neuropsychopharm3 Flashcards

(40 cards)

1
Q

What is the biochemical basis of depression?

A

Imbalance in biogenic amine neurotransmitter systems

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2
Q

Neurochemical effects of tricyclic antidepressants

A

Blockade of transmitter uptake – NE and 5-HT

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3
Q

What are the most commonly used anti-depressants? What are the two we need to know?

A

SSRIs –Fluoxetine and Sertraline

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4
Q

Common SE of SSRIs?

A

N/V, Insomnia, Nervousness, Sexual dysfunction

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5
Q

What is serotonin reaction and why can it occur?

A

In the presence of MAOI’s Include hyperthermia, muscle rigidity and CV collapse

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6
Q

What is SSRI Discontinuation syndrome?

A

Occurs within 1 to 7 days after stopping an SSRI; Most common with shorter acting drugs like sertraline; Symptoms include: dizziness, light-headedness, vertigo, anxiety, fatigue, h/a, tremor, visual disturbances

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7
Q

Clinical uses of SSRI’s:

A

MDD, OCD, Panic disorder, social phobia, PTSD, GAD, PMS

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8
Q

First SSRI on the market, Active metabolite with long half-life, Effects on drug metabolism

A

Fluoxetine

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9
Q

SSRI, Similar to fluoxetine with less effects on drug metabolism, shorter half-life

A

Sertraline

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10
Q

Blocks both serotonin and Norepinephrine uptake

A

SNRI

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11
Q

SNRI, 12-18 hour half-life, Use with caution in patients with liver disease Approved for use with fibromyalgia, diabetic neuropathy, back pain, and osteoarthritis pain

A

Duloxetine

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12
Q

Drugs without typical tricyclic structure or SSRI action; may or may not block catecholamine uptake

A

Atypical antidepressants

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13
Q

Atypical antidepressant; approved for nicotine withdrawal and seasonal disorder; blocks NE and dopamine uptake

A

Bupropion

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14
Q

Atypical antidepressant; blocks presynaptic alpha2 receptors in the brain; increases appetite

A

Mirtazapine

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15
Q

First highly effective drugs for the treatment of depression; now used secondarily to SSRI’s and other newer cmpds

A

Tricyclic antidepressants

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16
Q

Pharmacological properties of tricyclic antidepressants

A
  1. produces elevation of mood in depressed patients after 2-3 weeks 2. Decreases REM and increase stage 4 sleep 3. Prominent anticholinergic effects 4. Sedation 5. Cardiac abnormalities
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17
Q

Symptoms of overdose with TCA

A

hyperpyrexia, hyper/hypotension, seizures, coma, cardiac conduction defects

18
Q

Drug interactions with TCA’s

A

Guanethidine – blocks guanethidine uptake Sypathomimetic drugs – particularly indirect acting ones Effects on absorption and metabolism of other drugs

19
Q

Therapeutic uses of TCA’s

A

MDD, Enuresis in childhood; chronic pain (amitriptyline); OCD (Clomipramine)

20
Q

Two TCA’s we need to know and what they’re used for

A

Amitriptyline –> chronic pain Clomipramine –> OCD

21
Q

Block the oxidative deamination of naturally occurring biogenic amines like NE, DA and 5-HT and ingested amines

22
Q

Irreversible inhibitor of MAO

23
Q

What do you have to watch in your diet if you’re on MAOI’s?

A

Tyramine intake

24
Q

Major mental disorder characterized by derangement of personality and loss of contact with reality, delusions, hallucinations

25
Which dopamine receptor activates adenylyl cyclase?
D1 type
26
Which dopamine receptor inhibits adenylyl cyclase?
D2 type
27
Which two receptors do atypical antipsychotic drugs act on?
DA + 5HT2 receptors
28
Actions of typical antipsychotic drugs
Decrease psychotic behavior, sedation, extrapyramidal actions, neuroendocrine effects, orthostatic hypotension; weight gain; neuroleptic malignant syndrome
29
Prototype available typical antipsychotic drugs (Class)
Phenothiazines-- 3 subtypes based on side chain: Chlorpromazine, Thioridazine, Fluphenazine
30
Compounds with aliphatic side chains; low to medium potency, sedative, pronounced anticholinergic actions
Chlorpromazine
31
Compounds with piperidine side chains; low potency, sedative, less extrapyramidal actions, anticholinergic
Thioridazine
32
Compounds with piperazine side chains; high potency, less sedative, less anticholinergic, more extrapyramidal reactions
Fluphenazine
33
Butyrophenone Derivative, not chemically related to phenothiazines but pharmacologically similar to high potency piperzine derivatives
Haloperidol
34
Atypical Antipsychotics
Clozapine, Olanzapine, Risperidone, Quetiapine, Aripiprazole
35
Less extrapyramidal symptoms, May cause serious agranulocytosis, weight gain; Effects on negative symptoms
Clozapine
36
More potent 5-HT2 antagonist; few extra pyramidal symptoms; no agranulocytosis; weight gain and diabetes risk
Olanzepine
37
Combined dopamine and serotonin receptor antagonist; low incidence of extrapyramidal side effects
Risperidone
38
Structurally related to clozapine with effects on D2 and 5-HT2 receptors; some abuse potential
Quetiapine
39
D2 partial agonist -- approved as an adjunct in the treatment of depression
Aripiprazole
40
Uses of atypical antipsychotics
Acute psychotic episodes, chronic schizo, manic episodes, augmentation of antidepressant action, Tourette's, Antiemesis