Drugs Flashcards
4-aminopyridine
Fast potassium channel blocker that has been shown to improve axonal conduction of demyelinated fibers
Greatest affinity for Kv1.5 potassium channel
MOA in restoring peacemaking activity of purkinje cells
Phenobarbital
Increasing neuronal responsiveness to GABA, antiglutamate effects, and decreasing calcium flow into neurons
Bromide
Hyperpolarizes the neuronal membrane after traversing chloride channels
Benzodiazepines
Enhance GABA effects in the brain
Felbamate
Interfering with voltage gated sodium channels, antagonizing NMDA preferring glutamate receptors, and interfering with the binding of glycine
Gabapentin and pregabalin
Main MOA through inhibition of voltage gated neuronal calcium channels via specific binding of the drug to the alpha2delta-subunit of these channels. The inhibition of calcium flow reduces release of excitatory neurotransmitters including glutamate, noradrenaline, and substance P
Zonisamide
Blockage of T-type calcium and voltage gated sodium channels and binding to the chloride channel associated with GABA
Levetiracetam
Pyrrolidine-based
Main MOA specific binding to SV2A
Neuroprotective
Anti-kindling
Topiramate
Sulfamate substituted monosaccharide thought to work on multiple cell signaling mechanisms including enhancing GABAergic activity, inhibition of mainstream-evokes currents, and inhibition of carbonic anhydrase isoenzymes
Imepition
Imidazolinone derivative that is a low affinity partial agonist at the benzodiazepine site of GABAa receptors
Tricyclic antidepressants
Imipramine, protryptaline, amitryptaline
Block cellular NE reuptake in CNS
Imipramine also blocks serotonin reuptake
SSRI
Fluoxetine
Blocks serotonin reuptake
Selegiline
Monismine oxidase B inhibitor that increases CNS dopamine levels
Procainamide and mexilitine
Na channel blockers
Myokymia and neuromyotonia
Chlorpromazine
Phenothiazine derivative
Effects at D2 dopaminergic, M1 cholinergic, and a2 adrenergic receptors
Motion sickness