antidepressants 2 Flashcards

1
Q

Cognitive behavior therapy

and behavioral activation are alternatives to antidepressants when ?

A

major depression of mild to moderate severity

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2
Q

Psychological or behavioral treatment is not recommended as sole therapy when?

A

severe major depression

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3
Q

Class of drug that blocks the reuptake of serotonin at the serotonin reuptake pump of the neuronal membrane, enhancing the actions of serotonin on 5HT1A autoreceptors.

A

Selective serotonin-reuptake inhibitor (SSRI)

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4
Q

Class of drugs that can cause abnormal vision; decreased libido; abnormal ejaculation; rash; sweating and withdrawal symptoms

A

Selective serotonin-reuptake inhibitor (SSRI)

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5
Q

Sodium-dependent serotonin transporter inhibitor

Potassium voltage-gated channel inhibitor

5-hydroxytryptamine receptor 2C antagonist

Neuronal acetylcholine receptor subunit alpha-2, alpha-3, beta-4 antagonist

A

Fluoxetine

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6
Q

Sodium-dependent serotonin transporter inhibitor

Sodium-dependent noradrenaline transporter

5-hydroxytryptamine receptor 2A antagonist

Muscarinic acetylcholine receptor subunit M-1, M-2, M-3, M-4, M-5 antagonist

A

Paroxetin

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7
Q

Sodium-dependent serotonin transporter inhibitor

Sodium-dependent dopamine transporter

Sigma receptor

Increase in uterine adenocarcinomas in animals’ models

A

Sertraline

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8
Q

Sodium-dependent serotonin transporter inhibitor

Histamine receptor antagonist

Antagonism of muscarinic, histaminergic, and adrenergic receptors is thought to be associated with several anticholinergic, sedative, and cardiovascular effects of other psychotropic drugs

  • Pregnancy category C, excreted in human milk.
A

Citalopram

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9
Q

Class of drugs that inhibits the membrane pump for re-uptake of transmitter amines, such as norepinephrine and serotonin, thereby increasing their concentration at the synaptic clefts of the brain

A

Tricyclic tertiary amines (TCAs)

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10
Q

Class of drugs that can cause: cardiac symptoms, convulsions dilated pupils, reduced body temp, stupor, coma

A

Tricyclic tertiary amines (TCAs)
and
Tricyclic secondary amines (TCAs)

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11
Q

drug that is not recommended during pregnancy, is excreted into breast milk, and causes chromosome abnormalities

A

Amitriptyline

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12
Q

Sodium-dependent noradrenaline and serotonin transporters inhibitor.

5-hydroxytryptamine receptor 1A, 1C, 1D, 2A, 2C, 7 antagonist

Delta, Mu and kappa-type opioid receptors agonist

Nerve growth factor & BDNF/NT-3 growth factors receptor agonist

Adrenergic, Histamine, receptors antagonist

Potassium voltage gated channel antagonist

A

Amitriptyline

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13
Q

Drug that can cause severe hypotension, central nervous system depression, decreased the number of viable embryos, abnormal sperm and decrease the sperm motility

A

Doxepin

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14
Q

Sodium-dependent noradrenaline and serotonin transporters inhibitor.

Histamine receptor 1, 2 & 4 antagonist

5-hydroxytryptamine receptor 1A, 2A, 2B, 2C, 6.

Muscarinic acetylcholine receptor M1, M2, M3, M4 & M5 antagonist.

Adrenergic receptor Alpha-1A, 1B & 1D antagonist.

Potassium voltage-gated channel

A

Doxepin

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15
Q

Drug that can cause anticholinergic activity (blurred vision, increased intraocular pressure, hyperthermia, constipation), o Central nervous system and neuromuscular effects ( drowsiness, lethargy, fatigue, agitation, hallucinations), effects on GI tract, increase in pancreatic enzymes, and black tongue

A

imipramine

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16
Q

Infants whose mothers were receiving _________ antidepressants prior to delivery have experienced cardiac problems, irritability, respiratory distress, muscle spasms, seizures, and urinary retention

A

tricyclic

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17
Q

Class of drug that selectively blocks reuptake of norepinephrine (noradrenaline) from the neuronal synapse. It also inhibits serotonin reuptake, but to a lesser extent compared to tertiary amine TCAs.

A

Tricyclic secondary amines (TCA)

18
Q

Drug that can cause o Antimuscarinic activity (urine retention), cardiotoxicity, psychotoxic effects (induce manic episodes in bipolar)

A

Desipramine

19
Q

Sodium-dependent noradrenaline transporter antagonist

Sodium-dependent serotonin transporter antagonist

5-hydroxytryptamine receptor 1A, 2A, 2C antagonist

Adrenergic receptor beta-1, beta-2 and alpha-1 antagonist

Histamine H1 receptor antagonist

Muscarinic acetylcholine receptor M1, M2, M3, M4 & M5 antagonist

A

Desipramine

20
Q

Drug that can cause toxic effects ( Cardiac dysrhythmias, severe hypotension, shock, congestive heart failure) and Adverse effects (hypotension, postural hypotension, hypertension, Heart failure)

A

Nortriptyline

21
Q

class of drug that Inhibitions presynaptic uptake of catecholamines, thereby increasing their concentration at the synaptic clefts of the brain

A

Tetracyclic –> maprotiline

22
Q

Class of drug that can cause muscular twitching and rigidity, tremor, ataxia, convulsions, vertigo, mydriasis shock, deep coma

A

Tetracyclic –> maprotiline
and
Unicyclic –> bupropion

23
Q

Class of drug that that exerts its pharmacological effects by weakly inhibiting the enzymes involved in the uptake of the neurotransmitters norepinephrine and dopamine from the synaptic cleft, therefore prolonging their duration of action within the neuronal synapse and the downstream effects of these neurotransmitters.

