Pharm Flashcards
(31 cards)
Ropinirole
D2 R agonist used to tx PD
Pramipexole
D R agonist used to tx PD, relative D3 affinity
Rotigotine
D R agonist used to tx early PD. Skin patch
in PD, the ____ pathway predominates
indirect
5 strategies in PD pharm therapy
replace DA, stim D Rs, enhance DA release, inhibit DA metabolism, alter DA/Ach balance
Selegiline
MAO-B inhibitor. Tx PD. May have neuroprotective effects. Used when Ldopa response has declined. Little effect when used alone
Rasagiline
more potent MAO-B inhibitor. For combined therapy with levodopa in late stage PD or alone early in PD
Do not take meperidine, TCAs, SSRIs with
Selegiline
Metabolized by CYP1a2
Ropinirole - D R agonist (D2)
COMT inhibitors
entacapone, tolcapone - inhibit DA metab. increase bioavail of Ldopa, reduces fluctuations in response
only has peripheral COMT inhib effect
entacapone. Tolcapone is central and peripheral
AE tolcapone
increased liver enzymes and hepatic failure
Muscarinic antagonists used in PD
benztropine, diphenhydramine, trihexyphenidyl - early PD or adjunct to Ldopa
AE of musc antags for PD
typical anticholinergic effects, drows, inattention, confusion, delusions, halluc, mood change
Contraindications of musc antags used in PD
prostatic hyperplasia, OBD, glaucoma, avoid use with other drugs with antimusc effects (TCAs, antihistamines)
calcium channel blocker of the dihydropyridine class. It is usually prescribed for the treatment of high blood pressure in order to reduce the risk of stroke and heart attack. More recent research in animal models suggests that isradipine may have potential uses for treating Parkinson’s disease
Isradipine
Drugs for Huntingtons are aimed at
treating the depression - Fluoxetine, Carbamazepine. Reserpine and tetrabenazine (central dopamine depleting agents) may help with chorea - increase act of indir pathway by blocking D2)
mu R endogenous opioid peptide
endorphins > enkeph > dynorph
delta R endogenous opioid peptide
enkephalin
kappa R endogenous opioid peptide
dynorphin
main reservoir for opiate distribution
skeletal muscle
AE of opioids that do not demonstrate tolerance
miosis, constipation, convulsions. Moderate for bradycardia
increased CNS depression with opioids when given with
sedative hypnotics, antipsychotic tranquilizers, monoamine oxidase inhibitors (increased risk hyperpyrexic coma)
codeine converted to morphine via
CYP2D6