neuropsychopharm3 Flashcards

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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

A

MAOI’s

22
Q

Irreversible inhibitor of MAO

A

Phenelzine

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

A

Psychosis

25
Q

Which dopamine receptor activates adenylyl cyclase?

A

D1 type

26
Q

Which dopamine receptor inhibits adenylyl cyclase?

A

D2 type

27
Q

Which two receptors do atypical antipsychotic drugs act on?

A

DA + 5HT2 receptors

28
Q

Actions of typical antipsychotic drugs

A

Decrease psychotic behavior, sedation, extrapyramidal actions, neuroendocrine effects, orthostatic hypotension; weight gain; neuroleptic malignant syndrome

29
Q

Prototype available typical antipsychotic drugs (Class)

A

Phenothiazines– 3 subtypes based on side chain: Chlorpromazine, Thioridazine, Fluphenazine

30
Q

Compounds with aliphatic side chains; low to medium potency, sedative, pronounced anticholinergic actions

A

Chlorpromazine

31
Q

Compounds with piperidine side chains; low potency, sedative, less extrapyramidal actions, anticholinergic

A

Thioridazine

32
Q

Compounds with piperazine side chains; high potency, less sedative, less anticholinergic, more extrapyramidal reactions

A

Fluphenazine

33
Q

Butyrophenone Derivative, not chemically related to phenothiazines but pharmacologically similar to high potency piperzine derivatives

A

Haloperidol

34
Q

Atypical Antipsychotics

A

Clozapine, Olanzapine, Risperidone, Quetiapine, Aripiprazole

35
Q

Less extrapyramidal symptoms, May cause serious agranulocytosis, weight gain; Effects on negative symptoms

A

Clozapine

36
Q

More potent 5-HT2 antagonist; few extra pyramidal symptoms; no agranulocytosis; weight gain and diabetes risk

A

Olanzepine

37
Q

Combined dopamine and serotonin receptor antagonist; low incidence of extrapyramidal side effects

A

Risperidone

38
Q

Structurally related to clozapine with effects on D2 and 5-HT2 receptors; some abuse potential

A

Quetiapine

39
Q

D2 partial agonist – approved as an adjunct in the treatment of depression

A

Aripiprazole

40
Q

Uses of atypical antipsychotics

A

Acute psychotic episodes, chronic schizo, manic episodes, augmentation of antidepressant action, Tourette’s, Antiemesis