Watts Antidepressants Flashcards
what was the first antidepressant and what class?
imipramine
types of depression with percentages
reactive - 60%
major depressive disorder - 25%
bipolar affective - 15%
drug induced depression classes
antihypertensive
sedative hypnotics
anti-inflammatory/analgesics
steroids
biogenic amine hypothesis
reserpine depletes NE and 5HT
neuroendocrine hypothesis
overactive HPA and CRF
stress causes hypothalamus to release cortisol
antidepressants do what to CRF
reduce levels
CRF1 does what
arousal
anxiety
sexual dysfunction
sleep problems
activation of HPA axis
CRF2 does what
appetite suppression
neurotrophic hypothesis
depressed ppl have reduced BDNF and volume of hippocampus
antidepressants to what to BDNF
increase
increase in BDNF does what to dendritic sprouts
increase
MAO inhibitors mechanism of action
prevents degradation of NE and 5HT by mao
- increased amount of NE and 5HT packaged in vescicles
non selective MAO inhibitors
phenelzine
tranylcypromine
non selective MAO inhibitors are _________
irreversible
MAO B selective inhibitor
selegiline (reversible)
MAO A selective inhibitor
moclobemide
MAO side effects
headache
drowsiness
dry mouth
weight gain
orthostatic hypotension
sexual dysfunction
avoid what kind of foods with MAO
tyramine containing
orthosteric site is where what binds?
serotonin
indications for TCAs
depression, pain, panic, enuresis
patients more likely suicidal with what class
TCAs (2 weeks into treatment)
tertiary amines inhibit what
NE and 5HT via NET and SERT
tertiary amines also are antagonists at what
antihistamine
antimuscarinic
antiadrenergic
side effects of tertiary amines
weight gain
sedation
autonomic
(very strong)
also conduction of heart
tertiary amine drugs
imipramine
amitriptyline
clomipramine
doxepin
imipramine metabolized to what
desipramine (secondary amine)
amitriptyline metabolized to what
nortriptyline (secondary amine)
imipramine uses
ADHD
enuresis
clomipramine use
OCD (orgasm while yawning)
secondary amine drugs
desipramine
nortriptyline
maprotiline
secondary amines inhibit what mainly
NET
secondary amines side effects
less sedation
less weight gain
less CV
less anticholinergic
SSRI moa
serotonin transporters blocked
increased 5HT in synapse
side effects of SSRIs
N/V
headache
sexual dysfunction
anxiety
insomnia
SSRI discontinuation syndrome symptoms
brain zaps
dizzy
sweating
what can occur if SSRIs are given with MAOis or TCAs
serotonin syndrome:
restless, shiver, hyperthermia
treatment of serotonin syndrome
administration of serotonin antagonists (cyptoheptadine)
benzos to control movements
vilazodone MOA
SSRI + 5HT1A partial agonist
vartioxetine MOA
SSRI + 5HT1A partial agonist
vilazodone side effect profile
reduced sexual dysfunction compared to SSRIs
tetracyclic antidepressants
maprotiline
mirtazapine
maprotiline is a ____ inhibitor
NET
D2 antagonists will have what side effects
motor side effects
mirtazapine targets whwat
alpha 2 receptor antagonist
5HT antagonist
H1 antagonist
bupropiron is a _____
unicyclic antidepressant
bupropion inhibits what
DAT
NET
SERT
trazodone MOA
5HT2 antagonist
SERT inhibitor
(off label alpha 1, H1, 5HT2)
venlafxine use
GAD and panic disordewr
SNRIs
desvenlafaxine
venlafaxine
duloxetine
milnacipran
levomilnacipran
duloxetine treats what
peripheral neuropathy
milnacipran treats what
fibromyalgia
NSRI meds
reboxetine
atomoxetine
triple blockers block what
serotonin
norepinephrine
dopamine
SDNRIs
what is a triple blocker example
cocaine
NMDA antagonist drug
ketamine
esketamine
ketamine useful at what doses
subanesthetic
esketamine approved with what
oral antidepressant
post partum depression treatment
SSRI: fluoxetine/paroxetine
brexanolone
brexanolone MOA
resensitizes GABA-A receptors
what happens during pregnancy
increase in allopregnanolone
GABA-A receptors desensitize
non pharm options for depression
electroconvulsive
psychotherapy
hospitalization
fibanserin use
female sexual desire stimulate
originally developed as antidepressant
filbanserin targets
5HT1A agonist
5HT2A/C antagonist
(polypharmacology)
mania features
euphoria
high risk behavior
decrease sleep and appetite
aggressive
lithium mechanism
depletes PIP2 and IP3 so less Gq activation and recycling of PIP2
effectiveness of lithium
lag time- takes awhile bc we need to burn out the PIP2
valproic acid and valproate mechanism
increase GABA
block Na channels
block Ca channels
inhibit histone deacetylase
drugs that block Na inactive state
carbamazepine/oxcarbazepine
lamotrigine
topiramate