Pharm 4: Antiepileptic Agents Flashcards
List the 9 antiepileptic drugs which work as pre-synaptic voltage-gated Na+ channels blockers via enhanced fast inactivation.
1) Carbamazepine
2) Oxcarbazepine
3) Lamotrigine
4) Phenytoin
5) Rufinamide
6) Topiramate
7) Valproic acid
8) Zonisamide
9) Lacosamide
Which AED is unique in its ability to prolong fast inactivation of Nav ion channels and also enhance slow inactivation of Nav channels?
Lacosamide
Which 2 antiepileptic drugs are AMPA-receptor antagonists?
MOA?
- Topiramate
- Perampanel
MOA = bind AMPA receptor and block glutamate binding; channel doesn’t open –> AP does not propogate downstream
Which antiepileptic drug is an NMDA-receptor antagonist?
Felbamate
The pharmacological activity of AED Nav channel blockers is _______ and ________-dependent
State and Use-dependent
AED’s binding site is at the _________ side Nav channel ‘pore’
Interior
Which gate must be open for AED’s to access the pore of Nav channels?
Which states can this occur?
- Activation gate
- Open state and Fast-inactivated state
The probability of Nav blockade is proportional to what?
FREQUENCY of Nav channel opening and dose
Why do the AED’s that are Nav blockers act preferentially on the neurons involved in epileptic seizures?
The neurons involved will be firing at higher freqeuncy than normal, allowing more chances for these drugs to slip right in and bind
What is the water-soluble pro-drug of phenytoin which is given via IV and is an Nav channel blocker used as an antiepileptic?
Fosphenytoin
Which AED acts as a Nav channel blocker (fast inactivation), AMPA-receptor antagonist, and GABAA agonist?
Topiramate
What occurs when the post-synaptic GABAA receptor becomes occupied by GABA?
- Cl- channel opens
- Hyperpolarization occurs blunting AP propogation
What is the MOA of the AED, Tiagabine?
- Blocks pre-synaptic reuptake of GABA by blocking the GABA transporter, GAT-1
- Causes GABA to go post-synaptically, bind GABAA receptor leading to hyperpolarization and decreased AP propogation
What are the 3 MOA’s of Valproic acid used as a AED at the pre-synaptic GABA terminal?
1) Increase activity of glutamic acid decarboxylase, leading to increased GABA presynaptically
2) Inhibit GABA-T, which typically metabolizes GABA
3) Inhibit Succinic Semialdehyde Decarboxylase (SSD), which typically metabolized GABA
Which 2 AED’s inhibit the metabolism of GABA through the inhibition of GABA-T?
- Vigabatrin
- Valproic acid
Which drug in the barbiturate family gets metabolized to phenobarbital in the body?
Primidone
Where do Benzodiazepines bind the GABAA receptor and what effects does this have?
- Bind to a distinct site –> Allosteric change potentiate GABA binding
- Cl- channel opens with greater frequency
Where do Barbiturates bind the GABAA receptor and what is their effect?
- Bind a distinct site
- Increases the duration of Cl- channel opening
Of the GABAA receptor agonists used as AED’s which is more lethal at higher doses and why?
- Barbituates are more lethal due to being GABA INdependent
- Benzodiazepines are GABA-dependent
What are the 7 AED’s which act post-synaptically to potentiate GABAA-receptor Cl- currents?
1) Phenobarbital
2) Primidone
3) Clonazepam
4) Lorazepam
5) Diazepam
6) Clobazam
7) Topiramate
Which type of ion channel mediates the 3-Hz spike and wave activity in the thalamus which is the hallmark of absence (petit mal) seizures?
T-type Ca2+ channels