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52 Cards in this Set

  • Front
  • Back
what 4 things is serotonin involved in?
1. mood
2. food intake
3. sleep
4. sex/libido
what happens when you increase serotonin levels?
1. elevated mood
2. decrease food intake
3. increase sleep
4. decrease libido
what is the MOA of tricyclic antidepressants?
bind to the amine pumu and block pre-synaptic reuptake of 5HT and NE
which receptors do tricyclic antidepressants bind to ?
alpha-1 : orthostatic hypotension and syncope
2. histamine receptors : cause sedation
3. muscarinic receptors: anti SLUDE
what are the two main differences between tertiary amines and secondary amines?
tertiary amines : long acting, more selective at blocking 5HT reuptake
secondary amines : short acting, more selective at blocking NE reuptake
name 5 tertiary amines?
ACID T
amitryptyline, clomipramine, doxepin, imipramine, trimipramine
name 5 secondary amines?
DAMPN
amoxapine, desipramine, maprotiline, nortryptyline, protryptyline
what would you give a sleepy depression patient? secondary or tertiary?
secondary, it will increase NE more than 5 HT
Name six SSRIs?
citalopram, escitalopram,fluoxetine, fluvoxamine, paroxetine,sertraline ( SC PEFF)
Name three SNRI's ?
duloxetine, milnacipran, venlafaxine (DMV)
what are the five atypical drugs?
bupropion ( increases incidence of seizures), nefazodone , mirtazapine (sedation is an adverse effect due to blocking histamine receptor, also blocks 5HT2A, alpha1 and alpha2, reboxetine, trazadone( no cardiac or anticholinergic side effects
what is tyramine? why cant you take tyramine when you are on MAOi?
tyramine is a releaser of stored monoamines. if you block MAO and take tyramine you release all the stored NTs which can cause a hypertensive crisis and a patient can stroke out.
what is the MOA for lithium?
it gets in the way of sodium so action potential cannot start. that gives you a generalized neuronal dampening.
state 8 side effects of lithium?
1. arrhythmias
2. polyuria and polydipsia
3. nausea and vomiting
4. drug abuse ( place them on SSRI, MAOi, SNRI)
5. insomnia
6. weight gain
7. thyroid enlargement
8. increase in circulating PMNL ( reversible)
what are the three drug interactions for lithium?
1.use osmotic diuretic or acetazolamide for detoxification ( increased excretion of lithium)
2.loop diuretic or thiazide decrease excretion of lithium and can lead to toxicity.never use them.
3. NSAIDs indomethacin, naproxen, ibuprofen can diminish clearance and increase plasma levels leading to lithium toxicity.
which are the other three drugs used to treat bipolar depression?
1. lamotrigine ( blocks sodium channels and causes generalized neuronal dampening)
2. carbamazepine (anti convulsant, blocks Na channel)
3. valproic acid( anti convulsant, blocks Na channel)
what is tyramine? why cant you take tyramine when you are on MAOi?
tyramine is a releaser of stored monoamines. if you block MAO and take tyramine you release all the stored NTs which can cause a hypertensive crisis and a patient can stroke out.
what is the MOA for lithium?
it gets in the way of sodium so action potential cannot start. that gives you a generalized neuronal dampening.
state 8 side effects of lithium?
1. arrhythmias
2. polyuria and polydipsia
3. nausea and vomiting
4. drug abuse ( place them on SSRI, MAOi, SNRI)
5. insomnia
6. weight gain
7. thyroid enlargement
8. increase in circulating PMNL ( reversible)
what are the three drug interactions for lithium?
1.use osmotic diuretic or acetazolamide for detoxification ( increased excretion of lithium)
2.loop diuretic or thiazide decrease excretion of lithium and can lead to toxicity.never use them.
3. NSAIDs indomethacin, naproxen, ibuprofen can diminish clearance and increase plasma levels leading to lithium toxicity.
which are the other three drugs used to treat bipolar depression?
1. lamotrigine ( blocks sodium channels and causes generalized neuronal dampening)
2. carbamazepine (anti convulsant, blocks Na channel)
3. valproic acid( anti convulsant, blocks Na channel)
to which class do first generation antipsychotics belong to? what is their MOA?
phenothiazines, they are D2 receptor antagonists.
what are the three subclasses of phenothiazines? what are their D2 receptor affinities?
