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18 Cards in this Set

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amitriptyline
TCA
elavil
clomipramine
TCA
**labeled use for OCD
anafranil
desipramine
TCA
*most potent TCA
**high affinity for NET (not SERT)
***down-regulates alpha-1 & causes desensitization of alpha-2
Norpramin
doxepin
TCA
Sinequan
imipramine
TCA
*First clinically used
**Also indicated for bedwetting
Tofranil
protriptyline
TCA
**has unsaturated bridge in the middle ring (at the top)
Vivactil
Trimipramine
TCA
Surmontil
amoxapine
tetracyclic/unicyclic (which is why it looks totally different--> has the O and N in the ring)
*used in delusional depression (why?)
Ascendin

metabolite of loxapine (a benzazepine anti-psychotic)
Maprotiline
tetracyclic/unicyclic
Why is it special?
Has an ethylene bridge in its central ring
*Has the highest affinity and selectivity for NET
**associated with dose-dependent seizures compared to other TCAs
isocarboxazid
MAOI
Marplan
phenelzine
MAOI (nonselective)
Nardil
selegiline
MAOI (selective for MAO-B at low doses... at high doses= nonselective)
tranylcypromine
MAOI
Parnate
bupropion
tetracyclic/unicyclic
**smoking cessation
Wellbutrin
mirtazapine
tetracyclic/unicyclic
*has a clinical use for sedation
Remeron
nefazodone
5-HT2 antagonist

Common SEs= sedative & GI
Sexual SEs are rare
* black box warning for hepatotoxicity
trazodone
5-HT2 antagonist

Common SEs= sedative & GI

Sexual SEs are rare
Desyrel

*more sedative effect (unlabeled use as a hypnotic)

**rarely associated with priapism (longer than 8 hrs)
Explain the MOA of trazodone & nefazodone
5-HT2 antagonists

5-HT1a receptor is linked with depression & 5-HT2a/c are linked with sexual dysfunction, insomnia, anxiety

By blocking 5-HT2a, they are pushing more serotonin onto the 5-HT1a receptor--> increasing the antidepressant effect (also, this is the reason for the decreased sexual SEs seen with this medication, priapism, sedation)
At low doses, trazodone acts as a sedative

At high doses it acts as an antidepressant it also blocks the reuptake of 5HT (SERT)