Psychopharm Flashcards

(27 cards)

1
Q

When is Psychological treatment first line

A

Anxiety, OCD , mild-moderate depression

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2
Q

Examples of Typical Antipsychotics

A
  • Chlorpromazine
  • Haloperidol
  • Sulpride
  • Zuclopenthixol (clopixol)
  • Fluphenazine
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3
Q

Examples of Atypical Antipsychotics

A
• Lurasidone
• Olanzapine
• Quetiapine
• Risperidone
• Aripiprazole
• Amisulpride
-Clozapine
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4
Q

What is psychosis

A

Disorder of excess dopamine

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5
Q

What type of drugs are Antipsychotics

A

Dopamine Antagonists at D2 receptors

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6
Q

Do Antipsychotics affect negative symptoms

A

No

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7
Q

What are the Dopamine Pathways Relevant to Schizophrenia Syndromes

A

Positive - overactivity of mesolimbic pathway

Negative & cognitive - Dysfunction of mesocortical pathway

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8
Q

Adverse Affects of Antipsychotics

A

Mediated by dopamine antagonism
1- Nigrostriatal tract - Extra pyramidal side effects (EPSE) : Acute dystonia , Akathisia, tardive Dyskinesia, Parkinosonism
2- Tuberoinfundibular system –prolactin elevation

Mediated by other receptors 
• Serotonin
• Histamine
• Muscarinic
• Alpha adrenergic
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9
Q

Which side effects are more common with 2nd generation Antipsychotics , which drugs specifically

A

Metabolic Effects
• Weight gain
• Dyslipidaemia
• Type 2 diabetes

Specifically: Quetiapine, olanzapine and clozapine

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10
Q

Antidepressants Types

A

SSRIs : Selective serotonin reuptake inhibitors
SNRIs : serotonin and noradrenaline reuptake inhibitors
NASSAs : noradrenergic and specific serotinergic
MAQIs : monoamine oxidase inhibitors
TCAs: tricyclic antidepressants

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11
Q

SSRIs MOA

A

Block serotonin transport in synapse , blocking the reuptake of serotonin into neurons = increase serotonin activity

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12
Q

What causes Depression

A

Functional deficiency of monoamines ( serotonin and noradrenaline ) : research not verified

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13
Q

How do antidepressants work

A
  • Increase BDNF and stimulate neurogenesis = enhancing synaptic plasticity
  • moderates limbic system to reduce cognitive bias
  • increase serotinergic neurotransmission to modulate other neurotransmitter systems ( GABA , dopamine )

MOST effective with psychological and social interventions

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14
Q

What are Anxiolytics

A

Anxiety medications ; Benzodiazepines and GABA receptors

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15
Q

What is GABA-A receptor

A

important target for benzodiazepine and Z drugs

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16
Q

How do Benzodiazepines work

A

Increase affinity for GABA

  • binding site is between alpha and gamma subunits
  • different subunits will have different affects
17
Q

Uses of benzodiazepine

A
  • Anxiolytic
  • Hypnotic
  • Muscle relaxant
  • Anti-convulsant
  • Amnestic
18
Q

Benzodiazepine affect on subunits a1 to a6

A
  • α2 and 3: anxiolytic
  • α1 and 5: sedation, amnesia and ataxia
  • α1-6: anticonvulsant
19
Q

Side Effects of Benzodiazepines

A
  • Headaches
  • Confusion, amnesia
  • Ataxia
  • Dysarthria
  • Blurred vision
  • Paradoxical (disinhibition) reaction
  • At risk: children, LD, CNS disorder, impulsivity
  • Interaction with alcohol at GABA receptor
  • Overdose –rarely fatal alone but dangerous in combination with alcohol
20
Q

Where does alcohol interact

A

GABA receptor

21
Q

List drugs that act on GABA other than benzodiazepines

A
  • Z drugs
  • Barbituates
  • Flumazenil
  • Alcohol
22
Q

What are Z drugs

A

Ex: Zolpidem, zopiclone

  • Bind to benzodiazepine site at GABA-A receptor
  • Short onset of action
  • Specific to α-1 subtype –Hypnotic
  • Anticonvulsant and muscle relaxant only at high doses
  • Same Side effects as benzodiazepines
23
Q

What are barbiturates

A

Ex: Amobarbital, phenobarbital, thiopentone
- used only for severe insomnia, epilepsy, induction of
anaesthesia
- Highly addictive, dangerous in overdose

24
Q

What is Flumazenil

A

Competitive antagonist in benzodiazepine binding site

  • Displaces Benzodiazepine
  • Rapid onset of action but short half life
  • shouldn’t be used if benzodiazepine is being used to treat epilepsy
25
What can be used to treat benzodiazepines OD
Flumazenil
26
Where is Alcohol an antagonist
At Glutamate receptors
27
Why do barbituates have a higher risk of toxicity
Benzodiazepines : increase affinity of GABA = increase frequency of opening of chloride channels , can only act if GABA present Barbituates : increase duration chloride channels opening and can act in absence of GABA if at high doses = higher risk of OD