Q

Schizophrenia:

  • Acute or chronic?
  • Time of onset
  • Consequence on individual
A
  • Chronic disease
  • Onset in late adolescence/ early adulthood
  • Highly disabling to social and vocational functioning
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2
Q

The five symptom domains of schizophrenia

A
  1. Positive sx
  2. Negative sx
  3. Anxiety/depression
  4. Aggressive sx
  5. Cognitive sx

(focus on positive and negative sx)

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3
Q

Examples of “Positive sx” in schizophrenia and its “function” in the disease

A
  1. Delusion
  2. Hallucinations
  3. Abnormal behaviours (E.g. stereotypical)
  4. Thought disorder, incl. feeling that thoughts are controlled by outside agency

Function: Presentation of these sx most disturbing, leads to referral to psychiatrist and detection of schizo

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4
Q

Negative sx in Schizophrenia and its impact on the patient

A
  1. Withdrawal from social contacts
  2. Flattening of emotional responses

Impact: Negative sx most distressing (while positive sx characterised by lack of insight)

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5
Q

As Schizo progresses, which of the five symptoms of schizophrenia becomes dominant?

A

Negative sx

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6
Q

In 10% schizo cases, suicide occurs. Why is this so?

A

Schizo is frequently associated with depression

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7
Q

What are some possible secondary causes of negative sx?

A
  1. Depression
  2. Extrapyramidal sx (EPS)
  3. Environmental deprivation
  4. Positive sx
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8
Q

What are some examples of cognitive dysfunction of schizo. What is the cause of cognitive dysfunction in schizo patients?

A
  1. Impaired selective attention (unable to focus and retain info)
  2. Impaired working memory

Cause: The disease itself (i.e. persistent core feature of disease, no iatrogenic)

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9
Q

Why is the level of cognitive dysfunction important in treatment of schizo?

A

Helps predict level fo social and vocational functioning, hence treatment outcome. It is a better predictor than positive sx.

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10
Q

Factors that may lead to Schizo

A
  1. Genetic factors (mutationof various genes)

2. Environmental factors: related to neurodevelopmental abnormalities (e.g. maternal viral infections during preg)

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11
Q

What are some possible evidence showing “neurodevelopmental abnormalities” in Schizo Patients?

A
  • Onset in late adolescence/ early adulthood
  • Myelination of cortico-cortical pathways is abnormal
  • Enlarged ventricles, abnormalities in laminar organisation of cortical cells
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12
Q

State the three neurochemical theories of Schizo. What characteristic of Schizo do these theories attempt to explain?

A
  1. Dopamine Theory
  2. 5-HT Theory
  3. Glutamate Theory

These theories proposed are primarily theories of positive sx

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13
Q

Describe Dopamine Theory. How did dopamine theory come about?

A

D2 receptor activity is associated with Schizo

  1. Amphetamine, a dopaminergic, produces sx of acute schizo
  2. Drugs are D2 antagonists
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14
Q

Four dopamine pathways of the Brain and their functions. What pathways are the proposed drug targets?

A
  1. Nigrostriatal: Part of extrapyramidal motor system (affected in PD)
  2. Mesolimbic: Reward and emotion
  3. Mesocortical: Cognition and attention
  4. Tuberoinfundibular: Prolactin secretion into blood circulation

Drug targets: 2 and 3

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15
Q

Describe the 5-HT Theory in Schizo

A
  • Lysergic acid diethylamide (LSD), a 5-HT2 agonist, produces sx similar to acute Schizo
  • Many atypical antipsychotics have 5-HT2 antagonism
  • Hence excess 5-HT is associated with Schizo
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16
Q

Describe the Glutamate Theory in Schizo

A
  • Drugs blocking NMDA receptor chanel (e.g. PCP, ketamine) produce sx similar to acute Schizo
  • Hence NMDA receptor associated with Schizo
  • No clinically useful drugs yet
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17
Q

One of the most widely used TYPICAL antipsychotic

A

Haloperidol

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18
Q

Some examples of ATYPICAL antipsychotics

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A
  1. Amisulpride
  2. Clozapine
  3. Olanzapine
  4. Risperidone
19
Q

Similarity between Typical and Atypical antipsychotics

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A

Control positive symptoms

20
Q

One important difference between Atypical Antipsychotics over Typical Antipsychotics

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A

Atypical produce less extrapyramidal SE

21
Q

Other than D2 receptor, what are other receptor that Chlorpromazine binds to, hence its side effects and loss in popularity as an atipsychotic?

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A
  1. M1 receptor: Parasympatholytic effects (dry mouth, constipation, blurred vision)
  2. H1 receptor: Sedation, Weight gain
  3. Alpha-1 receptor: postural hypotension, dizziness (body unable to respond to orthostatic changes)
22
Q

Advantage of Haloperidol over Chlorpromazine

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A
  • Haloperidol does not block M1 and H-1 receptor

- Hence less SE

23
Q

Three examples of extrapyramidal SE in antipsychotic drugs. What is the mechanism leading to these SE?