A

Unicyclic –> bupropion

24
Q

class of drug that causes a Potentiation of neurotransmitter activity in the CNS. Inhibit the reuptake of both serotonin and norepinephrine with a potency greater for the 5-HT than for the NE reuptake process.

A

Norepinephrine Serotonin Reuptake inhibitors (NSRI)

25
Q

Class of drugs that can cause CNS depression, serotonin toxicity, Death at high doses

A

Norepinephrine Serotonin Reuptake inhibitors (NSRI)

26
Q

Class of drug that is a Full agonist at the mu-type opioid receptor.
This drug is thought to persistently alter glutamate receptor bursting of the hippocampal CA3 commissural associational synapse.

A

Norepinephrine Serotonin Reuptake Enhance (NSRE) —> tianeptine

27
Q

Class of drug thats Antidepressant effects work through the modulation of glutamate receptor activity (in the amygdala and the hippocampus )and affect the release of brain-derived neurotrophic factor (BDNF).

A

Norepinephrine Serotonin Reuptake Enhance (NSRE) —> tianeptine

28
Q

Class of drug that Reduces the hypothalamic-pituitary-adrenal response to stress, and thus prevents stress-related behavioral issues.

A

Norepinephrine Serotonin Reuptake Enhance (NSRE) —> tianeptine

29
Q

Class of drug that stimulates the uptake of serotonin (5-hydroxytryptamine; 5-HT), and 5-hydroxyindoleacetic acid (5-HIAA) in brain tissue.

A

Norepinephrine Serotonin Reuptake Enhance (NSRE) —> tianeptine

30
Q

Glutamate receptor 1 modulator

Mu-type opioid receptor agonist

5-hydroxytryptamine receptor 1A antagonist

D(3) dopamine receptor agonist

A

Norepinephrine Serotonin Reuptake Enhance (NSRE) —> tianeptine

31
Q

Class of drug that can cause GI symptoms, CNS symptoms (most common) and severe panic attacks, metorrhagia, suicide attempts

A

Norepinephrine Serotonin Reuptake Enhance (NSRE) —> tianeptine

32
Q

Class of drug that Exerts antagonist activity at presynaptic α2-adrenergic inhibitory autoreceptors and heteroreceptors in the central nervous system.
Strong antagonist of serotonin 5-HT2 and 5-HT3 receptors.
Peripheral α1-adrenergic antagonist.
Potent histamine (H1) receptor antagonist

A

Noradrenaline and Specific Serotonin Antidepressant (NaSSA) –> mirtazapine

33
Q

class of drug that can cause hepatocellular adenomas and carcinomas, thyroid follicular adenomas and cystadenomas / loss of fetus and is a preg. category C drug

A

Noradrenaline and Specific Serotonin Antidepressant (NaSSA)–> mirtazapine

34
Q

Class of drugs that Binds at 5-HT2 receptor, it acts as a serotonin agonist at high doses and a serotonin antagonist at low doses.
Blockage of serotonin reuptake by inhibiting serotonin reuptake pump at the presynaptic neuronal membrane.
Alpha-adrenergic blocking action and modest histamine blockade at H1 receptor

A

Atypical antidepressants / Serotonin modulators –> trazodone, nefazodone

35
Q

Class of drug that can cause life threatening hepatic failure, preapism, and hypotension

A

Atypical antidepressants / Serotonin modulators –> trazodone, nefazodone

36
Q

Class of drugs that is an Inhibitor and substrate of monoamine oxidase and Presents a similar structure to amphetamine which produce the effect on the uptake and release of dopamine, noradrenaline, and serotonin. Inhibit tyrosine aminotransferase, aromatic amino acid decarboxylase, and dopamine B-hydroxylase.

A

Mono Amine Oxidase Inhibitor (MAOI) –> Phenelzine
Isocarboxazid
Tranylcypromine

37
Q

Class of drugs: Inhibitor and substrate of monoamine oxidase

A

Mono Amine Oxidase Inhibitor (MAOI) –> Phenelzine
Isocarboxazid
Tranylcypromine

38
Q

Class of drug that can cause transient, mild and asymptomatic aminotransferase elevations, and of liver injury after 1-3 months of treatment

A

Mono Amine Oxidase Inhibitor (MAOI) –> Phenelzine
Isocarboxazid
Tranylcypromine

39
Q

Class of drugs that has Selective, reversible inhibition of MAO-A. This inhibition leads to a decrease in the metabolism and destruction of monoamines in the neurotransmitters. This results in an increase in the monoamines (serotonin, adrenaline, noradrenaline, dopamine)

A

Reversible Selected Mono Amine Oxidase Inhibitor (RIMA)–> moclobemide

40
Q

Class of drugs that Selectively inhibits serotonin reuptake in the central nervous system as well as acting as a partial agonist of 5HT-1A receptors

A

Serotonin partial agonist reuptake inhibitor –> Vilazodone

41
Q

class of drug that can cause effects on offspring to be reduced fetal weight, increased mortality, delayed maturation, and decreased fertility.

A

Serotonin partial agonist reuptake inhibitor –> Vilazodone