Drugs test 3 Flashcards
levodopa MOA
converted to dopamine by DOPA decarboxylase (in both the periphery and CNS) to act on D1 and D2 receptors
levodopa SAE
Nausea, arhythmia, orthostatic hypotension (peripheral toxicity)
Neuropsychiatric symptoms (central toxicity)
carbidopa MOA
peripheral DOPA decarboxylase inhibitor, which increases the bioavailability of levodopaand decreases the peripheral toxicities of levodopa
catechol-O-methyltransferase (COMT) MOA
converts levodopa to 3-OMD in the periphery and 3-MT in the CNS (neutralizes levodopa)
tolcapone MOA
peripheral and central COMT inhibitor (increases bioavailability of levodopa)
tolcapome SAE
hepatotoxicity
entacapone MOA
peripheral COMT inhibitor (increases bioavailability of levodopa)
amantadine MOA
increases dopamine synthesis/release and inhibits uptake
pramipexole
D3 receptor agonist
treat restless leg syndrome
ropinirole
D2 receptor agonist
treat restless leg syndrome
ropinirole SAE
may enhance impulse control disorders (gambling, shopping, hypersexuality)
selegiline MOA
monoamine oxidase B inhibitor (increases dopamine levels in CNS)
trihexyphenidyl MOA
M1 antagonist
improves tremor and rigidity
Benztropine MOA
M1 antagonist
improves tremor and rigidity
haloperidol MOA and uses
D2 receptor antagonist
chorea, psychosis, irritability