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A
  1. Acute Dystonias (involuntary contraction of muscles)
  2. Tardive Dyskinesia (involuntary stiff and jerky movements)
  3. Akathisia (inner restlessness)

Mechanism: Actions on extrapyramidal motor pathways (affects basal ganglia –> Striatum and substantia nigra)

24
Q

Describe acute dystonias caused by antipsychotics. During treatment, when does it occur? How does it occur? Is it reversible?

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A
  • Parkinsonism-like syndrome (e.g. cogwheel rigidity, tremor at rest)
  • Occurs within first few weeks of treatment and reversible when drug is stopped
  • May be caused by D2 antagonism in nigrostriatal pathway
25
Similarties and differences between Tardive Dyskinesia and Akathisia caused by antipsychotics?
Similarties: - Irreversible - Caused by upregulation or supersensitivity of D receptors in nigrostriatal system (due to initial blockade) Differences: - Akathisia, but not dyskinesia, correlates directly with duration on medication
26
Main difference between ATYPICAL and TYPICAL antipsychotics
Atypical has LESS severe extrapyramidal SE (but still have)
27
Other characteristics of ATYPICAL antipsychotics
1. Greater affinity at 5HT2 receptors 2. Greater affinity at D4 receptors 3. Mixed antagonism at a-adrenoceptors, H1-histamine receptors, M receptrs and 5-HT2 receptors
28
"Core" of most ATYPICAL antipsychotics (i.e. their main MoA)
Serotonin-dopamine antagonism (SDA)
29
Are there common receptor affinity between ATYPICAL antipsychotic drugs?
No. They have complex mixtures of actions
30
Rare but significant and fatal AE of Clozapine
Clozapine-induced agranulocytosis
31
SEs of ATYPICAL antipsychotics. Which drugs exhibits most of which SE?
1. Parasympatholytic: Clozapine, Olanzapine 2. Sedation due to H1 receptor antagonism: Clozapine, Olanzapine 3. Postural hypotension, reflex tachycardia: Risperidone
32
Describe the receptor binding of Amisulpride, which has an atypical pattern of receptor affinities for an atypical antipsychotic
- Selective D2/D3 antagonist | - (some 5-HT7 antagonism)
33
What advantages does the unique receptor affinities of amisulpride gives?
- Less SE due to selective D2/D3 antagonism | - Little a-adrenoceptor block, antihistaminergic and anticholinergic SE
34
Adverse effects of amisulpride
1. Increased prolactin secretion (due to blocked D2/D3 receptors in anterior pituitary gland) 2. Breast swelling, pain and lactation 3. Gynaecomastia in males
35
What is Aripiprazole's MoA?
- Partial Agonist of D2 & D3 receptors | - In presence of agonist, it exhibits antagonistic effects
36
An AE of ATYPICAL antipsychotics, that is significant and not reversible. - Which drugs may cause it? - Mechanism?
New onset or exacerbation of diabetes - Drugs: clozapine, Olanzapine, Risperidone - Exception: Amisulpride - Unknown mechanism
37
Which ATYPICAL antipsychotics causes Drug-induced Weight Gain? What is the possible mechanism(s)?
Drugs: 1. Clozapine 2. Olanzapine 3. Risperidone Possible mechanisms: - Sedation by H1 histamine antagonism = sedentary lifestyle - a-adrenoceptor and 5-HT2 antagonism on hypothalamus = altered feeding behaviour (does NOT explain for chlorpromazine)
38
Drug that is currently in experimental use to treat anorexia nervousa
Olanzapine
39
Ways in which ATYPICAL antipsychotics produce less EPS, and which drugs correspond to which way?
1. Potent 5-HT2A vs weak D2 antagonism: lower EPS, higher efficacy against negative sx - Clozapine, Olanzapine 2. High D4:D2 antagonism ratio favour actions in prefrontal cortex over striatum - Clozapine 3. High D3:D2 antagonism ratio favour actions on nucleus accumbens over striatum - Amisulpride 4. High D2:D1 antagonism ratio reduce impact of antagonism in striatum - Amisulpride, Risperidone
40
How does higher D2:D1 antagonism ratio confer less blockade on dopaminergic function?
- Presynaptic D2 are autoreceptors - Blockage of D2 inhibits negative feedback, allowing more dopamine to be released - Hence less complete blockade of dopaminergic function
41
Additional benefits of ATYPICAL antipsychotics compared to typical antipsychotics, and drugs that exhibit them
1. More effective against negative sx - Clozapine, Olanzapine, Risperidone 2. Better at mood stabilisation - Clozapine, Olanzapine, Risperidone 3. Ameliorate cognitive dysfunction better - Clozapine, Risperidone Note: These effects are still weak, only suitable for patients who start out with more severe negaitve sx
42
How effective are antipsychotic treatment?
- Some do not respond - Some remain severely disabled in social and occupational function - Some recover to near pre-illness levels of function - Few can have meds discontinued and retain near pre-illness levels of function Hence there is still need for improved antipsychotic drugs
43
Among the EPS SE caused by antipsychotics, which is/are reversible when the drug is stopped?
Dystonias
44
Examples of TYPICAL antipsychotics
1. Haloperidol 2. Chlorpromazine 3. Fluphenazine 4. Trifluoperazine
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