Licarbazepine

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Licarbazepine structure

Licarbazepine is a voltage-gated sodium channel blocker with anticonvulsant and mood-stabilizing effects. It is structurally and pharmacologically related to oxcarbazepine, a second-generation anticonvulsant used primarily in the management of epilepsy and bipolar disorder.

Pharmacology[edit | edit source]

Licarbazepine is an active metabolite of oxcarbazepine, which itself is a prodrug that exerts its therapeutic effects only after metabolism. Upon administration, oxcarbazepine undergoes reduction in the liver, resulting in the formation of licarbazepine and eslicarbazepine, its (S)-isomer. These metabolites are responsible for the anticonvulsant activity by blocking voltage-gated sodium channels, thereby stabilizing neuronal membranes and preventing excessive repetitive neuronal firing.

Mechanism of Action[edit | edit source]

Licarbazepine primarily exerts its effects by:

  • Blocking voltage-gated sodium channels (VGSC) in the central nervous system, reducing hyperexcitability in neurons.
  • Modulating excitatory neurotransmission, leading to decreased seizure activity and mood stabilization.
  • Inhibiting repetitive firing of neurons, which plays a critical role in preventing seizures and stabilizing mood in individuals with bipolar disorder.

Isomeric Forms[edit | edit source]

Licarbazepine exists in two isomeric forms:

  • (S)-(+)-licarbazepine, commonly known as eslicarbazepine, which is an active metabolite of eslicarbazepine acetate.
  • (R)-(-)-licarbazepine, which has less clinical significance compared to its (S)-isomer.

Both oxcarbazepine and eslicarbazepine acetate function as prodrugs, meaning they must be metabolized in vivo to their active forms (licarbazepine and eslicarbazepine, respectively) to exert therapeutic effects.

Clinical Uses[edit | edit source]

Licarbazepine is not available as a standalone medication but is the active component in the treatment of:

Metabolism and Excretion[edit | edit source]

  • Liver metabolism: Oxcarbazepine undergoes hepatic metabolism to form licarbazepine.
  • Renal excretion: The majority of the active metabolite is excreted unchanged in the urine.

Adverse Effects[edit | edit source]

Since licarbazepine is an active metabolite of oxcarbazepine, it shares similar side effects, including:

  • Dizziness and drowsiness
  • Hyponatremia (low blood sodium levels)
  • Fatigue and headache
  • Gastrointestinal disturbances (nausea, vomiting)
  • Skin rashes, including hypersensitivity reactions similar to carbamazepine (e.g., Stevens-Johnson syndrome)
  • Double vision (diplopia) and blurred vision

Related Compounds[edit | edit source]

Licarbazepine is closely related to:

  • Carbamazepine – The first-generation anticonvulsant from which oxcarbazepine was derived.
  • Oxcarbazepine – A second-generation carbamazepine derivative and prodrug of licarbazepine.
  • Eslicarbazepine – The (S)-isomer of licarbazepine, which is also an active metabolite of eslicarbazepine acetate.

See Also[edit | edit source]



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