1. aliphatics ( weakly selective)
2. piperdines ( intermediate selectivity)
3. piperazides ( highly selective)
name three aliphatic phenothiazines?
what is the main side effect?
chlorpromazine, promazine, trifluopromazine.
these drugs give autonomic side effects.
which receptors do aliphatic phenothiazines bind? what are the effects?
alpha 1 , histamine, muscarinic.
blocking alpha 1 results in orthostatic hypotension.
blocking histamine- sedation
blocking muscarinic- anti SLUDE
name two major drugs from the piperdine class?
mesoridazine and thioridazine.
what is the SE of piperdine class of drugs?
black box warning for cardiotoxicity, long QT interval which slows the heart.
name three drugs for the piperazide class? what are the SE of this class of drugs?
fluphenazine, perphenazine, trifluoperazine
extrapyramidal side effects, parkinson like SE,tardive dyskinesia and neuroleptic malignant syndrome.
what are butyrophenones?
its haloperidol, they have intermediate to high affinity for D2 receptors and thus have increased risk of extrapyramidal side effects.
name two thioxanthenes?
Chlorprothixene and thiothixene.
what are the advantages of second generation antipsychotics? whom are the atypicals meant for?
they have little or no D2 antagonism, hence no tardive dyskinesiaand drug induced parkinsonism. they are meant for patients with negative symptoms.
which are the three general atypicals? which one is not used much?
clozapine- not used much because of agranulocytosis.
Olanzapine and loxapine are other atypicals
what is the SE of piperdine class of drugs?
black box warning for cardiotoxicity, long QT interval which slows the heart.
name three drugs for the piperazide class? what are the SE of this class of drugs?
fluphenazine, perphenazine, trifluoperazine
extrapyramidal side effects, parkinson like SE,tardive dyskinesia and neuroleptic malignant syndrome.
what are butyrophenones?
its haloperidol, they have intermediate to high affinity for D2 receptors and thus have increased risk of extrapyramidal side effects.
name two thioxanthenes?
Chlorprothixene and thiothixene.
name three 5HT2A receptor antagonists?
Risperidone, Ziprasidone and Paliperidone
name three other heterocyclic antipsychotics?
Molindone, Pimozide and Quetiapine
which class of drugs will you give for hallucinations
5HT2A antagonists.
name a partial dopamine receptor agonist? what is it used for? what are its SE?
Aripriprazole. used to treat mania
may have some alpha 1 receptor antagonist activity and thus can cause orthostatic hypotension.
what are the 8 strategies used to treat parkinson disease?
1. direct replacement
2.dopamine releasers
3. MAO type B inhibitors
4. muscarinic antagonist
5. post synaptic DA receptor agonist
6. Vit E
7. COMT inhibitors
8. adjunct therapy
which drug combination is used for dopamine replacement?
Carbidopa / Levodopa
name a dopamine releaser?
Amantadine
Name a MAO type B inhibitor and its MOA?
Selegiline - blocks the action of MAO-B and causes more dopamine to be available. its metabolites are amphetamine and methamphetamine
name 2 muscarinic antagonists?
1. Trihexlphenidyl- inhibits Ach activity in key excitatory pathways
2. Benztropine - centrally acting anti-muscarinic
Name 4 dopamine receptor agonists? and their specificities?
Bromocriptine(D2 and partial D1), Pergolide (D2 and D1), Pramipexole ( highly selective D2), Ropinirole(highly selective D2).
name 2 COMT inhibitors and their drawback?
1. Entacapone
2. tolcapone
Black box warning for hepatotoxicity
name 3 drugs used in adjunct therapy
1. diphenhydramine ( for anticholinergic effects)
2. Ethopropazine ( for anticholinergic properties)
3. Procyclidine ( again anticholinergic, atropine like)
what 2 drug interactions do we keep in mind when treating parkinson's disease?
1. MAOI can lead to acute hypertensive episode and stroke
2. High Vit B6 increases GI dopa decarboxylase activity.
which is the drug of choice to treat huntington? what is its MOA? which drug is supplementary addition?
Baclofen, its a GABA B agonist. GABA B is found presynaptically that control the release of excitatory NTs.
which is the main drug for ALS treatment? what is its MOA?
Riluzole, its a glutamate antagonist and also causes decrease in release of glutamate.
Which other drugs are used for ALS apart from Riluzole?
Baclofen and muscarinic receptor antagonist like Dicyclomine, Flavoxate, Oxybutynin, Oxyphencyclimine, Trihexylphenidyl. muscarinic antagonist cause anti-SLUDE