Vigabatrin is an antiepileptic used in infantile spasms and refractory focal seizures. Its anticonvulsant mechanism is:
- A Inhibition of GABA reuptake via neuronal GAT-1 transporter
- B Blockade of the synaptic vesicle protein SV2A
- C Irreversible inhibition of GABA transaminase, increasing brain GABA concentrations ✓
- D Selective antagonism of AMPA-type glutamate receptors
Explanation
Vigabatrin irreversibly inhibits GABA-transaminase (GABA-T), the enzyme that degrades GABA, thereby raising CNS GABA levels. Tiagabine is the agent that blocks GAT-1 reuptake; levetiracetam binds SV2C; perampanel blocks AMPA receptors. Vigabatrin's major limiting toxicity, irreversible constriction of visual fields, mandates regular ophthalmologic monitoring during therapy.
Reference: Katzung Basic and Clinical Pharmacology, 15th ed.
High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP
Written and medically reviewed by the StethoPrep medical team.