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15 Cards in this Set
- Front
- Back
Ergotamine
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Ergot alkaloid with a.a. side chain
Partial agonist of alpha adrenoceptors Increases BP (vasoconstriction) Partial antagonist of 5HT1 |
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Dihydroergotamine
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Ergot alkaloid with a.a. side chain
Partial antag. of alpha adrenoceptors Antagonist and partial agonist of 5HT1 Safer than ergotamine because doesn't produce peripheral vasoconstrictor effects |
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Bromocriptine
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Ergot alkaloid with a.a. side chain
Agonist of DA receptors |
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Methysergide
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Ergot alkaloid with amine side chain
Antagonist of 5HT2 receptors Used for migraine prophylaxis |
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Sumatriptan
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5-HT1 agonist
Subq dose has rapid onset (10min) and relieves accompanying symptoms Oral dose gives relief in 1.5-2hr. Not recommended for patients with ischemic heart disease Short plasma T1/2 so headaches often recurr Take when symptoms start not at aura |
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Naratriptan
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5-HT1 receptor agonists
Higher bioavailability than oral sumatriptan and longer T1/2 Fewer recurrent HAs Tablet form |
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Rizatriptan
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Higher oral bioavailability than sumatriptan like Naratriptan
Has been shown to improve migraine-specific quality of life indices Fast onset (30 min) Tablet form can be dissolved on tongue |
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Zolmitriptan
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Better oral availability than sumatriptan
Proven best reliever of menstrual migraines Tablet Form |
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Treximet
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Sumatriptan/Naproxen combo
Constricts basilar artery and dura vasculature Inhibits synthesis of inflammatory mediators |
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Tacrine
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First ACHE Inhibitor
Assoc with hepatotoxicity and has to be given 4x/day Rarely used |
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Donepezil
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Cholinesterase Inhibitor for Mild-Mod/Sev Alz
1x/day regimen SIde effects of cholinergic overstimulation Selective for "acetyl" cholinesterase |
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Rivastigmine
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Cholinesterase Inhibitor for mild- mod/sev Alz
Inhibits "acetyl" and "butyryl" cholinesterase |
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Galantamine
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Cholinesterase Inhibitor
Activates central nicotinic receptors |
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Memantine
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NMDA receptor antagonist that decreases Glutamate excitotoxicity of neurons
Use in Mod-Sev Alz in combo with CHE Inhibitor |
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Dimebon
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Antihistamine used in Russia
Supposedly blocks toxic actions of Beta amyloid and modulates NMDA receptors through inhibiting Ca channels |